EHS Supervisor (Zhanjiang, GD, CN)

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Summary

Job Qualifications

About Discovery
Discovery from Charles River is industry-proven in the successful development of novel therapies, with over 350 patents and 80 preclinical drug candidates delivered to our sponsors in the past 17 years. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND. Our client-focused, collaborative approach creates true partnerships that anticipate challenges, overcome obstacles, and move us forward together on the journey of getting new drugs to market.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

R&D Researcher (Zhanjiang, GD, CN)

Job Summary

Job Qualifications

Vaccine Mandate

This position services client(s) that requires us to ensure our employees are fully vaccinated against COVID-19. We will require proof of vaccination from all employees servicing client(s) with COVID-19 Vaccination requirements.

About Insourcing Solutions
Charles River Insourcing Solutions℠ can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment. Insourcing Solutions℠ provides you with the ability to maintain control of your facility and expertise while leveraging available space.

About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

QA Specialist II (Mumbai, IN)

Job Summary

Responsible for assisting / performing facility, process, vendor and local validation activities to assure compliance with applicable federal, state, and local regulations as well as corporate policies, Good Manufacturing Practice (GMP), applicable ISO requirements and Standard Operating Procedures (SOP). Understand the voice of the customer and participate in identifying recommendations to the Quality Management. Assist in executing continuous improvement initiatives as supported by QMS metrics and/or site management. Approximately 5% of this role’s responsibilities are customer-facing (e.g. customer audit participation and correspondences via email and telephone).

DUTIES & RESPONSIBILITIES

Assure Charles River’s compliance with applicable federal, state, and local regulations as well as corporate policies to avoid any business interruptions. Communicate all identified compliance and quality risks to supervisor.
Perform compliance assessments of site and cross-site Quality Systems (process inspections/facility inspections/equipment and record review/computer validation activities; and/or training records) including review of client audit observations.
Review SOPs, protocols/batch records, reports, quality and regulated records (e.g. deviations, change controls, or CAPA) involving technically complex issues and processes for accuracy and compliance with all applicable regulations and internal policies.
Participate in the process for identifying recommendations to Operations and Quality Management for improvements in auditing of quality systems.
Participate in the preparation of study and QA files in preparation for sponsor site visits and regulatory inspections. May participate in the support of client site visits.
Assist in the development of recommendations for corrective and preventative actions to respond to client visit and regulatory inspection findings.
Participate in the execution of site-wide applicable regulations or standards (ISO/GLP/GMP) training sessions, as developed and approved by senior Quality Systems team members.
Participate in the preparation of support during regulatory inspections, as required.
Participate in the performance of internal facility inspections at planned intervals to evaluate effective control and maintenance of site quality systems. Maintain written and signed records of all audits and inspections as required and may sign records documenting the performance of audits and inspections and reporting to management.
Perform facility and equipment records and logbook reviews.
Where appropriate, approve customer test reports and participate in reagent release activities to support laboratory operations.
Assist in correction of any regulatory risk areas as identified by Senior Quality Systems team members.
Participate in inspections and audits of subcontractors, vendors, and suppliers of products and services.
Assist with analysis and collection of site Quality Metrics via QMS.
Assist with preparations for Quality Management Review (QMR).
Participate in the execution of identified process-improvement for dashboard analysis and analyze metric data for QMS.
Participate in execution of Quality Assurance projects.
Assist with providing basic regulatory training to operations personnel.
Provide timely responses to Customer inquiries to support their qualification / regulatory requests.

Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor’s degree (B.S. / BA.A.) or equivalent, preferably in a life science.
Experience: Minimum of 2 years in a Quality Assurance role.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Other: Some experience with Microsoft Office® applications. Position requires the individual to be able to communicate clearly, effectively and professionally; easily grasp instructions without follow-up; attention to detail and strong writing skills are essential.

PHYSICAL DEMANDS:

Must regularly operate a computer and occasionally operate other office productivity machinery such as a calculator, copy machine, and computer printer.
Must regularly communicate with employees/customers; must be able to exchange accurate information.
Must occasionally move about inside the office to access file cabinets, office machinery, etc.
May occasionally be required to wear protective clothing and equipment.

WORK ENVIRONMENT:

General office working conditions and/or laboratory/manufacturing areas.
The noise level in the work environment ranges from low to moderate.
May occasionally be required to work in tight or confined spaces.
May occasionally be exposed to high temperatures and humidity.

About Microbial Solutions
Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies.

With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

National Sales Manager (Mumbai, IN)

For nearly 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Summary

Own and deliver sales and service revenue targets for Charles River Microbial Solutions India.
Lead and oversee commercial and client-facing operations across India and neighboring countries (Sri Lanka, Nepal, Bangladesh, Myanmar, Bhutan, and Pakistan).
Define and align sales, field service, and technical service strategies with key stakeholders to drive revenue growth and customer retention.
Supervise, coach, and optimize sales team deployment and performance across the region.
Ensure timely and effective resolution of customer issues through a strong customer-centric approach, working closely with cross-functional teams.
To drive high customer satisfaction, business growth, safety initiatives and regulatory compliance.
Demonstrate the Charles River values of Care. Lead, Own and Collaborate.

Responsibilities

DUTIES AND RESPONSIBILITIES:

Provide annual forecasting and perform a regular review for the region as well as each individual sales territory.
Develop sales, pricing and distribution strategies, identify and capitalize on market opportunities, adjust strategies to reflect changing conditions.
Prepare and implement a comprehensive all India sales management plan to indicate target opportunities, potential new accounts, expansion of existing accounts and an analysis of competitor accounts.
Develop major and established customer accounts through customer service and production and support activities, to achieve upselling of products and use of products and services across the MS brands.
Attain revenue and objectives, and where possible increase revenue, in the assigned territory and or accounts.
Participate in regular co-travel with sales team, to provide coaching and feedback.
Ensure that specialists in the region are utilized in an efficient and effective manner
Initiate arrangement requests required for participation in trade or other convention programs.
Implements follow up and needs assessment for sales training
Establish and maintain sales training program for current employees and new hires within the region.
Manage activities of assigned group(s) to ensure optimum performance of the group/function.
Responsible for personnel management activities such as: scheduling, personnel actions (hiring, promotions, transfers, etc.), training and development, providing regular direction and feedback on performance, disciplinary actions and preparing and delivering annual performance and salary reviews.
Assist in the development of short- and long-range operating objectives, organizational structure, staffing requirements and succession plans.
Assist in the development and recommendation of departmental budget and authorize expenditures.
Develop and oversee the implementation of departmental training programs, including orientation.
Support the policy of equal employment opportunity through affirmative action in personnel actions.
Ensure adherence to pertinent regulatory requirements and to departmental policies, practices and procedures [SOPs, safety procedures etc].
Perform all other related duties as assigned.
Ensuring compliance to Business Code of Conduct and Ethics. Ensure compliance with all Company, Country, local, state, and federal regulations.
Ensure adherence to data privacy regulations within the Company and Corporate Global Data Privacy framework
Demonstrate the Charles River values of Care. Lead, Own and Collaborate
Perform all other related duties as assigned by the direct manager.

Job Qualifications

The following are minimum qualifications related to the National Field Technical Service Manager, MS India position:

Education: Bachelor’s degree (B.S. / B.A) or equivalent in life science . Master’s degree preferred. A second Business Administration qualification or Management certification would be an advantage.

Experience: Minimum 10 to 15 years relevant industry experience, with at least 5 of those years having direct client interface and team management .

Excellent interpersonal, customer relationship and leadership skills with experience working in a matrix organization.

This position requires frequent domestic and international travel.

Must be able to prioritize workload and manage multiple competing deadlines.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Laboratóriumi technikus (Veszprem, HU)

For 75 years, Charles River employees have worked to advance the discovery, development, and safe manufacture of new drug therapies, making a profound impact on global health. Our 20-year partnership with Boston Children’s Hospital takes this mission to the next level, supporting groundbreaking innovations that directly impact patient care. At Boston Children’s, their commitment to diversity drives the exceptional quality of care provided to patients from local communities to over 160 countries worldwide. This is your moment to become part of a family where unique talents and perspectives unite to change lives, including your own. Together, we’re shaping a healthier future through compassion, innovation, and opportunity.

Laboratóriumi technikus

Cégünk új munkavállalót keres Laboratóriumi technikus munkakörben.

Főbb feladatok, munkák:

o A vizsgálatokhoz használt vegyszerek, műszerek, laboreszközök használata
o A vizsgálatok előírás szerinti elvégzése és pontos dokumentálása
o Laboratóriumi munkához szükséges számítások elvégzése
o Általános laboratóriumi munkafolyamatok elvégzése

Az álláshoz tartozó elvárások:

o Minimum középfokú végzettség
o Felhasználói szintű számítástechnikai ismeretek
o Jó kommunikációs készség, csoportmunkára való alkalmasság
o Precíz, pontos munkavégzés, rugalmasság
o Alap laboratóriumi eszközök magabiztos használata
o Laboratóriumi munkavégzésben szerzett tapasztalat

Az állás betöltéséhez előnyt jelent:

o Vegyésztechnikusi képzettség vagy hasonló területen középfokú képzettség
o Szakirányú BSc. végzettség
o Tapasztalat steril munkavégzésben
o Angol nyelv minimum alapfokú ismerete
o Tapasztalat GLP környezetben

Egyéb juttatások:

Éves bónusz, Cafeteria, Nyelvtanulás támogatása, 13. Havi bér

Munkavégzés helye:

8200 Veszprém, Szabadságpuszta

At Charles River we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Bioanalytical assistant I-II 1 (Budapest, HU)

Job Summary

Responsibilities:

sample preparation (OE, LLE, SPE) for HPLC & LC-MS/MS
assisstance in bioanalytical method development and validation
preparation of solvents, eluents, sample dilutions, internal standard stock solutions
assisstance in quantitative concentration determination by starting sample sequences
assisstance in report writing
procurement of necessary consumables and tools
documantation in compliance with ISO9001 quality assurance system

We offer:

high-tech laboratory and equipment (12 mass specs, 2 HT ion sources, robots)
carreer at an international biotech company
competitive compansation based on skills and performance
outstanding benefits
enthusiastic colleagues

Job Qualifications

chemical technician or BSc in chemistry
2-5 years of recent laboratory experience with HPLC, LC-MS/MS
confident with chemical concentration calculations
medium level in English
administrative, precise, orderly, team-player, persistent, following rules, loyal

About Discovery
Discovery from Charles River is industry-proven in the successful development of novel therapies, with over 320 patents and 74 preclinical drug candidates delivered to our sponsors in the past 17 years. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND. Our client-focused, collaborative approach creates true partnerships that anticipate challenges, overcome obstacles, and move us forward together on the journey of getting new drugs to market.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Soigneur animalier / Assistant vétérinaire - F/H - Missions temporaires (Paris, FR)

Pendant de 70 ans, les employés de Charles River ont travaillé ensemble pour aider à la découverte, au développement et à la fabrication sûre de nouvelles pharmacothérapies. Lorsque vous rejoignez notre famille, vous aurez un impact significatif sur la santé et le bien-être des gens à travers le monde. Que vos antécédents soient en sciences de la vie, en finance, en informatique, en ventes ou dans un autre domaine, vos compétences joueront un rôle important dans le travail que nous effectuons. En retour, nous vous aiderons à bâtir une carrière dont vous pouvez vous sentir passionné.

Notre société, de dimension internationale, partenaire de l’industrie pharmaceutique, est leader dans la vente de produits et services précliniques.

L'activité Insourcing désigne la prestation de gestion d'animalerie, dans laquelle le client confie à Charles River le soin de réaliser les prestations définies dans un contrat au sein de ses installations adaptées à l'hébergement des animaux de laboratoire.

Au sein de plusieurs animaleries de laboratoire, implantées dans plusieurs départements, principale à Paris et Marseille (75, 91, 92, 13, 34, 33), nous recherchons des Animaliers / ASV - F/H pour renforcer nos équipes dans le cadre de missions intérimaires de remplacement de courte durée.

Missions principales

Réception des animaux (rongeurs)

Vérification des animaux à l’arrivée
Installation des animaux dans les cages
Etiquetage des cages, suivi journalier des mouvements de cages et de leur nombre

Entretien et soins des animaux

Observation des animaux et vérification de l’état clinique, application du programme d’enrichissement
Distribution de l’aliment, vérification de l’abreuvement
Préparation des animaux et du matériel (cages, biberons, couvercles) pour les transferts
Opérations de change des litières et nettoyage des cages, distribution de l’alimentation et de la boisson

Entretien du matériel et des locaux

Désinfection du matériel et des produits
Nettoyage des locaux en respectant les règles de prophylaxie et de biosécurité

Votre profil

De formation ASV ou équivalent, vous possédez une expérience dans ce domaine ou dans une activité en lien avec les rongeurs.
Vous aimez les animaux, êtes rigoureux, autonome et assidu(e) et appréciez le travail en équipe.

À propos des modèles et services de recherche
Indispensable dans la recherche fondamentale et la découverte, l'utilisation de modèles in vivo nous aide à cibler certaines maladies et à déterminer les voies d'intervention biologiques potentielles qui permettent de contrôler l'évolution de la maladie. En notre qualité de leader mondial dans la production et la distribution d'animaux de recherche de qualité supérieure, avec un modèle sur deux produit pour la recherche préclinique à l'échelle mondiale, nous sommes bien placés pour comprendre l'importance de cette étape. Grâce à nos sept décennies d'expérience, notre expertise est inégalée, ce qui nous permet de mettre à votre disposition le modèle parfait, y compris des options spécifiques à une maladie et pré-conditionnées, pour la recherche fondamentale et au-delà.

À propos de Charles River
Charles River est une organisation internationale de recherche de phase initiale sous contrat (ORC). Nous avons tiré parti de nos solides fondations dans le domaine de la médecine et de la science vétérinaire de laboratoire pour créer un portefeuille diversifié de services d'évaluation de découverte et de sécurité, conformes aux bonnes pratiques de laboratoire et autres, dans le but d'apporter à nos clients un soutien complet, de l'identification de cible au développement pré-clinique. Charles River propose également une gamme de produits et de services à l'appui des besoins en matière d'essais cliniques en laboratoire et des activités de fabrication de ses clients. Ce portefeuille considérable de produits et de services permet à nos clients de créer un modèle de développement de médicament plus flexible réduisant leurs coûts, accroissant leur productivité et améliorant leur efficacité, pour une mise sur le marché plus rapide.

Avec plus de 17 000 collaborateurs sur 90 sites dans 20 pays, nous sommes positionnés stratégiquement pour coordonner des ressources mondiales et appliquer des perspectives pluridisciplinaires à l'élaboration de solutions aux défis uniques de nos clients. Notre base de clientèle comprend des sociétés de biotechnologies et des laboratoires pharmaceutiques internationaux, des agences publiques, et des établissements hospitaliers, d'enseignement et de recherche partout dans le monde.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2019.

Les Laboratoires Charles River France sont engagés dans une politique en faveur de l’intégration et du maintien dans l’emploi des personnes en situation de handicap. Tous nos postes sont ouverts aux travailleurs handicapés et une attention particulière sera portée aux candidats en situation de handicap qui postuleront auprès de Charles River.

Pour plus d'information, consultez www.criver.com.

Sr. Data Engineer (REMOTE) (Hyderabad, IN)

Job Summary

At Charles River Laboratories, we’re transforming how we work by harnessing the power of AI, data, and digital innovation to accelerate the discovery and development of life-saving therapies. Our vision is to embed artificial intelligence and advanced analytics across every stage of our scientific and operational workflows—empowering our teams with smarter tools, seamless data, and actionable insights to deliver client-centric services and solutions that better serve our customers and, ultimately, improve patients’ lives.

As a Senior Data Engineer within our Enterprise Data and Analytics team, you’ll be at the forefront of a company-wide digital transformation. We’re looking for a forward-thinking engineer who brings deep technical expertise and a passion for building scalable, AI-ready data platforms. In this role, you’ll architect and implement modern data solutions that power intelligent applications, streamline operations, and deliver measurable business value. You’ll work closely with cross-functional teams to design robust pipelines, integrate diverse data sources, and enable advanced analytics and generative AI capabilities. This is a unique opportunity to shape the future of data engineering at Charles River and help unlock the full potential of data to drive innovation in the life sciences.

Key Responsibilities:

• Design, develop, and maintain scalable data pipelines and ETL processes using Azure Data Factory, Azure Data Bricks, and other Azure services.

• Implement and optimize data storage solutions using Azure Data Lake, Azure SQL Database, and Delta Lake to support analytics and reporting needs.

• Collaborate with data scientists, analysts, and business stakeholders to understand data requirements and deliver high-quality, reliable datasets.

• Ensure data security, compliance, and governance by applying best practices, role-based access control (RBAC), and encryption.

• Monitor and troubleshoot data workflows, ensuring performance, reliability, and cost-efficiency across Azure cloud environments.

• Automate data integration and transformation tasks using Azure Functions, Logic Apps, and scripting languages like Python.

• Mentor junior engineers and foster a collaborative team environment.

Job Qualifications

Essential Qualifications:

• Bachelor’s degree in computer engineering, Computer Science, or a related discipline

• 7+ years of experience in ETL design, development, and performance tuning using the Microsoft Stack in a multi-dimensional data warehousing environment.

• 7+ years of advanced SQL programming expertise (PL/SQL, T-SQL)

• 5+ years of experience in Enterprise Data & Analytics solution architecture

• 3+ years of experience in Python Programming

• 3+ years of hands-on experience with Azure, especially for data-heavy/analytics applications leveraging relational and NoSQL databases, Data Warehousing, and Big Data solutions.

• 3+ years of experience with key Azure services: Azure Data Factory, Data Lake Gen2, Analysis Services, Databricks, Blob Storage, SQL Database, Cosmos DB, App Service, Logic Apps, and Functions

• 2+ years of experience designing data models aligning with business requirements and analytics needs.

• 2+ years of experience defining and implementing data security standards, including encryption, auditing, and monitoring.

• Strong analytical skills and a passion for intellectual curiosity

Preferred Skills:

• 2+ years of experience setting up and operating data pipelines using Python or SQL

• Familiarity with DevOps processes (CI/CD) and infrastructure as code

• Knowledge of Master Data Management (MDM) and Data Quality tools

• Experience developing REST APIs using Java Spring Boot, Python

• Experience building and supporting AL/ML software solutions

• Familiarity with stream-processing systems (e.g., Event Hubs, Storm, Spark-Streaming)

• Experience with API integrations (RESTful, SOAP) for both internal and external systems to enhance data flow and automation.

• Experience working in Agile environments, familiarity with Agile tools like Jira or Azure DevOps.

• Experience in data and analytics within the Life Sciences industry is a plus.

About Corporate Functions
The Corporate Functions provide operational support across Charles River in areas such as Human Resources, Finance, IT, Legal, Sales, Quality Assurance, Marketing, and Corporate Development. They partner with their colleagues across the company to develop and drive strategies and to set global standards. The functions are essential to providing a bridge between strategic vision and operational readiness, to ensure ongoing functional innovation and capability improvement.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Senior Data & Dev Ops Engineer - Azure (REMOTE) (Hyderabad, IN)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.

Job Summary

If you're a Senior Data & DevOps Engineer who thrives at the intersection of cloud infrastructure, data engineering, and AI innovation, this is your opportunity to make a significant impact. In this role, you’ll serve as a trusted advisor and hands-on expert, partnering across business units and IT to architect and optimize our Azure-based enterprise data platform. You’ll mentor engineering teams, champion best practices, and drive automation and scalability through modern DevOps and data engineering tools. We’re looking for someone who brings deep expertise in the Microsoft Azure data ecosystem, a passion for building resilient, future-ready platforms, and a desire to shape the next generation of data and AI capabilities at Charles River. If you’re energized by solving complex challenges, influencing architectural decisions, and enabling transformative analytics, we’d love to connect with you.

Key Duties & Responsibilities

Build, administer and deploy key infrastructure within the Azure Cloud supporting a wide variety of technology solutions.
Working specifically with services in Azure such as Azure Data Lake, Azure Databricks, Azure SQL Data Warehouse, Azure Data Factory, Azure Service Bus, Azure Virtual Machines, Blob Storage, Azure SQL Database, Azure DNS, Virtual Network, Azure App Service.
Build core cloud infrastructure using Terraform (Infrastructure As Code).
Manage code, CI/CD pipelines and documentation via Azure DevOps platform.
Define and manage release workflows to update latest code to the corresponding environments.
Enable developers with automation of deployments and testing frameworks
Document, implement and audit security and access permissions for the data platform.
Monitor nightly data pipelines to meet SLAs.
Respond to alerts across many services related to the EDH platform providing timely and effective solutions.
Create and standardize user communications for operations failures.
Work within Agile squads delivering first in class technology solutions.

Job Qualifications

Education:

Bachelor’s degree in Computer Engineering, Computer Science or related discipline, Master’s Degree preferred

Experience (essential):

Minimum of 7 years related experience in Data and DevOps Engineering
Minimum 5 years hands-on experience building infrastructure and technology solutions within the Azure cloud. Experience with the following services is preferable Azure Data Lake, Azure
Databricks, Azure SQL Data Warehouse, Azure Data Factory, Azure Service Bus, Azure Virtual Machines, Blob Storage, Azure SQL Database, Azure DNS, Virtual Network, Azure App Service.
Hands on experience administering and using source control systems (GitHub, Azure DevOps).
Hands on experience developing and maintaining CI\CD pipelines (Azure DevOps preferable).
Hands on experience deploying cloud Infrastructure As Code.
Hands on experience automating processes using coded solutions (Powershell, Python preferable).
Experience working with Agile squads
Self-starter with the ability to work independently or as part of a project team.
Capability to conduct performance analysis, troubleshooting and remediation.
Interface with key customers from all functional areas.
Proven and recent experience of implementing solutions from requirements gathering and process design to functional production deployment.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Experience (essential):

Administering relational database management systems (RDMS).
Experience in ETL design, development, and performance tuning in general.
Experience managing and governing cloud costs.
Experience working with other public cloud technologies AWS, GCP.
Experience working with MS Fabric.
Experience working AI tool stack in Azure.

Other:

Excellent analytical and organization skills
Ability to understand and translate business and end user requirements
Excellent verbal and written communication skills
Ability to navigate ambiguity and define desired outcome
Strong attention to detail

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

Sr. Data API Engineer (REMOTE) (Hyderabad, IN)

Job Summary

As a Senior Data Engineer – API within our Enterprise Data and Analytics team, you’ll be a key driver of our digital transformation. We’re looking for a technically skilled and forward-thinking engineer who thrives on building scalable, secure, and high-performance data APIs that power intelligent applications across the enterprise. In this role, you’ll lead the design and implementation of modern data services that enable seamless integration, unlock real-time insights, and support advanced analytics and generative AI initiatives. You’ll collaborate with cross-functional teams to deliver solutions that enhance customer value, streamline operations, and accelerate scientific discovery. This is a unique opportunity to shape the future of data engineering at Charles River and help redefine how we deliver science and innovation to the world.

Key Responsibilities:

• Design, develop, and maintain RESTful and GraphQL APIs to support scalable, high-performance applications.

• Collaborate with data engineers and developers to create seamless integrations between APIs, data pipelines, and web applications.

• Build and maintain applications using frameworks like Java Spring Boot, Hibernate, Python Fast API, and ReactJS.

• Ensure system scalability, security, and reliability by implementing best practices in multi-threading, concurrency, and microservices architecture.

• Drive architectural decisions to optimize performance across application, data, and infrastructure domains.

• Develop and deploy solutions on Azure, utilizing tools like SQL Server, Redis, App Services, and API Management.

• Create and maintain test automation frameworks to ensure data quality and service reliability.

• Mentor junior engineers and foster a collaborative team environment.

Job Qualifications

Essential Qualifications:

• Bachelor’s degree in computer engineering, Computer Science or related discipline, Master’s Degree preferred

• 7+ years of software development experience in Big Data

• 7+ years of experience in modern programming languages - Java, Java-based frameworks (Spring, Maven), Python

• 3+ Years of experience in application, data, and infrastructure architecture disciplines

• 3+ years of experience with multi-threading, concurrency, and highly scalable Microservices and REST web Services

• Ability to work collaboratively in teams and develop meaningful relationships to achieve common goals

• Extensive experience with message driven software patterns such as Service Bus, Kafka, Tibco, EMS, and MQ

Preferred Skills:

• Experience working with other public cloud technologies Azure, AWS, GCP

• Strong communication skills to effectively present complex technical solutions to business and technical stakeholders.

• Experience in scripting languages (e.g., JavaScript, PowerShell, shell scripting, Regex).

• Experience building and supporting AL/ML software solutions

• Prior experience in the Life Sciences industry or working with data and analytics in a similar domain.

• Knowledge of test automation tools to validate data accuracy and system reliability.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Sr BI & Data Analyst (REMOTE) (Hyderabad, IN)

Job Summary

As a Senior BI & Data Analyst, you’ll be a key driver of insight and innovation within our Enterprise Data and Analytics team. We’re looking for a curious, detail-oriented professional who thrives on turning complex scientific and operational data into clear, actionable intelligence. In this role, you’ll lead the development of analytical solutions that illuminate critical KPIs, uncover performance trends, and support strategic decision-making across the business. You’ll partner closely with stakeholders to map business processes, align data solutions with real-world operations, and conduct deep-dive analyses that solve high-value challenges. This is a high-impact opportunity to shape how data informs strategy and contributes to our mission of creating healthier lives.

As a Sr. BI & Data Analyst you will be focused on:

Our team thrives on curiosity, collaboration, and a commitment to excellence. We work closely with cross-functional engineering and business partners to deliver impactful data and analytics solutions that shape the future of research and development.

In this role, primary responsibilities include:

• Analyzing complex scientific datasets to uncover meaningful insights and support strategic initiatives.

• Mapping key business process rules to ensure data solutions align with operational realities.

• Creating insight-driven solutions that bring visibility into critical KPIs and performance metrics.

• Conducting deep-dive analyses to solve challenging problems and support evidence-based recommendations.

• Engage Business Stakeholders at all levels to identify requirements for current and future products through ongoing interaction.

• Lead requirements workshops and User Acceptance Testing for new data, products and analytics solutions.

• Analyze business processes and develop business flow diagrams and data flow diagrams to support system design and optimization.

• Work cross-functionally with engineering, product, and business teams to ensure alignment and successful delivery.

• Data Profiling, mining, and data validation/testing to ensure data is fit for use by the business.

• Perform ad-hoc analysis and present results in a clear and user-friendly manner.

• Build strong business relationships that foster a collaborative and trusting approach and partnership.

Job Qualifications

Key Elements

We are looking for the following minimum qualifications for this role:

• Bachelor degree in Business Management, Computer Science or any related field.

• Master in Business Administration/ Information Systems/ Computer Science is an asset.

• Excellent analytical and problem-solving skills with the ability to approach challenges creatively.

• Ability to understand and make sense of complex datasets with a strong attention to detail

• Ability to translate requirements to well-written user stories to bridge the gap between business and technology.

• Strong business mindset with ability to collaborate with business partners to identify needs and opportunities for improved data management and delivery.

• Ability to see big picture and then identify key areas for deep analysis to support sound solutions.

• Self-driven and capable of working both independently and collaboratively within a team setting.

• Experience in life science or Biotechnology industry is a plus.

Technical Expertise required:

• Minimum of 5 years’ experience in writing complex SQL queries, data mining, data profiling, and data validation/testing;

• Minimum of 5 years’ experience as a Business Systems Analyst / Data Analyst specializing in the Data & Analytics discipline, preferably in a senior or lead role;

• Minimum of 5 years’ experience organizing and running User Acceptance Testing cycles and training with business users and stakeholders;

• Experience working with Data Visualization Tools like Power BI, Tableau, Looker, MicroStrategy

• Experienced working in Agile Software Development Methodology.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Facilities Coordinator (Mumbai, IN)

Job Summary

General management of all matters relating to Facilities for the day-to-day operation of the site in compliance with appropriate Regulatory, Statutory and Corporate standards. Responsibility for all services and facilities to the site. Management of Facilities, small projects, Equipment Calibration, EH&S, Security and all external Contractors.

DUTIES & RESPONSIBILITIES

Provide engineering/technical support and ensure efficient management and operation of the facility.
Direct the development of and ensure compliance with all quality systems, department policies, practices and procedures (SOPs, safety procedures and biosecurity protocols) including all external Regulatory Bodies in conjunction with QA department.
Overall responsibility for all plant, equipment, utilities, security, building services and pest control.
Manage the installation, maintenance, operation, repair and adjustments made to all equipment and Facilities e.g. (HVAC, pumps, boilers, air handling units, air compressors, etc.).
Maintain the facility to a high standard of housekeeping and manage external cleaning company within this area.
Support with relevant Global Facilities Depts personnel, the design, review in-house, value engineering and construction management for facility projects, and prepare capital expenditure template and related justification.
Oversee daily operational activities in Facilities and Equipment Calibration. Ensure all reporting staff and \ or Contractors understand their roles and responsibilities and their tasks are performed in accordance with site procedures.
Responsible for ensuring appropriate SOPs, protocols, reports etc are written by trained personnel and contain true and accurate information. Writing and\or approval of SOPs related to the activities in conjunction with QA department.
Overall management of all external contractor services to include quotations/costs, risk assessments, method statements and work permits in advance of work being carried out.
Work in conjunction with local security contractors and corporate security.
Manage the Technical "On-Call" Team activities
Any other duties/responsibilities requested by the Site Management.

H&S and Environment

To develop and co-ordinate the operation, development and organisation of safety, health and environmental systems at the site to include implementing policies, record keeping, monitoring and compliance.
Investigate, record and report {local and global} any incidents, accidents or dangerous occurrences as per company policy and legislation, take remedial action where required in addition to KPI development and management.
Management of the site Enablon safety reporting software tool.
To draft all required risk assessments and other practical requirements as necessary under Health & Safety legislation.
Point of contact on all Health & Safety and environmental matters for Staff and the Management Team.
Maintenance of the Life Saving Systems on-site as required by legislation with appropriate oversight of fire warden training as necessary.
Management of contractors regarding any/all on-site work which may affect Health and Safety while ensuring legal requirements surrounding permitting are in place.
Regular Health & Safety audits/inspections (internal & External) across the site in line with EHS approved inspection schedule,
To be responsible for ensuring that a safe working environment is maintained for all employees of CRL and visitors to the site, by observing all safety procedures and working methods, by making proper use of protective clothing and equipment and by reading, understanding and following all safety documents issued.
Energy Management: Overall responsibility to manage electricity, fuel, water, wastewater and waste from a budgetary and regulatory standpoint. Perform energy audits.

Equipment Calibration

Manage the Equipment Calibration activities on site
Complete Equipment Calibration or manage vendor calibration activities as per schedule and in accordance with Regulatory requirements
Have the ability to understand Equipment Calibration tasks on various types of instrumentation including temperature, pressure, humidity, volume, pH and conductivity analyzers
Suggest continuous improvement ideas for processes and Equipment Calibration activities
Maintain all documentation in an organized and controlled manner in compliance with GMP.
Provide Instrumentation/Equipment Calibration support to Facilities, Quality Assurance Team and Operations.
Represent, Communicate and Coordinate Equipment Calibration activities with Management, Testing Departments, Equipment Vendors, Service Suppliers and Clients.

Job Qualifications

- Education: Bachelor degree in Biological Science or related discipline required.
- Experience: 1-2 years of experience in Molecular, Microbiology, or Chemistry.
- QC Microbiology Lab experience particularly in the Pharma setting is an advantage
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
- Other: Must possess excellent communication and presentation skills and the ability to work cross-functionally. Proficient in the use of Microsoft Office applications

PHYSICAL DEMANDS:

- Lifting, Standing, working overhead and at height as required.
- Manual Work as required.
- Participate as Technical "On-Call" Team member.

WORK ENVIRONMENT:

- General Office Environment
- Frequent Outdoor work environment

For more information, please visit www.criver.com.

Sr. Technical Service Specialist (Mumbai, IN)

Job Summary

Responsible for technical support for Endosafe® (including automated NEXUS system), Accugenix® AxcessTM or Celsis™ and their associated systems. Support Endosafe®, AXCESSTM or Celsis™ product line development providing input and testing for new product design specifications, validation, and change controls. Support internal and external customers with new and changes to the above product lines. Drives the onboarding of new customers and continued customer satisfaction of our clients. Manage activities to help meet revenue targets and goals for the business.

ESSENTIAL DUTIES AND RESPONSIBILITIES

Maintain subject matter expertise in at least one of the Endosafe®, AxcessTM or Celsis™ portfolio.
Applies technical/scientific skills to develop existing accounts and compete for customers together with the Account Management team whether for products sales or services sales.
Provides technical leadership and supports customer onboarding, provide customer training, qualify leads, perform test demonstrations and help close new business opportunities during customer start up and continued account management.
Recommends or performs remedial actions to troubleshoot customer issues related to application, reagents and software for the assigned product line.
Establishes regular interface and communication with the Account Management and Field Service team to relay shared goals and targets; develop co-strategies to achieve defined targets; and work cohesively as a team to provide excellence in service to clients
Builds relationships with customers to influence the acceptance and use of MS portfolo
Supports internal training for new launches and changes to product lines under responsibility.
Responsible for the initial training and validation/application development support for customers, ensuring full and continued utilization of Microbial Solutions products.
Generates, reviews or revises related Standard Operating Procedures (SOPs) related to Technical Services.
Conducts seminars and hands-on workshops and support marketing educational activities related to portfolio.
Participates in investigations (e.g. root cause analysis, impact analysis, risk assessment, corrective actions etc) and assists QA department in the event of any or audits in area of specialization.
Participates and assumes support role in tradeshows and seminars.
Territory coverage: Singapore, South Korea, Australia, and distributors in Thailand, Vietnam, Malaysia and Indonesia.

General requirements

Maintains confidentiality of all Client information according to internal SOPs, Quality Service Agreements, and regulatory requirements.
Maintains appropriate records and documentation of activities to facilitate continuous compliance to ISO 9001, ISO/IEC 17025, cGMP, PIC/S, Company local & global SOPs and data integrity principles and requirements, where appropriate.
Actively seeks improvement within area of responsibility and takes necessary action to implement such improvements.
Adheres to Company Policies and Procedures, including Code of Ethics and to Health and Safety requirements.
Performs all other related duties as assigned.

Job Qualifications

Education: Minimally Bachelor’s degree (B.S.) or equivalent in Microbiology, Life Sciences, Biotechnology or any other related scientific discipline.
Experience: Minimum 5 years of relevant industry experience, preferably 3 of which should involve customer-facing responsibilities.
Understanding of Biology/Microbiology in the Pharma setting is an advantage
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Other: Must possess excellent communication and presentation skills. Proficient in the use of Microsoft Office applications

For more information, please visit www.criver.com.

Data & DevOps Engineer - Azure (Ahmedabad, IN)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

If you're a Data & DevOps Engineer who thrives at the intersection of cloud infrastructure, data engineering, and AI innovation, this is your opportunity to make a significant impact. In this role, you’ll serve as a trusted advisor and hands-on expert, partnering across business units and IT to architect and optimize our Azure-based enterprise data platform. You’ll work within engineering teams, champion best practices, and drive automation and scalability through modern DevOps and data engineering tools. We’re looking for someone who brings solid expertise in the Microsoft Azure data ecosystem, a passion for building resilient, future-ready platforms, and a desire to shape the next generation of data and AI capabilities at Charles River. If you’re energized by solving complex challenges, influencing architectural decisions, and enabling transformative analytics, we’d love to connect with you.

Duties and Responsibilities:
This position will serve on a high-performing team responsible for all cloud infrastructure components in the Charles River Laboratories Enterprise Data Hub (EDH) and a Microsoft Azure cloud-based warehousing and reporting solution supporting multiple applications across many business segments.

Build, administer and deploy key infrastructure within the Azure Cloud supporting a wide variety of technology solutions.
Working specifically with services in Azure such as Azure Data Lake, Azure Databricks, Azure SQL Data Warehouse, Azure Data Factory, Azure Service Bus, Azure Virtual Machines, Blob Storage, Azure SQL Database, Azure DNS, Virtual Network, Azure App Service.
Build core cloud infrastructure using Terraform (Infrastructure As Code).
Manage code, CI/CD pipelines and documentation via Azure DevOps platform.
Define and manage release workflows to update latest code to the corresponding environments.
Enable developers with automation of deployments and testing frameworks
Document, implement and audit security and access permissions for the data platform.
Monitor nightly data pipelines to meet SLAs.
Respond to alerts across many services related to the EDH platform providing timely and effective solutions.
Create and standardize user communications for operations failures.
Work within Agile squads delivering first in class technology solutions.

Job Qualifications

Education:

Bachelor’s degree in Computer Engineering, Computer Science or related discipline, Master’s Degree preferred

Experience (essential):

Minimum of 5 years related experience in Data and DevOps Engineering
Minimum 3 years hands-on experience building infrastructure and technology solutions within the Azure cloud. •Experience with the following services is preferable Azure Data Lake, Azure Databricks, Azure SQL Data Warehouse, •Azure Data Factory, Azure Service Bus, Azure Virtual Machines, Blob Storage, Azure SQL Database, Azure DNS, •Virtual Network, Azure App Service.
Hands on experience administering and using source control systems (GitHub, Azure DevOps).
Hands on experience deploying cloud Infrastructure As Code.
Experience working with Agile squads
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Experience (preferred):

Administering relational database management systems (RDMS).
Experience in ETL design, development, and performance tuning in general.
Experience managing and governing cloud costs.
Experience working with other public cloud technologies AWS, GCP.
Experience working with MS Fabric.
Experience working AI tool stack in Azure.

Other:

Excellent analytical and organization skills
Ability to understand and translate business and end user requirements
Excellent verbal and written communication skills
Ability to navigate ambiguity and define desired outcome
Strong attention to detail

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

For more information, please visit www.criver.com.

Testreq - Italy Walkthrough (Ahmedabad, IN)

Job Summary

test test test test

Job Qualifications

test test test

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

For more information, please visit www.criver.com.

Recrutements de talents - Administratif (Ahmedabad, IN)

Job Summary

About RightSource (Biologics Testing)

The biopharmaceutical industry is growing at an unprecedented pace which is simultaneously changing current testing methodologies. To keep up with the demand, we offer a flexible testing platform which can be deployed on-site at the client site to their exact needs. Our biologics testing lab...in a box…at the client site. RightSource℠ is completely managed and operated using our quality management system, SOP’s, methods, and best practices. It’s as if you shipped your samples to an outsourced lab but walked down the hall instead.

Our Biologics Testing Solutions offers a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

For more information, please visit www.criver.com.

Field & Instrumentation Service Engineer (Bangalore, IN)

Job Summary

Job Qualifications

Equal Employment Opportunity

For more information, please visit www.criver.com.

Customer Service Representative (Songdo, KR)

POSITION SUMMARY

Provide dependable quality customer service including responses to product or service inquiries, efficient order coordination and processing, and routine problem solving. This role also responsible for management of customer account.

DUTIES & RESPONSIBILTIES

To improve customer satisfaction, it is necessary to lead the better communication with customers and deliver accurate information.
Receive orders through “Service Cloud”, confirm delivery schedules, and process orders.
Complete all associated paperwork for shipment.
Communicate price quotations, products availability, and product information.
Use “WEHAGO” to issue the tax invoice to customer.
Create and manage customer accounts.
Respond to any basic and routine Endosafe® product and Microbial Identification Service inquiries.
Resolve basic and routine problems and customer complaints.
Follow-up complaints to ensure that customer expectations are satisfied. If necessary, coordinate the implementation of service improvements to prevent future complaints.
Remain proficient in all SOPs in areas of responsibility.
Perform all other related duties as assigned.

QUALIFICATIONS:

Education: Bachelor’s degree (B.A. /B.S.) or equivalent in business or related discipline.
Experience: No experience required.
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensures: None
Other:
- Working knowledge of all Microbial Solutions products and services
- Strong phone contact handling skills and active listening
- Customer orientation and ability to adapt/respond to different types of characters
- Excellent communication skills
- Proficient with MS Office and phone systems

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Associate - (EG) (Kingston, NY, US, 12401)

Job Summary

As an Animal Care Associate for our production site in Stone Ridge, NY, you will be responsible for the well-being of our research animals. Your contribution will ensure the health of our animals, as well as impact the lives of patients across the world.

* This is a temporary opportunity with the potential to be hired as a full-time, employee.

* Up to $500 sign on bonus (CRL employees not eligible)

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform routine animal husbandry duties and monitor daily health and welfare to maintain quality and health of animals.
Handle, transfer, and distribute animals, supplies and waste as needed to and from work area(s).
Monitor animal health by observing animal behavior, physical appearance, and physical environment. Identify and report any abnormal findings.
Responsible for collecting health monitoring swabs and following health monitoring schedules.
Perform physical environment housekeeping duties and production operations according to Good Manufacturing Practices (GMPs) and/or Standard Operating Procedures (SOPs).
Maintain recordkeeping pertaining to animal or supply area inventories.
Strictly follow all procedures necessary to maintain the barrier room barrier.
Use supplies according to safety guidelines. Perform all job-related duties in accordance with company safety procedures.
Colony Management
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

No experience required. On the job training will be provided.

Role Specific Information:

Location: Stone Ridge, NY
This is a temporary opportunity with the potential to be hired as a full-time, employee*
Schedule: Monday - Friday - 1st shift, some rotating weekends required. Early morning hours.
Up to $500 sign on bonus (CRL employees not eligible)
Benefits: 401K participation/Paid Sick Time and Paid Volunteer Time Off

The hourly pay rate for this position is $17.75.

About Research Models & Services
Fundamental to basic research and discovery is the use of in vivo models to help identify disease targets and determine potential biological pathways that regulate the condition. As the world’s leader in the production and distribution of the highest quality research animal, with 1 out of 2 animal models produced for preclinical research globally, we understand the importance of this step. With seven decades of experience, our expertise is unmatched, allowing us to provide you with the perfect model, including disease-specific and preconditioned options, for basic research and beyond.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Caretaker - Contratto a chiamata (GENOVA) (Genova, IT, 16163)

Da 75 anni, i dipendenti di Charles River hanno lavorato insieme per assistere alla scoperta, allo sviluppo e alla produzione sicura di nuove terapie farmacologiche. Quando si unisce alla nostra famiglia, avrai un impatto significativo sulla salute e il benessere di persone in tutto il mondo. Se il tuo background è in scienze della vita, finanza, IT, vendite o in un'altra area, le tue abilità avranno un ruolo importante nel lavoro che svolgiamo. In cambio, ti aiuteremo a costruire una carriera che puoi sentirti appassionata.

Job Summary

Per nostro cliente sito in Genova ricerchiamo uno stabularista.

La risorsa sarà inserita all'interno del team operante nella struttura e si occuperà di svolgere le mansioni relative alla gestione del laboratorio

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nel controllo delle procedure sperimentali;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature automatiche e carrelli

Job Qualifications

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro con contratto a chiamata

Disponibilità a lavoro nel week-end

Buona conoscenza del pacchetto office

Di cosa si occupa la Charles River

Charles River è un’organizzazione di ricerca a contratto (CRO) per le fasi precoci della ricerca farmacologica. Sulla base della nostra scienza e medicina degli animali da laboratorio abbiamo costituito e sviluppato un portafoglio diversificato di servizi di scoperta e di valutazione della sicurezza, sia GLP che non-GLP, per supportare i clienti a partire dall’identificazione del bersaglio fino allo sviluppo preclinico. Charles River offre inoltre una gamma di prodotti e servizi a supporto delle esigenze di analisi cliniche di laboratorio e delle attività di produzione dei nostri clienti laboratorio. L’utilizzo di questo portafoglio variegato di prodotti e servizi permette ai nostri clienti di creare modello di sviluppo dei farmaci più flessibile, che riduce i costi e migliora la produttività e l’efficienza al fine di ridurre i tempi di immissione sul mercato.

Con oltre 20.000 dipendenti in 90 strutture dislocate in 20 paesi in tutto il mondo, siamo posizionati strategicamente per coordinare le risorse a livello mondiale e applicare prospettive multidisciplinari per risolvere le sfide particolari dei nostri clienti. La nostra base clienti include aziende farmaceutiche di livello mondiale, aziende operanti nel settore delle biotecnologie ed enti governativi, nonché ospedali e istituzioni accademiche di tutto il mondo.

Alla Charles River, promuoviamo con convinzione il nostro ruolo nel miglioramento della qualità di vita delle persone. In tutto ciò che facciamo, siamo guidati dalla nostra missione, dalle nostre eccezionali competenze scientifiche e da una grande risolutezza e affrontiamo ogni giorno con la consapevolezza che il nostro lavoro contribuisce al benessere e al miglioramento della salute di molte persone in tutto il mondo. Abbiamo orgogliosamente ha collaborato allo sviluppo di ~85% dei farmaci approvati dalla FDA nel 2021.

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Technical Service & Research Supervisor (Cambridge, MA, US, 02142)

Job Summary

We are seeking an experienced Technical Services & Research Supervisor to join our Insourcing Solutions team, located in Cambridge, MA.

This individual will be responsible for direct supervision of Charles River Accelerator & Development Labs (CRADL) in vivo technical services group. Manages the day-to-day technical operations for a smooth execution of technical services across all CRADL sites in the market. Maintains performance and service levels consistent with and according to company’s and IS’s (Insourcing Solution) standards, as well as client contractual requirements. Liaises with clients to ensure satisfaction with technical staff’s performance.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

The following statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified.

Responsible for the daily technical operations, managing the end-to-end technical service delivery from client request to completion, while supervising a team of research associates and technicians.
Schedules, assigns and balances workload among the technical staff to fulfil service requests.
Serves as a liaison between the client and technical team to ensure client satisfaction
Promptly resolves client inquiries and issues through close collaboration with leadership
Accommodates varying workloads and work on weekends, holidays, and evenings to meet client needs; ensures resolution of “after-hour” emergencies as necessary.
Acts as subject matter expert in technical skills and basic animal welfare skills.
Leads the development efforts for new in vivo techniques to expand technical service offerings.
Supports technical services as needed by being able to perform and obtain competency/proficiency in the required in vivo procedures.
Conducts personnel training and competency/ proficiency assessments; maintains all related documentation.
Responsible for personnel management activities, including mentorship, hiring, promotions, training & development, providing regular direction and feedback on performance, delivering annual performance and salary reviews.
Recommends new or innovative techniques to improve productivity, increase efficiencies, and maintain quality standards.

.

Maintains an awareness of the financial status and impacts of technical operations.
Drives operational excellence by proactively resolving issues and fostering a culture of continuous improvement through staff training and process optimization.
Ensures in vivo study applications are performed in accordance with currently defined protocols and in a manner consistent with the Guide for the Care and Use of Laboratory Animals and all local, state, and federal requirements.
Participates in the development and implementation of organizational and function-specific SOPs, in compliance with all state, federal and industry requirements.
Monitors adherence to all policies, SOPs and all required documentation related to the department.Partners with the veterinarians, veterinary technicians, trainers, and the IACUC office to ensure compliance with biosecurity policies and procedures, IACUC required training, IACUC non-compliance and/or animal welfare concerns.
Report non-compliance or animal welfare concerns to the appropriate Animal Welfare Team member or IACUC office.
Serves as a role model to CRADL staff as it relates to CRL Core Values (CARE, LEAD, OWN, COLLABORATE). Provide leadership and motivation to all CRADL personnel.
Attends and participates in on-the-job and classroom training sessions; completes all assigned computer-based safety and professional development training.
Maintains required attendance level and adherence to work schedule in accordance with required staffing levels to ensure that assigned duties are completed.
Performs other duties as directed by management.

MINIMUM QUALIFICATIONS

Bachelor's degree (B.A./B.S.) or equivalent in animal or laboratory science, business, or related discipline.
Minimum four (4) years in the laboratory animal industry of which two (2) years is supervisory or lead technician experience.
Certification/Licensure: AALAS certification at the Laboratory Animal Technologist level (LATG) preferred.

The pay range for this position is $88,900K - 103,000K USD annually Please note that salaries vary within the range based on factors including experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technician III - (ABSL experience) (Cambridge, MA, US, 02139)

Job Summary

We are seeking an experienced Animal Care Technician III  to join our Insourcing Solutions team, located in Cambridge, MA.

As the ACTIII, you will maintain and monitor the health, production, post-operative care and physical environment of animal models within a ABLS2/ABSL3 facility.  

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Work with veterinarians and researchers while performing specialized techniques and procedures with the study of animal models infected with hazardous biological agents.
Perform duties involving specialized ABSL2/ABSL3 safety methods, procedures and sanitation of the animals' environment.
Use appropriate barrier techniques and applies knowledge of quarantine, isolation and containment procedures pertinent to ABSL2 and/or ABSL 3 required to prevent cross infection of animals during experiments and to prevent infection of the technicians and/or co-workers.
Those without ABSL3 experience will receive training.
Provide input into the creation/revision of SOPs and assist in implementation and training of new SOPs.
Perform animal procedures and veterinary technical support duties: including but not limited to blood collection, intramuscular or subcutaneous injections, organ collection, animal identification, sentinel collection, and animal treatment.
May provide environmental enrichment feed and other enrichment stimuli and/or provide behavioral assessments.
Perform animal husbandry which includes feeding, watering, and cleaning cages as required. Monitor animal health and adhere to health monitoring schedules.
Maintain accurate departmental animal housing/isolator or support area record keeping.
Regularly use and update animal inventory/census.
Receive animals and perform duties such as transporting, unloading/uncrating, transferring, weighing, inspecting and associated documentation.
Participate in planning/coordination of customer projects for department.
Operate and perform routine maintenance checks on automated rack washer and bulk autoclaves and other associated equipment (e.g. bedding disposal/dispenser, bottle filler).

MINIMUM QUALIFICATIONS

To qualify for this role, candidates must meet one of the following combinations of education and experience:

Bachelors of Science Degree in Animal Science/Biology or a related discipline and 2 years of related animal laboratory experience.
Associates of Science Degree in Animal Science/Biology or a related discipline and 3 years of related animal laboratory experience.
High School Diploma/GED and 4 years of related animal laboratory experience.
Experience working in an ABSL1 or ABSL2 facility.

PREFERRED QUALIFICATIONS:

LAT certification
Experience working in an ABSL3 facility.

The pay for this position is $26.83-$29.66 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Scientist I - Immunochemistry (Shrewsbury, MA, US, 01545)

Job Summary

ESSENTIAL DUTIES AND RESPONSIBILITIES:

•   Function independently as a Project Scientist, Principal Investigator, Contributing Scientist in the direction and execution of assigned studies in compliance with regulations as they apply to the conduct of preclinical and clinical research. Provide scientific expertise in study conduct, design, and interpretation.
•   Participate in and coordinate all phases of the study planning process with appropriate departments.
•   Develop assays, generate high-quality laboratory method, protocols, amendments, reports, and facilitate appropriate changes to study design for assigned projects and programs.
•   Review, interpret, integrate, and present data on assigned studies.
•   Writes and edits draft or final reports that document all study related procedures and results.
•   Analyze scientific problems, troubleshoot analytical methods and technical issues.
•   Function independently as the point of contact for the planning and execution of sponsor interaction related to assigned studies, including proposal management and study scheduling, conduct and reporting.
•   Provide prompt verbal or written communication with Sponsors on study related business.
•   Mentor technical staff in areas such as protocol interpretation, method development and refinement, study-related problem resolution, and execution of validation studies.
•   Provide technical and scientific guidance to the research staff.
•   Contribute to testing of new biomarker technologies or introduce improvements in existing technologies.

The pay range for this position is between $100,000 to $110,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
• Education: Bachelor's degree (B.S./B.A.) or equivalent in a scientific related discipline. Related Master's degree (M.S./M.A.) or PhD/DVM preferred.

• Experience: Minimum of 6 years related experience in the development and/or validation of biomarker, PK and ADA assays is preferred (eg: ligand binding assays, enzymatic assays, Luminex, Bioplex, MSD, Quanterix Simoa, ProteinSimple Ella). Experience in a contract research organization is preferred.

• Other: Understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good Laboratory Practices (GLPs), as appropriate. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and with standard laboratory calculations. Experience with Watson LIMS (preferred).

PHYSICAL DEMANDS:
• While performing the duties of this job, the employee is regularly required to talk, hear and work/ type at a computer.
• Specific vision abilities required by this job include close vision and the ability to adjust focus.

WORK ENVIRONMENT:
•   General office working conditions, the noise level in the work environment is usually quiet.
•   While performing the duties of this job the employee may occasionally be required to wear protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots), work near toxic or caustic chemicals, work with biohazards, and/or work with live animals with risk of exposure to allergens and/or zoonotic diseases.
•   The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors, and/or wet, humid and/or extreme temperature conditions.

COMMENTS:
• This position may require occasional travel.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technician I (Shrewsbury, MA, US, 01545)

Job Summary

Full Time - 40 Hours/Week - Tues-Say Day Shift

Responsible for performing operational, administrative and technical tasks to provide comprehensive care for all species of laboratory animals at the site, including: daily health observations, feeding/watering, sanitizing primary and secondary enclosures, environmental enrichment, handling and restraint and related tasks. Assist with the movement of animals and stocking of supplies. May serve as lead/primary technician and perform technical duties with guidance.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• May serve as lead/primary technician and perform technical duties with guidance.
• Handle, restrain, and provide care for all species of animals at the site.
• Observe animals for general health and overall well being.
• Clean primary enclosure and enclosure area for animals.
• Sanitize cages, enrichment devices and other related equipment.
• Measure and distribute feed to animals in accordance with established procedures.
• Provide environmental enrichment.
• Inspect feeding and watering devices for proper function.
• Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs).
• Review documentation of functions performed as part of quality control requirements.
• Perform quarantine & isolation procedures as they relate to husbandry tasks.
• Perform duties associated with the transportation, receipt, transfer and distribution of animals as assigned.
• Perform cagewash duties as assigned.
• Collect laboratory data and independently use equipment related to the collection of data.
• May perform basic veterinary technical and husbandry tasks with guidance, including the following:
o    Administration of various therapeutic measures by IV, IM, SQ, topical, oral routes, etc.
o    Bandage/wrapping techniques.
o    Nail/hoof/teeth clipping/trimming.
o    Venipuncture techniques.
o    Vaginal swabs.
o    Proficient animal restraint techniques.
o    Monitor critical care animals (i.e., place IVs, monitor fluids, etc.).
• Perform all other related duties as assigned.

The pay for this position is $20.00/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
• Education: High school diploma or General Education Degree (G.E.D.) required.
• Experience: Minimum of 6 months related experience in animal research and/or husbandry preferred or must have demonstrated full knowledge of competencies and positive performance at the previous level. Experience working in a regulated environment preferred.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: AALAS certification at the ALAT level preferred
• Other: Ability to handle common laboratory animal species. Basic knowledge of GLP regulations preferred. Ability to work on assignments that are semi-routine in nature in which ability to recognize deviation from accepted practice is required. Ability to receive and understand general instructions on routine work and detailed instructions on new assignments.

PHYSICAL DEMANDS:
• Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
• Must be able to perform procedures, which require, talking, hearing, standing or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
• Must be able to frequently firmly hold species while utilizing fine motor skills.
• Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

WORK ENVIRONMENT:
• Works in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles.
• The employee regularly works with live animals with risk of exposure to dander, allergens, zoonotic disease, and biohazards.
• The noise level in the work environment ranges from low to high depending upon the species housed.

COMMENTS:
• This position requires overtime, weekend, holiday, and/or after hours shift coverage, as needed.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Sample Management Technician I (Shrewsbury, MA, US, 01545)

Job Summary

Compile required documentation and package biological. samples for shipping. Responsible for managing the inventory of biological samples, study data and equipment within the Sample Management group.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

•Package biological samples and ensure accurate completion of all required documentation for the shipment (i.e: verify shipping lists against samples).

•Prepare shipping documentation and assist In preparation of CITES permits as needed. Fax shipping documentation to sponsors as needed.

•Prepare domestic and international packages according to applicable guidelines.

•Deliver packages to carrier/shipper as needed.

•Notify Study Directors, Study Supervisors, and sponsors of FedEx tracking numbers and verify that packages have arrived at their destinations.

•Handle all details required for shipment <if samples·(receiving, storage, inventory and verification) using Study protocol or Sponsor guidance documents.

•Log samples in and out of storage via LIMS system or other determined process (i.e.: manual data collection)-

•Manage check In/out process of samples required for analysis and return samples to the appropriate storage condition when analysis is complete.

•· May prepare sample inventories and sample verification for maintained, archived, and sample requests/receipts.

•Perform data-entry to maintain the database for biological samples inventory.

•Maintain freezer/refrigerator recording charts and all associated documentation.

•File study data and generate box labels.

•Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs).

•Perform all other related duties as assigned.

The pay for this position is between $21.00 and $23.00/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
•Education: High school diploma or General Education Degree (GED.) required.
•Experience: 1 year related experience in a life science laboratory preferred
•An equivalent com1;>1nation of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•Certification/Licensure: None.
Other: Must be detail oriented and have general familiarity with lab procedures; Good verbal and written communication skills required. Basic computer skills; familiarity with Microsoft Office and Excel software. Ability to organize and prioritizs1 work and meet timelines.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Environmental Health & Safety Associate (Shrewsbury, MA, US, 01545)

Job Summary

Administer and maintain the Safety Data Sheet (SDS), biowaste, and biological waste disposal programs. Maintain safety equipment and stock supplies, qualify and train staff in safety or environmental areas.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
⦁ Administer and maintain biowaste at Shrewsbury facility including waste profiling, permitting, manifesting, record keeping and reports.
⦁ Oversee transportation and maintain logs of biowaste material.
⦁ Maintain a preventative maintenance program within the confines of an annual budget.
⦁ Administer and maintain the environmental index and permit database, ensure up to date records for compliance for all regulatory agencies, and sponsor inspections.
⦁ Assist in the implementation and monitoring of company health and safety programs
⦁ Maintain all Safety Data Sheets (SDS), database and binders, perform scheduled inventory of products and document locations of products, data entry of all required SDS information into appropriate tracking database.
⦁ Conduct safety training classes as qualified and required
⦁ Assist in coordinating and scheduling of safety committee meetings.
⦁ Inventory, stock, and order safety supplies.
⦁ Perform respirator fit testing and monitor and review respirator monthly inspection and end of service logs.
⦁ Conduct inspections of safety shower and eyewash checks.
⦁ Assist site EH&S Manager with proactive risk assessment and mitigation programs for site laboratories, vivarium, offices and shared spaces.
⦁ Perform all other related duties as assigned.

The pay for this position is between $70,000 and $79,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
⦁ Education: High school diploma or General Education Degree (G.E.D.) required. Associates Degree (A.A./A.S.) or equivalent in environmental science, environmental engineering or related discipline preferred
⦁ Experience: 2 years related experience in a health & safety and or environmental position. Experience in regulatory environment preferred.
⦁ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
⦁ Certification/Licensure: None.
Other: Proficient in the use of computer network and standard office software applications. Knowledge of governmental safety and environmental regulations and chemical handling preferred.

PHYSICAL DEMANDS:
⦁ While performing the duties of this job, the employee is regularly required to talk, hear, and work/type at a computer.
⦁ While performing the duties of this job, the employee is occasionally required to walk, kneel or crouch, and use hands to handle, finger or feel objects, tools or controls.
⦁ While performing the duties of this job, the employee is occasionally required to lift, move and/or hold up to 50 pounds; this includes work materials and supplies.
⦁ Specific vision abilities required by this job include close vision and the ability to adjust focus.

WORK ENVIRONMENT:
⦁ General office working conditions, the noise level in the work environment is usually low to moderate.
⦁ While performing the duties of this job, the employee is occasionally required to wear protective clothing (goggles, face shield, surgical mask, respirator, cap, gloves, scrubs, boots).
⦁ While performing the duties of this job, the employee is occasionally exposed to fumes or airborne particles, unpleasant odors, wet, humid and/or extreme temperature conditions.
⦁ While performing the duties of this job, the employee is occasionally required to work with and/or near moving mechanical parts, sharp objects, toxic or caustic chemicals and biohazards, and is exposure to allergens and/or zoonotic diseases.

Comments:
This position requires overtime, weekend, holiday, and/or after hours shift coverage, as needed

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Habituation Technician I - Vet Services (Shrewsbury, MA, US, 01545)

Job Summary

Assist with performing appropriate acclimations for all animals to prepare them for study procedures. Assist with providing appropriate enrichments to the animals’ structural and social environments and provide opportunities for species-typical activities.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

⦁ Handle animals as required to perform acclimations that precondition animals for study procedures
⦁ Implement basic operant conditioning plans to modify animal behavior
⦁ Maintain, track and review data related to acclimation and enrichment programs

⦁ Receive deliveries of foodstuff items, label items, and ensure proper storage.
⦁ Assist with food prep and enrichment stock organization and cleanliness
⦁ Assist with providing appropriate enrichments to the animals’ structural and social environments and provide opportunities for species-typical activities.

⦁ Assist with the distribution for client specific enrichment per protocols
⦁ Assist with building and maintaining enrichment devices
⦁ Assist with evaluation of new enrichment devices and provide input on strategies for individually and socially housed animals.
⦁ Work closely with the veterinary and animal care staff to ensure proper animal care standards are maintained.
⦁ Maintain documentation for the Behavioral Management Program including data review

⦁ May be needed to provide support in other Lab Animal Medicine groups
⦁ Perform all other related duties as assigned.

The pay range for this position is $21.00 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
⦁ Education: GED + 1 year experience or Bachelors degree (preferred) or Associates degree (or equivalent in animal or life sciences or related discipline).
⦁ Experience: 1+ years experience in animal research and/or husbandry; multi-species experience preferred or must have fully satisfied technical and experience requirements for the previous level.
⦁ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
⦁ Certification/Licensure: AALAS certification at the ALAT level preferred
⦁ Other: Ability to handle common laboratory species. Proficient in basic technical skills and the operation of data collection equipment. Knowledge of GLP’s and other federal regulations and guidelines relating to the care of laboratory animals. Understanding of routine study design and protocols.

PHYSICAL DEMANDS:
⦁ While performing the duties of this job, the employee is regularly required to talk, hear and lift.
⦁ Must be able to regularly lift and manipulate up to 50 pounds on a repetitive basis each day over approximately 1 to 75 ft.
⦁ Must be able to regularly push wheeled carts weighing up to 1200 pounds on a repetitive basis each day over a distance of approximately 1 to 100 ft.
⦁ Duties require regularly standing for an average of 8 hours a day.
⦁ Must be able to regularly manipulate objects on shelves from one and one-half to six and one-half feet above the floor on a repetitive basis each day.
⦁ Must be able to regularly read, understand, and follow written procedures.
⦁ Must be able to occasionally work in spaces as narrow as 2 feet.
⦁ Must be able to frequently accurately record data by hand.
⦁ Must be able to perform procedures, which require, talking, hearing, standing or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
⦁ Must be able to frequently firmly hold species while utilizing fine motor skills.
⦁ Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

WORK ENVIRONMENT:
⦁ Works in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
⦁ The employee regularly works with live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
⦁ The noise level in the work environment ranges from low to high depending upon the species housed. Noise protection is provided.

Comments:
⦁ This position requires overtime, weekend, holiday, and/or after hours shift coverage, as needed.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Technician I - 2nd Shift (Shrewsbury, MA, US, 01545)

IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.

Job Summary

Full Time Position - Monday- Friday 2:30 - 11:00pm. Must be able to start within one month of offer date.

Charles River Laboratories is seeking a Research Technician I for our In Vivo (In Life) Team within our Safety Assessment site located in Shrewsbury, MA.

The Research Technician 1 will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods.

The following are minimum qualifications:

Education: High school diploma or General Equivalent Degree (G.E.D.). Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline.
Experience: 6 months to 1 year related experience in animal research and/or husbandry or must have fully satisfied technical and experience requirements for the previous level.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: ALAT preferred.
Other: Ability to handle common laboratory species. Proficient in basic technical skills and the operation of data collection equipment. Knowledge of GLPs and other federal regulations and guidelines relating to the care of laboratory animals. Basic understanding of study design and protocols.

The pay range for this position is $24.50 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

For more information, please visit www.criver.com. #LI-LH1

Veterinary Technician I (Shrewsbury, MA, US, 01545)

Job Summary

This is a Full Time position (40 hours/week) Sunday-Thursday.

BASIC SUMMARY:
Assist veterinary staff in the documentation and triage of all laboratory animal health cases. May also perform technical in-life procedures.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
Assist veterinary staff in the documentation and triage of all animal health cases noted by technical staff and/or Attending Veterinarian.
Perform routine veterinary technical and husbandry skills including the following:
Administration of various therapeutic measures by IV, IM, SQ, topical, oral routes, etc.
Bandage/wrapping techniques.
Nail/hoof/teeth clipping/trimming.
Venipuncture techniques.
Vaginal swabs.
Proficient animal restraint techniques.
Monitor critical care animals (i.e., place IVs, monitor fluids, etc.).
Perform animal follow-up observations or new findings as required.
Monitor animal health, visually, and by following detailed schedules.
Generate animal treatment records and perform, track and schedule follow-ups.
Maintain appropriate medical records for each animal in accordance with study and regulatory requirements. Assist in maintaining accurate record keeping procedures for the veterinary department.
Maintain and follow complex procedures to ensure appropriate animal health and treatment.
Assist in providing leadership, animal health training, and guidance to other laboratory personnel.
Assist in keeping inventory and stocking the vet rooms (i.e., drugs and supplies). Assist in organizing and maintaining the vet exam rooms.
May be responsible for tissue sampling, routine animal manipulations and administration of fluids or other treatments as required.
May perform routine technical and husbandry functions (general housekeeping) on studies and must adhere to safety procedures.
Assist in surgery and peri-surgery care, e.g. provide and monitor anesthesia, prepare surgical packs, administer supportive therapy.
Perform all other related duties as assigned.

The pay for this position is between $26.00 and $28.00 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
Education: Graduate of a collegiate veterinary technology program accredited by the American Veterinary Medical Association Committee on Veterinary Technician Education and Training Activities or equivalent program in veterinary technology.
Experience: 0-2 years related experience working with animals in a pre-clinical laboratory or clinical setting; experience working in a CRO with multi-species preferred
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above if the individual is credentialed as a Certified Veterinary Technician·.
Certification/Licensure: LVT license or CVT/RVT certification preferred. Uncertified candidates will be required to receive certification within 12-18 months or show that certification has been substantially completed. AALAS certification desired.
Other: Demonstrate understanding of Standard Operating Procedures. Excellent organizational, time management and recordkeeping skills. Basic word processing skills required. Excellent communication skills both written and verbal. Must be proficient in routine veterinary technical and husbandry techniques

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animalier contrôle de production - F/H - CDI week-end (Chatillon sur Chalaronne, 01, FR, 01400)

Le site de Chatillon sur Chalaronne est un établissement pharmaceutique pour le contrôle qualité (tests biologiques) et soumis aux Bonnes Pratiques de Fabrication (BPF) et aux current Good manufacturing Practice (cGMP).

Nous recherchons un Animalier contrôle de production F/H en CDI week-end et jours fériés pour un contrat de 5 heures par semaines à raison de 5h les dimanches matins et jours fériés, pour notre site de Châtillon sur Chalaronne (01400).

Au sein d’une unité de production, vous serez chargé(e) des tâches suivantes :

Missions principales

Réception des animaux

Vérification des animaux à l’arrivée
Installation des animaux dans les cages
Etiquetage des cages, suivi journalier des mouvements de cages et de leur nombre

Entretien et soins des animaux

Opérations de change des litières et nettoyage des cages, distribution de l’alimentation et de la boisson
Observation des animaux et vérification de l’état clinique
Préparation des commandes pour les clients

Entretien du matériel et des locaux

Désinfection, stérilisation du matériel et des produits
Nettoyage des locaux

Profil recherché

Vous êtes étudiant dans un domaine scientifique (biologie, pharmacie, vétérinaire, etc.), vous souhaitez acquérir une expérience dans une entreprise soutenant le développement de médicaments.
Vous êtes disponible tous les dimanches et jours fériés
Vous êtes rigoureux, de confiance et aimez travailler au contact des animaux.

Modalités contractuelles

Nous vous proposons un CDI de 5 heures par semaine : 5h le dimanche de 8h00 à 13h ainsi que les jours fériés.
Prime de transport, 13e et 14e mois, mutuelle et prévoyance, CE
Véhicule indispensable, site non accessible en transport en commun.

About RightSource (Biologics Testing)

For more information, please visit www.criver.com.

Learning and Process Enablement Lead (Wilmington, MA, US, 01887)

Job Summary

The Learning and Process Enablement Lead plays a critical operational role in ensuring CRL’s talent and learning processes run efficiently, consistently, and at scale. This role leads the execution engine that enables enterprise programs, including leadership development offerings, talent processes (performance, succession, engagement, careers/skills), assessment programs, learning delivery, digital roadmap and operational coordination.

This position manages a team of mid-career professionals (A2–A3) who coordinate and deliver enterprise programs, administer tools and assessments, support learning logistics, track completions, maintain reporting, and ensure communications and materials flow appropriately across GTM&D. The role partners closely with Talent Partners (strategic process owners), Talent Technology and Digital solutions leaders, Learning & Development program designers and owners and Well-being/Belonging leads to operationalize program and process strategy with speed, accuracy, and quality.

ESSENTIAL DUTIES AND RESPONSIBILITIES

Translate talent and learning process strategy into clear, repeatable operational workflows across the enterprise.
Lead learning delivery execution, including session setup, facilitator coordination, registration management, roster tracking, and course maintenance.
Manage assessment program operations (e.g., 360 assessments, team diagnostics). Support CVP in creating alignment with multiple stakeholders across many levels including HR executives, business executives, TM team, HRT teams, IT teams and others
Ensure quality, consistency, and timely delivery of all GTM&D processes and programs and coordinate enterprise talent processes such as performance cycles, OTR preparation, engagement administration, and career framework rollout.
Supervise A2–A3 staff providing learning operations, talent coordination, reporting, and administrative support.
Oversee communications, templates, calendars, and readiness materials.
Support Talent Partners by providing operational backbone for process execution.
Collaborate with Digital Solutions to ensure system configuration and workflows meet operational needs.
Partner with People Analytics on dashboards, metrics, and outcome reporting.
Identify opportunities to simplify, standardize, automate, and scale operational processes.

Job Qualifications

7+ years experience in L&D operations, HR program management, or talent operations.
Experience coordinating learning and talent management programs at scale.
Strong project management and organizational skills.
Demonstrated ability to lead mid-level professionals.
Experience collaborating across HR functions and COEs.
Strong communication and stakeholder management skills.
Ability to work in a fast paced environment.
Experience with SuccessFactors, Eightfold, and LMS administration preferred.
HR or project management certifications preferred.

Compensation Data

The pay rate for this role is $139,018 - $185,357 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Senior Business Development Executive - Cell Solutions (New England territory) (Wilmington, MA, US, 01887)

For over 40 years, Charles River Cell Solutions has worked to making a positive impact on the world by providing the highest quality cellular material and services to biotech and pharmaceutical companies and research organizations that are performing innovative research and developing novel cell-based therapies.

We recognize that our success depends on the vision and passion of our employees; that is why we are devoted to making Cell Solutions a rewarding and valuable place to work. We believe in making a difference, and at Cell Solutions, you will make a difference every day.

Job Summary

The Senior Business Development Executive is primary responsibility is to develop new business relationships and expand existing relationships by analyzing account potential; initiating, developing, and closing sales that drive profitable revenue growth. The Business Development Executive is directly responsible for achieving or exceeding quarterly and annual area sales targets and gross profit growth within an assigned geographic territory and various market segments such as Cell and Gene Therapy, Pharmaceutical, Biotechnology, Regenerative Medicine, Vaccine, and Academic R&D.

This position is remote and will work from a home office. Must live in the New England area and commutible within the territory.

Travel is expected to be 50% of the time.

Essential Responsibilities

•   Demonstrate technical, negotiation, and selling skills.
•   Work with management to develop, prepare, and implement a comprehensive territory business plan to identify new target accounts and target opportunities within an assigned geographic area to achieve quarterly and annual revenue targets.
•   Develop and maintain short- and long-term sales pipeline to consistently generate revenue.
•   Build team relationships with other Sales and Operational staff to maximize sales revenue and territory pipeline.
•   Serve as the voice of the customers in their territory by collecting and communicating VOC to Marketing to improve customer experience and anticipate market changes to adapt and respond to new product and service needs.
•   Enhance job knowledge by participating in local educational opportunities, reading professional publications, maintaining personal networks, and participating in professional organizations.
•   Work with management to prepare and provide accurate territory forecasts throughout the year to track achievements versus goals.
•   Comfortable working with ambiguity in a dynamic and changing environment.
•   Assist with updating and maintaining applicable databases (e.g., SalesForce.com)
•   Assist with executing other daily tasks or special projects, as assigned.
•   Independently travel to meet with current and prospective customers, attend vendor shows and seminars, and sales meetings. In person travel should achieve the goal of increasing revenue and building territory pipeline via prospecting, increasing brand awareness and building relationships and strategic partnerships with end users of the product portfolio.

Job Qualifications

To perform this job successfully, an individual must be able to perform each essential responsibility satisfactorily using the skills and abilities outlined in this job description. The requirements listed below are representative of the knowledge, skills, and abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
•   Strong communication and interpersonal skills
•   Organizational skills and attention to detail required
•   Well-developed math and business skills
•   High level of understanding of the market
•   Discretion in handling confidential and sensitive matters
•   Building and maintaining relationships with internal stakeholders and external customers
•   Closing skills
•   Ability to learn and understand highly technical content
•   Positive attitude and resilience
•   Ability to adapt and succeed in an evolving, dynamic environment
•   Independent decision making & problem-solving skills
•   Flexibility to work both autonomously and part of a larger team
•   Presentation skills

Education, Experience, and Licensure

•   Education: Bachelor’s degree (B.A./B.S.) or equivalent in a scientific, business or marketing related discipline; master’s degree preferred and/or Ph.D. preferred. Certified Sales Professional designation preferred.
•   Experience: 6-9 years previous experience in a similar sales role, preferably in selling to academic, biotechnology, or pharmaceutical researchers and organizations.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Familiar with primary human cells, stem cells, immunology, life science research, drug screen, toxicity test, cell-based assay, hematology, or flow cytometry

Compensation Data

The pay range for this position is $120K - $135K USD + commission + $5,000 sign on bonus. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Charles River Cell Solutions

Charles River Cell Solutions is a global leader and trusted brand in the customization of human-derived biological products and services for biomedical research, drug discovery, and cell and gene therapy development. Cell Solution’s vertically integrated solutions support preclinical research, clinical studies from phases 1 to 3, and commercialization with high-quality RUO and GMP-compliant starting material and apheresis collections.

In January 2020, HemaCare was acquired by Charles River Laboratories, an early-stage contract research organization (CRO). Combined with Charles River’s integrated, early-stage portfolio of discovery, safety assessment, and manufacturing support services, the acquisition creates a unique, comprehensive solution for researchers and cell therapy developers and manufacturers worldwide to help accelerate their critical programs from basic research and proof-of-concept to regulatory approval and commercialization. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs and enhances their productivity and effectiveness to increase speed to market. We work closely with our clients throughout the clinical process to maximize success and drive positive clinical outcomes.

Together, with over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical and biotechnology companies, government agencies, and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

At Cell Solutions, we are passionate about our role in improving the quality of people’s lives. We have proudly supported the development of 100% of the current commercially available FDA-approved immunocellular therapies. Our mission is to provide a best-in-class portfolio of high quality, customizable human cellular material and services to support drug discovery, scientific research, and cell therapy. This resonates from our employees and impacts our customers because we know that every day is an opportunity to advance discoveries and make a difference in someone’s life.

For more information, please visit www.criver.com.

Business Development Director - Biologics (Southeast territory) (Wilmington, MA, US, 01887)

Job Summary

We are seeking an experienced Business Development Director to support our growing Biologics business. This position is based in the Southeast US territory.

Ideal candidates will live in NC, GA, FL.

The following are the minimum requirements related to the Business Development Director position:

• Work closely with both the specialist sales staff and management teams to increase market share of both in-house and outsourced revenue spend at assigned accounts.
• With direction from management, generate account-specific sales strategies to sell all company products and services.
• Work with management to prepare and provide accurate account forecasts for assigned accounts/territories throughout the year to track achievements versus goals.
• Develop and qualify account leads through frequent customer contact and prospecting.
• Gather data on potential customers in their designated geographic region.
• Build relationships with customers to influence the acceptance and use of company products and services.
• Communicate available product and services and inform customers of new products and services in a timely manner.
• Handle initial inquires and qualify all prospective opportunities. Identify the drug development business model at these accounts and effectively communicate the value proposition of the company’s products and services.
• Work closely with the specialist sales staff to ensure that the customer has a cohesive and responsive team throughout the sales process
• Work with management to prepare and implement a comprehensive territory management plan to indicate target opportunities, potential new accounts, expansion of existing accounts and an analysis of competitor accounts.
• Gather data on marketing trends and competitive products and pricing.
• Utilize CRM to capture customer information.
• Complete all required sales documentation in a timely manner.
• Participate in sales meetings and trade shows as required.
• Share customer problems/concerns with all appropriate departments for quality resolution.
• Perform all other related duties as assigned.

Job Qualifications

• Education: Bachelor’s degree (B.A. /B.S.) or equivalent in life sciences, sales or related discipline.

• Experience: Minimum of 10 years of sales experience, preferably in life science industry with a solid scientific background. Also acceptable would be a minimum of 3 years of experience in sales with substantial scientific background (e.g. MS/PhD).

• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Senior, Business Development Executive - DSA (MA territory) (Wilmington, MA, US, 01887)

Job Summary

The Senior, Business Development Executive is responsible for achieving quarterly and annual sales bookings targets in assigned region for DSA (Discovery & Safety Assessment) divisional unit with primary focus on new business capture and growing share within subset of existing client base.

Sales territory is Massachusetts. Must live within the state or be commutable to MA territory.

Position will work remote from home office.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Identify and develop opportunities primarily new business to DSA followed by rapidly progressing them to close awards for earliest possible revenue impacts.
• Focus on share gain within existing client base in assigned territory by effectively communicating the differentiated value of the DSA portfolio.
• Rapidly establish new customer contacts and influence them for share gain potential.
• Collaborate with Client Services & Managers for rapid turnaround times on proposals/agreements, participate in the negotiation process as appropriate and follow through on sales execution.
• Manage all initial inquires and qualify prospective opportunities.
• Effectively utilize CRM (SFDC) to capture customer information to included but not limited to accurate pipelines and effective opportunity management and activity documentation.
• Work closely with the relevant subject-matter-expert to ensure that the customer has a cohesive and responsive experience throughout the buying journey.
• Proficient in knowledge of competitor profiles and is able to develop positioning to influence potential new customers.
• Take a lead Business Development role in relevant conference events and trade shows.
• Effectively communicated customer challenges/concerns with all appropriate departments for quality resolution.
• Prepare and implement a comprehensive territory management plan to indicate target opportunities, potential new accounts, expansion of existing accounts and an analysis of competitor share within existing accounts.
• Complete all sales, commercial and portfolio trainings as required to be fluent in DSA portfolio and ready to present to range of customer personas.
• Perform all other related duties as assigned.

Job Qualifications

• Education: Bachelor’s degree (B.A. /B.S.) or equivalent in life sciences, sales or related discipline.
• Experience: Minimum of 10+ years’ experience, preferably in commercial role(s) within life science industry.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Other: Excellent communication, negotiation, and presentation skills. Proficient in the use of standard office computer applications (word processing, spreadsheets, presentations, e-mail).

Compensation Data

The pay range for this position is $120K - $150K USD annually + commission. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Associate Director Commercial Finance DSA (REMOTE) (Wilmington, MA, US, 01887)

Job Summary

This role will drive business performance by enhancing the effectivity of global DSA Commercial. In turn this will generate sequential revenue growth, margin development and shareholder value.

The role necessitates a deep reach into the organization to deliver meaningful impact that enhances the operation through step change. This role requires leadership, strategic guidance, performance management, team collaboration, financial and management reporting acumen.

You will represent DSA Commercial Finance in regional and global forums. You have experience with running a business and your input is not limited to Finance. You can understand complex business models, implement them, drive change and lead with influence. You are comfortable in “pushing back” and driving unpopular decisions if needed.

Most importantly you are hands on, can deal with complex excel models, create pivots, charts, PowerPoint presentations, mine data in SAP/BI systems and at the same time lift from the detail and provide the “helicopter view”. You are a business partner and understand key developments in both commercial teams and at the operational sites not limited to Finance.

You understand the business just as well as Commercial leadership and partner with Commercial team members on a regular (daily) basis. You are accountable and take ownership in overall success within DSA not limited to finance.

You are comfortable presenting in multiple forums where you are at times not familiar with the audience. You can convey a sense of purpose, urgency and authority and collaboratively lead cross functional groups towards a common goal.

The role directs resources to support the overall execution of the commercial operation including go-to market strategy, action-oriented analysis and client benefiting process effectiveness.
You influence and develop project capabilities essential to the global commercial team.

Key efforts include commercial client processes and analytical tools optimization, reporting and measurement of KPI’s, and technology infrastructure design. Elevating the commercial function to deliver for both internal and external customers whilst providing strategic guidance to support Commercial direction setting.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Enhance Commercial Analytics: Produce new and enhanced meaningful management reporting including long-range forecasting KPI’s for senior management review and action.
• Pricing Models: Develop and evolve pricing insights and strategies to enhance profitability. Lead initiatives to advance novel analytical capabilities and insights.
• Price-volume-mix-analysis: Own revenue and margin analytics, including price-volume-mix-analysis.
• Enhance Data Integrity: Drive one source of truth of data consistency across systems and segmentations to support consistent and accurate reporting (CRM, ERP, BI systems etc).
• Deepen Forecast Insights: Reconciling and explaining client slippage in backlogs on a routine basis to identify client trends and patterns to improve forecast reliability.
• Client Forecast Evolution: Support the weekly, monthly, quarterly rolling forecast, annual plan submissions and sequentially enhance team understanding of client behavior.
• Commercial Business Partnering: Support analyzing Opportunities, Proposals and Bookings in the CRM with the Commercial function to generate sales focus.
• Enhance Commercial Analytics: Produce new and enhanced meaningful management reporting including long-range forecasting KPI’s for senior management review and action.
• Enhance Data Integrity: Drive one source of truth of data consistency across systems and segmentations to support consistent and accurate reporting (CRM, ERP, BI systems etc).
• Executive Reporting: Support forecast variance analysis, commentary, Business Review bridges.
• Strategic Planning: Deliver the annual long-range financial plan and strat planning cycle with executive leadership, helping advance the commercial direction and client strategy.

Job Qualifications

• Experience: Seven plus years of similar related experience in an international environment, background could be commercial sales or finance.
• FP&A/commercial finance exposure and P&L ownership.
• Education: Bachelor’s degree (BA/BS) in business or related discipline preferred.
• Qualified Accountant beneficial – CPA/ACCA/ICAS/ICAEW/CIMA or equivalent
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Skills: Demonstrated proficiency managing analytically rigorous initiatives. Advanced Excel and PowerPoint presentation abilities required.
• Tangible understanding and experience of ERP, Data Warehouse and Business Intelligence systems incl. financial reporting, PowerBI and CRM systems.
• Accustomed to communicating and reporting to senior management.
• Supervisory and/or people management experience advantageous.

COMMENTS:
- This position may require occasional domestic and/or international travel (e.g. to CRL or client venues).
- Position will work remote, from home office located in North America.

Compensation Data

The pay range for this position is $120K - 140K USD annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Veterinary Technician (Rodent) (Wilmington, MA, US, 01887)

Job Summary

We are seeking a Veterinary Technician I for our GEMS: Breed Department located in Wilmington, MA. The Veterinary Technician will assist veterinary staff in the monitoring, documentation and triage of all laboratory animal health cases. May also perform technical in-vivo procedures.

Great benefits including medical/dental/vision/401K/paid time off and much more.
Onsite gym.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Assist veterinary staff in the monitoring, documentation and triage of all animal health cases noted by animal husbandry and/or veterinary staff.
Perform routine veterinary technical skills including:
- Administration of various therapeutic measures by IV, IM, SQ, topical, oral routes, etc.
- Nail//teeth clipping/trimming.
- Venipuncture techniques.
- Vaginal, anal or oral swabs.
- Proficient animal restraint
- Monitor critical care animals
- Perform euthanasia
Perform animal follow-up observations or new findings as required.
Monitor animal health, visually, and by following detailed schedules.
Generate animal treatment records and perform, track and schedule follow-ups.
Maintain appropriate medical records for each animal in accordance with study and regulatory requirements.
Assist in maintaining accurate record keeping procedures for the veterinary department.
Maintain and follow complex procedures to ensure appropriate animal health and treatment.
Assist in providing leadership, animal health training, and guidance to other personnel.
Assist in keeping inventory and stocking the vet rooms (i.e., drugs and supplies).
Assist in organizing and maintaining the vet exam rooms.
May be responsible for tissue sampling, routine animal manipulations and administration of fluids or other treatments as required.
May perform routine technical and husbandry functions (general housekeeping) on studies and must adhere to safety procedures.
Assist in surgery and peri-surgery care, e.g. provide and monitor anesthesia, prepare surgical packs, administer supportive therapy.
Perform all other related duties as assigned.

Minimum Qualifications:

To qualify for this role, candidates must have one of the following combinations of educations/experience:

Bachelor’s Degree (B.A./B.S.) in a Vet Tech accredited program and/or a minimum 1 year of related experience.
Associate’s Degree (A.A./A.S.) in a Vet Tech accredited program and/or a minimum of 1-2 years of related experience.

In addition:

Graduate of a collegiate veterinary technology program accredited by the American Veterinary Medical Association Committee on Veterinary Technician Education and Training Activities or equivalent program in veterinary technology preferred.
AALAS Certification at the ALAT or higher level preferred; ALAT certification is required within 18-24 months
Competent with using a tablet computer for data entry and communication (emails, IM’s, etc)
The ability to develop knowledge of, respect for, and skills to engage with those of other cultures or backgrounds.
The ability to communicate clearly and effectively.
Must possess a high level of initiative and ability to work with minimal supervision
Proficient in computers (IE: MS Office Suite)
Competent with using a tablet computer for data entry and communication (emails, IM’s, etc)

The hourly pay rate for this position is $22.50.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Associate (GEMS) - EG (Wilmington, MA, US, 01887)

Job Summary

As an Animal Care Associate for our GEMS Breed Group in Wilmington, MA. The GEMS Animal Care Associate will learn how and continue to maintain and monitor the health, production, and physical environment of client or Charles River Laboratories (CRL) animals housed at CRL facilities. These environments may include isolators or individual ventilated cages (IVC).

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform entry-level husbandry tasks, including supplying food, bedding, water and environmental enrichment.
Maintain rat and mouse colonies, including setting up matings, weaning and sexing of offspring, genetic sampling of animals.
Handle rodents (mice and rats), including restraining of animals for collection of fecal pellets, ear/tail sampling as well as tagging animals for identification.
Observe animals for any abnormalities or common health issues.
Identify and select specific animals for customer shipments, genotyping, health monitoring, matings, transfers or other various tasks as needed.
Learn, understand, and comply with all Standard Operating Procedures (SOPs) with direct supervision and instruction for most processes/tasks.
Learn and strictly follow all animal welfare standards and biosecurity procedures necessary to maintain isolator integrity and animal health status, including the proper sterilization and entry of supplies/animals into isolators.
Be detailed-oriented and enter accurate data entry into Internet Colony Management (ICM).
Ensure compliance with all local, state and federal laws governing the use of research animals.
Ability to prioritize and execute daily tasks with guidance from supervisor(s).
Perform general housekeeping and adhere to EHS, safety, and ergonomic procedures.
General computer skills and ability to quickly learn required computer programs, databases and other applications (i.e. ICM and Microsoft Office)
Be able to learn to identify issues and communicate to management and learn the importance of our CRL DNA and core values.
Perform all other related duties as assigned.

Role Specific Information:

Location: Wilmington, MA
Schedule: Monday - Friday - 1st shift, no weekends required

MINIMUM QUALIFICATIONS

Experience: Entry-level, no previous experience required.
Sufficient computer knowledge to use a tablet computer and communicate using Microsoft Applications.
The ability to develop knowledge of, respect for, and skills to engage with those of other cultures or backgrounds.
The ability to communicate clearly and effectively.

PREFERRED QUALIFICATIONS

Certification/Licensure: AALAS certification at the ALAT or above.

The hourly pay rate for this position is $18.00.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technologist - EG (Wilmington, MA, US, 01887)

Job Summary

We are seeking an Animal Care Technologist for our GEMS-Breed Department located in Wilmington, MA.

The Technologist performs specialized production duties to maintain and monitor the health, production and physical environment of animals within isolators, micro-isolator cages or barrier rooms. Provides training to departmental staff on all technical skills and Standard Operating Procedures (SOPs).

This is temporary opportunity with the potential to become a regular Charles River Labs employee.

Some benefits include:

Paid sick time
401K participation with a company match
Paid volunteer time off
Use of our onsite gym

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Has substantial understanding and knowledge to perform husbandry tasks, including supplying food, bedding, water and environmental enrichment.
Proficient at maintaining rat and mouse colonies, including setting up matings, weaning and sexing of offspring, genetic sampling of animals, processing samples and other technical tasks as required.
Proficient at handling rodents (mice and rats), including restraining of animals for collection of fecal pellets, ear/tail sampling as well as tagging animals for identification.
Has substantial understanding and knowledge to observe animals for any abnormalities or common health issues.
Has substantial understanding and knowledge to identify and select specific animals for customer shipments, genotyping, health monitoring, matings, transfers or other various tasks as needed.
Learn, understand, and comply with all Standard Operating Procedures (SOPs). Able to complete new processes/tasks with minimal instruction.
Strictly follow all animal welfare standards and biosecurity procedures necessary to maintain isolator integrity and animal health status, including the proper sterilization and entry of supplies/animals into isolators.
Workload contains complex projects and requires judgement in resolving issues and/or in making recommendations. Be detailed-oriented and enter accurate data entry into Internet Colony Management (ICM).
Ensure compliance with all local, state and federal laws governing the use of research animals.
Ability to collaborate with others to train and mentor on knowledge and skills learned.
Ability to self-organize, plan and execute daily tasks.
Perform general housekeeping and adhere to EHS, safety, and ergonomic procedures.
Has substantial understanding of using general computer skills and ability to quickly learn and master required computer programs, databases and other applications (i.e. ICM and Microsoft Office)
Engage in studies, special projects, efficiency improvements, engagement opportunities, etc.
Identify issues and recommend potential solutions to management.
Able to effectively apply and incorporate CRL DNA into day-to-day work.
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

To qualify for this role, candidates must have one of the following combinations of educations/experience:

Bachelor’s Degree (B.A./B.S.) plus a minimum of 0-1 years of related experience.
Associate’s Degree (A.A./A.S.) plus a minimum of 1-2 years of related experience.
High School diploma or GED plus a minimum of 2-4 years related experience.

In addition:

Competent with using a tablet computer for data entry and communication (emails, IM’s, etc)
The ability to develop knowledge of, respect for, and skills to engage with those of other cultures or backgrounds.
The ability to communicate clearly and effectively.
Must possess a high level of initiative and ability to work with minimal supervision
Proficient in computers (IE: MS Office Suite)
Competent with using a tablet computer for data entry and communication (emails, IM’s, etc)

PREFERRED QUALIFICATIONS

AALAS certification at the ALATG.

The hourly pay rate for this position is $21.25.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Sr. Manager, Digital Media Channels (REMOTE) (Wilmington, MA, US, 01887)

Job Summary

The Sr. Manager, Digital Media Channels plays a critical role in both hands-on digital media execution and team capability development, serving as a subject matter expert across multiple paid digital channels. This role drives advanced campaign execution, optimization, and analysis across paid search, paid social, and programmatic display, with deep, current platform expertise in LinkedIn, Google, and Meta.

As a senior individual contributor and mentor, the Sr. Manager works closely with the Director, Digital Media Channels to bring global paid media strategy to life while also supporting, and training manager-level team members to achieve proficiency across multiple platforms. The role requires strong analytical skills, operational rigor, and the ability to balance hands-on execution with cross-functional collaboration in a global, matrixed environment.

Strategy Support & Advanced Execution
• Partner with the Director, Digital Media Channels to execute global paid media strategies across regions, businesses, and customer segments
• Own execution/configuration and SME-level analysis of complex, high-impact digital campaigns ensuring on-time, on-budget delivery
• Serve as a hands-on expert in LinkedIn Campaign Manager, Google Ads, and Meta Ads Manager, GoTo Meeting and other digital media platforms applying best practices and testing new platform capabilities
• Translate business objectives into channel-level strategies and execution plans that drive funnel performance and measurable outcomes

Campaign Optimization, Analytics & Reporting
• Lead advanced optimization efforts using dashboards, pacing tools, and platform insights to continuously improve performance
• Analyze large and complex data sets across channels to identify trends, risks, and opportunities
• Partner with digital strategy team members to review performance, validate attribution, and provide actionable insights and recommendations
• Ensure consistent use and refinement of reporting standards, dashboards, and documentation

Team Enablement & Coaching
• Act as a player–coach, mentoring manager-level employees to build proficiency across multiple digital media platforms
• Provide hands-on training, troubleshooting support, and platform best practices to elevate team capability and consistency
• Share case studies, learnings, and optimization frameworks to improve overall team performance
• Support onboarding and skill development through documentation, SOPs, and working sessions

Collaboration & Communication
• Collaborate closely with Global Strategic Marketing’s business unit, regional, and segment marketing teams
• Engage with stakeholders to understand business needs, align on priorities, and communicate performance and insights
• Maintain tight timelines and manage multiple simultaneous projects, proactively identifying risks and dependencies
• Participate in meetings with global team members, including occasional off-hours collaboration

Innovation & Continuous Improvement
• Stay current with platform changes, emerging trends, and industry best practices
• Identify opportunities to drive efficiency through automation, standardization, and scalable solutions
• Actively contribute ideas to improve processes, workflows, and campaign effectiveness

Job Qualifications

Experience
• Bachelor’s degree in marketing, digital marketing, business, or a related field. MBA a plus
• 6–8+ years of experience in B2B customer-focused digital marketing with life science, biotech, or pharma experience highly preferred
• Hands-on expertise across multiple paid media channels, with deep experience in at least two (paid social, paid search, programmatic display, webinar platforms (On24, GoTo))
• Current, hands-on experience managing campaigns in LinkedIn, Google, and Meta platforms
• Experience supporting revenue-, lead-, or demand-generation programs at scale
• Experience mentoring or training team members (formal people management not required)

Knowledge, Skills & Abilities
• Expert-level understanding of digital media campaign execution, optimization, and performance measurement
• Strong analytical and problem-solving skills, with the ability to synthesize insights from multiple data sources
• Advanced Excel skills and comfort managing campaigns at scale, including bulk uploads
• Experience with analytics and reporting tools (e.g., PowerBI, Adobe Analytics, Google Analytics)
• Experience with marketing automation platforms such as Pardot or Marketo is highly desired
• Exceptional communication skills, with the ability to translate data into clear recommendations
• Strong organizational, planning, and prioritization skills in a fast-paced environment
• Collaborative, proactive, and solution-oriented mindset

Compensation Data

The pay range for this position is $80K - $130K USD annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Senior Marketing Specialist - Research Models and Services (REMOTE) (Wilmington, MA, US, 01887)

Job Summary

The Senior Marketing Specialist will play an integral role in the execution of digital and outbound marketing programs to drive awareness and demand for the Research Models and Services business. This position is responsible for collaborating across several departments to gain insights in order to develop and execute marketing campaigns that promote and drive demand for our products.

Key Responsibilities

Strategic Campaign & Portfolio Support
• Develop and execute digital marketing campaigns aligned to business goals for the RMS (GEMS, RADS, IS) portfolio to drive product/service awareness, promotions, education, and sales, and provide feedback on ROI.
• Develop and execute targeted outbound lead generation programs to generate prospects and marketing qualified leads, and manage response flow/routing.
• Lead engagement with first-touch clients through the implementation of automated cadences, engagement studios, autoresponders.
• Identify opportunities and execute campaigns to increase pipeline conversion rates and velocity from prospect to MQL to SQL and opportunity through persona-based nurture campaigns.
• Develop webinar, in-person event, field/account-based marketing (ABM) activities, and online seminar marketing strategies and promotional materials across varied channels.
• Utilize data mining and lead generation software tools, publication reports, lead lists, LinkedIn, etc. to find and contact prospective new targets.
• Support monitoring of inbound Leads and routing to BDE team as required; includes leads generated from the Charles River website, events, Maestro, and other platforms (Scientist.com, Science Exchange).
• Manage channel content for organic and paid social and other paid media.
• Monitor, optimize, and develop web content to advance GEO/SEO visibility and ranking (i.e. product and service landing pages, collateral pages, thought leadership content)
• Independently and through collaboration with internal teams, research target audiences and industry competitors to identify positioning/differentiation opportunities, cross-reference keywords, and identify content/concepts that will inform strategic content decisions.
• Work within the CRM database to maintain updates to lead and sales stages, marketing statuses, and customer intelligence data.
• Assist with special projects and perform other duties as assigned.
• Maintain a working knowledge of all company product lines with more in-depth knowledge of business segment that is being supported.
• Ensure a competent and professional image to the customer and an accurate portrayal of business strategies both on the phone, email and at customer events.

Measurement & Reporting
• Utilize SFDC, Pardot and our marketing KPI Dashboard to monitor performance, evaluate effectiveness, quantify ROI and optimize for future projects.
• Where needed monitor datamining platforms (eg. Scileads) and set up alerts for key target persona companies and execute initial outreach as required. Triage responses to the sales team.
• Compile and present campaign results and insights to managers, marketing team, and stakeholders.

Cross-Functional Collaboration
• Collaborate with Product Management to research and develop Lead gen projects/campaigns for target products and client segments.
• Collaborate and assist with event specialists on virtual and in-person event logistics and management (webinars, seminars, workshops, chapter events, conferences, etc.).
• Collaborate across marketing, sales, and subject matter experts to engage and help develop persona-based and account-based marketing campaigns in the various customer segments to nurture new and existing clients. Such projects could include mail merge campaigns, creation of personalized marketing materials and the organization and running of bespoke client webinars.
• Maintain a working knowledge of all RMS product lines with more in-depth knowledge of the business segment that is being supported to be an educator to others.

Job Qualifications

To perform this job successfully, an individual must be able to perform each essential responsibility satisfactorily using the skills and abilities outlined in this job description. The requirements listed below are representative of the knowledge, skills, and abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
• Proven experience as a marketing specialist or a similar role
• Exceptional written and verbal communication, with deep channel specific writing expertise and a strong attention to detail
• Have a strong eye for copy that converts
• Commercial awareness partnered with a creative mind
• Strategic thinking and excellent analytical skills
• Excellent organizational, time management, and problem-solving skills
• Ability to work well under deadlines and pressure
• Ability to adapt to a fast-paced and ever-changing digital communication landscape
• Discretion in handling confidential and sensitive matters

Education, Experience, and Licensure
• Bachelor’s degree (B.A /B.S.) or equivalent in biological sciences, marketing, business, or related discipline.
• 3-5 years related experience in marketing or communications. An equivalent combination of education and experience may be accepted as a satisfactory substitute.
• Previous experience within a life science environment (e.g., biotech, pharmaceutical, preclinical drug development, CRO, or lab) required.

Technical Skills
• Knowledge in drug discovery and/or research animal model industry
• Strong knowledge of digital marketing channels, best practices, and tactics, including SEO/GEO, paid media, video, and social media.
• Experience in market research and voice of customer methods.
• Strong understanding of customer journeys and how to plan for and analyze success metrics across the marketing channels and stages of that journey.
• Demonstrable experience in marketing data analytics and tools.
• Strong Excel skills
• Solid computer skills, including MS Office, marketing software (Adobe Creative Suite, CRM)
• Ability to quickly learn new software and applications
• Strong Salesforce experience
• Canva experience a plus

Language Skills
Must have a good command of the English language and be able to communicate clearly and concisely in both written and verbal format.

Compensation Data

The pay range for this position is $75,000 - $95,000K USD annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Global Segment Marketing Manager - Pharma & Biotech (REMOTE) (Wilmington, MA, US, 01887)

Job Summary

The Segment Marketing Manager – Pharma & Biotech develops and executes enterprise-wide segment-specific marketing strategies that deepen Charles River Laboratories’ engagement with biopharma innovators, drive pipeline growth, and strengthen our leadership along the drug development continuum. This role owns segment-specific growth initiatives, customer insights translation, go‑to‑market (GTM) programs, and sales enablement for the Pharma & Biotech segment, ensuring alignment across functional partners and regions.

Key Responsibilities:

Segment Strategy & Customer Insights

Conduct market research, segment analysis, and competitive assessments; translate insights into actionable segment‑aligned strategies.
Support development of customer segmentation strategies and segment prioritization.

Value Proposition & Messaging

Develop segment-specific, enterprise-wide value propositions, workflows and messaging frameworks that reflect customer challenges and scientific/business drivers.
Ensure alignment with Charles River’s enterprise portfolio narrative and BU-led product/service narratives.

Integrated Campaigns, GTM Execution & Strategic Events

Build and execute integrated segment marketing campaigns across digital, ABM, events, media, and sales channels.
Translate segment strategy into tactical GTM plans and regional activation.
Partner with Events Marketing to shape and support strategic events that elevate Charles River’s leadership with Pharma & Biotech audiences.

Cross-Functional Leadership & Collaboration

Partner closely with BU Strategic Marketing, Regional Marketing, Digital Marketing, Events Marketing, and Sales Leadership.
Work closely with Global Key Account Managers (GKAMs) to align on segment insights, value propositions, and account‑specific messaging.
Ensure the segment’s voice is embedded across content, campaigns, events, KOL and customer engagement programs.

Sales Enablement

Develop tools such as segment playbooks, customer profiles, competitive briefs, and capability decks et al.

Measurement, Reporting & Optimization

Track performance referencing target KPIs such as pipeline contribution, lead quality, conversion rates, engagement metrics, and ROI.
Deliver insights and recommendations to refine strategy and optimize marketing investments

Job Qualifications

Required

Bachelor’s degree in life sciences, business, marketing, or related field.
5–8 years of experience in life sciences, biopharma, CRO/CDMO, or biotechs.
Experience in segment marketing, demand generation, or strategic marketing.
Strong analytical capabilities and comfortable working with data, segment insights, and VOC.
Demonstrated success by executing integrated campaigns and GTM programs.
Ability to collaborate effectively in a matrixed organization.

Preferred

MBA or advanced scientific degree.
Prior commercial (sales/marketing) experience supporting enterprise-scale portfolios and global customer segments.
Familiarity with biopharma R&D, CMC, regulatory, and QC workflows.
Knowledge of segmentation, value proposition development, CRM/marketing automation, and digital tools.

Core Competencies

Strategic execution
Customer-centric mindset
Cross-functional collaboration with commercial and scientific stakeholders
Analytical rigor
Communication excellence

Compensation Data

The pay range for this position is $95,000 - $120,000K USD annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Product Manager (Charleston, SC, US, 29425)

Job Summary

We are seeking an experienced Product Manager for our Microbial business unit. This position is remote.

This individual will lead the development, commercialization, and launch of instrument control and analytics software across our Microbial portfolio.
This responsibility includes extensive customer interactions for across the product lifecycle
This individual needs to have a high level of initiative and be comfortable working in a fast paced environment, taking decisions independently and bringing clarity
They will collaborate with cross functional teams including R&D, marketing, sales, and customer care as well as external partners
This position will be responsible for developing and driving the successful strategy, revenue and profitability of a specific product line from ideation to end-of-life.
This role has deep knowledge of the pharmaceutical and personal care products quality control testing markets including the regulatory and competitive landscape.
This role requires strategic thinking and excellent tactical execution with strong project management skills.

Job Qualifications

Education: Bachelor’s degree (B.A. /B.S.) or equivalent in life sciences or related discipline. MBA preferred.

Experience: 3-5 years or more experience in pharmaceutical or personal care products QC testing and/orexperience with services, analytical instrumentation, reagents and software.

Other: Exceptional presentation skills required.

Must be able to influence and manage resources/staff without direct reporting relationships.
Ability to multi-task, excellent written and verbal communication skills, organizational skills, and attention to detail required.
Must possess analytical thinking and problem solving skills and be able to prioritize and re-evaluate priorities as situations change.
Working knowledge of computer software (MS Word, MS Excel and databases) preferred.
Knowledge and experience of a pharmaceutical QC laboratory setting, including regulatory awareness of e.g. G&P, CSV, data integrity)
Knowledge and experience of software development or implementation or evaluation
Knowledge and experience of product management

The pay range for this position is $104k-110k. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

For more information, please visit www.criver.com.

Scientist I (Charleston, SC, US, 29407)

Job Summary

The Scientist I will contribute to analytical characterization of protein-based assay development by performing routine and complex laboratory analyses. This role supports method development, troubleshooting activities and execution of analytical testing to ensure high-quality data in support of research, development, and manufacturing programs. The ideal candidate has hands-on experience with protein chemistry techniques and enzymatic assays and thrives in a fast-paced, collaborative laboratory environment.

Key Responsibilities

• Perform protein characterization using techniques such as SDS PAGE, Western blotting, HPLC/UPLC (SEC, IEX, RP), capillary electrophoresis, mass spectrometry, and spectroscopy-based assays.
• Conduct sample preparation, data collection, analysis, and interpretation with high attention to detail.
• Support development, optimization, and qualification of analytical methods for proteins and endotoxins.
• Maintain accurate laboratory notebooks, electronic records, and documentation in compliance with internal quality standards and regulatory expectations.
• Collaborate with cross-functional teams to deliver high quality analytical results within project timelines.
• Communicate analytical results and technical insights to project teams and stakeholders.
• Troubleshoot analytical assays and laboratory instrumentation as needed.
• Assist in maintaining lab readiness, including instrument calibration, inventory management, and compliance with safety protocols.
• Maintain a high level of professional expertise by staying current with scientific and industry literature, technologies, and products.

Job Qualifications

Education: Bachelor's degree in a relevant field. Master's degree in Biochemistry, Chemistry, Molecular Biology, or related discipline preferred.
Experience: 3–5 years of hands-on protein analysis experience with a Bachelor's degree. 1+ years industry experience with a Master's degree. Experience working under GxP requirements a plus.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None.
Other: Strong organizational and documentation abilities, excellent communication and teamwork skills, ability to work independently in a dynamic environment while managing multiple tasks, highly collaborative and self-motivated teammate, ability to work productively under deadlines, high attention to detail, willingness to learn.

The pay range for this position is $70,000 - $80,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

For more information, please visit www.criver.com.

Product Manager (Charleston, SC, US, 29407)

Job Summary

We are seeking an experienced Product Manager for our Microbial business unit. This position is remote.
This position will be responsible for developing and driving the successful strategy, revenue and profitability of aspecific product line from ideation to end-of-life. This role has deep knowledge of the pharmaceutical and personalcare products quality control testing markets including the regulatory and competitive landscape. This rolerequires strategic thinking and excellent tactical execution with strong project management skills. Collaboratesacross the organization working closely with Sales, R&D, Operations and the Strategic Marketing teams. Prior Product/Project Management and Customer/Sales experience required.

Job Qualifications

The following are the minimum qualifications related to the Product Manager:

Education: Bachelor’s degree (B.A. /B.S.) or equivalent in life sciences or related discipline. MBA preferred.

Experience: 3-5 years or more experience in pharmaceutical or personal care products QC testing and/orexperience with services, analytical instrumentation, reagents and software.
Other: Exceptional presentation skills required. Must be able to influence and manage resources/staff withoutdirect reporting relationships. Ability to multi-task, excellent written and verbal communication skills,organizational skills, and attention to detail required. Must possess analytical thinking and problem solving skillsand be able to prioritize and re-evaluate priorities as situations change. Working knowledge of computersoftware (MS Word, MS Excel and databases) preferred.

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

Care - We show we care when we respect each other, our animals and the communities where we work and live, when we create a positive healthy workplace, when we are mindful of our compliance standards, and when we choose to do the right thing.

Collaborate -We collaborate when we partner with each other and promote teamwork, when we communicate clearly and effectively across the hall or around the globe, and when we welcome all forms of diversity and encourage inclusiveness.

Own - We act like owners when we hold ourselves accountable for our actions, when we respond to internal and external client needs with speed and accuracy, when we set and achieve meaningful goals, and when we strive towards continuous improvement.

Compensation Data

The pay range for this position is $104,000- $122,800. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Summer Associate (Charleston, SC, US, 29407)

Job Summary

The Summer Associate will support manufacturing operations through the following structured, value‑adding activities:

Production & Operational Support
Assist production teams on the shop floor with daily operational needs.
Collect and analyze production data (throughput, downtime, scrap, yield).
Support tracking/development of key performance indicators (KPIs) and production metrics.
Help identify inefficiencies and opportunities for process improvement.

Continuous Improvement & Lean Activities
Participate in Lean Manufacturing and continuous improvement initiatives.
Assist with time studies, process mapping, and value stream mapping.
Support 5S audits and standardization efforts.
Document improvement opportunities and support implementation tracking.

Quality & Engineering Support
Assist engineering and quality teams with data gathering and analysis.
Support root cause investigations for production or quality issues.
Participate in corrective and preventive action follow-ups.
Gain exposure to materials-related manufacturing considerations and controls.

Job Qualifications

Minimum Qualifications:

Education: High School Diploma or equivalent

Other: Effective communication and listening skills in a teamwork environment. Demonstrated ability to work on multiple projects with a strong attention to detail. Excellent organization skills

The pay for this position is $20.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

For more information, please visit www.criver.com.

Production Supervisor 1st Shift (Charleston, SC, US, 29407)

Job Summary

We are seeking a Production Supervisor for our Microbial Solution site in Charleston, SC. This is a 1st shift supervisory role for our PTS production team.

The primary functions of the Production Supervisor role is to provide direct daily supervision and review work of assigned departmental employees to ensure accuracy and to ensure adherence to pertinent departmental policies, practices, SOPs, safety procedures and biosafety protocols.

Assist in the coordination and scheduling of activities of the department through hands-on technical support, delegation of responsibility and/or authority to departmental subordinates.
Interview and select qualified non-exempt personnel. Recommend personnel actions, including hiring, promotions and raises; Partner with Human Resources and departmental management to assist in employee relations.
Identify training and development needs of direct reports; Assist in the development, implementation and delivery of departmental training programs; ensure that direct reports receive departmental orientation and necessary on-the-job training.
Monitor performance of direct reports. Provide regular coaching and counseling. Assist in preparation and delivery of salary and performance reviews of direct reports.
Ensure optimum performance of group function; Recommend and implement techniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.
Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor’s degree (B.A./B.S.) or equivalent in life sciences or related discipline.
Experience: 4-6 years related experience.
Certification/Licensure:
Other: Effective communication and interpersonal skills required. Demonstrated computer skills (data input, word processing) required.

Compensation Data

The pay range for this position is $75,000 to $85,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Senior Technologist / Team Lead 1 (Raleigh, NC, US, 27610)

JOB SUMMARY

As a Senior Technologist / Team Lead in Raleigh, NC, you will provide daily direction and operational guidance to ensure achievement of departmental goals and communicate progress to supervisor. You will perform specialized production duties to maintain and monitor the health, production and physical environment of animals within isolators, micro-isolator cages or barrier rooms. You will provide training to departmental staff on all technical skills and Standard Operating Procedures (SOPs). You will act as team leader for designated area(s).

ESSENTIAL DUTIES AND RESPONSIBILITIES

Provide daily direction, schedule, prioritize workload and review work of assigned group to ensure accuracy and adherence to pertinent departmental policies, SOPs, safety procedures and biosecurity protocols.
Provide leadership and motivation to departmental personnel.
Assist in ensuring optimum performance of group function. May recommend and implement techniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.
Coordination and scheduling of activities of the assigned group through hands-on technical support and delegation
Act as team leader for designated area, perform specific departmental projects, and coordinate other operations staff as directed.
Coordinate production and shipping activities of assigned group, including SOPs and OORs. Assist in the performance of production and shipping activities as necessary.
Responsible for complying with all SOPs pertaining to specific area. Provide input into the creation and revision of SOPs and assist with the implementation and training of new SOPs.
Perform specialized duties in the following areas: packing and shipping animals to customer; performing value added services; biospecimen orders and introducing supplies.
Perform production duties, ensuring proper breeding procedures and maintaining appropriate levels of assigned specialized rodent breeds, including inbred and outbred strains.
Monitor animal health by observing animal behavior, physical appearance, and physical environment. Identify and report any abnormal findings. Monitor animal health visually and by swabbing.
Monitor performance of team-members and provide daily feedback to supervisor. Assist with follow thru of disciplinary and personnel related concerns.
Assist with training and development of departmental staff on all levels of animal husbandry, production and tasks including feeding, watering and cleaning cages as required.
Assist with training and development of departmental staff on specialized tasks in the following areas; packing and shipping animals to customer; providing technical training to departmental personnel; performing value added services, biospecimen orders and introducing supplies.
Responsible for collecting health monitoring swabs and following health monitoring schedules.
Maintain the biosecurity of the animal physical environment by following SOPs related to introduction and removal of supplies/animals, isolator inspection and supply inspections.
Assist in the maintenance of physical environment, departmental equipment, and biosecurity in accordance with SOPs. Communicate findings and concerns to supervisor.
Maintain accurate departmental and isolator records.
Lead the preparation of reports, order inquiries, and completion of customer paperwork. Communicate with Customer Service department as needed.
Perform general housekeeping, adhere to safety procedures and follow ergonomic practices and stretching schedule.
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

Candidates must possess one of the following:

Bachelor’s in life sciences or related discipline and 1 year of demonstrated leadership responsibilities.
Associates degree in life sciences or related discipline and 2 years of demonstrated leadership responsibilities.
High school diploma or GED and 3 years of demonstrated leadership responsibilities.

ADDITIONAL QUALIFICATIONS:

Effective communication and interpersonal skills.
Demonstrated computer skills (data input, word processing).

PREFERRED QUALIFICATIONS:

ALAT certification

Salary Transparency

The pay range for this position is $22.00 - $32.00 / hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Assistant (Small Animal) (Raleigh, NC, US, 27610)

JOB SUMMARY

We are seeking a Research Assistant for the Global Animal Welfare department at Charles River Laboratories. As the Research Assistant, you will help collect and analyze data on rodent behavior. You will be working with rodents in high biosecurity areas where personal protective equipment (PPE) will be required.

*This is a temporary position for the summer only.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Observe and collect data on rodent behavior, including standing and observing rodents for extended periods of time in the vivarium.
Conduct literature searches on various topics related to animal behavior and welfare.
Conduct data entry and analyses as needed.
Write up research report for potential peer-reviewed publication.
Other duties as assigned.

MINIMUM QUALIFICATIONS

High School Diploma / GED required
Veterinary, graduate, or undergraduate student in animal science or related field
Experience working with animals
Understanding of animal behavior
Comfortable handling rodents
Past research experience preferred
Detail-oriented and reliable
Excellent communication skills

ROLE SPECIFIC INFORMATION

Location: Raleigh, NC
Pay: $17.75 - $22.00 / hour
Schedule: Monday through Thursday-9 hour shifts, Friday - 4 hour shift, all shifts beginning at a set start time between 4:00am-6:00am

The pay range for this position is $17.75 - $22.00 / hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Associate (Raleigh, NC, US, 27610)

JOB SUMMARY

As an Animal Care Associate for our production site in Raleigh, NC, you will be responsible for the well-being of our research animals. Your contribution will ensure the health of our animals, as well as impact the lives of patients across the world. You will perform routine animal husbandry and other production duties. You will also maintain supplies and environment of environmentally-controlled work area(s).

* This is a temporary opportunity with the potential to be hired as a full-time, employee.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform routine animal husbandry duties and monitor daily health and welfare to maintain quality and health of animals.
Handle, transfer, and distribute animals, supplies and waste as needed to and from work area(s).
Monitor animal health by observing animal behavior, physical appearance, and physical environment. Identify and report any abnormal findings.
Responsible for collecting health monitoring swabs and following health monitoring schedules.
Perform physical environment housekeeping duties and production operations according to Good Manufacturing Practices (GMPs) and/or Standard Operating Procedures (SOPs).
Maintain recordkeeping pertaining to animal or supply area inventories.
Strictly follow all procedures necessary to maintain the barrier room barrier.
Use supplies according to safety guidelines. Perform all job-related duties in accordance with company safety procedures.
Colony Management
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS:

No experience required. On the job training will be provided.

ROLE SPECIFIC INFORMATION:

Location: Raleigh, NC
Pay: $17.75 - $19.00 / hour
Schedule: Start times fall between 4:00am - 6:00 am, working 9 hour shifts Monday - Thursday and a 4 hour shift on Friday. Weekend rotation is required.

PHYSICAL DEMANDS

Regularly required to utilize a computer/tablet.
Regularly required to stand, use hands to finger, handle or feel objects, tools or controls; and reach with hands and arms.
Regularly required to stand and ascend/descend rolling platform ladder (up to six steps) to perform all tasks and procedures related to the job.
Regularly transports supplies, removes waste, and/or laboratory equipment while ascending/descending rolling platform stairs (up to six steps).
Regularly positions self (stoop, crouch, squat, sit, reach) to access and inspect small models and be able to assess their conditions and environment from various distances.
Regularly lifts and/or moves materials weighing up to 10 pounds and occasionally lifts and/or moves materials weighing up to 50 pounds.
May occasionally lift and/or move equipment and materials weighing 30-50 pounds, and equipment and materials weighing over 50 pounds with assistance.
Specific vision abilities required by this job include close vision, depth perception, and the ability to differentiate colors.
Regularly works with chemicals that require the use of respirators. Medical clearance is required prior to using respirators.

The pay range for this position is $17.75-$19.00 / hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Responsable d'équipe Immunologie - F/H - CDI (Evreux, FR, 27930)

Depuis plus de 75 ans, les employés de Charles River ont travaillé ensemble pour aider à la découverte, au développement et à la fabrication de nouvelles pharmacothérapies. Lorsque vous rejoignez notre famille, vous avez un impact significatif sur la santé et le bien-être des gens à travers le monde. Que vos antécédents soient en sciences de la vie, en finance, en informatique, en ventes ou dans un autre domaine, vos compétences jouent un rôle important dans le travail que nous effectuons. En retour, nous vous aidons à bâtir une carrière passionnante à nos côtés.

Qui sommes-nous ?

Le site Charles River d’Evreux est un site unique de 2 hectares, situé aux portes de la Normandie. Il offre un environnement scientifique innovant, dynamique et convivial où près de 500 personnes travaillent chaque jour dans l'objectif commun de participer au développement de pharmacothérapies, dans le respect du bien-être animal.

Le poste

Le service Immunologie recrute au sein du département Biomarkers un Responsable d’équipe (F/H) en CDI pour intégrer son équipe composée de 24 techniciens à compter de Juillet 2026.

Les missions

Sous la responsabilité du Responsable de Service Immunologie, vous assurerez l’encadrement des techniciens de laboratoires et aurez pour principales missions :

Organiser le fonctionnement quotidien du service en préparant le planning et en prenant en compte les compétences et ressources disponibles pour assurer l’adéquation entre la charge et le respect des délais d’études,
Maintenir le développement des compétences des équipes (fixation d’objectifs de développement, établissement du plan de formation, entretiens annuels, reconnaissance des succès…),
Suivre la gestion des temps de son équipe,
Être garant de l’animation et de la cohésion de son équipe,
Echanger régulièrement avec le responsable de Service ainsi que les services connexes pour le bon suivi de l’activité,
Être garant du respect des BPL, des procédures standards et de la bonne tenue du laboratoire,
Proposer des améliorations et participer à la rédaction de nouvelles procédures, ainsi que la mise au point de nouvelles techniques si applicables,
Lire les protocoles, avenants et notices en anglais,
Être leader dans la conduite du changement.

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 dans le domaine scientifique (biologie, biochimie, biologie moléculaire) et possédez d’une expérience confirmée en management d’équipe. Vous détenez idéalement des connaissances issues du milieu pharmaceutique et/ou en R&D.

Intéressé(e) par le travail de terrain, vous êtes curieux(se), force de proposition et rigoureux(se).

Vous savez rendre compte, expliquer et interpréter vos résultats. Vous savez communiquer clairement et adopter une position de leader.

Pour ce poste, la maitrise de l’anglais (écriture et lecture) et de l’informatique est nécessaire.

À propos de l'évaluation de sécurité

Charles River est une société engagée dans une démarche visant à aider ses partenaires à accélérer le développement préclinique de leurs médicaments avec des services d'évaluation de l'innocuité exceptionnels, des locaux utilisant des équipements à la pointe de la technologie et des conseils d'experts en matière de réglementation. Depuis la toxicologie spécialisée individuelle et les études permettant le dépôt d'une demande d'autorisation de nouveau médicament expérimental jusqu'aux formules sur mesure et à l'assistance totale pour les laboratoires, notre équipe chevronnée peut concevoir et exécuter des programmes qui anticipent les difficultés et évitent les blocages pour un parcours sans encombre et efficace jusqu'à la mise sur le marché. Chaque année, environ 300 études d'autorisation de nouveau médicament expérimental (dans le cadre du programme IDN, de l'anglais Investigational New Drug) sont réalisées dans nos centres d'évaluation de l'innocuité.

Avec plus de 20 000 collaborateurs sur 110 sites dans 20 pays, nous sommes positionnés stratégiquement pour coordonner des ressources mondiales et appliquer des perspectives pluridisciplinaires à l'élaboration de solutions aux défis uniques de nos clients. Notre base de clientèle comprend des sociétés de biotechnologies et des laboratoires pharmaceutiques internationaux, des agences publiques, et des établissements hospitaliers, d'enseignement et de recherche partout dans le monde.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Stage : vétérinaire - chargé de projets protocoles de socialisation - F/H - 6 mois (Evreux, FR, 27930)

Qui sommes-nous ?

L'équipe

Notre service Vétérinaire, au sein du département Toxicologie, regroupe une dizaine de personnes. L'équipe globale a pour mission principale d'assurer le bien-être général de nos animaux (physiologique et psychologique). La mission proposée visera à proposer des solutions d'amélioration afin de renforcer les protocoles de socialisation de nos animaux.

Votre quotidien

Faire un état des lieux des pratiques existantes
Rechercher de nouvelles pratiques et proposer un rapport détaillé (recherche bibliographique, étude de faisabilité, étude des coûts et bénéfices)
Mettre en place la/les pratiques validées (rédaction de procédures, formation des opérants, mise en place d'indicateurs de performance)

Pourquoi nous rejoindre ?

Actuellement en formation Bac +4/5, vous recherchez un stage dans un environnement de laboratoire dynamique et innovant. Vous avez un intérêt particulier pour l'amélioration continue et l'amélioration du bien-être animal.

Vous souhaitez intégrer un contexte international (anglais lu, écrit).

Sensible au respect des règles d'éthique et de sécurité, vous souhaitez mettre en oeuvre vos qualités d'observation, de rigueur et de force de proposition.

Modalités

Gratification de stage
Indemnités de transports (site non accessible en transports en commun)
Restaurant d'entreprise

À propos de l'évaluation de sécurité

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Animalier en Toxicologie Non-Rongeurs - F/H - CDD 9 mois (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Le département de Toxicologie recrute un Animalier (F/H) en CDD jusqu'au 26 décembre 2026 pour intégrer son équipe composée de 10 animaliers.

Les missions

Au sein du Département de Toxicologie, vous aurez pour principales missions sous la responsabilité du responsable d’équipe :

Participer à l’entretien des locaux (change de cages, matériel) et soins des animaux selon les règles d’hygiène et de sécurité et les bonnes pratiques de laboratoire
Réaliser progressivement certaines techniques sur toutes espèces (contention,…)
Assurer la saisie informatique des résultats
Appliquer les procédures standards et protocoles d’études avec toute la rigueur requise
Assurer un suivi et transmettre toutes informations sur tout évènement survenant au cours du travail

Qualifications souhaitées

Vous êtes titulaire d’un BEP/BAC type STL .
Vous êtes organisé(e) et vous appréciez le travail en équipe.
Vous êtes rigoureux(se), vous respectez les délais, les procédures et les consignes.

Conditions spécifiques du poste

Annualisation des heures : plage horaire standard (35H00) avec possibilité d’horaires décalées en fonction des roulements et du service.
Contact avec les animaux.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique, groupe : 2
Contrat : CDD de 09 mois - Non-cadre (accord de modulation 35h)
Salaire : A compter de 24 232€ bruts / an sur 13 mois
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de l'évaluation de sécurité

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Animalier en Toxicologie Non-Rongeurs - F/H - CDD 9 mois (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Le département de Toxicologie recrute un Animalier (F/H) en CDD jusqu'au 26 décembre 2026 pour intégrer son équipe composée de 10 animaliers.

Les missions

Au sein du Département de Toxicologie, vous aurez pour principales missions sous la responsabilité du responsable d’équipe :

Participer à l’entretien des locaux (change de cages, matériel) et soins des animaux selon les règles d’hygiène et de sécurité et les bonnes pratiques de laboratoire
Réaliser progressivement certaines techniques sur toutes espèces (contention,…)
Assurer la saisie informatique des résultats
Appliquer les procédures standards et protocoles d’études avec toute la rigueur requise
Assurer un suivi et transmettre toutes informations sur tout évènement survenant au cours du travail

Qualifications souhaitées

Conditions spécifiques du poste

Annualisation des heures : plage horaire standard (35H00) avec possibilité d’horaires décalées en fonction des roulements et du service.
Contact avec les animaux.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique, groupe : 2
Contrat : CDD de 09 mois - Non-cadre (accord de modulation 35h)
Salaire : A compter de 24 232€ bruts / an sur 13 mois
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de l'évaluation de sécurité

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Cuidador/a Animalario MAD (Madrid, M, ES, 28029)

Durante casi 75 años, los empleados de Charles River han trabajado juntos para ayudar en el descubrimiento, el desarrollo y la fabricación segura de nuevas terapias con fármacos. Cuando te unas a nuestra familia, tendrá un impacto significativo en la salud y el bienestar de las personas en todo el mundo. Ya sea que su experiencia sea en ciencias de la vida, finanzas, TI, ventas u otra área, sus habilidades desempeñarán un papel importante en el trabajo que realizamos. A cambio, te ayudaremos a construir una carrera que puedas sentir apasionada.

Charles River Laboratories España, S.A., empresa dedicada a la investigación y desarrollo experimental en biotecnología, necesita incorporar CUIDADORES/AS DE ANIMALARIO en Madrid.

• Jornada laboral de 40 h de lunes a viernes.

• Contrato laboral temporal por suplencia. Duración en función de la suplencia a cubrir.

• Incorporación inmediata.

• Formación remunerada a cargo de la empresa

Descripción de tareas

• Tareas de mantenimiento de animales con fines experimentales (cambio de jaula, rejilla y cobertor)

• Revisión de comida, agua y lecho

• Revisión del estado general de salud de los animales

• Desinfecciones de material de estabulación (racks ventilados, cabinas de cambio, jaulas, cobertores, etc.)

• Procesado de material de estabulación

• Mantenimiento de stocks de material en el área asignada

• Mantenimiento de registros ambientales (Tª, humedad, ciclos de luz, etc.)

• Mantenimiento de registros de tareas diarias según protocolos de trabajo

• Desinfección de salas de estabulación, pasillos, almacenes, zona de lavado, etc.

Requisitos

Experiencia 3 meses. Experiencia mínima de 3 meses, aunque formamos a nuestro propio personal.
Título CFGM
Técnico/a superior anatomía patológica y citodiagnóstico
Idioma español
Competencias / conocimientos: se valorará acreditación para funciones A y B o formación como ATV (asistente técnico veterinario)

Acerca de Charles River

Charles River es una organización de investigación por contrato (CRO) en fase temprana. Hemos ampliado nuestra oferta sobre la base de la medicina y ciencia con animales de laboratorio para desarrollar una cartera diversificada de servicios de descubrimiento y evaluación de la seguridad, tanto por medio de buenas prácticas de laboratorio (GLP) como sin ellas, para apoyar a los clientes desde la identificación de los objetivos hasta el desarrollo preclínico. Charles River también proporciona una serie de productos y servicios para apoyar las necesidades de pruebas de laboratorio clínico y actividades de fabricación de nuestros clientes. El uso de esta extensa cartera de productos y servicios permite a nuestros clientes para crear un modelo más flexible de desarrollo de fármacos, lo cual reduce sus costes y mejora su productividad y eficacia, logrando así incrementar la velocidad con la que llega al mercado.

Con más de 20,000 empleados en 90 centros de 20 países alrededor del mundo, nos encontramos posicionados estratégicamente para coordinar recursos internacionalmente y aplicar perspectivas multidisciplinarias de modo de resolver los desafíos únicos de nuestros clientes. Nuestra base de clientes incluye compañías farmacéuticas globales, compañías de biotecnología, agencias del gobierno, así como hospitales e instituciones académicas alrededor del mundo.

En Charles River, sentimos pasión con respecto al rol que cumplimos en mejorar la calidad de vida de las personas. Nuestra misión, nuestra ciencia de excelencia y nuestro fuerte sentido de propósito nos guía en todo lo que hacemos, y afrontamos cada día sabiendo que nuestro trabajo ayuda a mejorar la salud y el bienestar de muchas personas alrededor del mundo. Hemos apoyado con orgullo el desarrollo de ~85 % de los fármacos aprobados por la FDA en 2021.

En Charles River Laboratories, reconocemos y contratamos a todos los talentos. Somos una empresa comprometida con el principio de la diversidad y la inclusión y trabajamos diariamente en esta dirección.

Charles River España está comprometido con una política a favor de la integración y el empleo continuo de las personas con discapacidad. Todos nuestras vacantes están abiertas a trabajadores con discapacidad y se les dará especial consideración en los procesos de selección.

Para más información, visite www.criver.com.

Zootecnia de vivarios de investigación - Colaborador 1 1 1 1 (Madrid, M, ES, 28029)

Durante 75 años, los empleados de Charles River han trabajado juntos para ayudar en el descubrimiento, el desarrollo y la fabricación segura de nuevas terapias con fármacos. Cuando se une a nuestra familia, tendrá un impacto significativo en la salud y el bienestar de las personas en todo el mundo. Ya sea que su experiencia sea en ciencias de la vida, finanzas, TI, ventas u otra área, sus habilidades desempeñarán un papel importante en el trabajo que realizamos. A cambio, te ayudaremos a construir una carrera que puedas sentirte apasionada.

Resumen de trabajo

Acerca de Microbial Solutions

Nuestro grupo de negocios Microbial Solutions posee una exclusiva y completa cartera de productos y servicios de pruebas de endotoxinas, detección microbiana e identificación microbiana, que ha sido diseñada específicamente para cumplir con las necesidades complejas y siempre cambiantes de la industria. Ayudamos a los clientes a asegurar la seguridad y calidad del producto con soluciones de pruebas fáciles de usar pero robustas que satisfacen los requisitos regulatorios, apoyan el proceso de toma de decisiones críticas y mejoran las eficiencias operacionales.

Acerca de Charles River

Con más de 20,000 empleados en 110 centros de 20 países alrededor del mundo, nos encontramos posicionados estratégicamente para coordinar recursos internacionalmente y aplicar perspectivas multidisciplinarias de modo de resolver los desafíos únicos de nuestros clientes. Nuestra base de clientes incluye compañías farmacéuticas globales, compañías de biotecnología, agencias del gobierno, así como hospitales e instituciones académicas alrededor del mundo.

En Charles River, sentimos pasión con respecto al rol que cumplimos en mejorar la calidad de vida de las personas. Nuestra misión, nuestra ciencia de excelencia y nuestro fuerte sentido de propósito nos guía en todo lo que hacemos, y afrontamos cada día sabiendo que nuestro trabajo ayuda a mejorar la salud y el bienestar de muchas personas alrededor del mundo. Hemos apoyado con orgullo el desarrollo del 80% de los fármacos aprobados por la FDA en los últimos cinco años.

Para más información, visite www.criver.com.

Animal Caretaker -TORINO (Torino, IT, 10126)

Riepilogo del lavoro

Per nostro cliente sito in Torino ricerchiamo uno stabularista.

La risorsa sarà inserita all'interno del team operante nella struttura e si occuperà di svolgere le mansioni relative alla gestione del laboratorio

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nel controllo delle procedure sperimentali;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature automatiche e carrelli

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro full time o part-time

Disponibilità a lavoro nel week-end

Buona conoscenza del pacchetto office

Di cosa si occupa la Charles River

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

研究模型饲养- 支持类 1 1 1 1 1 1 (Changping District, BJ, CN, 100107)

近七十年来，查尔斯河员工一起努力协助新药治疗的发现，开发和安全生产。当您加入我们的家庭时，您将对全球人民的健康和福祉产生重大影响。无论您的背景是生命科学，金融，IT，销售还是其他领域，您的技能将在我们所执行的工作中发挥重要作用。作为回报，我们将帮助您建立一个您可以感受到激情的职业。

工作总结

关于企业职能部
企业职能部门为Charles River的运营提供了各领域的专业支持（如人力资源、财务、IT、法律、销售、质量保证、营销和企业发展）。他们与公司全球范围内的同事合作，制定和推动战略，并设立全球标准。这些职能对于衔接战略愿景和实际运营就绪度至关重要，能够确保持续性职能创新和能力改进。

关于Charles River
Charles River是一家早期药物研发授权研究机构（CRO）。我们的业务是建立在实验室动物医学和科学基础之上，我们开发多样化的发现和安全评估服务组合，包括与实验室管理规范（GLP）和非实验室管理规范有关的服务，以在从靶标鉴定到临床前开发的整个流程中为客户提供支持。Charles River还提供一套支持客户的临床实验室测试需求和制造活动的产品和服务。利用广泛的产品和服务组合，我们的客户可以创建更灵活的药物开发模式，从而降低成本、提高效率和功效，并加快上市速度。

我们在全球各地20个国家和地区拥有110家设施及20000多名员工，我们在战略上能够协调全球资源并采取多学科视角来解决客户面对的独特挑战。我们的客户群包括世界各地的全球性制药公司、生物技术公司、政府机构、医院和学术机构。

在Charles River，我们对在提高人们的生活质量方面所起的作用充满激情。我们的使命、优秀的科学专长和强烈的目标意识指导我们开展的所有业务，我们每天开展工作时都知道，我们在帮助改善世界各地人们的健康和安康。我们支持了2021年FDA批准的所有药物中约86％的药物的开发工作，我们为此感到自豪。

欲了解更多信息，请访问www.criver.com。

Cuidador/a Animalario BCN (Barcelona, B, ES, 08003)

Durante casi 75 años, los empleados de Charles River han trabajado juntos para ayudar en el descubrimiento, el desarrollo y la fabricación segura de nuevas terapias con fármacos. Cuando te unas a nuestra familia, tendrá un impacto significativo en la salud y el bienestar de las personas en todo el mundo. Ya sea que tu experiencia sea en ciencias de la vida, finanzas, TI, ventas u otra área, tus habilidades desempeñarán un papel importante en el trabajo que realizamos. A cambio, te ayudaremos a construir una carrera que puedas sentir apasionada.

Charles River Laboratories España, S.A., empresa dedicada a la investigación y desarrollo experimental en biotecnología, necesita incorporar CUIDADORES/AS DE ANIMALARIO en Barcelona.

• Jornada laboral de 40h de lunes a viernes.

• Contrato laboral temporal por suplencia. Duración en función de la suplencia a cubrir.

• Incorporación inmediata.

• Formación remunerada a cargo de la empresa

Descripción de tareas

• Tareas de mantenimiento de animales con fines experimentales (cambio de jaula, rejilla y cobertor)

• Revisión de comida, agua y lecho

• Revisión del estado general de salud de los animales

• Desinfecciones de material de estabulación (racks ventilados, cabinas de cambio, jaulas, cobertores, etc.)

• Procesado de material de estabulación

• Mantenimiento de stocks de material en el área asignada

• Mantenimiento de registros ambientales (Tª, humedad, ciclos de luz, etc.)

• Mantenimiento de registros de tareas diarias según protocolos de trabajo

• Desinfección de salas de estabulación, pasillos, almacenes, zona de lavado, etc.

Requisitos

Experiencia 3 meses. Experiencia mínima de 3 meses, aunque formamos a nuestro propio personal.
Título CFGM
Técnico/a superior anatomía patológica y citodiagnóstico
Idioma español
Competencias / conocimientos: se valorará acreditación para funciones A y B o formación como ATV (asistente técnico veterinario)

Acerca de Charles River

Para más información, visite www.criver.com.

Zootecnia de vivarios de investigación - Colaborador 1 1 1 1 1 (Barcelona, B, ES, 08003)

Resumen de trabajo

Acerca de Microbial Solutions

Acerca de Charles River

En Charles River, sentimos pasión con respecto al rol que cumplimos en mejorar la calidad de vida de las personas. Nuestra misión, nuestra ciencia de excelencia y nuestro fuerte sentido de propósito nos guía en todo lo que hacemos, y afrontamos cada día sabiendo que nuestro trabajo ayuda a mejorar la salud y el bienestar de muchas personas alrededor del mundo. Hemos apoyado con orgullo el desarrollo del 80% de los fármacos aprobados por la FDA en los últimos cinco años.

Para más información, visite www.criver.com.

Assistant Laboratory Manager (Singapore, SG)

JOB SUMMARY

The Assistant Lab Manager is responsible for the leadership of the microbiological contract services laboratory in Charles River Singapore and ensure that lab operates in accordance to ISO17025 and cGMP requirements. Assistant Lab Manager will serve as analytical lead in variety of projects which includes but not limited to method validation, method transfer, customized testing activities. In addition, this individual is responsible for directing the day-to-day project activity though interaction with technical personnel while gathering, analyzing and interpreting scientific data. He/She must ensure accurate and precise results are being achieved and properly reported.

ESSENTIAL DUTIES & RESPONSIBILITIES

Provides strong, independent technical leadership to technical personnel.
Lead, design and performs method development and validation of new test procedures for incoming projects.
Functions as Technical Reviewer for A2LA accredited tests and non-accredited tests.
Evaluates analytical results to form interpretations of data and renders scientific opinions for client-driven projects.
Serves as subject matter expert in area of specialization, established standards for regulatory compliance.
Serves as technical liaison with Customers with regards to technical services and performs Customer Site Visits where required.
Prepares documents including methods, procedures, standard operating procedures, study protocols, summary reports.
Assures that SOPs are in accordance to ISO 17025, cGMP and other regulatory requirements.
Provides problem-solving skills for test procedures and investigations within laboratory unit.
Responsible for notifying Quality Assurance and Senior Management of any compliance deficiencies or concerns in timely manner.
Monitor all proficiency-based testing and ensure compliance.
Participates in Internal Quality Audits, System Audits, Audits conducted by external agencies and Regulatory Authorities.
Participate in quarterly management review.
Drive process, quality and safety improvement initiatives within the department.
Provide coaching and mentoring to Technical personnel.
Supports the Laboratory Manager in all relevant functions

JOB REQUIREMENTS

Bachelor of Science or related degree, MSc. preferred but not essential.
Minimum 6 years relevant QC microbiological experience in regulated laboratory, minimum 2 of which should be in a supervisory role.
Experience in method validation, method transfer, qualifications activities in regulated laboratory.
Good knowledge of ISO17025, cGMP and other regulatory guidelines.
Good technical understanding and judgement.
Good interpersonal and communication skills across cultures.
Team player with ability to work in cross functional teams as well as independently depending on the requirement of task in hand.

For more information, please visit www.criver.com.

CW - Accountant (Singapore, SG)

SUMMARY

The role is responsible for the full spectrum of accounting in Singapore office. This includes managing day‑to‑day activities of the accounts department, such as maintaining the general ledger, preparing weekly and monthly financial reports, managing account receivable and payable, customer billing, managing staff claims, and closing of monthly financial book. The incumbent is expected to possess good accounting knowledge, and provide operational accuracy data to management for effective decision making.

ESSENTIAL DUTIES AND RESPONSIBILITIES
• Day-to-day duties and operations of the accounts department
• Management of capital and fixed assets, accounts payable, accounts receivables
• Preparation of IRAS GST submission
• General Ledger accounting
• Liaising with finance software vendor for maintenance and applications
• Perform revenue and expenditure variance analysis
• Prepares weekly and monthly financial reports, year-end closing, and annual audits
• Oversee internal control function and administration of financial policy
• Oversees stock entries and monthly stock-take
• Treasury Reporting
• Vendor Payment
• Accounts Receivable Management and Collection
• Handle full set of accounts
• Monitor revenue and expenditure transactions.
• Responsible for the preparation of audit reports for submission
• Coordinate the annual filing of statutory corporate documents with ACRA
• Assists in the preparation of annual Corporate tax return with external tax consultant
• Provide support and assistance for general administrative, finance and other general HR support as needed
• Perform billings to customers, generate weekly sales report, management of claims in Concur System, prepare monthly bank reconciliation

REQUIREMENTS
• Bachelor’s degree (B.A. /B.S.) or equivalent in Accounting.
• Experience: Five to Eight years related experience and/or training in Accounting, financial planning and analysis. Exchequer experience preferred. Strong US GAAP experience a must.
• Team player with positive working attitude and willingness to learn
• Ability to work independently and has good time management
• Proficient in written & spoken English, and MS Office applications

Equal Employment Opportunity

For more information, please visit www.criver.com.

Account Manager - Sydney, Remote (US)

SUMMARY

Responsible for selling and promoting Charles River Microbial Solutions products/services to assigned customers in New South Wales, ACT and South Australia - this is a remote position. Maintain and increase sales at new and existing accounts through proactive and outbound field account management.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Sell the company’s Endosafe, Accugenix and Celsis products/services to accounts by contacting both established customers and developing new prospects.
• Diligently maintain SFDC or any other Charles River CRM system, incl. adding customers and customer information, logging customer calls and meetings, creating and updating sales opportunities, and capturing marketing event leads.
• Maintain a working knowledge of all Endosafe, Accugenix and Celsis products, services and policies.
• Participate in all required specialized training for specific product/ service line(s)
• Develop an effective Territory Plan to ensure that all customers in the given territory are proactively engaged with on a regular basis.
• Manage a quarterly Territory Management Plan including opportunities and sales strategies.
• Attend customer conferences, networking events and other industry events to build contact lists, showcase our products and promote Charles River’s products and services.
• Maintain customer appointments and perform "cold" calls requiring professional business acumen.
• Conduct product demonstrations to potential customers as well as provide product training and support when needed.
• Research business and trade media to identify new potential customers in our industry
• Establish customer needs and requirements for Company products and services.
• Initiate all administrative details to execute the sales process flow.
• Share customer problems/concerns with your supervisor for quality resolution.
• Proactively and collaboratively engage with other internal departments
• From time to time, attend regional or international sales meetings.
• Perform all other related duties as assigned.

The following are minimum qualifications related to this position:

• Education: Bachelor’s degree (B.A. /B.S.) or equivalent in life sciences, sales or related field required. Master’s degree preferred.
• Experience: Minimum 5 years relevant industry experience, with at least 2 of those years having direct client interface.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
• Certification/Licensure: None.
• Other: Excellent interpersonal, customer relationship and leadership skill

Equal Employment Opportunity

For more information, please visit www.criver.com.

2026 Summer Intern - Immunology (US)

Job Summary

Responsible for routine laboratory procedures (e.g., animal care, facility cleaning, labeling, lab support basic procedures, etc.), facility/groundskeeping, and/or other administrative/IT functions, as assigned.

This is an onsite role in Ashland, OH. The pay range for this position is $15.00 - $17.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Must be authorized to work in the United States without requiring a Sponsor Visa.

Position is open to anyone, regardless of age, who meets the educational and experience requirements as posted

Job Qualifications

ESSENTIAL DUTIES AND RESPONSIBILITIES:

•   May perform area support cleaning, study set up, laboratory administrative functions, and/or basic animal husbandry.
•   May clean rooms and/or facility to include possible handling of biohazard materials.
•   May assist with use of balances and other laboratory equipment.
•   May perform basic facility/groundskeeping functions.
•   May perform administrative functions in various departments, including IT.
•   Use Good Laboratory Practice Regulations (GLP), SOP's and company policies when performing all job functions.
•   Perform all other related duties as assigned.

QUALIFICATIONS:

•   Education: Currently enrolled in a degree program
•   Experience: Pipette experience, scientific knowledge, Prior ELISA, flow cytometry, multiplex, or genetic toxicology experience.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Certification/Licensure: None
•   Other: Ability to handle common laboratory species in selected departments.

PHYSICAL DEMANDS:

•   Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals for the departments requiring such functions.
•   Must be able to perform procedures, which require, talking, hearing, standing or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
•   May be required to frequently firmly hold species while utilizing fine motor skills.
•   Specific vision abilities may be required by this job include close vision, color vision, depth perception, and the ability to adjust focus.
•   While performing the duties of any administrative-type functions, the employee may be assigned to regularly talk, hear and work/type at a computer.

Work Environment:

•   If assigned to works in a research environment, it may require use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
•   The employee may be required to work with live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
•   The noise level in the work environment ranges from low to high depending upon the species housed and department assigned, if applies.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Senior Event Specialist, APAC (Singapore, SG)

Job Summary

Charles River is seeking a Snr Events Specialist to support our portfolio in the APAC region. This remote-based role will work closely with both the corporate and regional commercial teams to deliver impactful, revenue-focused, and brand-aligned events. The Snr Events Specialist will own the regional tradeshow calendar, lead preshow planning to establish clear objectives, ensure flawless onsite execution, and evaluate performance to maximize return on investment.

Job Responsibilities

Research, plan, and execute a program of APAC focused tradeshows, and hosted events across the Charles River portfolio.
Serve as the primary liaison between internal stakeholders, external vendors, and event attendees to ensure successful delivery, whilst supporting revenue growth, and strengthening market presence.
Act as the subject matter expert and sole point of contact for APAC tradeshows and events.
Drive improvements in event lead quality and velocity, ensuring compliance with corporate standards for lead capture, processing, and best practices.
Partner with regional marketing and CRL creative to ensure all messaging and design are on-brand, strategically aligned, and tailored to the target audience.
Track, analyze, and report ROI metrics for each event; provide recommendations for continuous improvement to maximize impact and revenue outcomes.
Oversee all aspects of event planning and logistics, including vendor contracts, purchasing, shipping, and onsite coordination.
Collaborate with other CRL departments on projects that generate revenue and strengthen client relationships.
Perform other related duties as assigned.

Job Qualifications

Education: Bachelor’s degree (B.A. /B.S.) or equivalent or related discipline.
Experience: Four to six years related experience and/or training, including experience managing large tradeshows.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None.
Other: Proficiency in English is essential; multiple languages are advantageous. Knowledge of CRM systems, Smartsheet and Cvent or similar software/tools preferred

PHYSICAL DEMANDS:

While performing the duties of this job, the employee is regularly required to talk, hear and work/type at a computer.
Specific vision abilities required by this job include close vision and the ability to adjust focus.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to fostering a sense of belonging and work daily in this direction.

2026 Summer Intern - In Life (US)

Job Summary

Must be able to work from May 18th-Aug 7th, 2026
40 Hours/Week. Monday-Friday 8:30-5:00pm
Rate for this role is $17 per hour
Responsible for handling and restraining animals, clinical observations, monitoring food consumption and body weights, animal husbandry, and performing accurate data collection and reporting.

Position is open to anyone, regardless of age, who meets the educational and experience requirements as posted.

Must be eligible to work in the US without requiring a sponsor visa.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Observe animals for general health and overall well being.
Collect and record research data in compliance with Good Laboratory Practice Regulations (GLPs), study protocols and Standard Operating Procedures (SOPs).
Perform basic in-life technical procedures upon completion and sign-off of specific skill training. (e.g., clipping, handling, chipping, removals, body weight,).
Assist in cohabitation smears of all species.
Perform computer input under supervision.
Read basic study protocols and extract pertinent information.
Review documentation of data collected as part of quality control requirements.
Retrieve and view Standard Operating Procedures using appropriate database.
Use GLPs, SOPs, processes and company policies when performing all job functions.
Perform study preparation activities including cage tag generation, collection tube labeling and room setup.
Maintain clean work areas (e.g: laboratory area, primary enclosures, animal exam areas).
Receive animals (e.g., general health observation, sexing and identification) of all species.
May perform subcutaneous injections to administer sedatives to rabbits prior to euthanasia.
Perform all other related duties as assigned.

Job Qualifications

QUALIFICATIONS:

Education: High School Diploma or General Education Degree, must be enrolled in an undergraduate degree program.
Experience: None
Certification/Licensure: None
Other: Ability to handle common laboratory animal species. Basic knowledge of GLP regulations preferred. Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors. Able to quickly learn and utilize computer programs as needed; previous computer experience preferred

PHYSICAL DEMANDS:
Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform procedures, which require, talking, hearing, standing or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Must be able to frequently firmly hold species while utilizing fine motor skills.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

WORK ENVIRONMENT:

Works in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
The employee regularly works with live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to high depending upon the species housed.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

2026 Intern - Corporate Security (US)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

Including operations and commercial teams to produce a wide variety of deliverables focusing on the 5-year strategy of our business. Your insightful contribution and fresh perspective will help develop and expand our initiatives and assist you with acquiring presentation/communication skills and the knowledge of various industry/operational strategies. An Internship at Charles River Labs provides real world, hands-on experience for college students looking to gain knowledge and skills required for your career field of choice, while giving you an unparalleled internship experience. We are dedicated to ensuring our Co-op/Intern population can experience the ability to Grow, Perform, and Succeed during their time on board. Responsible for support with basic procedures, facility and/or other administrative/IT functions, as assigned.

This is a remote working opportunity.

Essential Duties and Responsibilities:

Working with our senior leadership teams to provide insights and deliverables to business leaders articulating our 5-year strategy.
Hands-on interaction with all stakeholders including, executives, senior leaders, SMEs, and certain external partners.
Culminate in a strategic planning presentation to the Executive Committee that you will listen in to and be tasked with follow-up actions.
The creation of PowerPoint decks and assisting with summarizing and/or researching relevant data. Opportunity to also work on the initial implementation of projects

Job Qualifications

Education: Student currently enrolled in an accredited college/ university bachelor’s degree program.
Experience: Prior security team experience (preferred).
Certification/Licensure: None expected, but certificates obtained during coursework are a plus.
Other: Proven trustworthiness and history of acting with integrity, taking pride in work, seeking to excel, being curious and adaptable, and communicating effectively. Solid written and verbal communication skills. Capable of working with diverse teams. Organized and punctual. Confident, but humble and willing to learn and take initiative.

Compensation Data:
The pay range for this position is $18/hour - $20/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certiﬁcations, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Addetto alla cura degli animali da laboratorio - MILANO (CALCO, IT, 23885)

Riepilogo del lavoro

For an important customer IS belonging to the world of research we are looking for an Animal Technician. The resource will be included in the team operating in the structure.

Animal Care and Colony Management: Provides feeding, watering, health checks, observes behavior, performs veterinary procedures and manages colonies.
Technical Support and Training: Trains users and new employees, assists research staff with animal procedures, and ensures compliance with SOPs and guidelines.
Operational Management and Documentation: Maintains animal records, collects data for management software, monitors environmental conditions, manages consumables and equipment, and supports budget preparation.
Cleaning and Safety: Performs cleaning and decontamination procedures, operates autoclaves, disposes of carcasses according to protocols, uses PPE, and prevents cross-contamination.
Compliance and Inspections: Ensures readiness for regulatory inspections, follows health, safety, and environmental rules, and collaborates with the manager to improve efficiency and quality of services.

Di cosa si occupa la Charles River

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Veterinario (CALCO, IT, 23885)

Riepilogo del lavoro

Selezioniamo un medico veterinario da inserire nell’ambito delle attività di ricerca e laboratorio presso la nostra sede di Calco.

La risorsa contribuirà al mantenimento degli standard di benessere animale e alla corretta applicazione delle normative vigenti, collaborando strettamente con il Veterinario Designato e con il personale tecnico-scientifico.

Requisiti:

Laurea in Medicina Veterinaria e iscrizione/disponibilità di iscrizione all'albo professionale;
Conoscenza della normativa relativa alla protezione degli animali utilizzati a fini scientifici;
Capacità organizzative, attitudine alla collaborazione in contesti multidisciplinari e predisposizione alla formazione continua.

Insourcing Solutions

Charles River Insourcing Solutions℠ è in grado di snellire la ricerca con efficienza operativa ed economica, grazie all’insourcing strategico di servizi di ricerca GMP, GLP e non-GLP che vanno dalla scoperta alla valutazione della sicurezza. Insourcing Solutions℠ offre al cliente la possibilità di mantenere il controllo della propria struttura e competenze, avvantaggiandosi nel contempo dello spazio a disposizione.

Di cosa si occupa la Charles River

Con oltre 20.000 dipendenti in 110 strutture dislocate in 20 paesi in tutto il mondo, siamo posizionati strategicamente per coordinare le risorse a livello mondiale e applicare prospettive multidisciplinari per risolvere le sfide particolari dei nostri clienti. La nostra base clienti include aziende farmaceutiche di livello mondiale, aziende operanti nel settore delle biotecnologie ed enti governativi, nonché ospedali e istituzioni accademiche di tutto il mondo.

Alla Charles River, promuoviamo con convinzione il nostro ruolo nel miglioramento della qualità di vita delle persone. In tutto ciò che facciamo, siamo guidati dalla nostra missione, dalle nostre eccezionali competenze scientifiche e da una grande risolutezza e affrontiamo ogni giorno con la consapevolezza che il nostro lavoro contribuisce al benessere e al miglioramento della salute di molte persone in tutto il mondo. Abbiamo orgogliosi di aver collaborato allo sviluppo dell' 80% dei farmaci approvati dalla FDA negli ultimi cinque anni.

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Addetto alla cura degli animali da laboratorio - MILANO (CALCO, IT, 23885)

Riepilogo del lavoro

For an important customer IS belonging to the world of research we are looking for an Animal Technician. The resource will be included in the team operating in the structure.

Animal Care and Colony Management: Provides feeding, watering, health checks, observes behavior, performs veterinary procedures and manages colonies.
Technical Support and Training: Trains users and new employees, assists research staff with animal procedures, and ensures compliance with SOPs and guidelines.
Operational Management and Documentation: Maintains animal records, collects data for management software, monitors environmental conditions, manages consumables and equipment, and supports budget preparation.
Cleaning and Safety: Performs cleaning and decontamination procedures, operates autoclaves, disposes of carcasses according to protocols, uses PPE, and prevents cross-contamination.
Compliance and Inspections: Ensures readiness for regulatory inspections, follows health, safety, and environmental rules, and collaborates with the manager to improve efficiency and quality of services.

Di cosa si occupa la Charles River

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Cagewash Technician I (Baltimore, MD, US, 21224)

Job Summary

We are seeking a Cagewash Technician for our Insourcing Solutions site located in Baltimore, MD.

As the Cagewash Technician, you will Provide cleaning and maintenance of laboratory animal caging, equipment and cage preparation areas as well as cleaning of animal support areas under minimal supervision. Provide quality assurance to the cagewash area.

Additional responsibilities include:

Dumps and scrapes soiled bedding from caging and prepares caging for cagewash under minimal supervision.
Sanitizes caging and related equipment using cage washers, pressure washer or hand washing as required.
Properly disposes of soiled bedding and waste in specified receptacles.
Cleans and sanitizes cage preparation and storage areas.
Monitors and records results of cagewash water temperature and cleaning results using provided supplies such as temperature dots/strips, cultures.
Ensures that all logbooks, checklists and other records are completed in a timely fashion.

Job Qualifications

The following are minimum requirements related to the Cagewash Technician position.

High school diploma or GED preferred
Experience and/or training working with animal husbandry preferred.

The pay for this position is $20.32 per hour.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Animal Care Technician I (Baltimore, MD, US, 21224)

Job Summary

We are seeking a Animal Care Technician I for our Insourcing Solutions site located in Baltimore, MD.

As the Animal Care Technician I, you will provide husbandry and veterinary assistance in a laboratory for small animals, as well as monitor animal health and report findings.

Additional responsibilities include:

Prepare caging for cagewash.
Perform daily animal health observations and report any abnormal conditions or behavior. Monitor and report irregularities in environmental conditions that may affect animals.
Clean assigned animal rooms, facility and animal care equipment, and associated animal facility areas. Obtain weekly animal census.
Ensure logbooks, checklists and other records are completed accurately in a timely fashion.
Provide environmental enrichment feed and other enrichment stimuli and/ or provide behavioral assessments.

Job Qualifications
The following are minimum requirements related to the Animal Care Technician I position:

High school diploma or GED preferred
AALAS certification at the ALAT level within one year of eligibility
1 year related experience in animal care
3 months working with lab animal species, most applicable rodents, preferred

The pay for this position is $20.32 USD per hour.

For more information, please visit www.criver.com.

Animal Caretaker I (Baltimore, MD, US, 21224)

Job Summary

We are seeking an Animal Caretaker to join our Insourcing Solutions team located in Baltimore, MD

As the Animal Caretaker, you will provide basic husbandry to rodents and lagomorphs, monitor environmental parameters for abnormalities and provide customer assistance to the investigative staff.

Additional responsibilities include:

- Perform daily animal husbandry duties to maintain quality and health of research animals, including: perform daily water bottle /automatic water line and cage checks; provide appropriate food and water; perform cage changing and/or cage cleaning.

- Monitor environmental parameters and maintain written records

- Assist with restraint and handling of various animal species.

- Receive, inspect, and put away incoming animals; as well as provide for sentinel animals in each rodent housing area.

- Operate equipment and perform general housekeeping.

Job Qualifications

The following are minimum requirements related to the Animal Caretaker position:

- AALAS certification at the ALAT level within one year of eligibility

- 1 year of related experience in animal care

- 3 months working with lab animal species (rodents), preferred

- High school diploma/ GED preferred

The pay for this position is $21.00 USD per hour.

For more information, please visit www.criver.com.

Animal Care Technician I (Baltimore, MD, US, 21224)

Job Summary

We are seeking an Animal Care Technician for our Insourcing Solutions site located in Baltimore, MD.

As the Animal Care Technician, you will provide husbandry and veterinary assistance in a laboratory for small animals, as well as monitor animal health and report findings.

Additional responsibilities include:

Prepare caging for cagewash.
Perform daily animal health observations and report any abnormal conditions or behavior. Monitor and report irregularities in environmental conditions that may affect animals.
Clean assigned animal rooms, facility and animal care equipment, and associated animal facility areas. Obtain weekly animal census.
Ensure logbooks, checklists and other records are completed accurately in a timely fashion.
Provide environmental enrichment feed and other enrichment stimuli and/ or provide behavioral assessments.

Job Qualifications
The following are minimum requirements related to the Animal Care Technician position:

High school diploma or GED
AALAS certification at the ALAT level within one year of eligibility
1 year related experience in animal care
3 months working with lab animal species, most applicable rodents, preferred

The pay for this position is $20.32 USD per hour.

For more information, please visit www.criver.com.

Cagewash Technician (Baltimore, MD, US, 21224)

Job Summary

We are seeking a Cagewash Technician for our Insourcing Solutions site located in Baltimore, MD.

Additional responsibilities include:

Dumps and scrapes soiled bedding from caging and prepares caging for cagewash under minimal supervision.
Sanitizes caging and related equipment using cage washers, pressure washer or hand washing as required.
Properly disposes of soiled bedding and waste in specified receptacles.
Cleans and sanitizes cage preparation and storage areas.
Monitors and records results of cagewash water temperature and cleaning results using provided supplies such as temperature dots/strips, cultures.
Ensures that all logbooks, checklists and other records are completed in a timely fashion.

Job Qualifications

The following are minimum requirements related to the Cagewash Technician position.

High school diploma or GED.
Experience and/or training working with animal husbandry preferred.

The pay for this position is $20.32 per hour.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Cagewash Technician I (EG) (Baltimore, MD, US, 21224)

Job Summary

We are seeking a Cagewash Technician for our Insourcing Solutions site located in Baltimore, MD.

Additional responsibilities include:

Dumps and scrapes soiled bedding from caging and prepares caging for cagewash under minimal supervision.
Sanitizes caging and related equipment using cage washers, pressure washer or hand washing as required.
Properly disposes of soiled bedding and waste in specified receptacles.
Cleans and sanitizes cage preparation and storage areas.
Monitors and records results of cagewash water temperature and cleaning results using provided supplies such as temperature dots/strips, cultures.
Ensures that all logbooks, checklists and other records are completed in a timely fashion.

Job Qualifications

The following are minimum requirements related to the Cagewash Technician position.

High school diploma or GED preferred
Experience and/or training working with animal husbandry preferred.

The pay for this position is $20.32 per hour.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Animal Caretaker I (EG) (Baltimore, MD, US, 21224)

Job Summary

We are seeking an Animal Caretaker I to join our Insourcing Solutions team located in Baltimore, MD

As the Animal Caretaker I, you will provide basic husbandry to rodents and lagomorphs, monitor environmental parameters for abnormalities and provide customer assistance to the investigative staff.

Additional responsibilities include:

- Monitor environmental parameters and maintain written records

- Assist with restraint and handling of various animal species.

- Receive, inspect, and put away incoming animals; as well as provide for sentinel animals in each rodent housing area.

- Operate equipment and perform general housekeeping.

Job Qualifications

The following are minimum requirements related to the Animal Caretaker I position:

- AALAS certification at the ALAT level within one year of eligibility

- 1 year of related experience in animal care

- 3 months working with lab animal species (rodents), preferred

- High school diploma/ GED preferred

The pay for this position is $21.00 USD per hour.

For more information, please visit www.criver.com.

Animal Care Technician I (EG) (Baltimore, MD, US, 21224)

Job Summary

We are seeking an Animal Care Technician I for our Insourcing Solutions site located in Baltimore, MD.

As the Animal Care Technician I, you will provide husbandry and veterinary assistance in a laboratory for small animals, as well as monitor animal health and report findings.

Additional responsibilities include:

Prepare caging for cagewash.
Perform daily animal health observations and report any abnormal conditions or behavior. Monitor and report irregularities in environmental conditions that may affect animals.
Clean assigned animal rooms, facility and animal care equipment, and associated animal facility areas. Obtain weekly animal census.
Ensure logbooks, checklists and other records are completed accurately in a timely fashion.
Provide environmental enrichment feed and other enrichment stimuli and/ or provide behavioral assessments.

Job Qualifications
The following are minimum requirements related to the Animal Care Technician I position:

High school diploma or GED
AALAS certification at the ALAT level within one year of eligibility
1 year related experience in animal care
3 months working with lab animal species, most applicable rodents, preferred

The pay for this position is $20.32 USD per hour.

For more information, please visit www.criver.com.

Account Manager (Yokohama-shi, 14, JP, 222-0033)

Job Summary

Responsible for achieving quarterly and annual sales targets for assigned region for all Charles River product and services into commercial accounts in a designated geographical region.

Duties & Responsibilities

Work with internal teams (TMDM, PM, Management, etc.) to increase market share and revenue at assigned accounts.
With direction from management, generate account-specific sales strategies to sell all company products and services.
Work with management to prepare and provide accurate account forecasts for assigned accounts/territories when required by management.
Develop and qualify account leads through frequent customer contact and prospecting.
Build relationships with customers to influence the acceptance and use of company products and services.
Communicate available product and services and inform customers of new products and services in a timely manner.
Handle initial inquires and qualify all prospective opportunities.
Effectively utilize CRM (SFDC) to capture customer information to included but not limited to accurate pipelines and effective opportunity management and activity documentation.
Work closely with the specialist sales staff to ensure that the customer has a cohesive and responsive team throughout the sales process
Proficient in knowledge of competitor profiles and is able to develop positioning to influence potential customers.
Consistently achieve all revenue targets
Proficient in selling the entire portfolio of Microbial Solutions Products and Services.

Complete all required sales documentation in a timely manner.
Participate in sales meetings and trade shows as required.
Share customer problems/concerns with all appropriate departments for quality resolution.
Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor’s degree (B.A. /B.S.) or equivalent in life sciences, sales or related discipline.
Experience: Minimum 2 years experience, preferably in life science industry.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: Valid driver’s license required.
Other: Excellent communication and presentation skills. Proficient in the use of standard office computer applications (word processing, spreadsheets, presentations, e-mail).

PHYSICAL DEMANDS:

Must regularly operate a computer and occasionally operate other office productivity machinery such as a calculator, copy machine, and computer printer.
Must regularly communicate with employees/customers; must be able to exchange accurate information verbally (in person and on the phone) and in writing.
Must occasionally move about inside the office to access file cabinets, office machinery, etc.

WORK ENVIRONMENT:

General office working conditions.
The noise level in the work environment is usually quiet.

Comments:

This position requires frequent domestic travel.

For more information, please visit www.criver.com.

Husbandry Group Leader (NHP) (Frederick, MD, US, 21701)

Job Summary

The NHP Quarantine Group Leader will assist the Supervisor with monitoring workflow and work assignments to assure required tasks are completed in assigned area. Serve as lead/primary technician and perform technical duties. Provide leadership and technical guidance and serve as a mentor to less experienced staff.

Work schedule: Tuesday- Saturday; 6:00am - 2:30pm

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Assign and direct employees to perform routine animal husbandry, area housekeeping/ sanitation and animal care to ensure animal welfare and high quality animal care.
Provide direction to department personnel; communicate and uphold company work standards, company policies and procedures, and department operating procedures by acting as a model for direct reports and peers.
Ensure accurate documentation of department activities and performance of personnel associated with department operations and the coordination of those tasks; audit department operations and documentation for accuracy, noting deviation.
Assist with training new team members in performing duties in compliance with the site’s Standard Operating Procedures and required forms.
Oversee adherence and proactively promote safety.
Perform procedures and tasks related to department or area operations, including support-related tasks and operations-related administrative tasks.
Deliver communications to animal husbandry staff concerning husbandry and shipment activities, receive information from Animal Care Supervisor(s) and Site Management Team and respond or channel communication to the proper recipient.
Provide backup as needed to Supervisor or Manager. Provide input on staffing actions (hiring/separation, performance appraisal, etc.)
Prepare paperwork for animal exports ensuring the safe packing, crating and loading of animals as well as animal import receiving documents following the delivery of an import. .
Provide backup for Facility Supervisor for animal import receipt and/or animal export. Provide oversight of the offloading and housing of animals and sanitation following an animal import, and/or the packing, loading and required paperwork for an animal export.
Perform animal husbandry and general housekeeping, which can include feed, watering, and cleaning cages as required. Monitor animal health visually and by performing contract lab testing, as directed by the veterinary staff, while adhering to safety procedures.
Perform all other related duties as assigned.

Job Qualifications

Education: High school diploma or General Education Degree (G.E.D.)
Experience: Three or more years of related experience and/or training in a laboratory animal facility

An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Certification/Licensure: AALAS certification at the Assistant Technician (ALAT) level required; certification at Technician (LAT) or Technologist (LATG) level preferred
Other: Continued education in the area of management/ leadership preferred. Must be proficient in all procedures and tasks related to department or area operations, including support-related tasks and operations-related administrative tasks.

PHYSICAL DEMANDS:

While performing the duties of this job, the employee is regularly required to stand and walk; use hands to finger, handle or feel objects, tools or controls; and reach with hands and arms.
The employee must be able to lift, hold and/or move up to 50 pounds; this includes equipment and animals.
Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and the ability to adjust focus.

WORK ENVIRONMENT:

While performing the duties of this job, the employee regularly wears protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots); works with biohazards; and works with live animals (small, medium and/or large) with risk of exposure to allergens and/or zoonotic diseases.
While performing the duties of this job, the employee is exposed to fumes or airborne particles, unpleasant odors, and wet, humid and/or extreme temperature conditions.
The noise level in the work environment is usually moderate.

The pay for this position is $30/hour. Please note that compensation varies based on factors including, but not limited to, experience, skills, education, and certifications.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Primate Technician I (Frederick, MD, US, 21701)

Job Summary

This is an entry-level position where you can gain experience and begin your career in life sciences. Training provided!

As a Primate Technician I, you will be responsible for the daily care of research animals. Your contribution will ensure the health and well-being of our animals, as well as impact the lives of patients across the world.

Work schedule: Sunday - Thursday, 6:00am - 2:30pm or Tuesday - Saturday, 6:00am - 2:30pm

Responsibilities:

Providing food and water
Inspect feeding and watering devices for proper function
Cleaning and sanitizing cages and enclosures
Observe animals for overall health and wellbeing
Assisting with the movement of animals
Log animal care data and maintain accurate records
Other assigned duties, including restocking supplies

Work Environment & Physical Demands:

Work is performed in an warm, climate controlled environment.
PPE (protective equipment) includes regular use of surgical mask, cap, goggles, face shield, scrubs, and boots.
The warm setting, physicality of the job duties, and use of personal protective equipment (PPE), when combined, frequently cause employees to become hot and sweaty.
Job duties require employee to regularly stoop, crouch, kneel, and reach up with hands and arms to perform repetitive tasks, and walk and stand for extended periods of time.
Employee must be able to regularly lift, hold and/or move up to 50 pounds.

Job Qualifications

If you possess the following qualities, we will train you in the rest:

High School Diploma or GED preferred, but not required
Animal care experience preferred
Previous experience in a physically demanding role
Previous experience maintaining records and complying with regulations and Standard Operating Procedures (SOPs)
Strong attention to detail
Enjoys being part of a team
Flexible and available to work holidays (on rotational basis) and overtime as needed

The starting pay for this position is $19.75 per hour.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

For more information, please visit www.criver.com.

Laboratory Animal Technician I (Ft. Detrick, MD, US, 21702)

Job Summary

We are seeking an experienced Laboratory Animal Technician to join our Insourcing Solutions team, located in Frederick, MD.

As the Laboratory Animal Technician, you will perform standard veterinary technical support for the NIAID Integrated Research Facility. Maintain performance levels consistent with and according to company standards at The National Institutes of Health.

Additional responsibilities include:

Reviews, comprehends and complies with all SOPs and quality assurance standards pertaining to specific areas. Cares for and maintains laboratory animals in accordance with the Animal Welfare Act and the Guide for the Care and Use of Laboratory Animals, as well as, NIH policies and Guidelines and other pertinent regulations and policies.

Works closely with Clinical Veterinarian(s) and Research Support Specialist(s) to perform daily health assessments, perform experimental manipulations and provide animal treatments as instructed by Clinical Veterinarian(s).

Performs technical functions required by research protocols utilizing rodents and nonhuman primates in infectious disease research.

Maintain individual health records for nonhuman primates and maintain accurate records of animal importations, health observations, and housing or support areas as required by Institute and facility.

Communicating with veterinary support staff, facility veterinarian(s), investigators and other staff members regarding the health of animals and experimental manipulations.

Performs daily colony health examinations and clinical observations of sick animals prior to reporting adverse findings to Clinical Veterinarian(s) and Research Support Specialists.

Duties continued

Provides technical support (e.g. animal handling and restraint, tail vein injections, collecting blood and other samples, perform injections, treatments, surgical preparation and post-operative observations and assist with research procedures as directed).

Familiarity with and the ability to use various forms of anesthetics and their means of application, including gas and injectable anesthetics.

Assist with various imaging modalities (e.g. CT/PET, CT/SPECT, MRI and XRAY) by providing patient monitoring and experimental manipulations.

Actively interacts with facility veterinarian(s) and investigators as required to solve customer requests, inquiries, and complaints and to provide technical assistance.

Assists with training animal facility staff in husbandry and technical procedures.

Performs animal husbandry - which can include feed, watering, and cleaning cages as required. Provide environmental enrichment and/or behavioral assessments.

Prepares and submits written reports, charts, logs and inventories as requested by management.

Operates equipment and uses supplies according to safety guidelines; performs general housekeeping and adheres to safety procedures. Complies with safety policies and procedures and MSDS guidelines, including those related to biohazards and radioactive substances.

Assists with the receipt, stocking and maintenance of supply inventories.

Maintains required attendance level and adheres to work schedule in accordance with required staffing levels in order to ensure that assigned duties are completed.

Performs other duties as assigned

Job Qualifications

Education: High school diploma or general education degree (GED) required. Possession of an Associate of Arts degree in Veterinary Technology or equivalent college level program is desired.

Experience: Three years’ experience in a laboratory animal facility, with experience relevant animal care, handling and technical experience required.

Certification/Licensure: AALAS certification at the Laboratory Animal Technician level (LAT) required.

Knowledge, Skills and abilities:

Basic knowledge of animal technical skills and ability to identify sick animals and provide medical treatment as prescribed. Ability to perform tail vein injections.
Computer literacy in word processing and database record keeping preferred.
Must be able to follow verbal and written instructions and exhibit interpersonal skills that are conducive to effective communication and that contribute to a congenial work environment. Maintain positive work atmosphere by behaving and communicating in a professional manner with clients, customers, coworkers, and supervisors.
Ability to read, write, speak and understand English.

Work Environment and Physical Demands

Physical Demands:

While performing the duties of this job, the employee is regularly required to stand and reach with hands and arms. The employee frequently is required to use hands to finger, handle, or feel objects, tools, or controls. The employee is occasionally required to stoop, kneel, crouch, or crawl. The employee is frequently required to type at a computer or typewriter.

The employee must regularly lift and/or move up to 50 pounds.

Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception, and the ability to adjust focus.

Work Enviroment:

While performing the duties of this job, the employee regularly works with computers, frequently works near moving mechanical parts; is exposed to fumes or airborne particles, laboratory animal caging of various species including mice, rats, other rodents, rabbits and nonhuman primates; is occasionally exposed to wet and/or humid conditions, toxic or caustic chemicals, biohazard materials/agents, infectious disease and risk of electrical shock.

This position requires working at Animal Biosafety Level 4 (ABSL-4) with animals infected with dangerous or toxic agents that pose a high individual risk or life-threatening disease, aerosol transmission, or related agent with unknown transmission.

Personnel must wear a positive pressure protective suit in the ABSL-4.

This position requires working near different imaging modalities including MR, PET/CT, SPECT/CT, X-ray and exposure to animals injected with radioactive isotopes. Must be able to work within a Magnetic Resonance Imaging suite.

The noise level in the work environment is usually moderate.

The pay rate for this position is $35 USD per hour. Please note that salary rates are based on varying factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Veterinary Technician (Poolesville, MD, US, 20837)

Job Summary

We are looking for a Veterinary Technician (Levels I, II) to join our Insourcing Solutions team located in Poolesville, MD. (See qualifications for each level)

In the Veterinary Technician (Levels I, II) role, you will assist with all activities required for supporting and maintaining the site animal colonies and Animal Study Protocols in support of the research program. Care for and maintain lab animals in accordance with all guidelines, policies, and regulations to ensure their health and welfare.

Additional responsibilities include:

Reviews, comprehends, and participates in the development of all SOP's and quality assurance standards pertaining to specific area. Cares for and maintains laboratory animals in accordance with Animal Welfare Act and the “Guide for the Care and Use of Laboratory Animals, as well as, NIH policies and Guidelines and other pertinent regulations and policies.
Communicate with animal care staff, co-workers, veterinary staff, supervisors, PI, and collaborators.
Provides veterinary technical and surgical support for NHPs (e.g. animal handling and restraint, collect blood and other tissues samples, perform injections, treatments, surgical preparation, pre-, peri-, and post-operative observations, anesthesia, intubations, placement of indwelling catheters, femoral, and necropsy).
Provides research support to investigators via Technical Request forms.
Operates and maintains a variety of medical equipment (e.g. blood gas analyzer, CBC machine, x-ray, anesthetic machines, EKG monitors, blood pressure recorders, IV pumps, surgical and dentistry instruments, irradiator and sterilizers).
Arranges, cleans and maintains procedure, treatment, and necropsy/procedure rooms.
Quality Control of treatment and procedure rooms including cleaning, supplies, and monitoring expirations dates.

Responsibilities continued:

Calculate drug dosages and administration frequencies.
Provides research support to investigators via Technical Request forms.
Accurately maintain electronic medical records and update treatment plans.
Monitors the environment and provides animal health surveillance as directed by facility veterinarian.
Assists in the maintenance and detailed documentation of accurate surgical, anesthetic and treatment procedures in the animal medical records and files. Assists in keeping medical records and files current through timely placement of information and supporting documents.
Quality Control of treatment and procedure rooms including cleaning, supplies, and monitoring expirations dates.
Provides limited support to the nonhuman primate environmental enrichment and psychological well-being plan, as needed in the absence of Behavioral staff.
Maintains and operates equipment and uses supplies according to SOPs and safety guidelines; performs general housekeeping and adheres to safety procedures. Complies with safety policies and procedures and MSDS guidelines, including those related to biohazards and radioactive substances.
Actively interacts with customers as required to solve customer requests, inquiries, and complaints and to provide technical assistance.
Maintains required attendance levels and adherence to work schedule in accordance with required staffing levels in order to ensure that assigned duties are completed.
Performs other duties as assigned.

Job Qualifications

Level I

Education: All candidates must possess a high school diploma or GED.

In addition, to qualify you must meet at least ONE of the following requirements:

AA in Veterinary Technology.
2-3 years' experience working with animals in biomedical research or companion veterinary medicine.
AALAS certification at the Laboratory Animal Technician (LAT) level.

Level II

Education: HS diploma or general education degree (GED) required. BS degree in Animal Science, Biology or similar, discipline or AA in Veterinary Technology preferred.
Experience: 3-5 years' experience working with animals (in biomedical research preferred), of which 1 year must be with non-human primates
Certification/Licensure: Eligible to take the AALAS Laboratory Animal Technician (LATG) certification.

The pay range for this position is $28.00 to $33.00 USD per hour.  Please note the range covers levels I - II, salary will depend on level, in addition to factors such as experience, skills, and certification.

Additional requirements

- Knowledge and technical skills related to animal health observations, treatments, husbandry and restraint of various animal species.
- Knowledge of general anatomy, biology and physiology of a variety of species.
- Knowledge and familiarity with operating room equipment (e.g. anesthesia machines, monitoring equipment, etc).
- Ability to calculate drug doses.
- Ability to work independently and within a team with minimal supervision; ability to multitask and exhibit good organizational skills
- Must be able to follow verbal and written instructions and exhibit interpersonal skills that are conducive to effective communication and that contribute to a congenial work environment. Maintain positive work atmosphere by behaving and communicating in a professional manner with clients, customers, coworkers, and supervisors
- Ability to read, write, speak and understand English.

Physical demands

While performing the duties of this job, the employee is regularly required to walk, stand; use hands to finger, handle, or feel objects, tools, or controls; and reach with hands and arms. The employee frequently is required to stoop, kneel, crouch, or crawl. The employee is occasionally required to sit.
The employee must regularly lift and/or move up to 50 pounds.
Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception, and the ability to adjust focus.

Work Environment

While performing the duties of this job, the employee is exposed to laboratory animal caging (non-human primates) and is regularly exposed to warm and/or humid conditions and chemicals.
The noise level in the work environment is usually moderate.
The employee works in various weather conditions.

For more information, please visit www.criver.com.

Laboratory Animal Technician (NHP) (Poolesville, MD, US, 20837)

Job Summary

We are looking for an Laboratory Animal Technician (Levels I, II) to join our Insourcing Solutions team located in Poolesville, MD. (See qualifications for each level)

As the Laboratory Animal Technician (Levels I, II) role, you will maintain, monitor, and document the health, well-being, and physical environment of animals on-site.

Additional responsibilities include:

Monitoring daily animal health and welfare while performing daily animal health observations.
Animal husbandry duties include daily water bottle /automatic water line and cage checks; provide appropriate food and water; environmental enrichment; perform cage changing and/or cage cleaning as required.
Maintain records related to the animal and facility functions; record animal health concerns and report as needed.
Assists with restraint, handling, and manipulation of various animal species.
Receive, inspect, and house incoming animals.
Other duties will include general housekeeping, in addition to reviewing, comprehending, and complying with all SOPs and quality assurance standards pertaining to specific area.

Job Qualifications:

Level I

Education: A high school diploma or GED (General Education Degree) is required.
Expereience: Experience with lab animals, specifically non-human primates, or any animal experience preferred but not required.
Certification/Licensure: Must be able to obtain the AALAS certification at the ALAT level within 6 months of eligibility.

Level II

Education: High school diploma or GED (General Education Degree) is required.
Experience: A minimum of one (1) years of experience relating to animal care and handling with NHP (non-human primates).
Certification/Licensure: Eligibility for AALAS (American Association of Laboratory Animal Science) certification at the ALAT (Assistant Laboratory Animal Technician) level required.

The pay for this position is $22.00 - 25.00 USD per hour.  Please note that salaries vary within the range based on factors including experience, skills, education, certifications, and location.

For more information, please visit www.criver.com.

Behavior Reseach Specialist II (Poolesville, MD, US, 20837)

Job Summary

We are looking for a Behavioral Research Specialist II to join our Insourcing Solutions team located in Poolesville, MD.

As the Behavioral Research Specialist II, you will maintain, monitor and provide the necessary care to meet the needs of lab animal psychological well-being and behavioral health under the guidance of the DVR program.

Additional responsibilities include:

Reviews, comprehends and complies with all SOP's and quality assurance standards pertaining to specific area.
Conduct behavioral assessments on NHPs as requested.
Establish pairs/social groups and monitor for compatibility. Maintaining the required goal of the QASP.
Use positive reinforcement to train animals for various husbandry and veterinary procedures.
Participate in discussions pertaining to enrichment.
Evaluate and implement novel behavioral data collection methodologies.

Responsibilities continued

Prepare for incoming shipments of NHPs and work with animal care managers/staff on adjustments to husbandry.
Organize and maintain related data and demonstrate proficiency using computer programs; able to enter and/or interpret data in spreadsheets for data analyses.
Perform all other duties as assigned by management.
Occasional work with other species (such as but not limited to varius ungulates and mice)

Job Qualifications

The following are minimum requirements related to the Behavioral Research Specialist I position:

Education: BS or MS (preferred) degree in a scientific discipline or have an AA degree and related practical experience.

Experience: Five years’ experience in a laboratory animal facility of which at least two (2) years preferred with NHP (non-human primates). Performing animal observations and behavior assessments highly desired; and an understanding of the applications of positive reinforcement training.

The pay for this position is $35.00 USD per hour.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us and BE THE DIFFERENCE!

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Associate Director Quality (Rockville, MD, US, 20850)

Job Summary

The Associate Director Quality is responsible for ensuring that Quality performance, compliance, and operational excellence are embedded and maintained across all strategic initiatives, GMP operations, and support functions at the Rockville site. This role provides leadership for Quality Operations Oversight, On‑the‑Floor Quality, and client‑facing Quality programs supporting the CDMO‑Rockville portfolio. The Associate Director leads, develops, and mentors Quality staff while providing strategic direction to maintain compliance with regulatory requirements in support of existing and new cell‑based gene therapy manufacturing.

Key Responsibilities:

Quality Leadership & Strategic Oversight

Serve as a strong, accountable leader who motivates, mentors, and develops the Quality team; sets clear expectations and drives ownership, performance, and continuous improvement.
Apply deep process knowledge and technical acumen—gene therapy preferred, biologics acceptable—to drive effective decision‑making, even in areas with limited historical precedent.
Represent Quality as an FDA‑facing subject matter expert and provide expertise to support preparation for regulatory inspections and client audits.
Promote a risk‑based, phase‑appropriate, and agile quality culture; demonstrate balanced judgment across Quality, operational timelines, and client needs.

Operational Quality Oversight

Ensure Quality deliverables for batch record review, lot disposition, and product release meet internal and external expectations and are executed in a timely, compliant, and client‑focused manner.
Oversee the review and approval of GMP records including batch production records, QC test reports, EM data, cleaning records, equipment and facility records, assay qualifications, stability protocols, and related documentation.
Manage execution of on‑the‑floor Quality operations, including walkthroughs of manufacturing, QC labs, storage, and material receiving areas to ensure GMP compliance.
Provide technical expertise during investigations; support data gathering, root‑cause analysis, and development of corrective and preventive actions (CAPA).

Client & Project Support

Monitor Quality support activities for client programs and ensure issues are escalated appropriately to maintain on‑time project delivery.
Partner with Manufacturing, Technical Operations, and cross‑functional stakeholders to resolve issues, identify root causes, and implement effective CAPA.
Act as a role model for effective problem‑solving and triage by demonstrating sound judgment, balanced risk assessment, and strong communication.

Quality Systems & Documentation

Oversee the revision, issuance, and tracking of controlled documents supporting bulk and sterile fill operations.
Perform and/or approve Quality Control data review, audit trail review, and other compliance checks.
Support cross‑training and participate in other Quality functions including Quality Systems, Training, Document Control, and Supplier Quality.
Contribute to internal and vendor audits; identify deficiencies and ensure timely closure of observations.
Drive continuous improvement initiatives that support self‑detecting, self‑correcting systems and operational excellence.

Leadership, Communication & Issue Resolution

Notify senior management of critical issues with potential impact to manufacturing timelines, offering feasible solutions and risk‑mitigation strategies.
Actively participate in hiring, onboarding, and developing new team members.
Ensure effective communication at all levels of the organization and with external clients.

Job Qualifications

BS/BA required; MS in a scientific or technical discipline preferred.
Minimum 8 years of Quality leadership experience in biologics, pharmaceuticals, or cell/gene therapy.
Experience with CDMO operations and/or gene‑modified or cell‑based therapies required.
Demonstrated experience reviewing QC test results and GMP batch records for clinical and commercial manufacturing.
Strong working knowledge of FDA, EMA, ICH regulations and industry best practices.
Experience with TrackWise or similar electronic Quality management systems preferred.
Excellent interpersonal, negotiation, and conflict‑resolution skills; able to influence across levels and functions.
Exceptional written and verbal communication skills.
Strong organizational capability to manage complex processes and competing priorities.
Proven ability to lead investigations, risk assessments, and CAPA programs.
Internal or external auditor experience.
Hands‑on, detail‑oriented, proactive, and able to make informed decisions in ambiguous situations.

Compensation Data

The pay rate for this role is $156,000 - $176,000 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Charles River’s CDMO Services

With over 20 years of experience and industry-leading expertise, Charles River’s cell and gene therapy Contract Development and Manufacturing Organization (CDMO) group supports biotechnology and pharmaceutical companies in advancing their complex programs from early development through commercialization. Our integrated, phase-appropriate CDMO capabilities—including plasmid DNA, viral vector, and cell therapy manufacturing—enable seamless development and faster timelines. With centers of excellence in the US and UK, we offer GMP-compliant and research-grade solutions, along with comprehensive analytical services and regulatory support. Whether clients need end-to-end development, standalone services, or insourced support, our CDMO team provides custom solutions to meet evolving program needs. From process development in Hanover to viral vector manufacturing in Rockville, large-scale cell therapy production in Memphis, and plasmid DNA services in Keele, we simplify the supply chain and accelerate cell and gene therapy breakthroughs.

About Charles River

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Cagewash Attendant I (14BS) (Bethesda, MD, US, 20892)

Job Summary

We are seeking a Cagewash Attendant I to join our Insourcing Solutions team located in Bethesda, MD.

As the Cagewash Attendant I, you will sanitize, maintain and repair animal cagewash materials.

Additional responsibilities include:

Follow SOPs and quality assurance standards
Perform routine preventative maintenance on cagewash and autoclaves
Maintain animal holding facilities clean and organized
Other tasks may include assist with receipt, stocking and maintenance of inventory supplies
Become involved in animal care and husbandry of multiple animal species

Job Qualifications

The following are minimum requirements related to the Cagewash Attendant I position:

High school diploma or GED preferred
Knowledge of detergent/disinfectant and operating knowledge of sanitization and sterilization equipment
Cagewash experience preferred
Must be successful in obtaining the ALAT (Assistant Lab Animal Technician) Certification within 1 year of eligibility.

The pay for this position is $20.32 USD per hour. Schedule: Monday through Friday 7AM-3:30PM.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Laboratory Animal Technician I (33) (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Laboratory Animal Technician I to join our Insourcing Solutions team located in Bethesda, MD.

As the Laboratory Animal Technician I, you will maintain and monitor the health, technical, and physical environments within the animal care facility. You'll work closely with the Clinical Veterinarians and Veterinary support staff to perform daily health assessments, clinical observations and providing treatments to the lab animals.

Additional responsibilities include:

Technical support: animal handling and restraint, weaning, timed mating, tail snips, ear tagging, injections (Sub-Q, IP, tail vein), blood/tissue collections (mandibular, tail vein, term bleed: IC or RO), treatments, microinjections, surgical preparations, and post-operative observations.
Familiarity with and ability to use various forms of anesthetic (Gas/Injectable).
Provide environmental enrichment feed, other enrichment stimuli as well as behavioral assessments.
Provide quality assurance to include animal health surveillance, HVAC, animal shipments, facility sanitation and other procedures.
Maintain accurate records of animal importations, breeding, and health checks.
Assist in assessing training needs; develop and present to staff and PIs.
Prepare and submit written reports, charts, logs, and inventories.

Job Qualifications

The following are minimum requirements for the Lab Animal Technician I:

High school diploma or GED.
A minimum of 3 years' lab animal facility experience performing animal husbandry and clinical support.
Must have LAT certification.
Schedule: Monday through Friday: 7AM-3:30PM, weekends and holidays if necessary.

The pay range for this position is $27 to $30 USD per hour.  Please note that salaries vary within the range based on factors including skills, certifications, and location.  

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Cagewash Attendant I (EG) (Bethesda, MD, US, 20892)

Job Summary

We are seeking a Cagewash Attendant I to join our Insourcing Solutions team located in Bethesda, MD.

As the Cagewash Attendant I, you will sanitize, maintain and repair animal cagewash materials.

Additional responsibilities include:

Follow SOPs and quality assurance standards
Perform routine preventative maintenance on cagewash and autoclaves
Maintain animal holding facilities clean and organized
Other tasks may include assist with receipt, stocking and maintenance of inventory supplies
Become involved in animal care and husbandry of multiple animal species

Job Qualifications

The following are minimum requirements related to the Cagewash Attendant I position:

High school diploma or GED preferred
Knowledge of detergent/disinfectant and operating knowledge of sanitization and sterilization equipment
Cagewash experience preferred
Must be successful in obtaining the ALAT (Assistant Lab Animal Technician) Certification within 1 year of eligibility.

The pay for this position is $20.32 USD per hour. Schedule: Monday through Friday 7AM-3:30PM.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technician I (EG) (Bethesda, MD, US, 20892)

Job Summary

We are seeking an Animal Care Technician I to join our Insourcing Solutions team located in Bethesda, MD.

As the Animal Care Technician I, you will work with our research animals to ensure they are well cared for.

Additional responsibilities include:
•   Providing food & water.
•   Ensuring cages are clean.
•   Performing and recording daily animal health checks.
•   Handing & restraining animals for injections
•   Learning & applying quality assurance standards
•   Examining new animals that arrive at the site & helping them to settle in
•   Learn & become involved in breeding of multiple animal species

Job Qualifications

The following are minimum requirements related to the Animal Care Technician I position:
• Six months of animal experience (e.g., dog walking, pet sitting, kennel attendant, vet assistant, farm hand, 4-H background, pet store worker)
• Must be successful in obtaining the ALAT (Assistant Lab Animal Technician) Certification within 1-2 years of eligibility

• High school diploma/GED preferred
 
The pay for this position is 22/hour USD per hour. 

Schedule: Monday through Friday 7AM-3:30PM. Must be available some weekend and holidays if necessary

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Breeder Technician (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Breeder Technician to join our Insourcing Solutions team, located in Bethesda, MD.

As a Breeder Technician, you will monitor daily animal health and welfare while performing duties to maintain the quality and health of research animals, to include but not limited to water bottle, cage, food, and water checks; cage changes; utilizing microisolator techniques, as required; and recording animal health concerns while reporting to veterinary staff.

Additional responsibilities include:

Maintain accurate records of animal breeding, health, and housing/isolator or support areas. Follow breeding and weaning procedures to ensure required production levels.
Perform technical support to include, but not limited to animal handling and restraint, weaning, tail snips, ear tagging, blood collection, tissue collection, time-mating, rodent breeding colony management as needed, as well as assist with research procedures.
Provide rodent identification using various techniques. Assist veterinary staff with providing blood collection, clinical and post-operative care, and observations. Ability to use an anesthesia machine and monitor anesthetized rodents.
Receive, inspect, and house incoming animals, and complete related receiving duties.
Perform cleaning and sanitation of work areas and facility equipment.
Provide customer service to research staff and complete submitted service requests.
General housekeeping.
Assist with receipt, stocking, and maintenance of supply inventories.

Job Qualifications

The following are minimum requirements related to the Breeder Technician position:

High school diploma or GED plus 3 years lab animal (rodent) experience or AA/AS degree plus 2 years lab animal (rodent) experience or BA/BS degree or higher and 1 year lab animal (rodent) experience.
AALAS certification eligibility at the LAT level required, existing LAT certification preferred.
Proficient in computer (MS Office Suite)

The pay range for this position is $25.00 USD per hour.

For more information, please visit www.criver.com.

Environmental Health & Safety Associate (Horsham, PA, US, 19044)

Job Summary

Responsible for managing the Environmental, Health &Safety (EH&S) Program for adherence to local, state, and federal regulations. Oversee all aspects of the Horsham Safety Program.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
⦁ Administer and maintain biowaste at facilities including waste profiling, permitting, manifesting, record keeping and reports.
⦁ Oversee transportation and maintain logs of biowaste material; ensure competency of digestor operators.
⦁ Administer and maintain the environmental index and permit database, ensure up to date records for compliance for all regulatory agencies, and sponsor inspections.
⦁ Assist in the implementation and monitoring of company health and safety programs
⦁ Maintain all Safety Data Sheets (SDS), database and binders, perform scheduled inventory of products and document locations of products, data entry of all required SDS information into appropriate tracking database.
⦁ Conduct safety training classes as qualified and required
⦁ Assist in coordinating and scheduling of safety committee meetings.
⦁ Inventory, stock, and order safety supplies.
⦁ Perform respirator fit testing and monitor and review respirator monthly inspection and end of service logs

Perform GEMBA walks of lab and support space
Conduct risk assessments for biohazradous and OEB agents
⦁ Conduct inspections of safety shower and eyewash checks.
⦁ Perform all other related duties as assigned.

The pay for this position is between $79,500 and $88,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
⦁ Education: High school diploma or General Education Degree (G.E.D.) required. Associates Degree (A.A./A.S.) or equivalent in environmental science, environmental engineering or related discipline preferred
⦁ Experience: 2 years related experience in a health & safety and or environmental position. Experience in regulatory environment preferred.
⦁ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
⦁ Certification/Licensure: OSHA certification preferred.
Other: Proficient in the use of computer network and standard office software applications. Knowledge of governmental safety and environmental regulations and chemical handling preferred.

Comments:
⦁ This position requires overtime, weekend, holiday, and/or after hours shift coverage, as needed.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Archives Customer Service AssociateI (Horsham, PA, US, 19044)

Job Summary

Responsible for client communication, billing, and marketing of Charles River Archiving services. Responsible for the placement and retrieval of archived material in a secure and controlled access archive. Maintain accurate summary of records. Update inventories for access and retrieval of archive materials. Interact with clients.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
⦁ Performs and documents all procedures, materials, and results in compliance with regulatory standards as applicable to protocols, reports and standard operating procedures.
⦁ Upholds archive security procedures and maintains the integrity of archived materials and client confidentiality.
⦁ Performs tasks including but not limited to, client contract generation, organizing, filing, and retrieving records.
⦁ Utilize the archival management system for client contract generation.
⦁ Communicate with internal and external clients as it relates to contracting and archiving.
⦁ Develops skills aligned with the needs of one operational area (transfer of ownership, local or global account manager, contract development, marketing).
⦁ Prepare archiving contracts and relevant documents to notify clients of archived study materials.
⦁ Assist clients with regulatory retention periods in collaboration with the archivist.
⦁ Oversee client communication and requests regarding archived material.
⦁ Monitor and track archiving business activities.
⦁ Perform all other related duties as assigned.

The pay range for this position is between $22.00 and $24.00 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
⦁ Education: High school diploma or General Education Degree (G.E.D.)/ Associate’s degree (A.A./A.S.) / or equivalent desired in business or administrative assistant discipline.
⦁ Experience: 0.5-2 year of customer service experience required. 1-2 year of office experience or administrative/inventory management training preferred. Marketing experience preferred.
⦁ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
⦁ Certification/Licensure: None.
⦁ Other: Proficient computer skills with departmental databases, word processing (Word), and spreadsheet programs (Excel). Must be organized, have attention to detail and possess good problem-solving and communication skills.

PHYSICAL DEMANDS:
⦁ Regularly communicate with employees/customers through various technologies, media, sources and contacts. Must be able to exchange accurate information.
⦁ Must regularly operate a computer and occasionally operate other office productivity machinery such as a calculator, copy machine, and computer printer.
⦁ Occasionally move about inside the office to access file cabinets, office machinery, etc.
⦁ Occasionally lift and carry up to 40 pounds (archived material) up and down stairs, laterally from shelf to shelf and from and to shelves of varying height; up to 5 feet high.

WORK ENVIRONMENT:
⦁ General office working conditions; the noise level is usually quiet.
⦁ May work from home with reliable internet and communication access.

Comments:
⦁ May occasionally be required to work overtime or come into the office for meetings or trainings.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Process Evaluation Technician I (Wayne, PA, US, 19087)

Job Summary

Under direct supervision, responsible for performing daily laboratory tasks as they relate to Process Evaluation Testing Services.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform daily laboratory operations.
Prepare materials and buffers used in projects.
Maintain inventories of all supplies/buffers used in projects.
Perform routine experiments, tests and procedures following well-defined guidelines.
Maintain a safe working environment by adhering to Company policies and procedures.
Follow all protocols, S0Ps, and cGMPs/cGLPs as they relate to specific tasks.
Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor's degree (B.A./B.S.) or equivalent in Biology or related discipline.
Experience: 0-1 years related experience in biological lab.
Certification/Licensure: None
Other: Knowledge of cGMPs or regulatory affairs pertaining to the pharmaceutical and biological industries is preferred. Must possess excellent interpersonal skills to maintain communication across biological functional groups. Able to communicate effectively in a group or one on one setting. Basic Microsoft Office skills are a plus.

The pay for this position is $24.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician I Molecular Biology (Wayne, PA, US, 19087)

Job Summary

Under direct supervision, responsible for performing daily laboratory tasks as they relate to Molecular Biology Testing Services.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Perform laboratory activities necessary for molecular biology testing including but not limited to;
• Reagent preparation including buffers, chemical solutions, complex mixtures and media preparations according to standard test methods.
• Perform tasks using aseptic techniques including work within a biological safety cabinet;
• Participate in the general maintenance of laboratory equipment;
• Conduct aseptic growth and/or manipulation of bacteria, yeast, virus and mammalian cells;
• Make detailed observations and accurately and precisely record data, summarize data for reports and document all activities performed in accordance with current Good Manufacturing Practice (cGMP)
• Perform a variety of molecular biology laboratory experiments, test and procedures including isolation and analysis of DNA and RNA, PCR, QF-PCR, restriction endonuclease digestion agarose gel electrophoresis, various blotting techniques and/or sequencing;
• Report results of experiments, test, and procedures and analyze data.
• Efficiently organize and plan daily activities
• Maintain a safe working environment by adhering to company policies and procedures.
• Follow all SOPs, STMs, and cGMP guidelines as they relate to specific tasks.
• Perform all other related duties as assigned.

Job Qualifications

• Education: Bachelor's degree (B.A./B.S.) or equivalent in Biology or related discipline.
• Experience: 0-1 years related experience in biological lab.
• Certification/Licensure: None
• Other: Knowledge of cGMPs or regulatory affairs pertaining to the pharmaceutical and biological industries is preferred. Must possess excellent interpersonal skills to maintain communication across biological functional groups. Able to communicate effectively in a group or one on one setting. Basic Microsoft Office skills are a plus.

The pay for this position is $24.70 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician I Microbiology (Malvern, PA, US, 19355)

Job Summary

Under direct supervision, responsible for performing daily laboratory tasks as they relate to Microbiology Testing Services.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Perform laboratory activities necessary for Microbiology testing including, but not limited to, reagent and media preparation, growth promotion of media and reagents and the practice of aseptic technique working within a biological safety cabinet.
• Perform routine laboratory maintenance including, but not limited to, cleaning of equipment, stocking of the laboratory and disposing of laboratory waste.
• Complete cleanroom gowning certification as necessary.
• Complete training on the performance of assays and/or environmental monitoring as assigned by their current Supervisor or Manager.
• Duties specific to Environmental Monitoring may include, but are not limited to:
• Oversee the general maintenance of all equipment related to the performance of Environmental Monitoring and schedule repairs as required. Perform any laboratory maintenance and/or monitoring as necessary.
• Responsible for the execution of both static and dynamic Environmental Monitoring and updating the EM Database.
• Perform preparation of sample material and all environmental and personnel isolates recovered during Environmental Monitoring for microbial identification, and updating the Microbial Identification Database.
• Duties specific to Sterile Services may include, but are not limited to:
• Perform bioburden and bioburden verification testing via pour plate and/or membrane filtration methods.
• Perform bacteriostasis and fungistasis testing via direct inoculation and/or membrane filtration.
• Perform sterility testing via direct inoculation and/or membrane filtration.
• Perform mycobacterium testing.
• Perform bacteriophage testing.
• Duties specific to Mycoplasma Testing may include, but are not limited to:
• Cultivable mycoplasma testing using broth and agar cultures following various compendia.
• Non-cultivable mycoplasma testing using indicator cell culture following various compendia.
• Perform mycoplasmastasis testing (inhibitory testing) following various compendia.
• Document all activities performed in notebooks, test batch records and/or forms in accordance with the current Good Manufacturing Practices.
• Perform all other related duties as assigned.

Job Qualifications

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Laboratory Assistant - Lab Support (Horsham, PA, US, 19044)

Job Summary

Perform basic laboratory and record-keeping tasks to support site operations.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
⦁ Clean and sanitize hallways, labs, and test article preparation rooms.
⦁ May be responsible for preparing simple lab solutions (ex. Bleach)
⦁ Monitor and maintain inventory of assigned areas (ex. PPE Stations, Hazard waste boxes, glassware, etc).
⦁ Order supplies for the lab and departments (ex. cleaning supplies, glassware, etc)
⦁ Pickup and deliver packages from receiving in a timely manner.
⦁ Assist with melting wax, printing labels for specimen collection.
⦁ Operate basic lab equipment and perform routine maintenance, as needed.
⦁ Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs).
⦁ Submit Work Orders for equipment or facility issues.
⦁ Prep cages, glassware and supplies for autoclaving.
⦁ Perform Pest Control checks of areas and document as per SOP.
⦁ Perform test article and control article discards under a fume hood.
⦁ Assist with the receipt and documentation of feed and bedding.
⦁ Perform and document weekly eye wash checks.
⦁ Assist in the breakdown and setup of study rooms.
⦁ Perform weekly census of animals.
⦁ Collaborate with technical staff in Operations, Pathology and Lab Sciences.
⦁ Assist in the archiving of non-study/study/ facility data (ex. cage wash forms).
⦁ Assist with clerical duties (ex. filing, making copies, etc.).
⦁ Perform all other related duties as assigned.

The pay range for this position is between $17.00 and $19.00 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
⦁ Education: High school diploma or General Education Degree (G.E.D.).
⦁ Experience: None
⦁ Certification/Licensure: None
⦁ Other: Must be detail-oriented and have general familiarity with lab procedures. Good verbal communication skills required. Basic computer skills; familiarity with Microsoft Office software.

PHYSICAL DEMANDS:
⦁ Employees must be able to regularly lift and move heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or supplies.
⦁ Must be able to regularly push wheeled carts weighing up to 1200 pounds on a repetitive basis each day over distances of approximately 1- 100 feet.
⦁ Must be able to perform procedures, which require standing or sitting for long periods of time.
⦁ Must be able to regularly move about the facility to access file cabinets, office machinery, and other buildings.
⦁ Regularly uses laboratory instruments.
⦁ Must be able to work in narrow spaces.
⦁ Must be able to wear safety equipment (PPE), as needed, according to OSHA regulations and company standards.
⦁ Must be able to regularly stoop, bend, kneel, stand or reach up with hands and arms to manipulate objects on shelves from one and one-half to six and one-half feet above the floor on a repetitive basis each day.
⦁ Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.
⦁ Must be able to communicate with employees, exchanging accurate information.
⦁ Must regularly move about inside the facility to access supplies which may require going up and down stairs.

WORK ENVIRONMENT:
⦁ Works in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, occasionally working within a walk-in refrigerator or freezer at noise levels ranging from moderate to loud.
⦁ The employee is regularly exposed to live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
⦁ The noise level in the general work environment ranges from low to loud depending upon the task being performed.

Comments:
⦁ This position requires overtime, weekend, holiday, and/or after hours shift coverage as needed.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Support Scientist I - Toxicology (Horsham, PA, US, 19044)

Job Summary

Responsible for providing scientific support to assist Study Directors with management of study conduct over the entire study life cycle.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
Provides scientific support to the Study Director team by assisting with many aspects of study conduct during the study life cycle, including planning and prioritization of deliverables to meet agreed deadlines.
Acquires knowledge of relevant processes and procedures established at Charles River Laboratories, Inc, including Standard Operating Procedures (SOPs).
Acquires knowledge of regulations and applicable Good Laboratory Practices (GLP).
Acquires knowledge of the study processes and the role of the Study Director.
Acquires knowledge of the animal ethical/IACUC process and the Quality Assurance (QA)/Quality Control (QC) process.
Attends study-related and/or department-related meetings to assure understanding of assigned projects including objectives, timelines, and reporting requirements.
May assist with reviewing draft protocols and amendments and preparing Animal Use Proposal Forms.
Participates in study oversights by observing various study procedures.
Prepares for client visits and participates in hosting clients while onsite.
Prepares study information summaries for Toxicokinetic Principal Investigators.
May assist with study investigations, documentation of deviations from the study plan/protocol or SOPs, preparation of summary data/tables for Sponsor updates and management of QA audits from Test Sites.
Assists with report finalization by initiating/completing finalization assessment forms, performing QC of final reports, and drafting/reviewing Common Technical Documents.
May assist with generation and review of historical control data.
May attend scientific meetings, conferences, or training courses to enhance job and professional skills.
May participate in cross-functional teams/working groups.
Performs all other related duties as assigned.

The pay range for this position is $28.00 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
Education/Experience: Master’s with 0-1 year experience or Bachelors with 2-3 years experience. Experience within a preclinical service environment is preferred. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None
Other: Advanced skills in spreadsheet, word processing, database, and publishing software (e.g.: MS Excel®, Word®, and Adobe® Acrobat® PDF software) preferred. Familiar with non-clinical study protocols/reports and GLP regulations. Strong written, verbal, analytical and communication skills.

PHYSICAL DEMANDS:
Must regularly operate a computer and occasionally operate other office productivity machinery such as a calculator, copy machine, and computer printer.
Must regularly communicate with employees/customers; must be able to exchange accurate information.
Must occasionally move about inside the office to access file cabinets, office machinery, etc.
The employee must occasionally lift and/or move up to 10 pounds.

WORK ENVIRONMENT:
General office working conditions; the noise level is usually quiet.
While performing the duties of this job, the employee may be exposed to animal-related allergens.
Laboratory and vivarium environment, as required.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Operaio stabularista (Milano) - Contratto a chiamata (MILANO, Milano, IT, 20122)

Riepilogo del lavoro

Per nostro cliente sito in Milano ricerchiamo uno stabularista con contratto a chiamata.

La risorsa sarà inserita all'interno del team operante nella struttura e si occuperà di svolgere le mansioni relative alla gestione del laboratorio

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nel controllo delle procedure sperimentali;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature automatiche e carrelli

Buona capacità comunicativa e di lavoro in team
Disponibilità a con contratto a chiamata

Disponibilità a lavoro nel week-end e festività

Buona conoscenza del pacchetto office

Di cosa si occupa la Charles River

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Addetto alla cura degli animali da laboratorio (Milano) - Contratto a chiamata (MILANO, Milano, IT, 20122)

Riepilogo del lavoro

Per nostro cliente sito in Milano ricerchiamo uno stabularista con contratto a chiamata.

La risorsa sarà inserita all'interno del team operante nella struttura e si occuperà di svolgere le mansioni relative alla gestione del laboratorio

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nel controllo delle procedure sperimentali;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature automatiche e carrelli

Buona capacità comunicativa e di lavoro in team
Disponibilità a con contratto a chiamata

Disponibilità a lavoro nel week-end e festività

Buona conoscenza del pacchetto office

Di cosa si occupa la Charles River

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Administrative Assistant - Temp (Horsham, PA, US, 19044)

Job Summary

Provide basic administrative support to manager(s) and their organizations.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
⦁ Receive and distribute mail. Take phone messages and handle routine matters as they arise.
⦁ Relay information and requests to department members and follow-up as needed.
⦁ Collate and distribute information.
⦁ Prepare routine documents and forms as requested.
⦁ With guidance, handle special projects and duties as needed (for example, data collection, report creation, database maintenance, contacting personnel for routine updates, etc.).
⦁ Establish and maintain files.
⦁ Make meeting and travel arrangements.
⦁ Answer routine/basic questions and provide assistance relating to office operations and established policies and procedures.
⦁ Assist with phone coverage for others as needed.
⦁ May greet visitors, set up and maintain management calendars, prepare expense reports, handle scheduling for one or more conference rooms, order office supplies, ensure office machinery is maintained and/or handle mail and shipping activities for the department.
⦁ Perform all other related duties as assigned.

The pay range for this position is between $23.00 and $25.00 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
⦁ Education: High School or G.E.D. and specialized secretarial training beyond High School. Associate’s degree (A.A. /A.S.) or equivalent from two year college preferred.
⦁ Experience: Zero to two years related experience.
⦁ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
⦁ Certification/Licensure: None.
⦁ Other: Ability to prioritize and multi-task. Good keyboarding skills, proficient in utilizing personal computer, e-mail and standard office software packages (word processing, spreadsheet, presentation, database).

PHYSICAL DEMANDS:
⦁ While performing the duties of this job, the employee is regularly required to talk, hear and is frequently required to work/type at a computer.
⦁ Specific vision abilities required by this job include close vision, distance vision, color vision and the ability to adjust focus.

WORK ENVIRONMENT:
⦁ General office working conditions.
⦁ The noise level in the work environment is usually quiet.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Analyst I- Bioanalytical Chemistry (Chemist) (Cleveland, OH, US, 44128)

Job Summary

We are seeking a Research Analyst I for our Bioanalytical Chemistry Team at our Safety Assessment site located in Cleveland, OH.

Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents.

Essential Functions (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:

Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team
Assist with laboratory maintenance functions
Independently perform laboratory support functions such as labeling and solution preparations
Assist with maintaining study specific inventory of consumables with oversight
Write both study and non-study deviations with minimal oversight
Actively participate in process improvement initiatives with oversight
Develop critical thinking, troubleshooting and time management skills aligned with needs of the operational area
Assist in execution of routine sample analysis studies with oversight
Assist in execution of method validation projects with oversight as needed
Operate laboratory instruments with complete oversight
Assist with data analysis in appropriate software for at least one analytical platform
Performs all other related duties as assigned

The starting pay for this position is $21.00/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Minimum of a Bachelor’s degree (BA/BS) or equivalent experience. No previous work experience required.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Basic familiarity with Microsoft Office Suite.
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice.
Ability to work under specific time constraints

Must be authorized to work in the United States without a sponsor visa, now or in the future.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Analyst I- Bioanalytical Chemistry (Chemist) (Cleveland, OH, US, 44128)

Job Summary

We are seeking a Research Analyst I for our Bioanalytical Chemistry Team at our Safety Assessment site located in Cleveland, OH.

Essential Functions (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:

Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team
Assist with laboratory maintenance functions
Independently perform laboratory support functions such as labeling and solution preparations
Assist with maintaining study specific inventory of consumables with oversight
Write both study and non-study deviations with minimal oversight
Actively participate in process improvement initiatives with oversight
Develop critical thinking, troubleshooting and time management skills aligned with needs of the operational area
Assist in execution of routine sample analysis studies with oversight
Assist in execution of method validation projects with oversight as needed
Operate laboratory instruments with complete oversight
Assist with data analysis in appropriate software for at least one analytical platform
Performs all other related duties as assigned

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Minimum of a Bachelor’s degree (BA/BS) in a scientific field.
Knowledge of a laboratory environment.
No previous work experience required.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Basic familiarity with Microsoft Office Suite.
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice.
Ability to work under specific time constraints
Must be authorized to work in the United States without a sponsor visa, now or in the future.

Must be authorized to work in the United States without a sponsor visa, now or in the future.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Testreq - Training Req (Parma, IT, 43122)

Job Summary

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Job Qualifications

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IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

Vaccine Mandate
Charles River is a U.S. Federal Contractor. As a result, we must follow the Presidential Executive Order to mandate vaccinations, and ensure our employees are fully vaccinated against COVID-19. Our main priority is the wellbeing, health, and safety of our people. We require proof of vaccination from all employees.

Anyone with requests for disability-related and/or religious exemptions should contact Talent Acquisition (crrecruitment_US@crl.com) so that information can be provided about the accommodation process at Charles River.

For more information, please visit www.criver.com.

Veterinary Technician I (Ashland, OH, US, 44805)

Job Summary

ESSENTIAL DUTIES AND RESPONSIBILITIES: (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:

Assist veterinary staff in the documentation and triage of all animal health cases noted by technical staff and/or Veterinarians.
Perform routine veterinary technical and husbandry skills including the following:
Administration of various therapeutic measures by IV, IM, SQ, topical, oral routes, etc.
Bandage/wrapping techniques.
Nail/hoof/teeth clipping/trimming.
Proficient animal restraint techniques.
Monitor critical care animals (e.g., place IVs, monitor fluids, etc.).
Daily walk through of animal rooms
Participate in colony management (biosurveillance, routine health monitoring, nail trims, etc.)
Animal observations, reporting abnormalities
Monitor animal health, visually, and by following detailed schedules.
Assist in maintaining accurate record keeping procedures for the veterinary department.
Assist in keeping inventory and stocking the vet rooms (e.g., drugs and supplies). Assist in organizing and maintaining the vet exam rooms.
May be responsible for tissue sampling, radiography, routine animal manipulations and administration of fluids or other treatments as required.
May perform routine technical and husbandry functions (general housekeeping) on studies and must adhere to safety procedures.
Assist in surgery and peri-surgery care, (e.g., prepare animals for surgery, prepare surgical packs, administer supportive therapy as directed).
Assistance in acclimation and behavior management of animals in our care.
Provide environmental enrichment for laboratory animals according to facility and Federal guidelines.
Participate in animal receipt as necessary.
Triage and recheck all animal species on site.
Participate in weekend assistant rotation.
Perform all other related duties as assigned.

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High school diploma or General Education Degree (G.E.D.) preferred. Graduate of a collegiate veterinary technology program accredited by the American Veterinary Medical Association Committee on Veterinary Technician Education and Training Activities or equivalent program in veterinary technology.
Experience: 0-2 years related experience working with animals in a pre-clinical laboratory or clinical setting; experience working in a CRO with multi-species preferred
Certification/Licensure: Licensed as a veterinary technician (RVT, LVT, CVT) is required, and you must be able to obtain an OH license. AALAS (ALAT) certification desired.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Other: Demonstrate understanding of Standard Operating Procedures. Excellent organizational, time management and recordkeeping skills. Basic word processing skills required. Excellent communication skills both written and verbal. Must be proficient in routine veterinary technical and husbandry techniques. Must work well with team members as well as function independently. Must be flexible with daily routine to meet demands of veterinary medical department.

Compensation Data

The starting pay for this position is $25.00 USD per hour. Please note that starting salaries vary based on factors including, but not limited to, experience, skills, education, certifications, and location

Equal Employment Opportunity

For more information, please visit www.criver.com.

Scheduling Coordinator II (Ashland, OH, US, 44805)

Job Summary

BASIC SUMMARY:

Maintain the scheduling and operation of the vivarium requiring the coordination of animal room availability, species availability, housing requirements and services of operating departments within the company to ensure optimal vivarium utilization. Application of skills and knowledge to assist in providing accurate information for proposals and general site capabilities. Key skills include excellent interpersonal and organizational skills, good comprehension skills, creative thinking skills, good writing skills, attention to detail, experience with good laboratory procedures, protocols, standard operating procedures, and regulatory laws/guidelines. Demonstration of creative problem solving and thinking skills to increase facility use and adaptation to client needs.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Provide technical support to managers, senior management, study directors and clients.
Knowledge, availability status and procurement of laboratory animal strains and species including the interaction with established vendors to acquire animal species in a timely manner.
Maintain and modify applicable scheduling programs and files.
Other duties as assigned by departmental management.

The starting pay for this position is $26.00 per hour. Please note that starting salaries vary based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:

Education: High School diploma or General Education Degree (G.E.D.), preferred. Associate’s degree (A.A./A.S.) or equivalent from two year college, recommended.
Experience: minimum of 3 years company experience.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None.
Must be authorized to work in the United States without a sponsor visa, now or in the future.
Other: Comprehensive knowledge of GLP and other federal regulations and guidelines pertaining to preclinical research. Comprehensive knowledge of creating, maintaining, and promoting optimal utilization of various database systems. Detail oriented.

PHYSICAL DEMANDS:

Repetitive dexterity/motion of hands and arms.
Good hand-eye coordination and vision.
Able to squat, bend or reach.
Able to walk at least 1 mile and stand for extended periods of time.
Able to lift up to 30lbs at a time.
While performing the duties of this job, the employee is regularly required to talk, hear and work/type at a computer.
Specific vision abilities required by this job include close vision and the ability to adjust focus.

WORK ENVIRONMENT:

General office working conditions, the noise level in the work environment is usually quiet.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Analyst I (Chemist), Bioanalytical Chemistry (Ashland, OH, US, 44805)

Job Summary

We are seeking a Research Analyst I (Bioanalytical Chemistry) for our Safety Assessment Group site located in Ashland, Ohio.

Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods.

Perform basic laboratory procedures and collect and record/document research data in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), study protocols and company policies/practices.
Under supervision may act as lead/primary technician on basic studies.
Basic Understand/Knowledge LCMS
Input, print and edit computer entries (e.g., laboratory data).
Prepare materials and data for shipment and archiving.
Receive samples and complete tracking documentation.
Review documentation of functions performed as part of quality control requirements.
Perform study preparation activities including collection tube labeling and room setup.
Maintain clean work areas.
Perform all other related duties as assigned.

The following are miminum requirements related to the Research Assistant I position.

Education: Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline required.
Experience: Zero to two years related experience in biology, chemistry/pharmacy, or similar lab environment GLP experience preferred.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None
Must be authorized to work in United States without a sponsor visa now or in the future.
Other: Proficient in basic technical skills and the operation of data collection equipment. Knowledge of GLPs and other federal regulations and guidelines. Basic understanding of study design and protocols; able to read basic study protocols and extract pertinent information. Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors. Able to quickly learn and utilize computer programs as needed; previous computer experiences preferred.

The pay range for this position is $21.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician I, Necropsy (Ashland, OH, US, 44805)

Job Summary

We are seeking a Technician I for our Necropsy team at our Safety Assessment site located in Ashland, Ohio. Candidate will be working 4/10's either Monday-Thursday or Tuesday-Friday 8a-630pm, weekend rotation, holiday rotation and overtime are required for this role.

A Technician I is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to conduct a study, which may include animal handling, euthanasia, and sedation; animal procedures including dissection; collection of samples and weights; laboratory preparation, set up and cleaning; preparation of laboratory solutions. The technician is working under close supervision to gain proficiency.

Essential Duties and Responsibilities: (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions
Train in on-boarding skills which may include animal handling, euthanasia, and sedation; animal procedures including dissection; collection of samples and weights; laboratory preparation, set up and cleaning; preparation of laboratory solutions. Specific skills will be based on each area’s training plan and business needs.
Prosect and perform functions in a time frame set by training group for core skill completion.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Learn and know anatomic terms
Receive, track, and prepare samples or materials, as required for department.
Perform all other related duties as assigned.

The pay for this position is $19/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High school diploma or General Education Degree (G.E.D.) preferred.
Experience: No previous experience required.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Must be authorized to work in the United States without a sponsor visa, now or in the future

Physical Demands

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform laboratory procedures, which require, talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

Work Environment

Works in a research laboratory environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from quiet to moderately noisy.

Comments

May occasionally work weekend/holidays and/or rotating on-call schedule.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician I, Animal Care (Ashland, OH, US, 44805)

We are seeking an experienced Animal Care Technician I for our Safety Assessment site located in Ashland, OH. Shift Monday-Friday 8am-430pm, every 4th weekend and every other holiday.

A Technician I – Animal Care Services is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to support a study which may include animal husbandry needs, animal handling, cage changes, equipment storage/tracking, wash systems, and water delivery system maintenance for various species throughout the site. The technician is working under close supervision to gain proficiency

ESSENTIAL DUTIES AND RESPONSIBILITIES: (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding skills which may include animal husbandry needs, animal handling, cage cages, equipment storage/tracking, wash systems, and water delivery system maintenance for various species throughout the site. Specific skills will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements. 
Use and maintain instrumentation and equipment.
Perform all other related duties as assigned.

The starting pay for this position is 18.00 per hour. Please note that starting salaries vary based on factors including, but not limited to, experience, skills, education, certifications, and location.

Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High school diploma, General Education Degree (G.E.D.), preferred.
Experience: No previous experience required.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating.
Must be authorized to work in United States without a sponsor visa now or in the future.

PHYSICAL DEMANDS:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform procedures, which require, talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Must be able to frequently firmly hold species while utilizing fine motor skills.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

WORK ENVIRONMENT:

Works in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles.
The employee regularly works with live animals with risk of exposure to dander, allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to high depending upon the species housed.

COMMENTS:

This position requires overtime, weekend, holiday, and/or after hours shift coverage, as needed.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician I-Histology-1st shift (Ashland, OH, US, 44805)

Job Summary

We are seeking a Technician I for our 1st shift Histology Team located in Ashland, OH.

A Histology Technician I is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to conduct a study, including various tasks within Pre-Trim with an introduction to Trimming. Technician is working under close supervision to gain proficiency.

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding tasks which includes GLP Training, Animal Welfare Training and New Hire Orientation. Specific tasks will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements. 
Use and maintain instrumentation and equipment.
Reading and understanding of protocols.
Excellent written and verbal communication skills. Knowledge of English.
Manage multiple tasks and priorities to achieve goals.
Ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Work under specific time constraints.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Perform all other related duties as assigned.

The pay rate for this position is $19/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High school diploma or General Education Degree (G.E.D.) preferred. 
Experience: No previous experience required.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Must be authorized to work in United States without a sponsor visa now or in the future.

Physical Demands:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform laboratory procedures, which require, talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

Work Environment:

Works in a research laboratory environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from quiet to moderately noisy.

Comments:

May occasionally work weekend/holidays and/or rotating on-call schedule.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Histology - Team Lead- 1st Shift (Ashland, OH, US, 44805)

Job Summary

BASIC SUMMARY:
Provide leadership, technical guidance, and serve as a mentor to less experienced staff. Assist supervisor/scheduler to prioritize workload of assigned group. Ensure schedule is prepared daily, accurately reflecting group and laboratory tasks and workload. Verify lab sections are prepared to complete the day’s work and confirm with management and scheduling. Perform technical duties as assigned.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Serve as a model as it relates to effective time management, communication, and utilization of resources.
•   Provide technical leadership.
• Ensure that there are adequate supplies of study-specified materials during study.
• Assist in study start up procedures: Target and LO study briefing.
• Understanding study requirements.
•   Contribute to department operations improvement in areas such as SOP revisions, laboratory space, and equipment.
• Review study protocols and provide recommendations to Research Associate (RA) on technical and logistical aspects of protocol design.
•   Relays pertinent study information to RAs when trends are noted and notifies scheduling when daily expectations are complete.
•   Assist technicians in the execution of all study-related activities.

The starting pay for this position is 25.00 per hour. Please note that starting salaries vary based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
•   Education: High School diploma or General Education Degree (G.E.D.), preferred.
•   Experience: 1-2 years of relevant experience.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Certification/Licensure: None, unless required by local government.
•   Excellent written and verbal communication skills.
•   Ability to manage tasks and priorities to achieve goals.
•   Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
•   Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
•   Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
•   Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
•   Ability to work under specific time constraints.

Must be authorized to work in United States without a sponsor visa now or in the future.

PHYSICAL DEMANDS:
•   Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
•   Must be able to perform laboratory procedures, which require, talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
•   Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
•   Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Scientist I, Toxicology (Ashland, OH, US, 44805)

Job Summary

Serve as a scientist in the conduct of assigned nonclinical research studies of basic to moderate complexity, to include study management, interpretation and reporting of study data, and assuring the regulatory compliance of these projects.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Serve as a study director in the direction and execution of assigned studies in compliance with GLP regulations as they apply to the conduct of nonclinical research.
Participate in proposal management and bid development process. Assist in the review of Letters of Commitment (LOC) in cooperation with client services.
Participate in and coordinate all phases of the study planning process with appropriate departments.
Generate high-quality protocols, amendments, and reports appropriate for assigned studies.
Review, interpret, integrate, and present data on assigned studies, using the assistance of senior scientific staff as appropriate.
Function as contact for the planning and execution of sponsor interaction related to assigned studies, including proposal management and study scheduling, conduct and reporting.
Provide technical and scientific guidance to the research staff.
Attend scientific meetings, conferences, and training courses to enhance job and professional skills.
Perform all other related duties as assigned.

The pay range for this position is between $87,000 to $93,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:

Education: Ph.D. or equivalent in toxicology or related scientific related discipline.
Experience: 0 – 1 year.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: N/A.
Other: Understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good Laboratory Practices (GLPs), as appropriate. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and with standard laboratory calculations.
Must be authorized to work in the United States without a sponsorship visa, now or in the future.

PHYSICAL DEMANDS:

While performing the duties of this job, the employee is regularly required to talk, hear and work/ type at a computer.
Specific vision abilities required by this job include close vision and the ability to adjust focus.

WORK ENVIRONMENT:

General office working conditions, the noise level in the work environment is usually quiet. Regularly enters vivarium laboratory areas, with proper utilization of protective laboratory.
While performing the duties of this job the employee may occasionally be required to wear protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots), work near toxic or caustic chemicals, work with biohazards, and/or work with live animals with risk of exposure to allergens and/or zoonotic diseases.
The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors, and/or wet, humid and/or extreme temperature conditions.

COMMENTS:

This position may require occasional domestic travel.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Scientist I, DART (Ashland, OH, US, 44805)

Job Summary

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Serve as a study director in the direction and execution of assigned studies in compliance with GLP regulations as they apply to the conduct of nonclinical research.
• Participate in proposal management and bid development process. Assist in the review of Letters of Commitment (LOC) in cooperation with client services.
• Participate in and coordinate all phases of the study planning process with appropriate departments.
• Generate high-quality protocols, amendments, and reports appropriate for assigned studies.
• Review, interpret, integrate, and present data on assigned studies, using the assistance of senior scientific staff as appropriate.
• Function as contact for the planning and execution of sponsor interaction related to assigned studies, including proposal management and study scheduling, conduct and reporting.
• Provide technical and scientific guidance to the research staff.
• Attend scientific meetings, conferences, and training courses to enhance job and professional skills.
• Perform all other related duties as assigned.

Job Qualifications

Education: Ph.D. or equivalent in toxicology or related scientific related discipline.
Experience: 0 – 1 year.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: N/A.
Other: Understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good Laboratory Practices (GLPs), as appropriate. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and with standard laboratory calculations.
Must be authorized to work in the United States without a sponsorship visa, now or in the future.

PHYSICAL DEMANDS:

While performing the duties of this job, the employee is regularly required to talk, hear and work/ type at a computer.
Specific vision abilities required by this job include close vision and the ability to adjust focus.

WORK ENVIRONMENT:

General office working conditions, the noise level in the work environment is usually quiet. Regularly enters vivarium laboratory areas, with proper utilization of protective laboratory.
While performing the duties of this job the employee may occasionally be required to wear protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots), work near toxic or caustic chemicals, work with biohazards, and/or work with live animals with risk of exposure to allergens and/or zoonotic diseases.
The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors, and/or wet, humid and/or extreme temperature conditions.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Analyst I (Chemist), Bioanalytical Chemistry (Ashland, OH, US, 44805)

Job Summary

We are seeking a Research Analyst I (Bioanalytical Chemistry) for our Safety Assessment Group site located in Ashland, Ohio.

Perform basic laboratory procedures and collect and record/document research data in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), study protocols and company policies/practices.
Under supervision may act as lead/primary technician on basic studies.
Basic Understand/Knowledge LCMS
Input, print and edit computer entries (e.g., laboratory data).
Prepare materials and data for shipment and archiving.
Receive samples and complete tracking documentation.
Review documentation of functions performed as part of quality control requirements.
Perform study preparation activities including collection tube labeling and room setup.
Maintain clean work areas.
Perform all other related duties as assigned.

The following are miminum requirements related to the Research Assistant I position.

Education: Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline required.
Experience: Zero to two years related experience in biology, chemistry/pharmacy, or similar lab environment GLP experience preferred.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None
Must be authorized to work in United States without a sponsor visa now or in the future.
Other: Proficient in basic technical skills and the operation of data collection equipment. Knowledge of GLPs and other federal regulations and guidelines. Basic understanding of study design and protocols; able to read basic study protocols and extract pertinent information. Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors. Able to quickly learn and utilize computer programs as needed; previous computer experiences preferred.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician I, Necropsy (Ashland, OH, US, 44805)

Job Summary

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions
Train in on-boarding skills which may include animal handling, euthanasia, and sedation; animal procedures including dissection; collection of samples and weights; laboratory preparation, set up and cleaning; preparation of laboratory solutions. Specific skills will be based on each area’s training plan and business needs.
Prosect and perform functions in a time frame set by training group for core skill completion.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Learn and know anatomic terms
Receive, track, and prepare samples or materials, as required for department.
Perform all other related duties as assigned.

The pay for this position is $19/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High school diploma or General Education Degree (G.E.D.) preferred.
Experience: No previous experience required.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Must be authorized to work in United States without a sponsor visa now or in the future.

Physical Demands

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform laboratory procedures, which require, talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

Work Environment

Works in a research laboratory environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from quiet to moderately noisy.

Comments

May occasionally work weekend/holidays and/or rotating on-call schedule.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Trainer I- Histology (Ashland, OH, US, 44805)

Job Summary

We are seeking a Trainer I for our Histology team at our Safety Assessment site located in Ashland, Ohio.

A Trainer I has substantial knowledge in basic tasks and is able to perform the intermediate tasks and procedures of the department training plan. The trainer is performing tasks independently which may include delivering, documenting, and reporting technical skill training and programs involving their training focus for basic skills. Tasks may include documenting and reporting technical skill training and programs involving their training focus for both basic and some advanced skills. Conduct classroom and on-job training sessions. The trainer assists with more advanced tasks that may include working with additional species, and/or specialized procedures to support the study and training needs.

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Perform basic training with little to no supervision.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use, maintain, and troubleshoot instrumentation and equipment.
Perform all other related duties as assigned.

The pay for this position is $23/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High school diploma or General Education Degree (G.E.D.), preferred.
Experience: 1-2 years of relevant experience.
Certification/Licensure: None
Demonstrated ability to consistently and effectively produce high quality results, interpret protocol requirements, troubleshoot quality issues, and record accurate study and departmental data.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Excellent written and verbal communication skills. Knowledge of English.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notifications.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to exercise independent decision-making and self-manage under the direction of a supervisor.
Ability to work extended hours beyond normal work schedule to include, but not limited to, evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Must be authorized to work in United States without a sponsor visa now or in the future.

Physical Demands

Employee must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform procedures, which require talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, wearing safety equipment (PPE) according to OSHA regulations and company standards.
Must be able to frequently hold species firmly while utilizing fine motor skills.
Specific vision abilities required by the job include close vision, color vision, depth perception and the ability to adjust focus.

Work Environment

Works in a research environment, which requires use of sharp tools, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles.
The employee may regularly work with live animals with the risk of exposure to allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to high depending on the species housed.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Technician I, Technical Operations (Ashland, OH, US, 44805)

Job Summary

We are seeking a Technician I, Technical Operations for our Safety Assessment site located in Ashland, OH. This is a full-time position that requires 5-9 weeks of training Tuesday-Friday 6am-430pm at $19/hour. After training the WEEKDAY shift is Tues-Fri 6am-430pm; every 4th weekend, every other holiday. We also have weekend shifts available. The weekend schedules are Friday-Sunday or Saturday-Monday 6am-630pm, every other holiday after training. There is a 10% pay differential for Saturday/Sunday hours only.

A Technician I is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to support a study, which may include animal handling, husbandry, observations, basic physiological indices, and data collection/recording to support each skill. The technician may occasionally perform basic skills independently but continues working under supervision to gain proficiency on skills still in development.

Ensure good welfare and humane care for all animals worked with through gentle, positive human animal interactions.
Train in on-boarding skills which may include animal handling, husbandry, observations, basic physiological indices, and data collection/recording to support each skill. Specific tasks will be based on each area's training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Ensure high levels of study quality to meet study goals.
Follow all PPE, safety, cleaning, and cross-contamination elimination practices.
Maintain appropriate communication with other personnel.
Support team-mates, technicians, and members of other departments.
Follow direction from team leaders, trainers, research associates and supervisors.
Use and maintain instrumentation and equipment according to SOPs.
Perform all tasks per SOP, BOP, and/or protocols.
Perform all other related duties as assigned

The starting pay for this position is 19.00 per hour. Please note that starting salaries vary based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High school diploma or General Education Degree (G.E.D.) preferred.
Experience: No previous experience required. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None.
Excellent written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

Physical Demands:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform laboratory procedures, which require, talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

Work Enviornment:

Work in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
The employee regularly works with live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to high depending upon the species housed.

Comments:

This position requires overtime, weekend, holiday, and/or after hours shift coverage, as needed.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technicien de laboratoire - H/F - CDD 12 mois (Saint-Nazaire, FR, 44600)

Qui sommes-nous ?

Le site Charles River Saint-Nazaire est spécialisé dans la mise en place de tests de Bioanalyse pour supporter le développement de nouveaux médicaments des phases précliniques aux essais cliniques de phase IV. Le site emploie environ 65 personnes et est doté d’équipements de dernière génération (LC-MS/MS). Il est accrédité par les différentes autorités habilitées pour ce type d’établissement.

Le poste

Notre Laboratoire Chromatographie recrute un Technicien de Laboratoire Chromatographie (F/H) en CDD 12 mois, basé sur le site de Saint-Nazaire (44).

Les missions

Vous ferez partie d’une équipe dans laquelle votre rôle sera la réalisation technique d’études de bioanalyse sur de nouveaux médicaments en développement. Ces médicaments sont de natures diverses incluant les principes actifs, les métabolites, les petits biomarqueurs tels que certaines vitamines, hormones ou acides aminés, des anticorps thérapeutiques, des ADC, des oligonucléotides, des vaccins, des peptides.

Vos principales responsabilités incluront :

Réaliser des analyses en utilisant diverses techniques d'extraction (précipitation de protéine, extraction en phase solide (SPE), liquide (LLE, SLE), digestion enzymatique, immunocapture, extraction par précipitation de protéines, extraction en phase solide) et LC-MS/MS pour quantifier les molécules d'intérêt
Manipuler et analyser des échantillons biologiques conformément aux bonnes pratiques de laboratoire (BPL) et bonnes pratiques cliniques (BPC)
Participer à la conception et la rédaction de méthodes de bioanalyse et de procédures
Participer à la gestion du laboratoire en collaboration avec ses collègues

Qualifications souhaitées

Vous êtes titulaire d'un Bac + 2 minimum (biochimie ou chimie) avec une expérience de 2 ans minimum :

Expérience en préparation d’échantillons biologiques
Expérience en chromatographie/spectrométrie de masse (LC-MS/MS)
Et/ou biochimie/immunochimie/biologie moléculaire et souhaitant évoluer vers les techniques de LC-MS/MS.

Vous avez idéalement une bonne connaissance des BPL / BPC et/ou avez travaillé dans un contexte qualité/réglementaire (suivi et respect de procédures et consignes).
Vou êtes rigoureux(se), autonome et à l'aise avec les outils informatiques.
La compréhension de l’anglais est un plus.

Modalités contractuelles

Convention collective de l’Industrie Pharmaceutique : Groupe 3
Contrat : CDD non-cadre (+ 6 RTT annuels)
Salaire : Rémunération sur 12 mois à partir de 25K€ (brut annuel selon profil et expérience)
Prise en charge de la mutuelle à 60% et Tickets Restaurant

Merci de vous assurer de joindre une lettre de motivation à votre CV quand vous postulez.

À propos de l'évaluation de sécurité

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Alternance : Chargé de mission HSE - F/H (Saint-Nazaire, FR, 44600)

Qui sommes-nous ?

Vous êtes étudiant dans une formation QHSE ? Vous recherchez un contrat d'apprentissage avec des missions opérationnelles et polyvalentes ?

Nous recherchons pour la rentrée 2026, notre futur(e) alternant(e), Chargé(e) de mission HSE.

Missions et responsabilités :

- Participer à l'animation et au déploiement des politiques Hygiène, Sécurité et Environnement (HSE) ; communiquer, sensibiliser, former et faire appliquer.
- Contribuer à la mise en oeuvre des projets HSE, notamment ceux en lien avec la prévention des risques et des accidents.
- Participer à l'analyse des accidents et presqu'accidents (enquêtes, suivi des plans d'actions).
- Apporter un appui dans les volontés d'améliorations et d'évolutions en matière d'hygiène, de sécurité, d’environnement et de conditions de travail (études de postes, EPI, protections collectives, évolutions de process, etc.).
- Participer à la rédaction et la mise à jour de la documentation HSE en lien avec la réglementation et les pratiques de l’entreprise.
- Contribuer à l'identification des risques dans les différents secteurs de l'entreprise et la mise à jour des documents associés.
- Participer à la mise en place et au suivi des indicateurs HSE (reporting accidents/incidents).
- Participer aux inspections HSE dans les zones de travail.
- Suivre la conformité du matériel de sécurité et des EPI.

Votre profil :

- Etudiant(e) en recherche d'un apprentissage pour sa formation de niveau Bac+4/5
- Faire preuve de dynamisme, d'organisation et de rigueur
- Bonne maitrise de l'anglais (écrit et oral)

Modalités :

Convention collective de l'industire pharmaceutique
Contrat : apprentissage

À propos de l'évaluation de sécurité

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Stage : Chargé de projet programmation système automatisé de laboratoire - F/H - 6 mois (Saint-Nazaire, FR, 44600)

Qui sommes-nous ?

L'équipe

Dans le cadre du développement de nouveaux médicaments, notre département Bioanalyse, composé de 42 personnes, a pour mission de développer, valider et appliquer des méthodes d'analyse pour le contrôle d'échantillons biologiques prélevés sur des animaux et humains. Au sein du service Chromatographie, vous intégrerez l'équipe en charge de l'innovation et de l'automatisation des méthodes analytiques. L'objectif est de réduire les tâches manuelles, améliorer la fiabilité des résultats et accélérer les flux de travail en laboratoire.

Votre quotidien

Participer à la vie du laboratoire
Se former à l'utilisation de nos automates de préparation d'échantillons
Analyser les processus actuels et identifier les étapes automatisables
Développer et mettre en production de nouvelles méthodes automatisées sur les différentes plateformes
Rédiger des procédures et supports techniques pour les utilisateurs

Pourquoi nous rejoindre ?

Actuellement en formation Bac +4/5, vous recherchez un stage dans un environnement scientifique, innovant et international. Vous souhaitez développer vos compétences en instrumentation analytique et programmation.

Sensible au respect des règles d'éthique et de sécurité, vous savez travailler en équipe, vous êtes adaptable, flexible et rigoureux(se).

Modalités

Gratification de stage
Indemnités de transports (site non accessible en transports en commun)
Tickets restaurants

À propos de l'évaluation de sécurité

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Stage : Chargé de production et planification - F/H - 6 mois (Saint-Nazaire, FR, 44600)

Qui sommes-nous ?

L'équipe

Notre service Administration recherche un stagiaire pour une mission de 6 mois. L'objectif principal est de moderniser ou remplacer l'outil actuel de planification pour garantir une meilleure flexibilité, mise à jour, et communication avec les autres systèmes IT (RPM).

Votre quotidien

Analyser le/les besoins
Analyser l'existant
Proposer des solutions (analyse investissement en temps, en coûts et en moyens)
Conceptualiser l'outil
Déployer l'outil et éventuellement former/créer un guide opérationnel

Pourquoi nous rejoindre ?

Actuellement en formation Bac +4/5, vous recherchez un stage qui mêlera gestion de projets et techniques de gestion de production. Des compétences IT seront nécessaires pour mener à bien cette mission : Pack Office, VBA à minima. La connaissance et l'utilisation de l'IA en supplément sera un atout.

Vous souhaitez intégrer un contexte international (anglais lu, écrit, parlé).

Sensible au respect des règles d'éthique et de sécurité, vous souhaitez mettre en oeuvre vos qualités d'observation, de rigueur et de force de proposition.

Modalités

Gratification de stage
Indemnités de transports (site non accessible en transports en commun)
Tickets restaurants

À propos de l'évaluation de sécurité

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Technicien de laboratoire - CDD 12 mois - H/F (Saint-Nazaire, FR, 44600)

Technicien de laboratoire Chromatographie - CDD 12mois - H/F

Notre Laboratoire Chromatographie recrute un Technicien de Laboratoire Chromatographie - H/F en CDD 12 mois, basé sur le site de Saint-Nazaire (44). Le site est spécialisé dans la mise en place de tests de Bioanalyse pour supporter le développement de nouveaux médicaments des phases précliniques aux essais cliniques de phase IV. Le site emploie environ 65 personnes et est doté d’équipements de dernière génération (LC-MS/MS). Il est accrédité par les différentes autorités habilitées pour ce type d’établissement.

Missions

Vos responsabilités incluront (sans être exhaustif) :

Réaliser des analyses en utilisant diverses techniques d'extraction (précipitation de protéine, extraction en phase solide (SPE), liquide (LLE, SLE), digestion enzymatique, immunocapture, extraction par précipitation de protéines, extraction en phase solide) et LC-MS/MS pour quantifier les molécules d'intérêt
Manipuler et analyser des échantillons biologiques conformément aux bonnes pratiques de laboratoire (BPL) et bonnes pratiques cliniques (BPC)
Participer à la conception et la rédaction de méthodes de bioanalyse et de procédures
Participer à la gestion du laboratoire en collaboration avec ses collègues

Qualifications attendues

Bac + 2 minimum (biochimie ou chimie) avec une expérience de 2 ans minimum :

Expérience en préparation d’échantillons biologiques
Expérience en chromatographie/spectrométrie de masse (LC-MS/MS)
Et/ou biochimie/immunochimie/biologie moléculaire et souhaitant évoluer vers les techniques de LC-MS/MS.

Idéalement bonne connaissance des BPL / BPC et/ou travail dans un contexte qualité/réglementaire (suivi et respect de procédures et consignes).
Rigoureux, autonome et à l’aise avec les outils informatiques.
La compréhension de l’anglais est un plus.

Modalités contractuelles

Convention collective de l’Industrie Pharmaceutique : Groupe 3
Contrat : CDD non-cadre (+ 6 RTT annuels)
Salaire : Rémunération sur 12 mois à partir de 25K€ (brut annuel selon profil et expérience)
Prise en charge de la mutuelle à 60% et Ticket Restaurant

Merci de vous assurer de joindre une lettre de motivation à votre CV quand vous postulez.

À propos de l'évaluation de sécurité

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Product manager - Celsis (Kaarst, DE, 41564)

Job Summary

We are seeking an experienced Product Manager for our Microbial business unit site located in Kaarst, Germany. This position is largely remote with Kaarst, Germany, as the office site. This position will be responsible for developing and driving the successful strategy, revenue and profitability of a specific product line from ideation to end-of-life. This role has deep knowledge of the pharmaceutical and personal care products quality control testing markets including the regulatory and competitive landscape. This role requires strategic thinking and excellent tactical execution with strong project management skills. Collaborates across the organization working closely with Sales, R&D, Operations and the Strategic Marketing teams. Prior Product/Project Management and Customer/Sales experience required.

Essential Duties And Responsibilities

Your expertise will play a crucial role in driving our sales success and fostering strong relationships with customers and industry stakeholders.

Job Qualifications

Education: Bachelor’s degree (B.A. /B.S.) or equivalent in life sciences or related discipline. MBA preferred.

Experience: 3-5 years or more experience in pharmaceutical or personal care products QC testing and/or experience with services, analytical instrumentation, reagents and software. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Must possess excellent communication and presentation skills in English.

Proficient in the use of standard office computer applications (word processing, spreadsheets, presentations, e-mail).

It requires regular travel, that might be done by car. A valid driver’s license is required.

Must be able to influence and manage resources/staff without direct reporting relationships. Ability to multi-task, excellent written and verbal communication skills, organizational skills, and attention to detail required. Must possess analytical thinking and problem solving skills and be able to prioritize and re-evaluate priorities as situations change.

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, paid time off, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Stage Qualité opérationnelle - H/F - 6 mois (Ecully, FR, 69130)

Pendant près de 75 ans, les employés de Charles River ont travaillé ensemble pour aider à la découverte, au développement et à la fabrication sûre de nouvelles pharmacothérapies. Lorsque vous rejoignez notre famille, vous aurez un impact significatif sur la santé et le bien-être des gens à travers le monde. Que vos antécédents soient en sciences de la vie, en finance, en informatique, en ventes ou dans un autre domaine, vos compétences joueront un rôle important dans le travail que nous effectuons. En retour, nous vous aiderons à bâtir une carrière dont vous pouvez vous sentir passionné.

Résumé du travail

Charles River recrute un(e) Stagiaire Qualité Opérationnelle - H/F - pour une durée d'environ 6 mois, sur notre site d'Ecully (69), labellisé Great Place to Work pendant 4 années consécutives.

Dans un contexte d’évolution de nos activités qualité et de transformation des pratiques du site vers une approche basée sur le risque, nous souhaitons accueillir un(e) stagiaire qui contribuera à soutenir nos équipes tout en participant à un projet majeur d'implémenation de qualification des équipements de laboratoire via cette approche. Vous intégrerez l’équipe Qualité (Qualité Opérationnelle & QMS) et travaillerez sous la responsabilité du/de la Responsable Release & Qualité Opérationnelle.

VOS MISSIONS PRINCIPALES :

70 % – Projet : Application et Pilotage d’un nouveau process de qualification des équipements de laboratoire

Vous serez acteur(trice) d’un projet stratégique visant à déployer un processus harmonisé de qualification des équipements. Vous contribuerez notamment à :

Participer à la définition, la formalisation et la structuration du nouveau processus de qualification.
Contribuer à la création, révision et mise en œuvre des URS (User Requirements Specifications) pour les équipements concernés.
Participer à l’analyse de risques associée aux équipements, en utilisant des méthodologies reconnues (type FMEA, grille de criticité, analyse de défaillances…).
Assurer le suivi de charge, la planification et l’avancement des tâches auprès des laboratoires utilisateurs.
Contribuer à l’harmonisation des pratiques et accompagner les équipes dans l’appropriation du nouveau process.
Identifier les points de blocage et proposer des actions correctives et préventives.
Préparer un reporting régulier sur l’état d’avancement, les risques et les priorités du projet.

Ce projet vous permettra de développer une vision globale de la gestion de parc équipement, des exigences réglementaires associées, et d’acquérir une solide expérience en gestion de projet qualité.

30 % – Approbation qualité des rapports Accugenix®

(Principalement lors des périodes de congés et de pics d’activité)

Vérifier et approuver les rapports d’analyse Accugenix® (laboratoire d'analyses et d'identifications microbiennes)
Contrôler leur conformité par rapport aux exigences internes et réglementaires.
Contribuer au maintien de la continuité opérationnelle du service d’approbation qualité.

VOTRE PROFIL :

Vous êtes idéalement :

En 6ᵉ année de Pharmacie, ou
En 2ᵉ année de Master en école d’ingénieur ou cursus spécialisé (qualité, biotechnologies, santé, procédés…).

Une première expérience en qualité, qualification/validation, gestion de risques ou amélioration continue dans le secteur de la santé serait un plus.

Sens de l’organisation et rigueur
Bonnes capacités d’analyse et de synthèse
Intérêt pour la qualification d’équipements et l’évaluation des risques
Aisance relationnelle, goût pour le travail en équipe
Appétence pour les projets d’amélioration continue
Bon niveau d’anglais écrit, indispensable dans notre contexte international

A pourvoir dès que possible.

Saisissez cette opportunité d'intégrer une entreprise dynamique dans le cadre d'un environnement de travail et d'une culture certifiés Great Place To Work, et rejoignez des équipes passionnées et impliquées pour contribuer aux efforts que nous accomplissons chaque jour pour améliorer la santé et le bien-être du plus grand nombre possible de personnes.

À propos de Microbial Solutions
Notre groupe Microbial Solutions dispose d'un portefeuille très complet de services de test d'endotoxines, et de services et produits de détection et d'identification de microbes sans égal, qui a été spécialement conçu pour répondre aux besoins complexes et changeants de l'industrie. Nous aidons nos clients à garantir la qualité et l'innocuité de leurs produits grâce à des solutions de test faciles à utiliser et néanmoins extrêmement fiables qui sont conformes aux exigences réglementaires, qui sont axées sur le processus de prise de décisions critiques et qui visent à améliorer l'efficacité opérationnelle.

Avec plus de 20 000 collaborateurs sur 90 sites dans 20 pays, nous sommes positionnés stratégiquement pour coordonner des ressources mondiales et appliquer des perspectives pluridisciplinaires à l'élaboration de solutions aux défis uniques de nos clients. Notre base de clientèle comprend des sociétés de biotechnologies et des laboratoires pharmaceutiques internationaux, des agences publiques, et des établissements hospitaliers, d'enseignement et de recherche partout dans le monde.

Pour plus d'information, consultez www.criver.com.

Assistant(e) service clients - H/F - 5 mois (Ecully, FR, 69130)

Résumé du travail

Nous recrutons sur notre site d'Ecully (69), labellisé Great Place to Work pour la quatrième année consécutive, un(e) Assistant(e) service clients - H/F - en CDD pour une durée prévisionnelle de 4.5 mois.

Le poste

Vous intégrerez une équipe de 7 assistant(e)s service clients afin de satisfaire et fidéliser les clients en prenant en charge leurs demandes liées à l'importance et l'exportation et en apportant un soutien commercial aux équipes vente.

Missions

Prendre en charge la gestion administrative et le suivi des commandes
Traiter les commandes EU et export
Assurer le support commercial auprès des équipes ventes
Entretenir le contact clients et la relation clients
Gérer les réclamations clients

Qualifications souhaitées

Bac +2 en Commerce international ou expérience professionnelle équivalente
Expérience professionelle de 3 ans minimum sur un poste similaire, ayant idéalement impliquée l'utilisation du logiciel SAP
Connaissances en export
Maitrise du français, de l'anglais, et de l'italien
Organisation, rigueur, sens du service clients et aisance relationnelle sont vos principaux atouts

Modalités contractuelles

Contrat CDD à partir de mi Avril 2026 jusqu'au 1er Septembre 2026
35 heures, horaires variables
Salaire annuel à partir de 31 375 €
Primes de transport et titres restaurant
Intéressement
Convention collective de l'industrie pharmaceutique : groupe 4

Dans le cadre de sa politique de recrutement, Charles River s'engage à respecter les principes d'égalité des chances et de non-discrimination tout au long du process.

Pour plus d'information, consultez www.criver.com.

Assistant(e) service clients - H/F - 5 mois (Ecully, FR, 69130)

Job Summary

Le poste

Missions

Prendre en charge la gestion administrative et le suivi des commandes
Traiter les commandes EU et export
Assurer le support commercial auprès des équipes ventes
Entretenir le contact clients et la relation clients
Gérer les réclamations clients

Profile and Requirements

Qualifications souhaitées

Bac +2 en Commerce international ou expérience professionnelle équivalente
Expérience professionelle de 3 ans minimum sur un poste similaire, ayant idéalement impliquée l'utilisation du logiciel SAP
Connaissances en export
Maitrise du français, de l'anglais, et de l'italien
Organisation, rigueur, sens du service clients et aisance relationnelle sont vos principaux atouts

Modalités contractuelles

Contrat CDD à partir de mi Avril 2026 pour une durée de 4,5 mois environ
35 heures, horaires variables
Salaire annuel à partir de 31 375 €
Primes de transport et titres restaurant
Intéressement
Convention collective de l'industrie pharmaceutique : groupe 4

Dans le cadre de sa politique de recrutement, Charles River s'engage à respecter les principes d'égalité des chances et de non-discrimination tout au long du process.

À propos de Microbial Solutions

Notre groupe Microbial Solutions dispose d'un portefeuille très complet de services de test d'endotoxines, et de services et produits de détection et d'identification de microbes sans égal, qui a été spécialement conçu pour répondre aux besoins complexes et changeants de l'industrie. Nous aidons nos clients à garantir la qualité et l'innocuité de leurs produits grâce à des solutions de test faciles à utiliser et néanmoins extrêmement fiables qui sont conformes aux exigences réglementaires, qui sont axées sur le processus de prise de décisions critiques et qui visent à améliorer l'efficacité opérationnelle.

À propos de Charles River

Charles River est une organisation internationale de recherche de phase initiale sous contrat (ORC). Nous avons tiré parti de nos solides fondations dans le domaine de la médecine et de la science vétérinaire de laboratoire pour créer un portefeuille diversifié de services d'évaluation de découverte et de sécurité, conformes aux bonnes pratiques de laboratoire et autres, dans le but d'apporter à nos clients un soutien complet, de l'identification de cible au développement pré-clinique. Charles River propose également une gamme de produits et de services à l'appui des besoins en matière d'essais cliniques en laboratoire et des activités de fabrication de ses clients. Ce portefeuille considérable de produits et de services permet à nos clients de créer un modèle de développement de médicament plus flexible réduisant leurs coûts, accroissant leur productivité et améliorant leur efficacité, pour une mise sur le marché plus rapide.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Chef de Projet Environnement - F/H - CDI (L'Arbresle, FR, 69592)

Le poste

Afin de rejoindre et compléter l’expertise de notre service HSE (4 personnes), nous recherchons un Chef de Projet Environnement / HSE (F/H) en CDI sur notre site de Saint-Germain-Nuelles (69).
Rattaché(e) au Responsable HSE, vous jouerez un rôle clé dans la définition et la mise en œuvre de la politique Environnement du groupe : conformité réglementaire, réduction de l’empreinte écologique et accompagnement des projets de développement durable.

Les missions

1. Gestion de Projets Environnement

Déployer et animer la politique Environnement du site en cohérence avec les orientations du Groupe
Concevoir, suivre et actualiser les plans d’actions environnementaux : énergie, eau, déchets, solvants, émissions…
Piloter les projets environnementaux structurants : BEGES, décret tertiaire, mobilité douce, sobriété hydrique, réduction carbone,...
Accompagner les projets internes ayant un impact environnemental, garantir leur performance ainsi que leur conformité
Suivre les indicateurs et proposer des axes d’amélioration continue, en intégrant innovations et meilleures pratiques du secteur

2. Conformité réglementaire & audits

Veiller au respect des exigences réglementaires : dossier ICPE, plan de gestion des solvants, plan de sobriété hydrique, ATEX,...
Actualiser les dossiers réglementaires du site
Identifier, analyser et prévenir les risques environnementaux
Contribuer à la qualité, l’exhaustivité et la mise à jour de la documentation HSE (EvRP/DU, fiches sécurité, plans de prévention…)
Réaliser et/ou coordonner audits internes, audits réglementaires et visites HSE

3. Culture HSE & prévention

Sensibiliser, former et accompagner salariés et sous‑traitants sur les enjeux HSE
Développer une culture environnementale forte
Contribuer aux programmes d’hygiène, de sécurité et de protection de l’environnement
Encourager les initiatives internes en matière d’environnement et de développement durable
Proposer des améliorations pour renforcer les pratiques et méthodes, et soutenir la dynamique d'amélioration continue sur la HSE

Profil recherché

Vous êtes diplômé(e) d’un Bac+5 ou ingénieur en HSE et disposez d’au moins 3 ans d’expérience en environnement industriel réglementé.
Vous maîtrisez les réglementations HSE, ainsi que les méthodes de gestion de projet, d’analyse environnementale, de prévention des risques et de développement durable.
Vous connaissez les référentiels liés à l’amélioration environnementale, aux ERT et aux sites industriels classés.
Rigoureux(se), autonome et adaptable, vous aimez travailler en équipe et savez mobiliser vos interlocuteurs.
Vos qualités relationnelles et pédagogiques vous permettent de fédérer autour des enjeux HSE.
Un niveau d’anglais courant (oral et écrit) est requis pour évoluer dans notre environnement international.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique, groupe : 6
Contrat : CDI cadre (forfait jours + RTT)
Salaire : A compter de 40000€ bruts / an sur 14 mois, selon profil + Bonus
Avantages : Indemnités de transport, accord de télétravail, primes de participation et d’intéressement, mutuelle prise en charge à 60 %, restaurant d’entreprise, CSE
Site non accessible en transports en commun : un moyen de locomotion personnel est indispensable

À propos de Research Models & Services

Indispensable dans la recherche fondamentale et la découverte, l'utilisation de modèles in vivo nous aide à cibler certaines maladies et à déterminer les voies d'intervention biologiques potentielles qui permettent de contrôler l'évolution de la maladie. En notre qualité de leader mondial dans la production et la distribution d'animaux de recherche de qualité supérieure, avec un modèle sur deux produit pour la recherche préclinique à l'échelle mondiale, nous sommes bien placés pour comprendre l'importance de cette étape. Grâce à nos sept décennies d'expérience, notre expertise est inégalée, ce qui nous permet de mettre à votre disposition le modèle parfait, y compris des options spécifiques à une maladie et pré-conditionnées, pour la recherche fondamentale et au-delà.

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Technicien Polyvalent de Maintenance (rythme 3x8) - F/H - CDI (L'Arbresle, FR, 69592)

Depuis plus de 75 ans, les salariés de Charles River travaillent ensemble pour aider à la découverte, au développement et à la fabrication de nouvelles pharmacothérapies. Lorsque vous rejoignez notre famille, vous avez un impact significatif sur la santé et le bien-être des gens à travers le monde. Que vos antécédents soient en sciences de la vie, en finance, en informatique, en ventes ou dans un autre domaine, vos compétences jouent un rôle important dans le travail que nous effectuons. En retour, nous vous aidons à bâtir une carrière passionnante à nos côtés.

Le site Charles River

Implanté au cœur de la vallée de l’Azergues sur 14 hectares, le site Charles River de Lyon est un environnement scientifique unique où près de 1000 collaborateurs contribuent chaque jour au développement de nouvelles pharmacothérapies. Le site propose un cadre de travail innovant, dynamique et convivial, avec un engagement fort en matière de bien‑être animal.

Le poste

Dans un contexte technique exigeant, afin de relever nos défis opérationnels quotidien, nous recherchons un Technicien Polyvalent de Maintenance (F/H) en CDI (rythme 3x8) afin de renforcer notre équipe composée de 8 personnes.
Vous jouerez un rôle central dans la continuité de fonctionnement du site en assurant la maintenance de premier niveau des installations, la surveillance des paramètres environnementaux, la bonne distribution des énergies et la sécurité du site et des personnes, notamment en dehors des horaires de journée.

Les missions

1/ Gestion Technique Centralisée (GTC)

Prendre en compte les alarmes GTC et réaliser les interventions nécessaires
Relayer les informations et consignes
Mettre à jour les documents d’enregistrement
Contacter l’astreinte en cas de panne

2/ Chaufferies

Assurer la maintenance préventive et curative des chaudières vapeur et équipements annexes
Réaliser les essais quotidiens des sécurités chaudières
Effectuer les analyses d’eau et relevés de consommation
Mettre à jour les cahiers et registres de chaufferie

3/ Maintenance générale

Réaliser le préventif hebdomadaire sur les Centrales de Traitement d’Air (CTA)
Intervenir sur la maintenance curative de premier niveau sur l’ensemble des installations techniques du site

4/ GMAO

Gérer les appels urgents 24h/24
Rédiger les Demandes de Service via le logiciel de GMAO pour les interventions réalisées en journée

5/ Sécurité du site et des personnes

Prendre en charge les alarmes intrusion
Assurer les premiers secours en dehors des heures ouvrées
Intervenir en premier niveau lors du déclenchement du Plan d’Opérations Interne (POI)

Conditions spécifiques du poste

Ce poste se réalise sur un cycle 3x8 incluant polyvalence et flexibilité. Vous serez amené(e) à travailler certaines nuits, week-ends et jours fériés.
Travail 6 jours consécutifs sur un principe de roulement : 2 matins (5h-13h) ; 2 après-midis (13h-21h) ; 2 soirs (21h-5h) + 4 jours de repos

Profil recherché

Issu(e) d’une formation en maintenance ou d’un CAP/BEP technique, vous justifiez d’une première expérience sur un poste similaire.
Titulaire du permis B, vous disposez idéalement des habilitations suivantes : Conducteur de chaudière (niveau 2) et électrique avec le niveau BE Manoeuvre-BS-HOV.
Vous êtes à l'aise avec les outils informatiques

Au-delà de vos compétences techniques, vous êtes rigoureux(se), responsable et méthodique, capable de garder votre sang‑froid face aux imprévus.
Vous savez travailler seul mais êtes aussi à l'aise dans un fonctionnement en équipe. Votre flexibilité constitue un véritable atout dans l’organisation du travail en cycle 3x8.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : CDI non-cadre (1561h/an)
Salaire : A compter de 27 600 € bruts / an sur 14 mois + prime forfaitaire 3x8 sur 12 mois
Avantages : Indemnités de transport, primes de participation et d’intéressement, mutuelle prise en charge à 60 %, restaurant d’entreprise, CSE

À propos de Research Models & Services

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Au sein des laboratoires Charles River, nous reconnaissons et recrutons tous les talents. Nous sommes une entreprise attachée au principe de mixité, de diversité et d’inclusion et œuvrons quotidiennement en ce sens. Les Laboratoires Charles River France sont engagés dans une politique en faveur de l’intégration et du maintien dans l’emploi des personnes en situation de handicap. Tous nos postes sont ouverts aux travailleurs handicapés et une attention particulière sera portée aux candidats en situation de handicap qui postuleront auprès de Charles River.

Pour plus d'information, consultez www.criver.com.

Animalier contrôle de production - F/H - CDI week-end (L'Arbresle, FR, 69592)

Nous recherchons un Animalier Contrôle de production H/F - en CDI week-end et jours fériés pour 6 heures d'intervention par semaine : 3h les samedis matins, 3h les dimanches matins.

Vous serez intégré au sein d'une équipe et travaillerez en autonomie sur différentes espèces de rongeurs (rats, souris, cobayes) sur notre site des Oncins basé à l'Arbresle (69).

Missions principales

Observer les animaux (rongeurs) selon les consignes préalablement transmises adaptées à chaque projet ;
S’assurer du bien-être des animaux et alerter en cas de nécessité ;
Distribuer l’aliment et vérifier l’abreuvement ;
Nettoyer les lieux d’hébergement et les locaux en respectant les règles d'hygiène et de biosécurité ;
Garantir la mise à jour des registres de suivi.

Profil

Idéalement étudiant en filière scientifique
Vous êtes rigoureux, de confiance et aimez travailler au contact des animaux
Vous êtes à l'aise avec les outils informatiques
Vous avez à cœur l'éthique animale, êtes autonome, proactif et avez le sens du travail en équipe.

Informations contractuelles

Formation au poste inclue.
Nous vous proposons un CDI avec le Rythme de travail suivant : 6h/ semaine les samedis, dimanches matin (3h/jour) et éventuellement les jours fériés.
Prime de transport, 13e et 14e mois, Intéressement, participation, mutuelle et prévoyance, CE,
Localisation : Saint Germain Nuelles (69) – Site non accessible en transport en commun - Moyen de locomotion indispensable.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Technicien de Laboratoire en Immunologie - F/H - CDD 9 mois (Saint Germain Nuelles, FR, 69210)

Depuis plus de 75 ans, les salariés de Charles River travaillent ensemble pour aider à la découverte, au développement et à la fabrication de nouvelles pharmacothérapies. En rejoignant notre famille, vous aurez un impact significatif sur la santé et le bien-être des gens à travers le monde. Que vos antécédents soient en sciences de la vie, en finance, en informatique, en ventes ou dans un autre domaine, vos compétences joueront un rôle important dans le travail que nous effectuons. En retour, nous vous aiderons à bâtir une carrière passionnante à nos côtés.

Qui sommes-nous ?

Le site Charles River de Lyon est un site unique de 14 hectares, situé dans la vallée d'Azergues. Il offre un environnement scientifique innovant, dynamique et convivial où près de 1000 personnes travaillent chaque jour dans l'objectif commun de participer au développement de pharmacothérapies, dans le respect du bien-être animal.

Le poste

Dans le cadre d'un remplacement au sein de notre Laboratoire d'Evaluation Biologique (LEB), nous recherchons un Technicien de Laboratoire en Immunologie (F/H) en CDD pour une durée de 9 mois. Vous intégrerez un département scientifique dynamique et en constante évolution, composé de techniciens, opérateurs et directeurs d'études. Sous la responsabilité de votre manager, vous travaillerez plus spécifiquement dans une équipe de 9 personnes dédiées à l'analyse technique des biomarqueurs.

Les missions

Réaliser des Immunoessais en plaque de type ELISA/ECLIA/Multiplexin dans les activités suivantes : Dosages de Biomarqueurs, Immunogénicité des vaccins, Dosages pharmacocinétiques, Dosages ADA (Anti-Drug-Antibodies)
Réaliser les lyses, marquages cellulaires et titrations d'Anticorps pour l'activité Immunophénotypage
Réaliser le traitement et analyse informatique des échantillons sur la plateforme : Cytométrie en flux
Être capable d'accepter ou non des résultats biologiques en respectant des critères d'acceptation
Être capable de comprendre et d'accepter des résultats obtenus selon une courbe de calibration en respectant des critères d'acceptation
Réaliser la compilation informatique des résultats obtenus pour les différentes études
Réaliser la maintenance sur les appareils/automates utilisés dans les différentes activités
Réaliser les traitements et reprises des échantillons provenant des animaleries avant stockage au laboratoire

Conditions spécifiques du poste

Amplitude horaire : 7h/18h avec planning à la semaine
Permanences matin, soir et week-ends sur la base du volontariat

Qualifications souhaitées

Issu(e) d'une formation de niveau bac+2 minimum dans le domaine de la biologie, vous connaissez tout ou partie des techniques utilisées dans notre laboratoire : ELISA ; ECLIA ; Multiplexin ; ELISPOT ; Cytométrie en flux.

Vous aimez le travail en équipe mais êtes également capable d'évoluer en autonomie.

Vous savez vous organiser et réaliser vos missions avec rigueur.

La connaissance des BPL ou autres référentiels qualité est un atout.

Le groupe étant international, des bases en anglais sont indispensables. Un bon niveau serait un plus.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : CDD Non-cadre (accord de modulation 35h)
Salaire : A compter de 25 500 € bruts / an sur 13 mois
Prise en charge de la mutuelle à 60%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté, etc.
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Technicien de Laboratoire en Pathologie Clinique - F/H - CDI (Saint Germain Nuelles, FR, 69210)

Qui sommes-nous ?

Le poste

Afin de renforecer notre équipe Pathologie Clinique au sein du Laboratoire d'Evaluation Biologique (LEB), nous recherchons un Technicien de laboratoire en Pathologie Clinique (F/H) en CDI.

Les missions

Réaliser les dosages et expérimentations dans les activités suivantes : Hématologie, Coagulation, Biochimie, Examens urinaires.
Être capable d'accepter ou non des résultats biologiques en respectant des critères d'acceptation.
Réaliser des immunoessais en plaque de type ELISA/ECLIA/Multiplexin dans les activités suivantes : Dosages de Biomarqueurs, Immunogénicité des vaccins, Dosages pharmacocinétiques, Dosages ADA (Anti-Drug-Antibodies)
Etre capable de comprendre et d'accepter des résultats obtenus selon une courbe de calibration en respectant des critères d'acceptation
Réaliser la compilation informatique des résultats obtenus pour les différentes études.
Réaliser la maintenance sur les appareils/automates utilisés dans les différentes activités.
Réaliser les traitements et reprises des échantillons avant stockage au laboratoire.
Superviser, contrôler et réaliser les envois d'échantillons vers d'autres sites

Conditions spécifiques du poste

Amplitude horaire : 7h/18h avec planning à la semaine
Permanences matin, soir et week-ends sur la base du volontariat

Qualifications souhaitées

Vous aimez le travail en équipe mais êtes également capable d'évoluer en autonomie.

Vous savez vous organiser et réaliser vos missions avec rigueur.

La connaissance des BPL ou autres référentiels qualité est un atout.

Le groupe étant international, des bases en anglais sont indispensables. Un bon niveau serait un plus.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : CDD Non-cadre (accord de modulation 35h)
Salaire : A compter de 25 500 € bruts / an sur 13 mois
Prise en charge de la mutuelle à 60%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté, etc.
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Pour plus d'information, consultez www.criver.com.

Stage : Assistant Ingénieur - Projets Digitaux & Automatisation - F/H - 6 mois (Saint Germain Nuelles, FR, 69210)

Qui sommes-nous ?

L'équipe

Vous intégrerez l’équipe européenne Business Process Improvement, dont la mission est d’optimiser et transformer les processus internes à travers des projets digitaux, des démarches d’amélioration continue et de conduite du changement.

Dans ce cadre, nous recherchons un Assistant Ingénieur – Projets Digitaux & Automatisation F/H pour une durée de 6 mois afin de venir renforcer l’équipe sur des sujets à forte composante informatique, data et low-code/no-code.

Votre quotidien

- Analyser les besoins métiers et contribuer à la formalisation des cahiers des charges fonctionnels
- Concevoir, développer et déployer des solutions digitales basées sur la Power Platform (Power BI, Power Automate, Power Apps…)
- Participer à la gestion de projet : planification, suivi d’avancement, analyse des risques, comités projet, clôture et retours d’expérience
- Structurer et maintenir la documentation technique et fonctionnelle
- Assurer le support et la maintenance des solutions développées, dans une logique d’amélioration continue
- Collaborer avec des équipes internationales dans un contexte multiculturel et anglophone

Pourquoi nous rejoindre ?

Étudiant(e) en formation Bac+5 (école d’ingénieur, informatique, data, systèmes d’information, ou équivalent)
Fort intérêt pour les technologies digitales, l’automatisation et les solutions low-code / no-code
À l’aise avec la logique algorithmique, l’analyse et la modélisation de processus
Curieux(se), structuré(e), avec un bon esprit de synthèse et de résolution de problèmes
À l’aise dans le travail en mode projet et en équipe
Niveau d’anglais professionnel requis (environnement européen).

Modalités

Gratification de stage
Indemnités de transports (site non accessible en transports en commun)
Restaurant d'Entreprise

À propos de Safety Assessment

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Technicien expérimentation végétale - F/H - CDI (Montboucher-sur-Jabron, 26, FR, 26740)

Le poste

Notre Business Unit "Crops & Chemicals" assure des essais sur l'efficacité et les résidus de produits phytopharmaceutiques dans une multitude de cultures protégées et de grandes cultures, en Europe.

Depuis notre base de Montboucher sur jabron, pour compléter l’équipe et réaliser les essais sur le périmètre Sud-Est de la France, nous recherchons un nouveau Technicien Expérimentateur végétal (F/H) en CDI. Accompagner par votre manager local, vous travaillerez pour le respect des délais, de la qualité imposée et de la satisfaction de nos clients.

Les missions

Conduire les études et essais terrain dans le respect des protocoles, des procédures et des principes BPL (étude de faisabilité, recherche du site, réception des tests items, application(s), prélèvement (récolte), stockage, finalisation des données brutes (météo, température),
Enregistrer et maintenir les données brutes,
Réaliser les contrôles et opérations de maintenance du matériel d’expérimentation,
Réaliser tout ou partie des techniques spécifiques des études,
Assurer le suivi des études en relation avec le responsable et alerter en cas de besoins.

Qualifications souhaitées

Vous êtes titulaire d’un diplôme de niveau bac ou bac+2 dans les domaines de l’agriculture ou similaire.
Vous avez des expériences en production agricole, en sélection végétale ou en expérimentation phytosanitaire.
En plus du travail sur le terrain (application des produits et récolte), votre rigueur vous permet d’être responsable de l’enregistrement des données brutes.
Vous savez travailler en toute autonomie, organiser et prioriser vos activités, communiquer efficacement.
L’équipe étant internationale et la documentation en anglais, un niveau d’anglais courant est indispensable pour ce poste.

Conditions du poste

Activité saisonnière (forte: printemps-été/faible: hiver)
Travail le Week-end possible.
Déplacements en autonomie à prévoir

Modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : CDI non-cadre (accord de modulation 35h)
Salaire : A compter de 26 000€ bruts / an sur 13 mois
Prise en charge de la mutuelle à 60%, primes de repas, CSE
Primes d’intéressement/participation, accord d’ancienneté, accord de télétravail,...
Des déplacements quotidiens sur une zone importante sont à prévoir – permis de conduire indispensable

À propos de Safety Assessment

À propos de Charles River

Pour plus d'information, consultez www.criver.com.

Animalier - F/H - CDI Week-End (Bordeaux, 33, FR, 33000)

Qui sommes-nous ?

L’activité Insourcing Solutions (IS) correspond à la prestation de gestion complète d’animaleries. Dans ce modèle, les clients confient à Charles River la réalisation de l’ensemble des services définis dans un contrat, directement au sein de leurs installations dédiées à l’hébergement et au soin des animaux de laboratoire. L’IS garantit ainsi un haut niveau d’expertise, de conformité réglementaire et de continuité de service, tout en permettant aux équipes scientifiques de se concentrer sur leurs activités de recherche.

Le poste

Vous souhaitez contribuer au bien‑être animal et évoluer au sein d’un environnement scientifique international ?
Nous recrutons un(e) Animalier(ère) en CDI week‑end pour intervenir dans une animalerie dédiée aux rongeurs sur le site de l’un de nos clients de Bordeaux (33).

En binôme, chaque samedi (et certains jours fériés), vous interviendrez 2h30 sur une plage entre 8h et 13h, afin d'assurer la surveillance des animaux et de leur environnement.

Les missions

Observer les animaux (rongeurs) selon les consignes préalablement transmises adaptées à chaque projet
S'assurer du bien-être des animaux et alerter en cas de nécessité
Vérifier l'aliment et l'abreuvement, les compléter si nécessaire
Relever et contrôler la température et l'hygrométrie
Nettoyer les lieux d'hébergement
Garantir la mise à jour des registres de suivi

Qualifications recherchées

Vous êtes disponible tous les samedis et une formation scientifique serait un plus pour ce poste.

Motivé(e), impliqué(e) et attentif(ve) au bien‑être animal, vous savez travailler aussi en équipe qu'en toute autonomie.

Fiable, rigoureux(se) et responsable, vous respectez les consignes et identifiez rapidement les situations nécessitant une alerte.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique, groupe : 2
Contrat : CDI temps partiel (2h30/semaine, samedi + jours fériés)
Salaire : 1856,06€ bruts/mois (à équivalent temps plein), sur 14 mois
Avantages : Indemnités de transport, primes de participation et d’intéressement, mutuelle prise en charge à 60 %, CSE

À propos d'Insourcing Solutions

Insourcing Solutions℠ de Charles River peut rationaliser la recherche en favorisant l'efficacité opérationnelle et les économies de coût grâce à son processus stratégique de réalisation en interne pour les services de recherche GMP, GLP et hors GLP, depuis la découverte jusqu'à l'évaluation de l'innocuité. Insourcing Solutions℠ vous offre la possibilité de continuer à contrôler votre espace de travail et à rester maître de votre expertise tout en tirant le meilleur parti possible de l'espace disponible.

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Addetto alla cura degli animali da laboratorio - ROVERETO (contratto a chiamata) (Rovereto, IT, 36068)

Riepilogo del lavoro

Per nostro cliente sito in Rovereto ricerchiamo un Animal Caretaker con contratto a chiamata

La risorsa sarà inserita all'interno del team operante nella struttura e si occuperà di svolgere le mansioni relative alla gestione del laboratorio

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nel controllo delle procedure sperimentali;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature automatiche e carrelli;

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro con contratto a chiamata
Buona conoscenza del pacchetto office

Insourcing Solutions

Di cosa si occupa la Charles River

Alla Charles River, promuoviamo con convinzione il nostro ruolo nel miglioramento della qualità di vita delle persone. In tutto ciò che facciamo, siamo guidati dalla nostra missione, dalle nostre eccezionali competenze scientifiche e da una grande risolutezza e affrontiamo ogni giorno con la consapevolezza che il nostro lavoro contribuisce al benessere e al miglioramento della salute di molte persone in tutto il mondo. Abbiamo orgogliosi di aver collaborato allo sviluppo dell' 80% dei farmaci approvati dalla FDA negli ultimi cinque anni.

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Addetto cura animali da laboratorio - ROVERETO (contratto a chiamata) (Rovereto, IT, 36068)

Riepilogo del lavoro

Per nostro cliente sito in Rovereto ricerchiamo un Animal Caretaker con contratto a chiamata

La risorsa sarà inserita all'interno del team operante nella struttura e si occuperà di svolgere le mansioni relative alla gestione del laboratorio

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nel controllo delle procedure sperimentali;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature automatiche e carrelli;

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro con contratto a chiamata
Buona conoscenza del pacchetto office

Insourcing Solutions

Di cosa si occupa la Charles River

Alla Charles River, promuoviamo con convinzione il nostro ruolo nel miglioramento della qualità di vita delle persone. In tutto ciò che facciamo, siamo guidati dalla nostra missione, dalle nostre eccezionali competenze scientifiche e da una grande risolutezza e affrontiamo ogni giorno con la consapevolezza che il nostro lavoro contribuisce al benessere e al miglioramento della salute di molte persone in tutto il mondo. Abbiamo orgogliosi di aver collaborato allo sviluppo dell' 80% dei farmaci approvati dalla FDA negli ultimi cinque anni.

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Supply Chain Manager (Memphis, TN, US, 38118)

Job Summary

The Supply Chain Manager - Inventory & Logistics performs and oversees all activities related to storage, issuance and shipping of both raw materials, finished drug products and our client-specific materials. This role involves cross functional development of late-stage clients both internally as well as externally (client facing), inventory management, and review & improvement of master data, standard operating procedures to support procurement, inventory strategies, and maintaining client & regulatory requirements regarding shipment of drug product delivery.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

· Develop new inventory dashboards for client health and measure KPIs for late phase and commercial clients.

· Accountable for all aspects of supply chain with oversight on Inventory Planning, Warehousing, Shipping and receiving for all clients

· Manage and refine process and communication of final drug product deliveries according to client and regulatory requirements between the business & client ensuring the supply chain department executes to commitments and deadlines

· Responsible for development and implementation of procedures and training logistics

· Responsible for constructing and maintaining dashboards for inventory levels, expiry reports and cycle counts etc.

· Support the production plan/schedule by aligning material delivery times, and accurate inventory levels

· Collaborate with purchasing and supply chain teams to ensure timely availability of raw materials and cost-effective inventory

· Assists in generating/revising departmental documentation to include SOP's, Work Instructions, deviation notices, etc.

· Identify and implement improvements in planning to enhance cost-effectiveness and operational efficiency.

· Attend and lead internal cross functional meetings on behalf of supply chain, as well as attend and lead client facing meetings

· Communicate regularly with key stakeholders, including sales, logistics, and quality control teams, regarding schedule changes and production status.

· Maintain accurate documentation and reports related to production planning

· Oversight of client shipment and coordination as well as client facing requirements

· Follows all established safety guidelines for dealing with biohazardous and biological materials.

-Maintains cleanliness and orderliness of all department-owned areas at all times.

· Hire associates (when applicable) and develop those associates via performance metrics

· Perform all other duties as assigned.

Job Qualifications

-Bachelor's degree preferred.

· Minimum 5 years of managerial experience in an FDA regulated shipping, manufacturing, or warehousing environment.

· SAP experience highly preferred

· GMP experienced preferred

· Familiarity with dangerous goods shipping requirements (IATA)

· Reliable transportation and ability to drive between multiple facilities

· Ability to coach and lead a team

· Ability to multi-task and quickly refocus as priorities change in a fast-paced environment.

· Exemplary verbal and written communication skills and the ability to interact effectively with other departments, management, and clients.

· Experience with Microsoft Outlook, Access, Word, and Excel required.

· Willingness and ability to work off-shifts and weekends as job demands dictate.

· Ability to work a rotating on-call shift.

· Ability to lift 35 pounds without assistance.

About Charles River’s CDMO Services

About Charles River

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Principal Scientist, Process Development (Memphis, TN, US, 38118)

Job Summary

The Principal Scientist Process Development is a leadership role focused on driving scientific innovation and strategy within Process Development. The Principal Scientist leads research projects, develops new scientific approaches, and mentors junior scientists. The Principal Scientist will work across various teams, build collaborations, and contribute to the company's scientific strategy and goals. The Principal Scientist will lead functional areas dedicated to technology development activities, as well as coordinate functional activities and manufacturing support for clinical/commercial bioprocesses. The position entails presenting at and leading internal departmental and cross-functional meetings and the expectation of reviewing and approving technical reports, and possibly also scientific publications, patent applications, and regulatory submissions. The Principal Scientist must possess strong technical expertise and significant technical and hands on experience and have skills and experience leading scientific groups that can analyze data, interpret results, and contribute to important decisions based on data. The position entails the ability to manage direct reports and experience leading and mentoring teams in a senior management role while also being able to lead collectively in a larger team and organizational environment. The position will participate in client-facing discussions and key business decisions.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Design and execute experiments to support process development, including cell therapy process optimization, technology development, and process modelling.
• Lead and manage scientific projects or workstreams: This can include designing experiments, overseeing the development and execution of studies, and analyzing and interpreting data.
• Contribute to strategy and decision-making: Provide expert input to shape research direction, influence cross-functional teams, and contribute to regulatory submissions and internal reports.
• Collaborate and communicate: Work closely with internal and external stakeholders, including other scientists, project teams, and regulatory bodies, to achieve project goals, share knowledge, and represent Charles River Laboratories in the scientific community.
• Mentor and develop others: Coach and manage junior scientists, fostering a collaborative and high-performing team environment.
• Provide scientific leadership and direction for research programs, often focusing on a specific therapeutic area or technology.
• Lead or contribute to research projects, from early discovery to late-stage development, often involving the application of cutting-edge technologies in cell therapy.
• Work effectively with multidisciplinary teams, including researchers, clinicians, and commercial teams.
• Represent the company in scientific forums, build external collaborations, and stay abreast of scientific advancements.

Job Qualifications

• Bachelor’s degree with 19+ years of experience, Master’s degree with 14+ years of experience, or PhD with 8+ years of experience.
• Experience leading groups or departments in biopharmaceutical, bioprocessing, analytical, and/or drug product or process development.
• Experience with relevant small to large scale bioprocessing equipment.
• Experience with relevant processes as they pertain to cell therapy.
• Experience working in CDMO or CRO industry.
• Experience in a client-facing role.

The pay range for this position is $152,493 - $170,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Charles River’s CDMO Services

About Charles River

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Supervisor QC Microbiology (Memphis, TN, US, 38118)

Job Summary

Supervisor QC Microbiology requires working knowledge of Environmental Monitoring of Good Manufacturing Practices (GMP) cleanrooms including how to appropriately and effectively complete investigations of excursions. Familiarity with compendial microbiological testing methods for sterility, mycoplasma, endotoxin, etc., and experience with culturing and identifying various microorganisms (bacteria, yeast, fungi) by different methods (stains, PCR, etc.), is essential.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

•   Leads all activities associated with daily operations of the QC Micro Department
•   Oversee the performance of QC Analyst providing support and guidance by coaching areas of growth and development and recognizing and rewarding successes
•   Reviews and maintains documentation and records for accuracy and compliance
•   Prepare for and actively participate in internal and external audits, investigations, and reporting
•   Provide direction and technical expertise to Micro team
•   Utilize common problem-solving tools and methodologies in processes and procedures for root cause analysis and resolution
•   Seek to understand and operate within the department budget, cost and profitability restraints, and ensure that materials meet regulatory requirements
•   Ensure timely response and closure of customer complaints
•   Conducts and leads meetings and communications effectively
•   Prepares and facilitates reporting, as requested by QC Micro Leadership Team
•   Manages KPI performance, goals, and objectives
•   Issues and traces necessary deviations, change controls, CAPAs, related to QC Micro Department
•   Review and approve QC Micro data for accuracy and compliance to applicable SOPs and Test Methods
•   Supports and coordinates special projects and other assignments related to QC Micro Department
•   Must be able to report onsite, work flexible hours, split shifts, during weekends and holidays as the operations of the business requires
•   Perform other duties as assigned

Job Qualifications

•   Bachelor's degree in biology or relevant scientific discipline
•   3-4 years of relevant Microbiology experience preferred or equivalent combination of education and experience
•   Ability to supervise and manage the schedule of Analysts
•   Ability and desire to take initiative on department-wide improvement projects and drive to completion.
•   Experience performing and managing performance of Environmental Monitoring of GMP cleanrooms.
•   Ability to process large amounts of paperwork in a timely and efficient manner.
•   Previous experience supervising/scheduling staff for a 24/7 operation desired.
•   Experience with microbiology laboratory design requirements, setting up/equipping, and inventorying.
•   Experience in culturing microbes and use of various classical microbiology and biochemical techniques such as gram stain, streak plate, spread plates etc.
•   Experience in data/statistical analysis, data trending, reporting results and presenting data in group and client meetings.
•   Excellent writing skills. Ability to draft Standard Operating Procedures (SOPs), protocols, reports, etc. Ability to write deviations, Environmental Monitoring investigations, OOS reports, CAPAs.
•   Understanding of cGMP/GLP regulations as well as excellent GDP (documentation skills).
•   Familiarity with relevant FDA, EMA, ICH, USP and EP guidelines and regulations associated with the quality control of aseptic processes, biologic/cell therapies in general and the environmental monitoring and operation of cleanrooms, specifically.
•   Excellent interpersonal skills and willingness to work interdepartmentally with QC, Manufacturing and Quality Assurance.
•   Ability to multitask, problem solve and troubleshoot as necessary.

Compensation Data

The pay range for this position is $76,000 - $82,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Charles River’s CDMO Services

About Charles River

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician I - In Vivo Ops Support - 2nd Shift (Mattawan, MI, US, 49071)

Job Summary

We are seeking a Technician I at our Safety Assessment site located in Mattawan, MI. The pay for this position is $20/hour plus shift differential and benefits. Working hours for 2nd Shift : 2:00pm to 10:30pm with possible late stays.

A Technician I – Technical Operations is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to conduct a study, which may include animal handling/restraint, housing maintenance, and feeding procedures; collecting data, observing the animals for health status, and body weight measurements; administering doses by various methods, conducting euthanasia, and/or biological specimen collections for analysis. The technician is working under close supervision to gain proficiency.

Successful Candidates will possess the 6 Cs of Success:

Character – Unquestionable integrity. Respect for all.
Coachable –Eager to receive feedback. Open to making improvements.
Commitment– Dedicated to our animals, our clients/studies, our team.
Collaborative – Team player. Eager to help.
Communicative – Proactively asks questions. Provide complete answers.
Competent – Continuously and proactively hones and expands skill sets.

Job Qualifications

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Ensure good welfare and humane care for all animals worked with through gentle, positive human animal interactions.
Train in on-boarding skills which may include animal handling, husbandry, observations, basic physiological indices, and data collection/recording to support each skill. Specific tasks will be based on each area's training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Maintain appropriate communication with other personnel.
Use and maintain instrumentation and equipment according to SOPs.
Capable of repetitive gripping, pinching, lifting, carrying, pushing, and pulling. Job requires ability to independently routinely lift or carry up to 50lbs, or team lift weights exceeding 50lbs.
Ability to perform repeated twisting, bending, and reaching; exposure to hot and/or humid environments.

QUALIFICATIONS:

Education: High school diploma or General Education Degree (G.E.D.), required. Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred.
Experience: No previous experience required.
Excellent written and verbal communication skills.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule includes evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to ensure that a safe working environment is maintained observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Must be authorized to work in United States without a sponsor visa now or in the future.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician I - Molecular Imaging (Mattawan, MI, US, 49071)

Job Summary

HOURLY RATE: The pay range for this position is $20.00 - $21.50. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

SCHEDULE: Monday - Friday, 8:00am - 4:30pm

We are seeking a Research Technician for our Molecular Imaging Team located in Mattawan, MI.

A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives.

Job Qualifications

The following are minimum requirements related to the Research Technician position:

Minimum: High School Diploma or GED
Experience: Zero - 6 months
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Basic familiarity with Microsoft Office Suite.
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice.
Ability to work under specific time constraints
Must be authorized to work in the United States without a sponsor visa, now or in the future.

The pay range for this position is $20-21.50/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician - Molecular Imaging (Mattawan, MI, US, 49071)

Job Summary

SCHEDULE: Monday - Friday, 8:00am - 4:30pm

We are seeking a Research Technician for our Molecular Imaging Team located in Mattawan, MI.

A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives.

Job Qualifications

The following are minimum requirements related to the Research Technician position:

Minimum: High School Diploma or GED
Experience: Zero - 6 months
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Basic familiarity with Microsoft Office Suite.
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice.
Ability to work under specific time constraints
Must be authorized to work in the United States without a sponsor visa, now or in the future.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician I - Clinical Pathology (Mattawan, MI, US, 49071)

Job Summary

We are seeking a Technician I for our 2nd shift Clinical Pathology Team in Mattawan MI.

A Technician I – Clinical Pathology is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to conduct a study, which may include biological sample management including labeling, delivery, aliquoting, processing, and verification; cleaning of lab and equipment; preparation, staining, and consolidation of slides. The technician is working under close supervision to gain proficiency.

The pay for this position is $20/hr USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

The work schedule for this role is Monday - Friday from 2:30PM - 11:00PM.

Essential Duties and Responsibilities

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding skills which may include biological sample management including labeling, delivery, aliquoting, processing, and verification; cleaning of lab and equipment; preparation, staining, and consolidation of slides. Specific skills will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Perform all other related duties as assigned.

Job Qualifications

Education: High school diploma or General Education Degree (G.E.D.) required. Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred.
Experience: No previous experience required.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills. Knowledge of English.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician I, Animal Care - Equipment Repair and Fabrication (Mattawan, MI, US, 49071)

Job Summary

We are seeking a Animal Care Technician I at our Safety Assessment site located in Mattawan, MI. The pay for this position is $19/hour plus benefits.

A Technician I is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to support a study which may include animal husbandry needs, animal handling, cage cages, equipment storage/tracking, wash systems, and water delivery system maintenance for various species throughout the site. The technician is working under close supervision to gain proficiency.

Essential Duties and Responsibilities

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding skills which may include animal husbandry needs, animal handling, cages, equipment storage/tracking, wash systems, and water delivery system maintenance for various species throughout the site. Specific skills will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Perform all other related duties as assigned.

Job Qualifications

Education: High school diploma, General Education Degree (G.E.D.), preferred.
Experience: No previous experience required.

An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Certification/Licensure: None.
Other:

Excellent written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and
Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician I - Surgery and Efficacy - Surgery OR (Mattawan, MI, US, 49071)

Job Summary

We are seeking an experienced Technician 1 – Surgery and Efficacy for our Surgery OR Team in Mattawan MI.

A Technician 1 is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives.

The pay for this position is $20/hr USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Essential Duties and Responsibilities

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding skills which may include animal handling/restraint, housing maintenance, and feeding procedures; collecting data, observing the animals for health status, and body weight measurements; administering doses by various methods, conducting euthanasia, and/or biological specimen collections for analysis. Specific skills will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Perform all other related duties as assigned.

Job Qualifications

The following are minimum Qualifications related to the Technician 1 position.

HS/GED/Bachelor's degree (preferred, not required) with no experience; contract research organization experience preferred.
Ability to communicate verbally and in writing.
Basic familiarity with Microsoft Office Suite.
Computer skills, commensurate with Essential Functions and including ability to learn a validated system.
Ability to work extended hours beyond normal work schedule to include, but not limited to, evenings, weekends, extended shifts and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Ability to lift/move up to 30 pounds regularly and up to 60 pounds frequently.
Physically able to wear personal protective equipment (PPE) to include properly fitted respirator.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Security Officer - 3rd Shift - Rotating Weekends (Mattawan, MI, US, 49071)

Compensation Data

This position offers $19.00/hr as a starting wage alongside a 15% shift differential for all hours worked on the alternative shift.

Job Summary

We are seeking an experienced full-time Security Officer for the 3rd Shift Security team in Mattawan, MI.

A Security Officer is responsible for: following established procedures and guidelines; monitoring and ensuring compliance with company security and safety policies; monitoring all access to the facility by checking and issuing security badges; monitoring security, safety and integrity of buildings and environs; responding to any unusual circumstances; protecting facility from unwanted actions or espionage; and providing a safe and secure environment for employees, clients, visitors and animals.

The pay for this position is $19.00/hr USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Essential Duties and Responsibilities

Greet, screen, record and allow visitors and employees admittance to the site in accordance with company procedures.
Monitor security systems and/or environmental systems and investigate and/or report any incidents.
Report all unauthorized persons to the proper authorities and initiate action to protect employees, animals, products, and physical site. In so doing, the incumbent should not place him or herself in harm’s way.
Ensure the physical safety and security of the facility by enforcing company policies and procedures; provide a deterrent and detection factor for wrongful activity; conduct patrols and monitor the status of the physcial security measures; and monitor the critical building systems.
Physically walk the facility grounds to complete visual inspection of site security on regularly scheduled tours.
Document all security department activity and generate incident reports as necessary.
Monitor facility equipment during tours and report equipment failure, reset alarms as instructed and/or assist in minor repair as directed. Provide effective secondary communications during business hours; and primary communications during non-business hours.
Contact emergency personnel as required and in accordance with company procedures.
Assist in directing appropriate emergency response efforts when required.
Perform all other related duties as assigned.

Job Qualifications

HS/GED degree with 2- 3 years of experience, with at least six to twelve months of related security experience and/or training; contract research organization experience preferred. Driver’s license is required.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Basic familiarity with Microsoft Office Suite.
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice.
Ability to work under specific time constraints.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Autopsy Technician I (Mattawan, MI, US, 49071)

Job Summary

We are seeking an experienced Technician I – Necropsy for our Pathology Services Team in Mattawan MI.

A Technician I – Necropsy is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to conduct a study, which may include animal handling, sedation; animal procedures including dissection; collection of samples and weights; laboratory preparation, set up and cleaning; preparation of laboratory solutions. The technician is working under close supervision to gain proficiency.

The pay for this position is $20/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

The work schedule for this role is: Monday - Friday 8:00AM to 4:30PM with a weekend/holiday rotation and overtime, as necessary.

Essential Duties and Responsibilities

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions
Train in on-boarding skills which may include animal handling, sedation; animal procedures including dissection; collection of samples and weights; laboratory preparation, set up and cleaning; preparation of laboratory solutions. Specific skills will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Learn and know anatomic terms
Receive, track, and prepare samples or materials, as required for department.
Perform all other related duties as assigned.

Job Qualifications

Education: High school diploma or General Education Degree (G.E.D.) required. Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred.
Experience: No previous experience required.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

Physical Requirements

The functions of this role require to be able to physically:

lift/move up to 60 pounds regularly, possibly over the head
stand for extended periods of time
walk long distances across the facility, possibly up to 10 miles per day on concrete floors
remain seated for extended periods of time
utilize meticulous fine-motor skills
work while wearing personal protective equipment (PPE)
work in close proximity to rodents and rabbits that may result in sensitization to allergens or exacerbate preexisting allergies

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Preclinical Autopsy Technician I (Mattawan, MI, US, 49071)

Job Summary

We are seeking an experienced Technician I – Necropsy for our Pathology Services Team in Mattawan MI.

The pay for this position is $20/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

The work schedule for this role is: Monday - Friday 8:00AM to 4:30PM with a weekend/holiday rotation and overtime, as necessary.

Essential Duties and Responsibilities

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions
Train in on-boarding skills which may include animal handling, sedation; animal procedures including dissection; collection of samples and weights; laboratory preparation, set up and cleaning; preparation of laboratory solutions. Specific skills will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Learn and know anatomic terms
Receive, track, and prepare samples or materials, as required for department.
Perform all other related duties as assigned.

Job Qualifications

Education: High school diploma or General Education Degree (G.E.D.) required. Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred.
Experience: No previous experience required.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

Physical Requirements

The functions of this role require to be able to physically:

lift/move up to 60 pounds regularly, possibly over the head
stand for extended periods of time
walk long distances across the facility, possibly up to 10 miles per day on concrete floors
remain seated for extended periods of time
utilize meticulous fine-motor skills
work while wearing personal protective equipment (PPE)
work in close proximity to rodents and rabbits that may result in sensitization to allergens or exacerbate preexisting allergies

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Research Technician (Temporary- Potential Permanent) (Mattawan, MI, US, 49071)

Job Summary

We are seeking Temporary to Potential Permanent Animal Research Technician at our Safety Assessment site located in Mattawan, MI. The pay for this position is $20/hour plus benefits.

A Technician is responsible for assisting management, scientists, veterinarians and study related items. The technician performs basic skills independently and continues to work under supervision to gain proficiency on skills still in development. They administer substances to animals, perform husbandry duties including cleaning/transporting caging and providing food and water; perform observations of animals to determine morbidity/mortality; collect and handle data and specimens.

Training Schedule:

Week 1: Tuesday-Friday 8:00AM – 4:30PM

Week 2+: Monday-Friday 7:00AM* – 3:30PM* All roles and shifts require flexibility to work extended hours outside of scheduled shift based on business need, sometimes with short notice.

Potential Permanent Schedules: May vary based on business need and available roles to include:

Monday – Friday with weekend and holiday rotations 07:00AM* – 3:30PM*
Sunday – Thursday with holiday rotations 07:00AM* – 3:30PM*
Tuesday – Saturday with holiday rotations 07:00AM* – 3:30PM*

All roles and shifts require flexibility to work extended hours outside of scheduled shift based on business need, sometimes with short notice.

Successful Candidates will possess the 6 Cs of Success:

Character – Unquestionable integrity. Respect for all.
Coachable – Eager to receive feedback. Open to making improvements.
Commitment – Dedicated to our animals, our clients/studies, our team.
Collaborative – Team player. Eager to help.
Communicative – Proactively asks questions. Provide complete answers.
Competent – Continuously and proactively hones and expands skill sets.

Job Qualifications

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Ensure good welfare and humane care for all animals worked with through gentle, positive human animal interactions.
Train in on-boarding skills which may include animal handling, husbandry, observations, basic physiological indices, and data collection/recording to support each skill. Specific tasks will be based on each area's training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Maintain appropriate communication with other personnel.
Use and maintain instrumentation and equipment according to SOPs.
Capable of repetitive gripping, pinching, lifting, carrying, pushing, and pulling. Job requires ability to independently routinely lift or carry up to 50lbs, or team lift weights exceeding 50lbs.
Ability to perform repeated twisting, bending, and reaching; exposure to hot and/or humid environments.

QUALIFICATIONS:

Education: High school diploma or General Education Degree (G.E.D.), required. Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred.
Experience: No previous experience required.
Excellent written and verbal communication skills.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule includes evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to ensure that a safe working environment is maintained observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Research Technician - 2nd Shift (Mattawan, MI, US, 49071)

Job Summary

We are seeking a Technician I at our Safety Assessment site located in Mattawan, MI. The pay for this position is $20/hour plus shift differential and benefits.

Successful Candidates will possess the 6 Cs of Success:

Job Qualifications

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Ensure good welfare and humane care for all animals worked with through gentle, positive human animal interactions.
Train in on-boarding skills which may include animal handling, husbandry, observations, basic physiological indices, and data collection/recording to support each skill. Specific tasks will be based on each area's training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Maintain appropriate communication with other personnel.
Use and maintain instrumentation and equipment according to SOPs.
Capable of repetitive gripping, pinching, lifting, carrying, pushing, and pulling. Job requires ability to independently routinely lift or carry up to 50lbs, or team lift weights exceeding 50lbs.
Ability to perform repeated twisting, bending, and reaching; exposure to hot and/or humid environments.

QUALIFICATIONS:

Education: High school diploma or General Education Degree (G.E.D.), required. Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred.
Experience: No previous experience required.
Excellent written and verbal communication skills.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule includes evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to ensure that a safe working environment is maintained observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Must be authorized to work in the United States without a sponsor visa, now or in the future

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

BTA / Biologielaborant /BSc als Lab Technician (m/w/d) - Viral Clearance (Cologne, NW, DE, 51105)

Seit fast 75 Jahren arbeiten die Mitarbeiter von Charles River zusammen, um bei der Entdeckung, Entwicklung und sicheren Herstellung neuer Arzneimitteltherapien zu helfen. Wenn Sie sich unserer Familie anschließen, haben Sie einen bedeutenden Einfluss auf die Gesundheit und das Wohlbefinden der Menschen auf der ganzen Welt. Ob Ihr Hintergrund in Life Sciences, Finanzen, IT, Vertrieb oder einem anderen Bereich ist, Ihre Fähigkeiten werden eine wichtige Rolle bei der Arbeit spielen, die wir durchführen. Im Gegenzug helfen wir Ihnen, eine Karriere zu bauen, die Sie begeistern wird.

Für die Abteilung Virus Clearance am Standort Köln suchen wir zur Erweiterung des Labor-Teams ab sofort unbefristet eine/n

BTA / Biologielaborant / B.Sc. Biologie-Biotechnologie
als Lab Technician (m/w/d)

Unterstütze uns bei:

der äußerst sorgfältigen, zuverlässigen und selbständigen Durchführung und Dokumentation von Virussicherheitsstudien (Viral clearance studies) nach GLP
der Organisation und Ausführung vielfältiger Methoden (z.B. Virusfiltrationen, Inaktivierungen und Chromatographien) zur Validierung von Herstellungsprozessen biologischer Arzneimittel im Rahmen dieser Studien
dem Umgang mit Chemikalien und Laborgeräten
der Durchführung von zellkulturbasierten Assays und deren Auswertung mittels Lichtmikroskopie
den Prozessdurchführungen mit Viren der Gefahrstufen BSL-2 und BSL-3**
der Betreuung und Sicherstellung der Pflege und Aufrechterhaltung des GLP-Systems u.a. Pflege und Wartung von Laborgeräten, sowie deren Qualifikation und dem Erstellen von Standardarbeitsanweisungen
der Betreuung von nationalen und internationalen Kunden während ihres Aufenthaltes in unseren Laboren, z.B. bei der Benutzung von Geräten und bei sicherheitsrelevanten Fragen
https://www.criver.com/products-services/biologics-testing-solutions/viral-clearance-and-tse-clearance-studies?region=3696

Überzeuge uns durch:

eine erfolgreich abgeschlossene Ausbildung als Biologisch-technischer Assistent / Biologielaborant oder ein erfolgreich abgeschlossenes Bachelorstudium in Biologie / Biotechnologie / verwandten Naturwissenschaften
Freude am Umgang mit Laborgeräten und experimentellen Aufbauten
erste Erfahrungen im Umgang mit Zellkulturen inkl. sterilem Arbeiten (wünschenswert)
Kenntnisse in Methoden zur Proteinaufreinigung, sowie chromatographischen Methoden (wünschenswert)
die Fähigkeit zu sehr strukturierten, zielorientierten und konzentrierten Arbeiten unter Einhaltung enger Zeitlinien
ausgeprägtes Verantwortungsbewusstsein, Organisationsfähigkeit, hohe Verlässlichkeit und Flexibilität
Team- und Kommunikationsfähigkeit
Dienstleitungsorientierung
Gute Kenntnisse von Microsoft Office (Word, Excel) sowie gute deutsche und englische Sprach- und Schriftkenntnisse setzen wir voraus.

Wir bieten Dir:

eine unbefristete Stelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten internationalen Unternehmen
eine intensive Einarbeitung
ein Gleitzeitsystem
diverse Benefits
eine aktive Mitgestaltung Deines Tätigkeitsfeldes in einem motivierten Team und
eine angemessene Vergütung

Haben wir Dein Interesse geweckt?

Wenn ja, bewirb Dich bitte unter der Job-ID 231849 über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a-b

40699 Erkrath

Vorangehen - Wir gehen voran, wenn wir unsere Absichten und Werte entwickeln und unsere Kompetenz teilen, wenn wir für die Zukunft planen und Wandlungsfähigkeit und Flexibilität zeigen, wenn wir Innovation ermöglichen und die großartige Arbeit anderer schätzen.

Sorgfalt - Wir beweisen Sorgfalt, wenn wir einander, unsere Tiere und das gesellschaftliche Umfeld, in dem wir arbeiten und leben, respektieren, wenn wir einen positiven, gesunden Arbeitsplatz schaffen, wenn wir unsere Compliance-Standards einhalten, und wenn wir stets das Richtige tun.

Zusammenarbeit - Wir arbeiten zusammen, wenn wir klar und effizient in unserem direkten Umfeld ebenso wie weltweit kommunizieren, andere einbeziehen und unterschiedliche Ideen schätzen, wenn wir unseren Kunden zum Erfolg verhelfen und das Teamwork fördern und wenn wir allumfassend und ganzheitlich denken und handeln.

Verantwortung - Wir handeln wie Eigentümer, wenn wir Verantwortung für unsere Handlungen übernehmen, wenn wir auf interne und externe Kunden mit Geschwindigkeit und Genauigkeit reagieren, wenn wir sinnvolle Ziele setzen und erreichen und wenn wir nach kontinuierlicher Verbesserung streben.

Biologics Testing Solutions

Mit über 50 Jahren Erfahrung und bewährter regulatorischer Kompetenz kann die Charles River Biologics-Gruppe sich den Herausforderungen von Biotech- und Pharma-Unternehmen weltweit stellen. Wir unterstützen mit Dienstleistungen wie Kontaminations- und Verunreinigungstests, Proteincharakterisierung, Bioassays, virale Clearance-Studien sowie Stabilitäts- und Chargenfreigabeprogrammen Kunden während des gesamten biologischen Entwicklungszyklus, von der Einrichtung und Charakterisierung von Zellbanken bis hin zu präklinischen und klinischen Studien und der Markteinführung von Produkten. Ganz gleich, ob Kunden eigenständige Dienstleistungen, ein maßgeschneidertes Testpaket oder In-house-Support benötigen, unsere Biologics-Gruppe kann für jeden Bedarf eine maßgeschneiderte Lösung entwickeln. Jedes Jahr werden mehr als 20.000 biologische Testberichte und über 200 lizenzierte Produkte von unserem Biologics-Team ausgesendet.

Über Charles River

Charles River ist ein auf die Frühphase der Wirkstoffentwicklung spezialisiertes Auftragsforschungsunternehmen (CRO). Wir haben auf der Grundlage unserer Erfahrungen mit Versuchstiermedizin und -wissenschaft ein vielseitiges Portfolio von Discovery- und Sicherheitsprüfungsdienstleistungen aufgebaut, sowohl mit Good Laboratory Practice (GLP) und ohne GLP, um Kunden von der Wirkstoffidentifikation bis zur präklinischen Entwicklung zu unterstützen. Charles River bietet auch eine Reihe von Produkten und Dienstleistungen für klinische Labortestbedürfnisse und Herstellungsaktivitäten. Die Nutzung dieses breiten Portfolios von Produkten und Dienstleistungen ermöglicht unseren Kunden, ein flexibleres Medikamentenentwicklungsmodell zu entwickeln, wodurch die Kosten gesenkt, die Produktivität erhöht und die Markteinführung beschleunigt wird.

Mit über 20.000 Mitarbeitern in 110 Standorten in 20 Ländern rund um den Globus sind wir strategisch positioniert, weltweite Ressourcen zu koordinieren und multidisziplinäre Projekte für die Entwicklung und Herausforderungen unserer Kunden zu entwickeln. Unsere Kundenbasis umfasst globale Pharmaunternehmen, Biotechnologieunternehmen, Behörden und Krankenhäuser sowie akademische Institutionen in der ganzen Welt.

Charles River setzt sich leidenschaftlich für die Verbesserung der Lebensqualität ein. Unsere Mission, unsere exzellente Wissenschaft und unser Engagement für einen sinnvollen Einsatz unserer Kapazitäten leiten uns in allem, was wir tun. Wir beginnen jeden Tag in dem Wissen, dass unsere Arbeit die Gesundheit und das Wohlergehen von vielen Menschen weltweit nutzt. Wir sind stolz darauf, dass wir die Entwicklung von etwa 86% der von der FDA in 2021 zugelassenen Medikamente unterstützt haben.

Bei Charles River Laboratories erkennen wir alle Talente an und stellen sie ein. Wir sind ein Unternehmen, das sich dem Grundsatz der Vielfalt und Inklusion verpflichtet hat und täglich in diese Richtung arbeitet.

Weitere Informationen finden Sie unter www.criver.com.

BTA / Biologielaborant / BSc als Lab Technician II (m/w/d) - Viral Clearance (Cologne, NW, DE, 51105)

Für die Abteilung Virus Clearance am Standort Köln suchen wir zur Erweiterung des Labor-Teams ab sofort unbefristet eine/n

BTA / Biologielaborant / B.Sc. Biologie-Biotechnologie
als Lab Technician II (m/w/d)

Unterstütze uns bei:

der äußerst sorgfältigen, zuverlässigen und selbständigen Durchführung und Dokumentation von Virussicherheitsstudien (Viral clearance studies) nach GLP
der Organisation und Ausführung vielfältiger Methoden (z.B. Virusfiltrationen, Inaktivierungen und Chromatographien) zur Validierung von Herstellungsprozessen biologischer Arzneimittel im Rahmen dieser Studien
dem Umgang mit Chemikalien und Laborgeräten
der Durchführung von zellkulturbasierten Assays und deren Auswertung mittels Lichtmikroskopie
den Prozessdurchführungen mit Viren der Gefahrstufen BSL-2 und BSL-3**
der Betreuung und Sicherstellung der Pflege und Aufrechterhaltung des GLP-Systems u.a. Pflege und Wartung von Laborgeräten, sowie deren Qualifikation und dem Erstellen von Standardarbeitsanweisungen
der Betreuung von nationalen und internationalen Kunden während ihres Aufenthaltes in unseren Laboren, z.B. bei der Benutzung von Geräten und bei sicherheitsrelevanten Fragen
https://www.criver.com/products-services/biologics-testing-solutions/viral-clearance-and-tse-clearance-studies?region=3696

Überzeuge uns durch:

eine erfolgreich abgeschlossene Ausbildung als Biologisch-technischer Assistent / Biologielaborant oder ein erfolgreich abgeschlossenes Bachelorstudium in Biologie / Biotechnologie / verwandten Naturwissenschaften
Mindestens drei Jahre Berufserfahrung als BTA / Biologielaborant / B.Sc. Biologie-Biotechnologie
Freude am Umgang mit Laborgeräten und experimentellen Aufbauten
Erfahrungen im Umgang mit Zellkulturen inkl. sterilem Arbeiten (wünschenswert)
Erste theoretische und praktische Kenntnisse im Bereich Chromatographie mit ÄKTA und der Bedienung von ÄKTA-Systemen (wünschenswert)
die Fähigkeit zu sehr strukturierten, zielorientierten und konzentrierten Arbeiten unter Einhaltung enger Zeitlinien
ausgeprägtes Verantwortungsbewusstsein, Organisationsfähigkeit, hohe Verlässlichkeit und Flexibilität
Team- und Kommunikationsfähigkeit
Dienstleitungsorientierung
Gute Kenntnisse von Microsoft Office (Word, Excel) sowie gute deutsche und englische Sprach- und Schriftkenntnisse setzen wir voraus.

Wir bieten Dir:

eine unbefristete Stelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten internationalen Unternehmen
eine intensive Einarbeitung
ein Gleitzeitsystem
diverse Benefits
eine aktive Mitgestaltung Deines Tätigkeitsfeldes in einem motivierten Team und
eine angemessene Vergütung

Haben wir Dein Interesse geweckt?

Wenn ja, bewirb Dich bitte unter der Job-ID 231149 über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a-b

40699 Erkrath

Biologics Testing Solutions

Über Charles River

Weitere Informationen finden Sie unter www.criver.com.

Wissenschaftler (m/w/d) als Scientist (Cologne, NW, DE, 51105)

Wir bei Charles River setzen uns mit Leidenschaft dafür ein, die Lebensqualität der Menschen zu verbessern. Unser Auftrag, unsere wissenschaftliche Führungsrolle und unser starkes Zielbewusstsein leiten uns bei allem, was wir tun und wir gehen jeden Tag mit dem Wissen an, dass unsere Arbeit dazu beiträgt, die Gesundheit und das Wohlbefinden von Menschen auf der ganzen Welt zu verbessern.

Für die Abteilung Virus Clearance am Standort Köln suchen wir ab sofort befristet für 2 Jahre in Vollzeit

einen

Wissenschaftler als Study Director (m/w/d)

Du hast 2–3 Jahre Erfahrung im regulierten Labor und möchtest Verantwortung übernehmen? Dann bist du bei uns genau richtig!

Deine Aufgaben

Planung, Betreuung und Dokumentation von GLP-konformen Virus-Sicherheitsstudien (viral clearance studies)
Unterstützung des technischen Personals bei der Durchführung der Studien
Umgang mit infektiösem Material, Zellkulturen und Viren unter GLP-Bedingungen
Mitwirkung bei der Pflege und Weiterentwicklung unseres GLP-Systems (Standardarbeitsanweisungen, Gerätequalifikation, Validierungen)
Enge Zusammenarbeit und Kommunikation mit in- und ausländischen Kunden

Das bringst Du mit

Masterabschluss (M.Sc.) in Biologie, Biotechnologie, Chemie oder vergleichbar
2–3 Jahre Erfahrung in GLP-Laboren oder regulierten Studien
Kenntnisse in Virologie, Zellkultur, Proteinaufreinigung
Erste Erfahrung mit Chromatographie-Anlagen (z. B. Äkta) wünschenswert
Strukturiert, zuverlässig und teamfähig, mit Organisationstalent und Verantwortungsbewusstsein
Sehr gute Deutsch- und Englischkenntnisse
Sicherer Umgang mit Microsoft Office

Wir bieten Dir

Unbefristete Vollzeitstelle mit abwechslungsreichen, anspruchsvollen Aufgaben
Intensive Einarbeitung in das Study Director-Aufgabengebiet und GLP-System
Flexible Arbeitszeiten und Möglichkeit zur Mitgestaltung deines Tätigkeitsfeldes
Arbeit in einem motivierten Team mit spannenden Projekten

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte über unser Karriereportal https://jobs.criver.com/ unter der Job-ID 232651 mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15 A-B
40699 Erkrath

Wir alle bei Charles River teilen eine große Leidenschaft, wenn wir unsere gemeinsame Mission verfolgen: Wir wollen ein gesünderes Leben schaffen. Die Möglichkeit, im Leben von Menschen auf der ganzen Welt etwas zu bewirken, ist das, was uns jeden Tag aus dem Bett treibt. Stell dir vor, du könntest deine Talente einsetzen, um neue Entdeckungen und klinische Durchbrüche voranzutreiben, die die Gesundheit der Menschen weltweit verbessern. Deshalb ist eine Karriere bei uns so viel mehr als nur ein Job. Es ist eine zielgerichtete Reise.

Biologics Testing Solutions

Weitere Informationen finden Sie unter www.criver.com.

Seasonal Help - EG (Spencerville, OH, US, 45887)

Job Summary

BASIC SUMMARY:

ESSENTIAL DUTIES AND RESPONSIBILITIES:

May perform area support cleaning, study set up, laboratory administrative functions, and/or basic animal husbandry.
May clean rooms and/or facility to include possible handling of biohazard materials.
May assist with use of balances and other laboratory equipment.
May perform basic facility/groundskeeping functions.
May perform administrative functions in various departments, including IT.
Use Good Laboratory Practice Regulations (GLP), SOP’s and company policies when performing all job functions.
Perform all other related duties as assigned.

The starting pay for this position is $15.00 per hour. Please note that starting salaries vary based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:

Education: H.S. diploma preferred.
Experience: None
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None
Other: Ability to handle common laboratory species in selected departments.
Must be authorized to work in the United States without a sponsorship visa, now or in the future.

PHYSICAL DEMANDS:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals for the departments requiring such functions.
Must be able to perform procedures, which require, talking, hearing, standing or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
May be required to frequently firmly hold species while utilizing fine motor skills.
Specific vision abilities may be required by this job include close vision, color vision, depth perception, and the ability to adjust focus.
While performing the duties of any administrative-type functions, the employee may be assigned to regularly talk, hear and work/type at a computer.

WORK ENVIRONMENT:

If assigned to works in a research environment, it may require use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
The employee may be required to work with live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to high depending upon the species housed and department assigned, if applies.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

In Vivo Technician I (Spencerville, OH, US, 45887)

Job Summary

We are seeking an In Vivo Technician I for our In Vivo Team at our Safety Assessment site located in Spencerville, OH.

A Technician I is in training to perform and become proficient in on-boarding tasks, procedures, and cooperating in a team environment. The technician is learning basic tasks required to conduct a study, which may include collecting and recording data in the performance of studies. Responsible for handling and restraining animals, clinical observations, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. The technician is working under close supervision to gain proficiency

Essential Functions (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding tasks which may include animal handling, sexing, and restraint on multiple species as well as feeding, watering, husbandry of multiple species. Clinical observations, acclimation observations, and body weight determination on multiple species as well as qualitative and quantitative food consumption. Specific tasks will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Perform all other related duties as assigned.

The pay for this position is $19/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High school diploma or General Education Degree (G.E.D.) preferred. Associate (A.A./A.S.) or Bachelor’s degree (B.A./B.S.) or equivalent in a biological science, desired.
Experience: No previous experience required.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills. Knowledge of English.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.

Must be authorized to work in the United States without a sponsor visa, now or in the future.

Physical Demands:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform procedures, which require, talking, hearing, standing or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Must be able to frequently firmly hold species while utilizing fine motor skills.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus

WORK ENVIRONMENT:

Work in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
The employee regularly works with live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to high depending upon the species housed.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Laborhilfe (m/w/d)- Erkrath / Quereinsteiger willkommen (Erkrath, NW, DE, 40699)

Am Standort Erkrath suchen wir zur Erweiterung des Labor-Teams ab sofort unbefristet

eine/n

Lab Assistant / Laborhilfe (m/w/d)

Als Laborhilfe bist du für die ordnungsmäßige, praktische Durchführung der mit den Prüfungen im Zusammenhang stehenden Aufgaben und Arbeiten im Labor unter Einhaltung interner Vorgaben verantwortlich.

Unterstütze uns bei:

Auffüllen und Entsorgung von Verbrauchsmaterialien
Reinigung von mikrobiologischen Sicherheitswerkbänken, CO2-Inkubatoren, Tiefkühlgeräten, Zentrifugen o. ä. Laborgroßgeräten
Überprüfung von Sicherheitseinrichtungen
Herstellung von Puffern und Materialien
Bestellungen und Kontrolle des Warenbestands
Fachgerechte Inaktivierung und Entsorgung von Laborabfällen
der Betreuung und Sicherstellung der Pflege und Aufrechterhaltung des Qualitätssicherungs-Systems (GMP)

Bist du der/die Richtige für uns?

Möchtest du einen wichtigen Beitrag in der Entwicklung von Medikamenten leisten?
Hast du erste Berufserfahrung, oder suchst einen Neu-, Quereinstieg
Bist du am biotechnologischen Arbeitsumfeld interessiert und bringst Neugierde mit?
Bist du strukturiert und zielorientiert?
Hast du ein ausgeprägtes Verantwortungsbewusstsein, kannst dich gut organisieren und bist verlässlich und flexibel?
Arbeitest du gerne im Team?
Hast du Interesse an Computersystemen?
Sprichst du Deutsch und etwas Englisch?

Wir bieten Dir:

eine Stelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten Unternehmen
eine intensive Einarbeitung
flexible Arbeitszeiten
eine aktive Mitgestaltung Deines Tätigkeitsfeldes in einem motivierten Team
eine angemessene Vergütung

.

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 232280 über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a-b
40699 Erkrath
Email: RecruitBPS@crl.com

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

Vaccine Mandate

For more information, please visit www.criver.com.

Wissenschaftler (m/w/d) als Scientific Officer - GTS (Erkrath, NW, DE, 40699)

Für die Abteilung Genetic Testing Services am Standort Erkrath suchen wir ab sofort unbefristet eine/n

Wissenschaftler*in als Scientific Officer (m/w/d)

Unterstütze uns bei:

der Durchführung von molekularbiologischen Analysen (Routine)
der eigenständigen Einleitung, Durchführung und Betreuung von Transfer & Validation Aufträgen
der Verbesserung der bestehenden Methoden und Ablaufe
die Etablierung von neuen Methoden und Verfahren
den Laborarbeiten mit GVOs und Biostoffen bis hin zur Risikogruppe S1
der Unterstützung der Scientific Officer bei der Bearbeitung von internen Dokumenten wie BOPs und Laborablaufplänen
der Erstellung von Auswertungs- und Trackingsheets mit Hilfe von Excel oder Smartsheet,
der eigenständigen Überprüfung von Labordokumentation sowie der Auswertung und Zusammenfassung von Analyseergebnissen
der Organisation und Pflege der Analysendaten in einer Datenbank in Verbindung dem LTM (Laboratory Testing Management) System
Betreuung des technischen Personals bei der Durchführung von Analysen
Zusammenarbeit mit in- und ausländischen Kunden
Bearbeitung von wissenschaftlichen Fragestellungen, Kundenanfragen sowie Freigabe von Analysenergebnissen

Überzeuge uns durch:

Ein abgeschlossenes Studium der Naturwissenschaften oder vergleichbare Qualifikation
Wissenschaftliche Expertise (praktisch und theoretisch) im Molekularbiologischem Bereich speziell im Bereich PCR und real time PCR
Sehr strukturiertes, detailorientiertes und zielorientiertes Arbeiten unter Einhaltung enger Zeitlinien
Wünschenswert wären Erfahrungen mit Tiermodellen
Service und Kundenorientierung
Sehr gute Kenntnisse von Microsoft Office sowie gute Deutsch- und Englischkenntnisse

Wir bieten Dir:

Eine Vollzeitstelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten internationalen Unternehmen
Eine intensive Einarbeitung
Flexible Arbeitszeiten
Eine aktive Mitgestaltung Deines Tätigkeitsfeldes in einem motivierten Team und
Eine angemessene Vergütung

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 232816 über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15 A-B
40699 Erkrath

For more information, please visit www.criver.com.

Mitarbeiter Probenmanagement, Wareneingang & Versand (m/w/d) - Pharma / Labor (Erkrath, NW, DE, 40699)

Für die Abteilung Operations Support am Standort Erkrath suchen wir ab sofort unbefristet

eine / einen

Mitarbeiter (m/w/d) Wareneingang und Versand & das Probenmanagement

Du behältst den Überblick, wenn Proben und Warensendungen bei Charles River in Erkrath eintreffen: Du nimmst sie an, prüfst sie und sorgst dafür, dass alles zur richtigen Zeit am richtigen Ort ist. So unterstützt du aktiv die Entwicklung und Prüfung neuer Medikamente in unseren Laboren.

Vorkenntnisse in der Logistik sind von Vorteil, aber kein Muss – wir freuen uns ausdrücklich auch über motivierte Quereinsteiger*innen.

Deine Aufgaben

Annahme eingehender Kundenproben für unsere GMP-Analytik, inklusive der Registrierung in unseren Laborinformations-Management System (LIMS)
Bereitstellung von Proben für die analytischen Labore
Ordnungsgemäßen Lagerung und Entsorgung von Proben im zentralen Prüfsubstanzlager
Organisation und Verwaltung des zentralen Warenlagers (Bestellung, Annahme, Erfassung, Ausgabe)
Sicherstellung und Überwachung des Warenbestandes
Versand von Prüfsubstanzen, Waren und Dokumenten einschließlich der Sendungsanmeldung
der Vorbereitung und Abwicklung von Sendungen
der Zusammenarbeit mit den operativen Einheiten und dem Projektmanagement als zentrale Anlaufstelle für Prüfsubstanz-Management, Versand & Logistik

Du bist die richtige Person für uns, wenn:

Du Erfahrung im Wareneingang,Versand oder der Logistik
Du an einem biotechnologischen oder pharmazeutischen Arbeitsumfeld interessiert bist
Du zielorientiert und strukturiert arbeitest
Du ein ausgeprägtes Verantwortungsbewusstsein hast
Du dich gut organisieren kannst und kannst gleichzeitig flexibel Situationen reagieren
Du sehr gute Deutsch- und grundlegende Englischkenntnisse hast

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 232829 über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a-b
40699 Erkrath
Bei Fragen bitte an RecruitBPS@crl.com wenden

Wir alle bei Charles River Laboratories teilen eine große Leidenschaft, wenn wir unsere gemeinsame Mission verfolgen: Wir wollen ein gesünderes Leben schaffen. Die Möglichkeit, im Leben von Menschen auf der ganzen Welt etwas zu bewirken, ist das, was uns jeden Tag aus dem Bett treibt. Stell dir vor, du könntest deine Talente einsetzen, um neue Entdeckungen und klinische Durchbrüche voranzutreiben, die die Gesundheit der Menschen weltweit verbessern. Deshalb ist eine Karriere bei uns so viel mehr als nur ein Job. Es ist eine zielgerichtete Reise.

BTA / Biologielaborant (m/w/d) - Bioassays & Zellkultur (GMP) (Erkrath, NW, DE, 40699)

Für die Abteilung Bioassays unserem Standort in Erkrath suchen wir ab sofor und befristet für zwei Jahre eine*n

BTA / Biologielaborant (m/w/d) Bioassays & Zellkultur

als

Senior Lab Technician I

Du arbeitest gern präzise, verantwortungsvoll und mit modernen bioanalytischen Methoden? Du bringst Erfahrung in Zellkultur, Bioassays oder regulierten Laborprozessen mit und möchtest in einem GMP-Umfeld den nächsten Schritt machen?

Dann werde Teil unseres Teams im Bereich Bioassays an unserem Standort in Erkrath - für die Dauer von 2 Jahren.

Zu Deinen Aufgaben zählen:

In dieser Position übernimmst Du eine wichtige Rolle in der Durchführung und Sicherstellung von zellbasierten Bioassays im GMP-Umfeld.

Durchführung von zellbasierten Bioassays im Rahmen von Routineprüfungen unter GMP-Bedingungen
Unterstützung von Scientists bei der Planung, Vorbereitung und dem Abschließen von Prüfungen
Mitwirkung bei der Bearbeitung interner GMP-Dokumente (z.B. SOPs und Abweichungen)
Eigenständige Prüfung der Labordokumentation
Auswertung, Zusammenfassung und Dokumentation von Analyseergebnissen
Fachliche Unterstützung des technischen Personals bei der Durchführung von GMP-Prüfungen
die Pflege und Aufrechterhaltung des GMP-Systems im Laboralltag
Verantwortung für Geräte und Infrastruktur im LAborbereich
Mitarbeit bei Gerätequalifikationen, Validierungen und weiteren qualitätssichernden Maßnahmen
Laborarbeiten mit Zellkulturen und Viren der Risikogruppe S1 und S2

Das bringst Du mit:

abgeschlossene Ausbildung als BTA / Biologielaborant / CTA / MTA / MTLA (m/w/d) oder
ein naturwissenschaftliches Studium (B.Sc. oder M.Sc) in Biologie, Biochemie ö.ä.
praktische Laborerfahrung in mindestens einem der folgenden Bereiche: Zellbiologie / Zellkultur, Bioassays, Immunologie, regulierte Laborprozesse
sorgfältige, strukturierte und zuverlässige Arbeitsweise
sehr gute Deutsch- und gute Englischkenntnisse
Erfahrung im GMP-regulierten Umfeld

Auch wenn du nicht alle Punkte erfüllst: Bewirb dich gerne, wenn du praktische Laborerfahrung in Zellkultur, Bioassays oder qualitätsgesicherten Prozessen mitbringst.

Das erwartet Dich

Befristete Festanstellung für 2 Jahre
Strukturierte Einarbeitung in ein spannendes Laborumfeld
Verantwortungsvolle Aufgaben im Bereich Bioassays & Zellkultur
Kollegiales Team mit enger Zusammenarbeit zwischen Labor und Wissenschaft
Möglichkeit zur fachlichen Weiterentwicklung im Bereich Bioassays, GMP und Qualitätsprozesse

Haben wir Dein Interesse geweckt?

Wenn ja, bewirb dich bitte unter der Job-ID 232799 über unser Karriereportal https://jobs.criver.com/ mit deinem Lebenslauf und Motivationsschreiben.

Wir freuen uns auf deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a-b
40699 Erkrath
Email: RecruitBPS@crl.com

BTA / Biologielaborant /BSc als Lab Technician (m/w/d) - Genetic Testing Services (Erkrath, NW, DE, 40699)

Für die Abteilung Genetic Testing Services am Standort Erkrath suchen wir ab sofort und unbefristet

eine/n

BTA / Biologielaboranten / B.Sc. Biologie-Biotechnologie

als Lab Technician (m/w/d)

Zu Deinen Aufgaben gehören:

Laborarbeiten mit Prüfmaterialien und -Substanzen
selbständige Durchführung und Dokumentation bioanalytischer Methoden
die Auswertung der Ergebnisse nach Kapillargelelektrophorese mit Hilfe entsprechender Software, sowie Ergebnisauswertung nach real time PCR.
Erstellung von prüfungsbezogenen und übergreifenden Dokumente über das LTM (laboratory testing management) System
Durchführung aller Arbeiten unter Einhaltung von Sicherheitsstandards und internen Vorschriften.
Allgemeine Labororganisatorische Aufgaben wie Erstellen von Business Operation Standard (BOB) – Arbeitsanweisungen, Pflege von Laborgeräten und Bestellung von Laborreagenzien/-materialien
der Kommunikation mit internen / externen Kunden (GTS).

Das bringst Du mit:

eine erfolgreich abgeschlossene Ausbildung als Biologisch-technischer Assistent / Biologielaborant (m/w/d) oder ein erfolgreich abgeschlossenes Studium zum Bachelor of Science im Bereich Biologie / Biotechnologie / Biochemie etc.
strukturiertes, zielorientiertes Arbeiten unter Einhaltung enger Zeitlinien, Verantwortungsbewusstsein, Verlässlichkeit, hohes Sicherheitsempfinden und Teamfähigkeit
hohe Lernbereitschaft zur Weiterbildung
hohe Leistungsbereitschaft
fähig Entscheidungen zu treffen
fähig zur kritischen Selbstreflexion
ausgeprägtes Informations- und Kommunikationsverhalten (intern und extern)
fähig Konflikte zu lösen
Gute Kenntnisse von Microsoft Office (Word, Excel, PowerPoint) sowie gute deutsche und englische Sprach- und Schriftkenntnisse setzen wir voraus

Wir bieten Dir:

eine unbefristete Stelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten internationalen Unternehmen
flexible Arbeitszeiten
eine aktive Mitgestaltung des Tätigkeitsfeldes in einem motivierten Team
eine angemessene Vergütung
eine intensive Einarbeitung mit Onboarding Programm
kostenfreie Parkplätze / Fahrkostenzuschuss
Fortbildungsmöglichkeiten
Engagement Programm

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 230696 über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a
40699 Erkrath
Bei Fragen bitte an RecruitBPS@crl.com wenden

Biologics Testing Solutions

Über Charles River

Weitere Informationen finden Sie unter www.criver.com.

BTA / Biologielaborant / BSc als Lab Technician (m/w/d) - Biosafety (Erkrath, NW, DE, 40699)

Für die Abteilung Biosafety am Standort Erkrath suchen wir ab sofort unbefristet in Vollzeit eine/n

Biologisch-Technischen Assistenten (BTA) /

Biologielaboranten / B.Sc. Biologie-Biotechnologie

als Lab Technician (m/w/d)

Zu Deinen Aufgaben zählen:

Laborarbeiten mit Zellkulturen, Mykoplasmen und Viren
der Nachweis von Viren und Mykoplasmen in biologischen Probenmaterialien
selbständige Durchführung und Dokumentation bioanalytischer Methoden
Erstellung von prüfungsbezogenen und übergreifenden Dokumenten
allgemeine Laborarbeiten, z.B. Gerätewartungen
Arbeiten und Dokumentation unter GMP-Bedingungen
Pflege und Aufrechterhaltung des GMP-Systems
Erstellen von Standardarbeitsanweisungen

Das bringst Du mit:

eine Ausbildung als Biologisch-technischer Assistent / Biologielaborant (m/w/d) oder ein Studium zum Bachelor of Science im Bereich Biologie / Biotechnologie / Biochemie etc.
Wünschenswert sind praktische Kenntnisse im Bereich Zellkultur, Virologie und / oder Mikrobiologie
Team- und Kommunikationsfähigkeit
Dienstleistungsorientierung
gute Kenntnisse von Microsoft Office (Word, Excel, PowerPoint) sowie gute Deutsch und Englischkenntnisse setzen wir voraus

Wir bieten Dir:

eine Stelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten Unternehmen
eine intensive Einarbeitung
flexible Arbeitszeiten
eine aktive Mitgestaltung Deines Tätigkeitsfeldes in einem motivierten Team und
eine angemessene Vergütung

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 231573 über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a-b
40699 Erkrath
Bei Fragen bitte an RecruitBPS@crl.com wenden

For more information, please visit www.criver.com.

Senior Lab Technician I Bioassays (m/w/d) (Erkrath, NW, DE, 40699)

Für die Abteilung Bioassays unserem Standort in Erkrath suchen wir ab sofor und unbefristet einen

Wissenschaftlichen Assistenten (m/w/d)

als Senior Lab Technician I

Zu Deinen Aufgaben zählen:

die Durchführung von zellbasierten Bioassays (Routine) in einem GMP-Umfeld
die Unterstützung von Wissenschaftler*innen (Scientists) bei der Planung, Vorbereitung und dem Abschließen von Prüfungen
die Unterstützung von Wissenschaftler*innen bei der Bearbeitung von internen Dokumenten wie Abweichungen und SOPs
die eigenständige Überprüfung der Labordokumentation sowie die Auswertung und Zusammenfassung von Analyseergebnissen
die Betreuung des technischen Personals bei der Durchführung von GMP-Prüfungen
die Pflege und Aufrechterhaltung des GMP-Systems
die Erstellung von Standardarbeitsanweisungen, Verantwortlichkeiten für Geräte und Infrastruktur, Mitarbeit an Qualifikationen von Geräten, Validierungen, etc.
Laborarbeiten mit Zellkulturen und Viren (Risikogruppe S1 und S2)

Überzeuge uns durch:

ein abgeschlossenes Studium der Naturwissenschaften (Bachelor oder Master / Diplom) oder eine erfolgreich abgeschlossene Ausbildung als Biologisch-Technischer Assistent / Biologielaborant mit mindestens 2 Jahren Berufserfahrung in relevanten Bereichen
praktische Erfahrungen in den Bereichen Zellbiologie, Immunologie und/oder Bioassays
wünschenswert sind Erfahrungen im Bereich Molekularbiologie / PCR
gute mathematische und biostatistische Kenntnisse sind von Vorteil
Verantwortungsbewusstsein, Organisationsfähigkeit, hohe Verlässlichkeit und Flexibilität
sehr strukturiertes, detail- und zielorientiertes Arbeiten unter Einhaltung enger Zeitlinien
Belastbarkeit, Team- und Kommunikationsfähigkeit
Service- und Kundenorientierung
hohe Leistungsbereitschaft und Motivation zur Weiterbildung
gute Kenntnisse von Microsoft Office (Word, Excel) sowie gute deutsche und englische Sprach- und Schriftkenntnisse setzen wir voraus
Kenntnisse in den Qualitätssicherungsstandards GMP sind von Vorteil aber keine Voraussetzung

Wir bieten Dir:

eine unbefristete Stelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten internationalen Unternehmen
eine intensive Einarbeitung
flexible Arbeitszeiten
eine aktive Mitgestaltung des Tätigkeitsfeldes in einem motivierten Team und
eine angemessene Vergütung

Haben wir Dein Interesse geweckt?

Wenn ja, bewirb dich bitte unter der Job-ID 231708 über unser Karriereportal https://jobs.criver.com/ mit deinem Lebenslauf und Motivationsschreiben.

Wir freuen uns auf deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a-b
40699 Erkrath
Email: RecruitBPS@crl.com

For more information, please visit www.criver.com.

Oproepkracht Lab Loket - Test Substance Registration (TSR) (Den Bosch (S-Hertogenbosch), NL, 5231 DD)

Flexibele baan in het laboratorium – ideaal naast studie of gezin

Heb jij een tussenjaar, loop je studievertraging op of zoek je als ouder werk dat past binnen schooluren?
Ben je netjes, betrouwbaar en werk je graag gestructureerd? Dan zijn wij op zoek naar jou!

Voor ons Test Substance Registration lab in ‘s-Hertogenbosch zoeken wij een

Oproepkracht Lab Loket

Afdeling:

De afdeling Chemie bestaat uit ongeveer 150 medewerkers verdeeld over de eenheden Analytische en Fysische Chemie, Bioanalyse en Test Item Receipt and Formulation. Ons onderzoek is divers en we onderzoeken een veelheid aan stoffen in een modern laboratorium. Ons onderzoek is erop gericht om veilig gebruik van nieuwe stoffen mogelijk te maken.

Team:

Jaarlijks ontvangt het team Test Substance Registration vele test materialen die onder de juiste condities worden opgeslagen, beheert en geregistreerd.

Wat is je rol?

Ons werk is vergelijkbaar met een ziekenhuisapotheek: gefocust, nauwkeurig, betekenisvol.

Als oproepkracht help jij je collega’s mee in het praktische en het administratieve werk.

Je zorgt ervoor dat de testmaterialen klaarstaan voor onze Analisten. Een verbindende én onmisbare rol tussen het team en het lab.

Wat ga je doen?

Testmaterialen voorbereiden zodat onderzoekers hun studies tijdig kunnen uitvoeren;
Alles nauwkeurig vastleggen (benodigde TM handling uitvoeren en documenteren; voor en na wegen van TM) volgens SOP/ GLP;
Correct opslaan; werkplek schoonmaken en klaarzetten voor de volgende dag;
Rustig en zelfstandig werken, met het TSR-team beschikbaar voor training en ondersteuning.

Wanneer werk je?

Doordeweeks, flexibel op oproepbasis;
Goed te combineren met studie of werken tijdens schooluren.

Je profiel:

Min. MBO 3 / 4 opleiding als Laborant of Apothekersassistent;
Bekend met basis laboratorium werk en apparatuur;
Je bent precies, zorgvuldig en betrouwbaar;
Solistische workflow en toch graag samenwerkend wanneer nodig;
Flexibel inzetbaar op oproepbasis doordeweeks;
Engels is een pré.

Wat wij bieden:

Een passend uurloon (inclusief vakantie-uren en vakantiegeld);
Reiskostenvergoeding van €0,23 per km (max. 100 km per dag);
Praktische GLP-ervaring binnen een internationale CRO;
Gestructureerde inwerktraining door het TSR-team.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to fostering a sense of belonging and work daily in this direction.

Oproepkracht Biotechniek (weekend en vakanties) EG (Den Bosch (S-Hertogenbosch), NL, 5231 DD)

Job Summary

�� Volg jij een studie met een proefdiermodule waarbij je artikel 13F kunt behalen?
En wil je alvast praktijkervaring opdoen bij een internationaal gerenommeerde organisatie binnen de life sciences? Dan hebben wij de perfecte (bij)baan voor jou!

Over de afdeling

De afdeling Toxicologie telt ruim 200 collega’s die onderzoek doen naar de veiligheid van nieuwe en bestaande medicijnen en chemische stoffen. Onze teams zijn betrokken, collegiaal en werken intensief samen. De sfeer is professioneel, maar ook gezellig – we helpen elkaar en dragen samen verantwoordelijkheid voor het welzijn van de dieren en de kwaliteit van het onderzoek.

Jouw rol

Als oproepkracht in de weekenden en vakanties ondersteun je de dagelijkse verzorging van de dieren en lever je een waardevolle bijdrage aan lopende studies. Je werkt onder begeleiding van ervaren biotechnici, waardoor je on-the-job training krijgt en steeds meer leert over werken volgens Good Laboratory Practice (GLP) en het naleven van dierwelzijnsregels (AAALAC-standaarden).

Wat ga je doen?

Verzorgen van de dieren en bijdragen aan lopende studies

Werken in een team waarin samenwerking en kwaliteit centraal staan

Meewerken in een moderne onderzoeksomgeving waar je veel kunt leren van ervaren collega

Wat vragen we van jou?

Je volgt een MBO-opleiding tot biotechnicus of een HBO-opleiding met een minor of specialisatie Proefdierkunde, waarbij je aantoonbaar al gestart bent met deze minor .(Kandidaten die de minor Proefdierkunde nog niet zijn gestart, komen helaas niet in aanmerking voor deze functie.)

Je bent beschikbaar in weekenden, vakanties en op oproepbasis (rooster wordt vooraf gedeeld)

Je bent collegiaal, sociaal en een echte teamspeler

Je kunt ook zelfstandig werken en verantwoordelijkheid nemen

Je bent flexibel en denkt proactief mee

Long Description

Wat bieden wij jou?

Een passend uurloon (inclusief vakantie-uren en vakantiegeld)

Reiskostenvergoeding van €0,23 per km (max. 100 km per dag)

Een waardevolle (bij)baan in een state-of-the-art laboratorium

On-the-job training door ervaren biotechnici

De kans om al tijdens je studie relevante werkervaring op te doen in jouw vakgebied

Interesse?

Wil jij je studie combineren met praktijkervaring in de life sciences? Solliciteer dan nu via onze career site: Charles River Carrières - Nederland Home of neem contact op met her-recruitment@crl.com voor meer informatie.

Zet jouw eerste stap in de wereld van biotechniek bij Charles River

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to fostering a sense of belonging and work daily in this direction.

Animal Technician I (Stilwell, KS, US, 66085)

Job Summary

Charles River Laboratories (CRL) is seeking an Animal Technician to join our Integrated Toxicology (ITox) team at the Kansas City (CR-KAN) Site. This site is the first of its kind, bridging CRL’s Discovery and Safety Assessment business units, while bringing automation to standard lead optimization toxicology study models to deliver rapid study results to our clients. When you join, you will have a significant impact on the health and well-being of people across the globe. The technician is learning basic skills required to conduct a study, which include animal husbandry needs, animal handling/restraint, housing maintenance, feeding procedures; collecting data, observing the animals for health status, body weight measurements; administering doses by various methods, conducting euthanasia, and/or biological specimen collections for analysis.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Ensure good welfare and humane care for all animals, using gentle and positive human-animal interactions.
Perform basic skills of the department including animal handling/restraint, housing maintenance, and feeding procedures; collecting data, observing the animals for health status, and body weight measurements; administering doses by various methods, conducting euthanasia, and/or biological specimen collections for analysis. Specific skills will be based on each area’s training plan and business needs
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Perform all other related duties as assigned.

The pay range for this position is $20/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:

Education: High school diploma, General Education Degree (G.E.D.), preferred.
Experience: No previous experience required. Experience working with/around animals is preferred. Experience in a role requiring physical labor a plus.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Must be authorized to work in the United States without a sponsor visa, now or in the future

PHYSICAL DEMANDS:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform laboratory procedures, which require, talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

WORK ENVIRONMENT:

Work in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
The employee regularly works with live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to high depending upon the species housed.

COMMENTS:

This position requires overtime, weekend, holiday, and/or after hours shift coverage, as needed.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technical Training - Associate (Stilwell, KS, US, 66085)

Job Summary

Charles River Laboratories (CRL) is seeking a research analyst to join our integrated toxicology (ITox) team at the Kansas City site. This site is the first of its kind, bridging CRL’s Discovery and Safety Assessment business units, while bringing automation to standard lead optimization toxicology study models to deliver rapid study results to our clients. When you join our team, you will have a significant impact on the health and well-being of people across the globe

A Technical Trainer I is responsible for providing technical skills instruction for staff including skills within in-vivo operations, basic clinical pathology sample processing, and animal euthanasia. This includes providing and/or coordinating technical training, conducting skill proficiency assessments, maintaining training documentation, and providing feedback to training program governance representative(s) and managers of the trainees.

The pay range for this position is $25-$27/hour. Please note that hourly rates vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

ESSENTIAL DUTIES AND RESPONSIBILITIES

Coordinate staff technical training based on needs identified through collaboration with functional line management; conduct training, including cross-training, where applicable; assess trainee knowledge/skills acquisition and evaluate trainee competence to perform required tasks.
Document training progress and completion; coordinates and monitors training conducted by other subject-matter experts.
Review work performed by trainees (including data collected as part of the job) and address minor deficiencies and escalate more notable deficiencies to department management.
Provide feedback about trainee progress to trainee and department management.
Review, update, and /or create training materials; obtain input for content and appropriate instructional design from other subject-matter experts, as applicable.
Perform assessments of staff technical skills to verify that correct and consistent practices are used; identify skill gaps and provide or coordinate refresher training, as needed.
Assist learning professionals with design and implementation of training programs and knowledge/skills assessments.
Other duties as assigned.

Job Qualifications

Education and Experience: HS/GED/Bachelor’s degree with 1-4 years of relevant experience.
Certification/Licensure: ALAT certification preferred.
Demonstrated proficiency in required departmental technical skills; previous training experience preferred.
Demonstrated knowledge of department processes and procedures.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Basic familiarity with Microsoft Office Suite.
Computer skills, commensurate with Essential Duties and Responsibilities, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Must be authorized to work in the United States without a sponsor visa, now or in the future

PHYSICAL DEMANDS

Must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform laboratory procedures, which require talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

WORK ENVIRONMENT

Work in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
Regularly works with live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
Noise level in the work environment ranges from low to high depending upon the species housed.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician I - Necropsy (Stilwell, KS, US, 66085)

Job Summary

A Technician I is in training to perform and become competent in on-boarding skills, procedures, and cooperating in a team environment. Post-Life minimally includes administrative functions and activities within Necropsy and Histology. Within these laboratories, this individual may support the handling of tissues and organs, trimming tissues, embedding, measuring organ weights; microtomy, slide preparation, staining; inventory and quality control, and shipping of tissues. Additionally, the technician may support euthanasia and sedation; animal procedures including dissection; collection of samples and weights; laboratory preparation, set up and cleaning; preparation of laboratory solutions. The technician is usually working closely with a trainer or buddy but becoming more independent.

Essential Duties and Responsibilities:

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding skills which may include handling tissues and organs, trimming tissues, embedding, measuring organ weights; microtomy, slide preparation, staining; inventory and quality control, and shipping of tissues. Specific skills will be based on each area’s training plan and business needs.
Train in on-boarding skills which may include animal handling, euthanasia, and sedation; animal procedures including dissection; collection of samples and weights; laboratory preparation, set up and cleaning; preparation of laboratory solutions. Specific skills will be based on each area’s training plan and business needs.
Collect, document, review, and verify data in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Learn how to use and maintain instrumentation and equipment.
Learn and know anatomic terms.
Receive, track, and prepare samples or materials, as required for department.
Perform all other related duties as assigned.

Job Qualifications

Education: High school diploma or General Education Degree (G.E.D.) required. Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred.
Experience: No previous experience required.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

PHYSICAL DEMANDS:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform laboratory procedures, which require, talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

WORK ENVIRONMENT:

Work in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
The employee regularly works with live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to high depending upon the species housed.

COMMENTS:

This position requires overtime, weekend, holiday, and/or after hours shift coverage, as needed.

The pay rate for this position is $20/hour.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Addetto alla cura degli animali da laboratorio - PADOVA (full-time) (Padova, IT, 35121)

Riepilogo del lavoro

Per nostro cliente sito in Padova ricerchiamo un Animal Caretaker part-time

La risorsa sarà inserita all'interno del team operante nella struttura e si occuperà di svolgere le mansioni relative alla gestione del laboratorio

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nel controllo delle procedure sperimentali;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature automatiche e carrelli;

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro con contratto part-time
Buona conoscenza del pacchetto office

Insourcing Solutions

Di cosa si occupa la Charles River

Alla Charles River, promuoviamo con convinzione il nostro ruolo nel miglioramento della qualità di vita delle persone. In tutto ciò che facciamo, siamo guidati dalla nostra missione, dalle nostre eccezionali competenze scientifiche e da una grande risolutezza e affrontiamo ogni giorno con la consapevolezza che il nostro lavoro contribuisce al benessere e al miglioramento della salute di molte persone in tutto il mondo. Abbiamo orgogliosi di aver collaborato allo sviluppo dell' 80% dei farmaci approvati dalla FDA negli ultimi cinque anni.

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Animal Care Associate (Hollister, CA, US, 95023)

JOB SUMMARY

We are seeking Animal Care Associates for our Breed Department in Hollister, CA. As an Animal Care Associate, you will perform routine animal husbandry and other production duties. You will also maintain supplies and environment of environmentally-controlled work area(s).

* This is a temporary opportunity with the potential to be hired as a full-time, employee.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform routine animal husbandry duties and monitor daily health and welfare to maintain quality and health of animals.
Handle, transfer, and distribute animals, supplies and waste as needed to and from work area(s).
Monitor animal health by observing animal behavior, physical appearance, and physical environment. Identify and report any abnormal findings.
Responsible for collecting health monitoring swabs and following health monitoring schedules.
Perform physical environment housekeeping duties and production operations according to Good Manufacturing Practices (GMPs) and/or Standard Operating Procedures (SOPs).
Maintain recordkeeping pertaining to animal or supply area inventories.
Strictly follow all procedures necessary to maintain the barrier room barrier.
Use supplies according to safety guidelines. Perform all job-related duties in accordance with company safety procedures.
Colony Management
Perform all other related duties as assigned.

QUALIFICATIONS:

No experience required. On the job training will be provided.

PHYSICAL DEMANDS:

Regularly required to utilize a computer/tablet.
Regularly required to stand, use hands to finger, handle or feel objects, tools or controls; and reach with hands and arms.
Regularly required to stand and ascend/descend rolling platform ladder (up to six steps) to perform all tasks and procedures related to the job.
Regularly transports supplies, removes waste, and/or laboratory equipment while ascending/descending rolling platform stairs (up to six steps).
Regularly positions self (stoop, crouch, squat, sit, reach) to access and inspect small models and be able to assess their conditions and environment from various distances.
Regularly lifts and/or moves materials weighing up to 10 pounds and occasionally lifts and/or moves materials weighing up to 50 pounds.
May occasionally lift and/or move equipment and materials weighing 30-50 pounds, and equipment and materials weighing over 50 pounds with assistance.
Specific vision abilities required by this job include close vision, depth perception, and the ability to differentiate colors.
Regularly works with chemicals that require the use of respirators. Medical clearance is required prior to using respirators.

The pay range for this position is $18.00-$19.50 / hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Senior Environmental Health, Safety & Sustainability Specialist (Hollister, CA, US, 95023)

JOB SUMMARY

We are seeking a Senior Environmental Health, Safety & Sustainability Specialist to support our Production site in Hollister, CA. In this role, you will be responsible for implementing/maintaining the Environmental, Health, Safety & Sustainability (EHS&S) Program(s) for adherence to local, state, and federal regulations. You will also identify and mitigate potential hazards to reduce/eliminate risk exposure.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Establish, administer, update and manage EHS&S programs to meet company Global Operating Framework standards and ensure compliance with regional, state and federal safety and environmental regulatory agencies.
Maintain and ensure timely reporting of safety and environmental data, documentation, permits and licenses to all applicable regulatory agencies. Assess new regulatory standards and identify program changes to meet new requirements.
Leverage the existing safety and environmental training within the company’s Learning Management System (LMS) to deliver training to employees and develop site/business specific training as necessary.
Develop the facility inspection program for department and site management to conduct documented safety walkthroughs to identify findings and provide technical support to implement solutions. Document information in company Management Information System (Enablon).
Lead the site risk assessment program, develop a training program and tool to identify work hazards, assess the risk and implement effective controls using the hierarchy of controls model.
Utilize change management practices to implement new programs and processes.
Track hazardous waste (Resource Conservation and Recovery Act - RCRA) and medical waste disposal records including waste profiling, permitting, and manifesting.
Maintain all documentation and submit records to agencies as necessary for reporting requirements.
Assist management team in emergency response and function as EHS&S Emergency Coordinator for 24-hour incident response.
Support the investigation, root cause analysis and corrective/preventative action plan of proactive safety and incident reports. All details need to be documented and tracked in company Management Information System (Enablon).
Serve as Chairperson of Safety Committee(s), provide guidance on EHS&S issues to staff, and provide summary reports of notes to management team.
Describe procedures and produce written documentation as proof of compliance to clients and federal and state investigators. Coordinate communications to regulatory agencies and client inspections on EHS&S-related matters.
May assist in development of departmental budget and development of EHS&S programs and metrics.
Develop sustainability initiatives to protect employees and the environment while promoting responsible business practices.
Possess knowledge of biosafety, chemical safety, industrial hygiene, and overall environmental awareness.
Coordinate efforts to educate employees and provide site guidance on ergonomics.
Ensure adherence to pertinent regulatory requirements and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols].
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

Candidates must possess one of the following:

Associate's Degree (A.A./A.S) in Environmental Science, Occupational Health and Safety, Environmental Engineering or related discipline AND seven (7) years of related experience in Environmental Health, Safety & Sustainability.

Bachelor’s degree (B.A./B.S.) in Environmental Science, Occupational Health and Safety, Environmental Engineering or related discipline AND five (5) years of related experience in Environmental Health, Safety & Sustainability.

Additional Qualifications:

Knowledge and application of environmental health and safety regulations and familiarity with EHS&S regulatory agencies’ protocols (e.g., OSHA, EPA, DEP, DOT, NRC, etc.).
Industrial hygiene skills and ergonomic program experience are preferred. Knowledge of governmental safety and environmental regulations and chemical handling preferred.
Ability to interpret federal and state regulation and apply them to address compliance solutions as required.
Hands-on experience in an industrial or manufacturing work environment.
Demonstrated ability to interpret/apply required federal or state regulations and manage multiple/changing priorities with many interruptions.
Excellent communication skills both verbal and written, project management skills, and strong time management and organizational skills are required.
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system. Proficiency in MS Office suite including Excel, Word, PowerPoint, and Project.
Effective writing, organizational and time management skills.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints

PREFERRED QUALIFICATIONS:

Hazardous Waste Operations and Emergency Response Training
Certified Safety Professional certification
Ability to speak Spanish

SALARY TRANSPARENCY

The salary range for this position is $115,000 - $130,000 / annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technician I (San Diego, CA, US, 92121)

Job Summary

We are seeking an Animal Care Technician I to join our Insourcing Solutions team, located in San Diego, CA.

As the Animal Care Technician I, you will observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Perform routine husbandry tasks such as feeding, watering, cage changing, and cleaning of equipment and rooms to maintain a safe and compliant environment. Support animal health and welfare by accurately reporting concerns collaborating with veterinary staff, ensuring all work aligns with institutional, state, and federal guidelines.

Additional responsibilities include:

Cage Wash
Operate a washer for cleaning and sanitizing animal cage supplies through automatic processes.
Operate autoclave machine to sterilize caging equipment and instruments for the animals.
Maintain documentation for QA including but not limited to temperature strips, room environmental reports and logs, dish washer and/or autoclaving logs.
Handle, transfer, and deliver animals, supplies (caging, gasses, dry ice, liquid nitrogen), and waste as needed to and from work area(s).
Perform daily cage duties including recycling and scheduled santiation procedures.
Animal Care
- Review and comprehend relevent SOPs, BOPs, and quality standards at the entry level, applying them to routine animal care and facility tasks under supervision. Demonstrate basic understanding and consistency in following written procedures.
- Monitor daily animal health and welfare while performing daily animal health observations.
- Perform animal husbandry duties to maintaing quality and health of research animals, to include performing daily water bottle and cage checks; provide appropriate food and water; perform cage changing and/or cage cleaning as required; record animal health concerns per SOP and/or specified protocols.
- Dispose of biological, hazardous, and animal facility waste following established procedures.

Additional Information

- Operate equipment and use supplies according to safety guidelines; perform general housekeeping (i.e. check pest traps, common area cleaning, testing eye wash stations and emergency showers) and adhere to safety procedures.
- Assist with receiving and housing incoming animals under supervision based on site needs.
- Cage card distribution including but not limited to printing cage cards for incoming shipments and requests from clients.
- Collect census data from animal cages and assist with uploading manual or handheld scanner data into approved software.
- Assist with monitoring client row assignments in shared animal holding rooms to ensure racks/rows are labeled and assigned correctly per facility needs.
Report non-compliance or animal welfare concerns to the appropriate Animal Welfare Team member or IACUC office.
Maintain an organized and clean work environment including but not limited to animal rooms, common areas such as corridors, cage washrooms, procedure rooms, anterooms, storage areas and grounds by cleaning at prescribed intervals following established procedures.
Training and Development:
- Attend and participate in on-the-job and classroom training sessions and complete all assigned computer-based safety and professional development training by predetermined due dates.
- Communicate procedural questions and self-identified training deficiencies to team lead or supervisor.
Maintain required attendance level and adherence to work schedule in accordance with required staffing levels in order to ensure that assigned duties are completed.
Perform all other related duties as assigned.

Job Qualifications

Required:
• Education: High school diploma, General Education Degree (G.E.D.)

Preferred:
• Education: Bachelor’s degree (B.A./B.S.) in animal or life sciences field preferred
• Experience: Directly related laboratory animal experience in a laboratory animal facility preferred.
• Certification/Licensure: Assistant Laboratory Animal Technician (ALAT) certification from AALAS preferred.

The pay range for this position is $20.50 - 22.00 USD per hour. Please note that salaries vary within the range based on factors including skills, certifications, and location.

Physical Demands & Work Environment

• While performing the duties of this job, the employee is routinely required to move about inside the facility, communicate, and operate a computer. The employee is routinely required to stand; walk; use hands to finger, handle, or feel objects, tools, or controls; and reach with hands and arms. The employee frequently is required to stoop, kneel, crouch, or crawl. The employee is occasionally required to sit.
• The employee must regularly lift and/or move items weighing up to 50 pounds independently and occasionally lift and/or move items weighing up 100 pounds with assistance.
• Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception, and the ability to adjust focus.
• While performing the duties of this job, the employee is required to use personal protective equipment (PPE) including gloves, protective clothing, and eye protection.

• Work in a busy research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles.
• The employee is occasionally exposed to wet and/or humid conditions and risk of electrical shock.
• Work with animal species including rodents with risk of exposure to animal allergens, zoonotic disease, and biohazards.
• The noise level in the work environment is usually moderate.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Senior Data Scientist (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

At Charles River Laboratories, we’re transforming how we work by harnessing the power of AI, data, and digital innovation to accelerate the discovery and development of life-saving therapies. Our vision is to embed AI and advanced analytics across every stage of our scientific and operational workflows, empowering our teams with smarter tools, seamless data, and actionable insights to deliver client-centric services and solutions that better serve our customers and, ultimately, improve patients’ lives.

As a Senior Data Scientist and a member of our Enterprise Data & Analytics engineering team, you will play a pivotal role in this transformation. You’ll lead the design, development, and deployment of data-driven and AI-powered solutions that enhance customer value, streamline operations, and create meaningful, data-informed experiences for our employees. Through advanced analytics and generative AI, you’ll help Charles River unlock new possibilities in how we deliver science, innovation, and impact to our clients and the patients they serve.

In this role, primary responsibilities include:

Lead end-to-end data science initiatives, including data exploration, model development, validation, implementation, and support for mission-critical applications;
Collaborate closely with cross-functional data teams to automate data science pipelines and integrate models into business workflows and digital platforms;
Partner with business units in a consultative and collaborative manner, advising on the most effective approaches to leverage data science and Generative AI technologies to deliver innovative, high-impact solutions.

Key Elements

We are looking for the following minimum qualifications for this role:

Master’s with a minimum of 5 years’ experience or Bachelor’s with a minimum of 7 years’ experience in Data science, Computer science, Statistics, Operations research, applied mathematics, applied physics or any related field;
Excellent analytical and problem-solving skills with the ability to approach challenges creatively;
Strong communication skills to translate the findings into actionable business recommendations through rich data visualization;
Familiar with Agile methodologies and tools;
Self-driven and capable of working both independently and collaboratively within a team setting;
Experience in or strong understanding of the life science industry, particularly in leveraging data science to support operational excellence, is preferred.

Technical Expertise required:

5+ years’ hands-on experience processing, analyzing and modeling large and complex data sets;
3+ years’ experience with the full Machine Learning product lifecycle, with a demonstrated ability to take initiative and ensure proactive delivery of project milestones;
5+ years’ experience working with development toolsets such as SQL, PySpark, Python, Pandas or Scala;
Experience with Generative AI technologies for scientific document reading, summarization, and generation, including prompt engineering, retrieval pipelines, and LLM fine-tuning for domain-specific applications.

Role Specific Information:

Location: Remote (Must be located in Canada);
Annual bonus based on performance;
Schedule: Daytime between Monday and Friday;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Paid development training;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
4 weeks’ Vacation & 10 Personal day policy.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Scientifique principal des données (Montreal (Senneville), Quebec, CA, H9X 3R3)

Pendant 75 ans, les employés de Charles River ont travaillé ensemble pour aider à la découverte, au développement et à la fabrication sûre de nouvelles pharmacothérapies. Lorsque vous rejoignez notre famille, vous aurez un impact significatif sur la santé et le bien-être des gens à travers le monde. Que vos antécédents soient en sciences de la vie, en finance, en informatique, en ventes ou dans un autre domaine, vos compétences joueront un rôle important dans le travail que nous effectuons. En retour, nous vous aiderons à bâtir une carrière dont vous pouvez vous sentir passionné.

Sommaire de l'emploi

Chez les Laboratoires Charles River, nous transformons notre façon de travailler en exploitant la puissance de l’IA, des données et de l’innovation numérique pour accélérer la découverte et le développement de thérapies qui sauvent des vies. Notre vision est d’intégrer l’IA et l’analytique avancée à chaque étape de nos flux de travail scientifiques et opérationnels, en donnant à nos équipes des outils plus intelligents, des données fluides et des informations exploitables afin de fournir des services et des solutions centrés sur le client qui répondent mieux aux besoins de nos clients et, en fin de compte, améliorent la vie des patients.

En tant que Scientifique sénior de données et membre de notre équipe d'ingénierie Enterprise Data & Analytics, vous jouerez un rôle central dans cette transformation. Vous dirigerez la conception, le développement et le déploiement de solutions basées sur les données et propulsées par l’IA qui augmentent la valeur pour les clients, optimisent les opérations et créent des expériences significatives et éclairées par les données pour nos employés. Grâce à l'analytique avancée et à l'IA générative, vous aiderez Charles River à explorer de nouvelles possibilités dans la manière dont nous offrons science, innovation et impact à nos clients et aux patients qu'ils servent.

Dans ce poste, les principales responsabilités incluront:

Diriger des initiatives de science des données de bout en bout, incluant l'exploration des données, le développement de modèles, la validation, la mise en œuvre et le support pour des applications essentielles à la mission;
Collaborer étroitement avec des équipes de données interfonctionnelles pour automatiser les pipelines de science des données et intégrer les modèles aux flux de travail commerciaux et aux plateformes numériques;
Travailler en partenariat avec les unités commerciales de manière consultative et collaborative, en conseillant sur les approches les plus efficaces pour exploiter la science des données et les technologies d'IA générative afin de fournir des solutions innovantes et à fort impact.

Élémentc clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Maîtrise avec un minimum de 5 ans d'expérience ou Baccalauréat avec un minimum de 7 ans d'expérience en Science des données, Informatique, Statistiques, recherche opérationnelle, mathématiques appliquées, physique appliquée ou tout domaine connexe;
Excellentes compétences analytiques et en résolution de problèmes avec la capacité d'aborder les défis de manière créative;
Solides compétences en communication pour traduire les résultats en recommandations commerciales exploitables grâce à une visualisation des données riche;
Familiarité avec les méthodologies et outils Agile;
Autonome et capable de travailler à la fois de manière indépendante et collaborative au sein d'une équipe;
Une expérience dans l'industrie des sciences de la vie ou une solide compréhension de celle-ci, en particulier dans l'utilisation de la science des données pour soutenir l'excellence opérationnelle, est préférable.

Expertise technique requise :

Plus de 5 ans d'expérience pratique dans le traitement, l'analyse et la modélisation de ensembles de données volumineux et complexes;
Plus de 3 ans d'expérience avec le cycle de vie complet des produits d'apprentissage automatique, avec une capacité démontrée à prendre des initiatives et à assurer la livraison proactive des jalons de projet;
Plus de 5 ans d'expérience avec des outils de développement tels que SQL, PySpark, Python, Pandas ou Scala;
Expérience des technologies d'IA générative pour la lecture, le résumé et la génération de documents scientifiques, y compris l'ingénierie de prompts, les pipelines de récupération et le réglage fin des LLM pour des applications spécifiques à un domaine.

Informations spécifiques au poste:

Localisation: Télétravail (Doit être localisé au Canada);
Bonus annuel basé sur la performance;
Horaire: De jour en semaine, du lundi au vendredi;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Formations de développement payées;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
4 semaines de vacances et 10 jours de congé personnel.

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

À propos de l'évaluation de la sécurité
Charles River est une société engagée dans une démarche visant à aider ses partenaires à accélérer le développement préclinique de leurs médicaments avec des services d'évaluation de l'innocuité exceptionnels, des locaux utilisant des équipements à la pointe de la technologie et des conseils d'experts en matière de réglementation. Depuis la toxicologie spécialisée individuelle et les études permettant le dépôt d'une demande d'autorisation de nouveau médicament expérimental jusqu'aux formules sur mesure et à l'assistance totale pour les laboratoires, notre équipe chevronnée peut concevoir et exécuter des programmes qui anticipent les difficultés et évitent les blocages pour un parcours sans encombre et efficace jusqu'à la mise sur le marché. Chaque année, environ 300 études d'autorisation de nouveau médicament expérimental (dans le cadre du programme IDN, de l'anglais Investigational New Drug) sont réalisées dans nos centres d'évaluation de l'innocuité.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Senior Data Developer (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Senior Data Developer within our Enterprise Data and Analytics team, you’ll be at the forefront of a company-wide digital transformation. We’re looking for a forward-thinking engineer who brings deep technical expertise and a passion for building scalable, AI-ready data platforms. In this role, you’ll architect and implement modern data solutions that power intelligent applications, streamline operations, and deliver measurable business value. You’ll work closely with cross-functional teams to design robust pipelines, integrate diverse data sources, and enable advanced analytics and generative AI capabilities. This is a unique opportunity to shape the future of data engineering at Charles River and help unlock the full potential of data to drive innovation in the life sciences.

In this role, primary responsibilities include:

Design, develop, and maintain scalable data pipelines and ETL processes using Azure Data Factory, Azure Data Bricks, and other Azure services;
Implement and optimize data storage solutions using Azure Data Lake, Azure SQL Database, and Delta Lake to support analytics and reporting needs;
Collaborate with data scientists, analysts, and business stakeholders to understand data requirements and deliver high-quality, reliable datasets;
Ensure data security, compliance, and governance by applying best practices, role-based access control (RBAC), and encryption;
Monitor and troubleshoot data workflows, ensuring performance, reliability, and cost-efficiency across Azure cloud environments;
Automate data integration and transformation tasks using Azure Functions, Logic Apps, and scripting languages like Python;
Mentor junior engineers and foster a collaborative team environment.

Key Elements

We are looking for the following minimum qualifications for this role:

Bachelor’s degree in computer engineering, Computer Science, or a related discipline;
7+ years of experience in ETL design, development, and performance tuning using the Microsoft Stack in a multi-dimensional data warehousing environment;
7+ years of advanced SQL programming expertise (PL/SQL, T-SQL);
5+ years of experience in Enterprise Data & Analytics solution architecture;
3+ years of experience in Python Programming;
3+ years of hands-on experience with Azure, especially for data-heavy/analytics applications leveraging relational and NoSQL databases, Data Warehousing, and Big Data solutions;
3+ years of experience with key Azure services: Azure Data Factory, Data Lake Gen2, Analysis Services, Databricks, Blob Storage, SQL Database, Cosmos DB, App Service, Logic Apps, and Functions;
2+ years of experience designing data models aligning with business requirements and analytics needs;
2+ years of experience defining and implementing data security standards, including encryption, auditing, and monitoring;
Strong analytical skills and a passion for intellectual curiosity.

Preferred Skills:

2+ years of experience setting up and operating data pipelines using Python or SQL;
Familiarity with DevOps processes (CI/CD) and infrastructure as code;
Knowledge of Master Data Management (MDM) and Data Quality tools;
Experience developing REST APIs using Java Spring Boot, Python;
Experience building and supporting AL/ML software solutions;
Familiarity with stream-processing systems (e.g., Event Hubs, Storm, Spark-Streaming);
Experience with API integrations (RESTful, SOAP) for both internal and external systems to enhance data flow and automation;
Experience working in Agile environments, familiarity with Agile tools like Jira or Azure DevOps;
Experience in data and analytics within the Life Sciences industry is a plus.

Role Specific Information:

Location: Remote (Must be located in Canada);
Annual bonus based on performance;
Schedule: Daytime between Monday and Friday;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
4 weeks’ Vacation & 10 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Développeur.se de données sénior (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

Chez Charles River Laboratories, nous transformons notre façon de travailler en exploitant la puissance de l'IA, des données et de l'innovation numérique afin d'accélérer la découverte et le développement de thérapies qui sauvent des vies. Notre vision est d'intégrer l'intelligence artificielle et l'analytique avancée à chaque étape de nos flux de travail scientifiques et opérationnels — offrant à nos équipes des outils plus intelligents, des données fluides et des informations exploitables pour fournir des services et des solutions centrés sur le client, afin de mieux répondre aux besoins de nos clients et, ultimement, d'améliorer la vie des patients.

En tant que Développeur.se de données sénior au sein de notre équipe Enterprise Data and Analytics, vous serez à l'avant-garde d'une transformation numérique à l'échelle de l'entreprise. Nous recherchons un ingénieur visionnaire qui apporte une expertise technique approfondie et une passion pour la création de plateformes de données évolutives et prêtes pour l'IA. Dans ce rôle, vous concevrez et mettrez en œuvre des solutions de données modernes qui alimentent des applications intelligentes, optimisent les opérations et génèrent une valeur commerciale mesurable. Vous travaillerez en étroite collaboration avec des équipes interfonctionnelles pour concevoir des pipelines robustes, intégrer des sources de données variées et permettre des capacités avancées d'analyse et d'IA générative. Il s'agit d'une occasion unique de façonner l'avenir de l'ingénierie des données chez Charles River et d'aider à libérer le plein potentiel des données pour stimuler l'innovation dans les sciences de la vie.

Dans ce poste, les principales responsabilités incluront:

Concevoir, développer et maintenir des pipelines de données et des processus ETL évolutifs en utilisant Azure Data Factory, Azure Databricks et d'autres services Azure;
Implémenter et optimiser des solutions de stockage de données en utilisant Azure Data Lake, Azure SQL Database et Delta Lake pour soutenir les besoins en analyse et en rapports;
Collaborer avec les scientifiques de données, les analystes et les parties prenantes de l'entreprise pour comprendre les exigences en matière de données et livrer des ensembles de données fiables et de haute qualité;
Assurer la sécurité, la conformité et la gouvernance des données en appliquant les meilleures pratiques, le contrôle d'accès basé sur les rôles (RBAC) et le chiffrement;
Surveiller et résoudre les problèmes des flux de données, en garantissant performance, fiabilité et rentabilité dans les environnements cloud Azure;
Automatiser les tâches d'intégration et de transformation des données en utilisant Azure Functions, Logic Apps et des langages de script comme Python;
Encadrer les ingénieurs juniors et favoriser un environnement d'équipe collaboratif.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Baccalauréat en Ingénierie informatique, en Informatique ou dans toute discipline connexe;
Plus de 7 ans d'expérience dans la conception, le développement et l'optimisation des performances d'ETL en utilisant le Microsoft BI Stack dans un environnement de data warehousing multidimensionnel;
Plus de 7 ans d'expertise avancée en programmation SQL (PL/SQL, T-SQL);
Plus de 5 ans d'expérience dans l'architecture de solutions d'analyse et de données d'entreprise;
Plus de 3 ans d'expérience en programmation Python;
Plus de 3 ans d'expérience pratique avec Azure, en particulier pour des applications lourdes en données/analyses utilisant des bases de données relationnelles et NoSQL, le data warehousing et des solutions Big Data;
Plus de 3 ans d'expérience avec les services clés d'Azure : Azure Data Factory, Data Lake Gen2, Analysis Services, Databricks, Blob Storage, SQL Database, Cosmos DB, App Service, Logic Apps et Functions;
Plus de 2 ans d'expérience dans la conception de modèles de données alignés sur les exigences commerciales et les besoins analytiques.

Compétences idéales :

Plus de 2 ans d'expérience dans la mise en place et l'exploitation de pipelines de données en utilisant Python ou SQL;
Familiarité avec les processus DevOps (CI/CD) et l'infrastructure en tant que code;
Connaissance de la gestion des données de référence (MDM) et des outils de qualité des données;
Expérience dans le développement d'API REST en utilisant Java Spring Boot, Python;
Expérience dans la création et le support de solutions logicielles d'IA/ML;
Familiarité avec les systèmes de traitement en flux (par ex., Event Hubs, Storm, Spark-Streaming);
Expérience avec les intégrations d'API (RESTful, SOAP) pour les systèmes internes et externes afin d'améliorer le flux de données et l'automatisation;
Expérience de travail dans des environnements Agile, familiarité avec des outils Agile comme Jira ou Azure DevOps;
Une expérience en données et analytique dans l'industrie des sciences de la vie est un atout.

Informations spécifiques au poste:

Localisation: Télétravail (Doit être localisé au Canada);
Bonus annuel basé sur la performance;
Horaire: De jour en semaine, du lundi au vendredi;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
4 semaines de vacances et 10 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Animalier·ère (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Animalier·ère - Aucune Experience requise

Tu as toujours rêvé de travailler avec les animaux dans une compagnie qui participe à la recherche de médicament pour sauver des vies? Bonne nouvelle! Nous cherchons actuellement un.e Animalier.ère à temps-plein pour notre site de Senneville (QC). Tu n’as pas besoin d’expérience préalable car nous avons une équipe de formation exceptionnelle qui va tout t’apprendre!

En tant qu’Animalier·ère pour notre équipe de Toxicologie situé au site de Senneville (QC), vous serez responsable du bien-être de tous nos animaux de recherche. Votre réussite assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Nettoyer les salles d’animaux;
Nettoyer les cages d’animaux;
Manipuler les animaux.

Éléments Clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Tu aimes travailler physiquement (lever des charges de 20-25 lbs);
Tu es capable de suivre des instructions précises;
Tu aimes les animaux.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire: 19 $ de l’heure avec des primes de :
- Soirée : 2.50$;
- Fin de semaine : 2.75$;
- Heure supplémentaire : Temps et demi;
- Fériés : Temps Double.
Horaire: Heure de début majoritairement vers 9h-10h. Fin de semaine en rotation et jours fériés. Selon les besoins, il pourrait y avoir du temps supplémentaire de soir ou de nuit;
Poste permanent, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Animal Care Attendant (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

Animal Care Attendant - No Experience needed

Have you always dreamed of working with animals in a company that participates in drug research to save lives? Good news! We are currently looking for a full-time Animal Care Attendant for our Senneville (QC) site. You don't need any previous experience because we have an exceptional training team who will teach you everything!

As an Animal Care Attendant for our Toxicology team at the Senneville (QC) site, you will be you will be responsible for the well-being of our laboratory animals. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Cleaning the animal rooms;
Cleaning the animal cages;
Handling animals.

Key Elements

If you have the following qualifications, we'll train you for the rest:

You like to work physically (lifting loads of 20-25 lbs);
You are able to follow precises instructions;
You like animals;

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Salary: $19 per hour with primes of :
- Evenings: $2.50;
- Weekend: $2.75;
- Overtime: Time and a half;
- Holidays: Double time;
Schedule: Start time mostly around 9-10AM. Weekend rotations and holidays with overtime on evenings or nights when needed;
Permanent position, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technicien·ne - Histologie (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Technicien·ne en Histologie

En tant que Technicien·ne en histologie pour notre équipe située à Senneville, vous serez responsable de préparer les tissus pour des fins d’évaluation microscopique. Votre réussite assurera le bon déroulement de nos recherches, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Effectuer certaines activités d’histologie telles que : dissection, décalcification, circulation des tissus, enrobage, coupe, coloration, contrôle de qualité, immunohistochimie, histomorphométrie et numérisation de lames microscopique.
Préparer le matériel nécessaire demandé par les procédures.
Opérer les équipements de laboratoire nécessaire.
Préparer les réactifs chimiques.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes:

Diplôme collégial en Science, en Biotechnologie ou toutes autres disciplines en lien avec la science.
Capable de faire preuve d’une grande minutie.
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).
La compréhension de la lecture en anglais est obligatoire. Le bilinguisme français et anglais est préférable.

Informations spécifiques au rôle:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique.
Salaire : 21.50$/hrs.
Bonus annuel basé sur la performance.
Horaire flexible, selon les besoins de l’entreprise vous devrez être disponible de jour, de soir, de fin de semaine ainsi que les jours fériés. Les heures régulières de travail sont de 8h à 16h15, mais peuvent être appeler à changer en fonction des études en cours.
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe, C’EST VOTRE MOMENT!

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Technician - Histology (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

Technician Histology

As a Histology Technician for our team located in Senneville, you will mainly be responsible to prepare tissues for microscopic analysis. Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Perform histology activities such as: dissection, decalcification, processing, embedding, cutting, staining, quality control, and immunohistochemistry, histomorphometry, and slides scanning.
Prepare necessary material requested by procedures.
Operate necessary laboratory equipment.
Prepare chemical reagents.

Key Elements

We are looking for the following minimum qualifications for this role:

Collegial Diploma in Science, Biotechnology, or any other related field.
Able to demonstrate a high level of attention to details.
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).
Understanding of written English is mandatory. Bilingualism French and English is preferable.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station
Salary: $21.50/hrs.
Annual bonus based on performance plan.
Flexible schedule, depending on the needs you must be available to work during days, evening, weekends, and holidays. Regular working hours are 8 am to 4:15 pm but may be subject to change depending on current studies.
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us, THIS IS YOUR MOMENT!

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician, Necropsy (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

Prosector - Necropsy

As a Technician for our Necropsy team located in Senneville, you will mainly be responsible for performing the post-mortem examination of animals while following the ethical regulations and directives from study plans. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Dissecting and evaluating animal tissues for pathologists;
Weigh and document all abnormalities of the organs;
Euthanize animals prior to performing the necropsy.

Key Elements

We are looking for the following minimum qualifications for this role:

Collegial Diploma in Animal Health (any other Biology related field) or Bachelor’s degree in biology or any other Animal Science related field;
Dissection experience (asset);
Ability to work in a team environment, independently, and detail-oriented;
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).
Reading and writing English is required. Bilingualism French and English is preferable.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Salary: $22/hrs;
Annual bonus based on performance;
Schedule: Daytime schedule, Monday to Friday. Depending on the needs, you may have to do weekends rotations and overtime;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Employee and family assistance program;
3 weeks’ Vacation & 5 Personal day policy;
Access to a doctor and various health professionals (telemedicine);
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Paid development training;
Free gym on site
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technicien·ne, Nécropsie (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

Prosecteur·trice - Nécropsie

En tant que Technicien·ne pour notre équipe de Nécropsie située à Senneville, vous serez responsable d'effectuer les examens post-mortem des animaux tout en suivant les règlements éthiques et les directives des plans d'étude. Votre réussite assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Effectuer les dissections et évaluer les tissus des animaux pour les pathologistes;
Peser et documenter toutes les anomalies des organes;
Euthanasier les animaux avant de procéder à la nécropsie.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes:

Diplôme collégial en Santé animale (ou toutes autres disciplines en lien avec la Biologie) ou Baccalauréat en Biologie ou toutes autres disciplines en lien avec la Science animale;
Expérience en dissection (atout);
Capacité à travailler en équipe;
Être autonome et minutieux;
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).
La lecture et l'écriture de l'anglais sont requis. Le bilinguisme français et anglais est préférable.

Informations spécifiques au rôle:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire: 22$/hrs;
Bonus annuel basé sur la performance;
Horaire: Horaire de jour en semaine du lundi au vendredi. Selon les besoins de l’entreprise vous pourriez avoir à effectuer des rotations de fin de semaine et du temps supplémentaires;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Programme d'aide aux employés et à leur famille;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Formations de développement payées;
Gym gratuit sur place;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Bioanalysis Analyst (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As an Analyst for our Bioanalysis team located at the Senneville site, you will be involved in the analysis of samples using various techniques to evaluate the safety of a compound.

In this role,responsibilities may include:

Conduct technical assays using various extraction techniques (protein precipitate extraction, solid phase extraction) and LC-MS/MS to quantify molecules of interest, , in compliance with the Good Laboratory Practice (GLP) and FDA regulations
Handle and analyze biological samples
Validate the analysis of samples, in a multidisciplinary laboratory using a variety of extraction techniques, manual assays, automated equipment and analytical instruments
Work closely with the Scientific team.

Key Elements

If you have the following qualifications, we will train you for the rest:

DEC in science or B.Sc. in science (chemistry or biochemistry)
Experience with LC-MS/MS
Team player with a collaborative and positive approach
English reading comprehension is mandatory. Bilingualism in French and English is preferred

Role Specific Information

Location: Senneville / Free parking / Free shuttle service from Ste-Anne-de-Bellevue train station and John Abbott College to the Senneville site
Salary: $23.50/hrs
Schedule: Daytime schedule, Monday to Friday
Permanent full-time position as of the hiring, 37.5hrs per week

Why Charles River?

Competitive benefits upon hire. We pay up to 85% of premiums (medical & dental coverage)
Paid development training
Employee and family assistance program
24/7 access to a doctor and various health care professionals (telemedicine)
3 weeks’ Vacation & 5 Personal day policy
Numerous organized social activities

If you want to contribute to the well-being of our communities, not only across the country, but around the world, join the team.This is Your Moment.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Analyste bioanalyse (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant que Analyste pour notre équipe de Bioanalyse situé au site de Senneville, vous participerez à l'analyse d'échantillons en utilisant différentes techniques pour évaluer la sécurité d'un composé.

Dans ce rôle, les responsabilités peuvent inclure:

Effectuer des analyses techniques en utilisant diverses techniques d'extraction (extraction par précipitation de protéines, extraction en phase solide) et LC-MS/MS pour quantifier les molécules d'intérêt, conformément aux bonnes pratiques de laboratoire (BPL) et aux règlements de la FDA
Manipuler et analyser des échantillons biologiques
Validation de l'analyse des échantillons, dans un laboratoire multidisciplinaire en utilisant une variété de techniques d'extraction, de tests manuels, d'équipements automatisés et d'instruments analytiques
Travailler en étroite collaboration avec l'équipe Scientific.

Éléments Clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Titulaire d'un DEC en sciences ou d'un B.Sc. en sciences (chimie ou biochimie)
Experience avec LC-MS/MS
Avoir l'esprit d'équipe et une approche collaborative et positive
La compréhension de la lecture en anglais est obligatoire. Le bilinguisme français et anglais est préférable

Informations spécifiques au poste

Localisation : Senneville / Stationnement gratuit / Nous offrons un service de navette depuis la gare de Ste-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville
Salaire : 23,50$/hr
Horaire : Horaire de jour en semaine du lundi au vendredi.
Poste permanent temps plein dès l’embauche, 37.5hrs par semaine

Pourquoi Charles River?

Avantages compétitifs dès l'embauche. Nous prenons en charge jusqu'à 85 % des primes (couverture médicale et dentaire).
Formation de développement rémunérée
Programme d'aide aux employés et aux familles
Accès 24/7 à un médecin et à divers professionnels de la santé (télémédecine)
3 semaines de vacances et 5 jours de congés personnels
Nombreuses activités sociales organisées

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Director Analytics Development (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

Are you passionate about data architecture and analytics solutions? Do you thrive in leading high-performing teams while staying hands-on with cutting-edge technologies? If so, join Charles River’s global Data & Analytics organization as our next Director, Data Analytics.

We are seeking a strategic yet technical leader to manage a team of Data Analysts and Analytics Engineers, driving enterprise analytics initiatives that deliver actionable insights across global business functions. This role combines leadership, solution design, and stakeholder engagement to enable scalable reporting and data-driven decision-making.

In this role, primary responsibilities include:

Lead & Mentor: Manage and develop a team of 4–7 Data Analysts and Analytics Engineers, fostering a culture of collaboration, innovation, and continuous improvement;
Strategic Planning: Partner with business and IT leadership to define the analytics strategy and roadmap, aligning with enterprise data initiatives;
Hands-On Delivery: Contribute to solution design and development, including data modeling, Power BI/Fabric reporting, and integration with enterprise data platforms;
End-to-End Execution: Drive projects from requirements gathering and process design through to production deployment in a cloud environment;
Business Partnership: Translate complex business challenges into analytical solutions, present insights and recommendations to senior stakeholders, and champion data-driven decision-making;
Technical Product Ownership: Act as product owner within Agile teams, ensuring delivery of high-quality, scalable analytics solutions;
Standards & Best Practices: Define UX and data visualization standards, optimize processes, and promote adoption of modern tools and technologies;
Global Collaboration: Manage initiatives across multiple time zones, primarily U.S.-based teams, in a matrix environment.

Key Elements

We are looking for the following minimum qualifications for this role:

Education: B.Sc./M.Sc. in Computer Science, Mathematics, or related field; Master’s preferred;
Leadership Experience: Proven track record of building and leading high-performing technical teams in a data or analytics organization. At least 5 to 7 years’ experience;
Technical Expertise:
- - Advanced Power BI and Microsoft Fabric experience, including SSAS design and expert DAX skills. At least 7 years’ experience;
  - Strong knowledge of Azure cloud services and data integration architectures. At least 7 years’ experience;
  - Hands-on experience with data visualization, report development, and enterprise data modeling. At least 7 years’ experience;
Business Acumen: Ability to analyze complex business challenges and translate them into actionable solutions. At least 7 years’ experience;
Methodologies: Skilled in Agile practices and managing multiple concurrent initiatives under tight deadlines. At least 3 years’ experience;
Experience with Python and data science concepts (preferred);
Deep understanding of data warehousing and BI analytics (preferred);
Familiarity with SAP or similar ERP systems (preferred).

Role Specific Information:

Location: Remote (Must be located in Canada);
Annual bonus based on performance;
Schedule: Daytime between Monday and Friday;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Stock option available;
We offer competitive benefits and advantages from day one to support your well-being;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
4 weeks’ Vacation & 10 Personal day policy.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Directeur.trice du développement analytique (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Êtes-vous passionné par l’architecture des données et les solutions analytiques? Aimez-vous diriger des équipes performantes tout en restant directement impliqué avec les technologies de pointe? Si c’est le cas, joignez-vous à l’organisation mondiale Données et Analytique de Charles River en tant que notre prochain Directeur.trice, Analyse de Données.

Nous recherchons un leader stratégique et technique pour gérer une équipe d’analystes de données et d’ingénieurs en analytique, en pilotant des initiatives analytiques à l’échelle de l’entreprise qui fournissent des informations exploitables à travers les fonctions commerciales mondiales. Ce rôle combine leadership, conception de solutions et engagement des parties prenantes afin de permettre la production de rapports évolutifs et la prise de décisions basée sur les données.

Dans ce poste, les principales responsabilités incluront:

Leadership et mentorat : Gérer et développer une équipe de 4 à 7 analystes de données et ingénieurs en analytique, en favorisant une culture de collaboration, d'innovation et d'amélioration continue;
Planification stratégique : Collaborer avec les dirigeants des affaires et des TI pour définir la stratégie et la feuille de route analytique, en alignement avec les initiatives de données de l'entreprise;
Livraison pratique : Contribuer à la conception et au développement de solutions, y compris la modélisation des données, le reporting Power BI/Fabric et l'intégration avec les plateformes de données d'entreprise;
Exécution de bout en bout : Piloter des projets depuis la collecte des exigences et la conception des processus jusqu'au déploiement en production dans un environnement cloud;
Partenariat d'affaires : Transformer des défis complexes en solutions analytiques, présenter des insights et des recommandations aux parties prenantes de haut niveau, et promouvoir la prise de décision fondée sur les données;
Propriété technique du produit : Agir en tant que propriétaire de produit au sein d'équipes Agile, en garantissant la livraison de solutions analytiques de haute qualité et évolutives;
Normes et meilleures pratiques : Définir les normes UX et de visualisation des données, optimiser les processus et promouvoir l’adoption d’outils et de technologies modernes;
Collaboration mondiale : Gérer des initiatives à travers plusieurs fuseaux horaires, principalement des équipes basées aux États-Unis, dans un environnement matriciel.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Éducation : B.Sc./M.Sc. en informatique, en mathématiques ou dans un domaine connexe ; un master est préféré ;
Expérience en leadership : Antécédents prouvés dans la constitution et la direction d'équipes techniques performantes au sein d'une organisation axée sur les données ou l'analytique. Au minimum 5 à 7 ans d’expérience;
Expertise technique :
- - Expérience avancée en Power BI et Microsoft Fabric, y compris la conception SSAS et une maîtrise de DAX. Au minimum 7 ans d’expérience;
  - Solide connaissance des services cloud Azure et des architectures d'intégration de données. Au minimum 7 ans d’expérience;
  - Expérience pratique en visualisation de données, développement de rapports et modélisation de données d'entreprise. Au minimum 7 ans d’expérience;
Sens des affaires : Capacité à analyser des défis commerciaux complexes et à les traduire en solutions concrètes. Au minimum 7 ans d’expérience;
Méthodologies : Compétences en pratiques Agile et gestion de plusieurs initiatives simultanées dans des délais serrés. Au minimum 3 ans d’expérience;
Expérience en Python et concepts de science des données (préférée) ;
Compréhension approfondie de l'entreposage de données et de l'analytique BI (préférée) ;
Familiarité avec SAP ou des systèmes ERP similaires (préférée).

Informations spécifiques au poste:

Localisation: Télétravail (Doit être localisé au Canada);
Bonus annuel basé sur la performance;
Horaire: De jour en semaine, du lundi au vendredi;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Option d’achat d’actions disponible;
Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
4 semaines de vacances et 10 jours de congé personnel.

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Director Data Development (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Director Data Development for our Enterprise Data Analytics team, you’ll be joining a purpose-driven team aligned with our mission: Together We Create Healthier Lives. We’re looking for visionary, self-driven leader to help expand its reach across all business lines. This is your opportunity to shape how we integrate, govern, and elevate data quality to fundamentally transform how Charles River operates through data science and advanced analytics.

In this role, primary responsibilities include:

Develop and executed a data engineering strategy aligned with enterprise goals and digital transformation;
Collaborate with stakeholders to define a unified data architecture and scalable roadmap;
Promote innovation through emerging technologies and platform enhancements;
Establish governance frameworks and best practices for data consistency and compliance;
Architecte enterprise-scale data platforms using Microsoft Azure tools (Data Factory, Databricks, Data Lake, Event Hubs);
Lead advanced Databricks implementations for large-scale processing, ML workflows, and real-time analytics;
Enable actionable insights via semantic models and Power BI enterprise reporting;
Built robust data pipelines for high-volume ingestion, transformation, and distribution.
Direct a high-performing team, ensured 99.9%+ uptime, and drove automation and DevOps for operational efficiency.

Key Elements

We are looking for the following minimum qualifications for this role:

Bachelor's degree in computer science, Mathematics, or related fields;
7+ years of experience in technology leadership, with a proven track record of building, mentoring, and scaling high-performing engineering teams;
7+ years of hands-on Data engineering experience;
7+ years of data warehousing and ETL tools experience;
10+ years of progressively responsible experience in information technology;
Deep expertise in database and data architecture, with demonstrated experience in designing robust dimensional data models;
Experience with Finance Reporting Modernization;
Experience with enterprise platforms such as Salesforce or SAP.

Role Specific Information:

Location: Remote (Must be located in Canada);
Annual bonus based on performance;
Schedule: Daytime between Monday and Friday;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Stock option available;
We offer competitive benefits and advantages from day one to support your well-being;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
4 weeks’ Vacation & 10 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Directeur.trice du développement des données (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Directeur.trice du développement des données pour notre équipe d'Analyse de données d'entreprise, vous rejoindrez une équipe motivée par un but en accord avec notre mission : Ensemble, nous créons des vies plus saines. Nous recherchons un leader visionnaire et autonome pour aider à étendre notre portée à travers toutes les lignes d'affaires. C'est votre opportunité de façonner la manière dont nous intégrons, gouvernons et améliorons la qualité des données pour transformer fondamentalement le fonctionnement de Charles River grâce à la science des données et à l'analyse avancée.

Dans ce poste, les principales responsabilités incluront:

Élaborez et exécutez une stratégie d'ingénierie des données alignée sur les objectifs de l'entreprise et la transformation numérique;
Collaborez avec les parties prenantes pour définir une architecture de données unifiée et une feuille de route évolutive;
Promouvoir l'innovation grâce à des technologies émergentes et des améliorations de plateforme;
Établir des cadres de gouvernance et des meilleures pratiques pour la cohérence des données et le respect des normes;
Architecturez des plateformes de données à l'échelle de l'entreprise en utilisant les outils Microsoft Azure (Data Factory, Databricks, Data Lake, Event Hubs);
Dirigez des implémentations avancées de Databricks pour le traitement à grande échelle, les flux de travail ML et l'analyse en temps réel;
Activez des informations exploitables via des modèles sémantiques et des rapports d'entreprise Power BI;
Construire des pipelines de données robustes pour l'ingestion, la transformation et la distribution à volume élevé;
Dirigez une équipe performante, assuré un temps de disponibilité de 99,9 % ou plus, et instauré l'automatisation et le DevOps pour l'efficacité opérationnelle.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Baccalauréat en Informatique, Mathématiques ou dans toutes autres domaines connexes;
Plus de 7 ans d'expérience en leadership technologique, avec un bilan prouvé dans la construction, le mentorat et le développement d'équipes d'ingénierie performantes;
Plus de 7 ans d'expérience pratique en ingénierie des données;
Plus de 7 ans d'expérience avec des outils d'entreposage de données et d'ETL;
Plus de 10 ans d'expérience de responsabilité progressive en technologie de l'information;
Expertise approfondie en bases de données et architecture de données, avec une expérience démontrée dans la conception de modèles de données dimensionnels robustes;
Expérience en modernisation des rapports financiers;
Expérience avec des plateformes d'entreprise telles que Salesforce ou SAP.

Informations spécifiques au poste:

Localisation: Télétravail (Doit être localisé au Canada);
Bonus annuel basé sur la performance;
Horaire: De jour en semaine, du lundi au vendredi;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Option d'achat d'actions disponible;
Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
4 semaines de vacances et 10 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Associate Director Commercial Finance DSA (REMOTE) (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

This role will drive business performance by enhancing the effectivity of global DSA Commercial. In turn this will generate sequential revenue growth, margin development and shareholder value.

Responsibilities

Enhance Commercial Analytics: Produce new and enhanced meaningful management reporting including long-range forecasting KPI’s for senior management review and action.
Pricing Models: Develop and evolve pricing insights and strategies to enhance profitability. Lead initiatives to advance novel analytical capabilities and insights.
Price-volume-mix-analysis: Own revenue and margin analytics, including price-volume-mix-analysis.
Enhance Data Integrity: Drive one source of truth of data consistency across systems and segmentations to support consistent and accurate reporting (CRM, ERP, BI systems etc).
Deepen Forecast Insights: Reconciling and explaining client slippage in backlogs on a routine basis to identify client trends and patterns to improve forecast reliability.
Client Forecast Evolution: Support the weekly, monthly, quarterly rolling forecast, annual plan submissions and sequentially enhance team understanding of client behavior.
Commercial Business Partnering: Support analyzing Opportunities, Proposals and Bookings in the CRM with the Commercial function to generate sales focus.
Enhance Commercial Analytics: Produce new and enhanced meaningful management reporting including long-range forecasting KPI’s for senior management review and action.
Enhance Data Integrity: Drive one source of truth of data consistency across systems and segmentations to support consistent and accurate reporting (CRM, ERP, BI systems etc).
Executive Reporting: Support forecast variance analysis, commentary, Business Review bridges.
Strategic Planning: Deliver the annual long-range financial plan and strat planning cycle with executive leadership, helping advance the commercial direction and client strategy.

Qualifications

Experience: Seven plus years of similar related experience in an international environment, background could be commercial sales or finance.
FP&A/commercial finance exposure and P&L ownership.
Education: Bachelor’s degree (BA/BS) in business or related discipline preferred.
Qualified Accountant beneficial – CPA/ACCA/ICAS/ICAEW/CIMA or equivalent.
Skills: Demonstrated proficiency managing analytically rigorous initiatives. Advanced Excel and PowerPoint presentation abilities required.
Tangible understanding and experience of ERP, Data Warehouse and Business Intelligence systems incl. financial reporting, PowerBI and CRM systems.
Accustomed to communicating and reporting to senior management.
Supervisory and/or people management experience advantageous.

COMMENTS:
- This position may require occasional domestic and/or international travel (e.g. to CRL or client venues).
- Position will work remote, from home office located in North America.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Directeur(trice) associé(e) - Finance commerciale mondiale (Télétravail) (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Ce rôle vise à stimuler la performance de l’entreprise en améliorant l’efficacité de l’équipe mondiale DSA Commerciale. Cela générera une croissance séquentielle des revenus, une amélioration des marges et une valeur accrue pour les actionnaires.

Le poste exige une forte capacité d’influence au sein de l’organisation afin de produire un impact significatif et d’appuyer des transformations opérationnelles. Il nécessite du leadership, des conseils stratégiques, la gestion de la performance, la collaboration interéquipes ainsi qu’une solide expertise en matière de rapports financiers et de gestion.

Vous représenterez le groupe de Finance Commerciale DSA dans divers forums régionaux et mondiaux. Vous avez une expérience concrète en gestion d’entreprise et votre apport ne se limite pas aux finances. Vous pouvez comprendre des modèles d’affaires complexes, les mettre en œuvre, piloter le changement et diriger par influence. Vous êtes à l’aise de « vous opposer » ou de soutenir des décisions impopulaires lorsque nécessaire.

Plus important encore, vous êtes très opérationnel, capable de gérer des modèles Excel complexes, créer des tableaux croisés dynamiques, des graphiques, des présentations PowerPoint, extraire des données dans SAP/BI et, en parallèle, prendre de la hauteur pour offrir une vue d’ensemble stratégique. Vous êtes un partenaire d’affaires qui comprend les développements clés tant au sein des équipes commerciales que des sites opérationnels, sans vous limiter au volet financier.

Vous comprenez l’entreprise aussi bien que la direction commerciale et collaborez régulièrement (quotidiennement) avec les membres de l’équipe Commerciale. Vous êtes responsable et vous vous appropriez le succès global de DSA, au-delà de la fonction Finance.

Vous êtes à l’aise de présenter dans divers forums, parfois devant des publics que vous ne connaissez pas. Vous savez transmettre un sens du but, de l’urgence et de l’autorité tout en menant de façon collaborative des groupes interfonctionnels vers un objectif commun.

Ce rôle dirige les ressources nécessaires à l’exécution des opérations commerciales, incluant la stratégie de mise en marché, l’analyse orientée vers l’action et l’efficacité des processus apportant de la valeur aux clients. Vous influencez et développez les capacités de projet essentielles à l’équipe commerciale mondiale.

Responsabilités

Les principales responsabilités incluent l’optimisation des processus commerciaux liés aux clients et des outils analytiques, la production de rapports et la mesure des indicateurs de performance (KPI), ainsi que la conception d’infrastructures technologiques. L’objectif est d’élever la fonction commerciale afin de mieux servir les clients internes et externes, tout en fournissant des conseils stratégiques pour orienter la direction commerciale.

Amélioration des analyses commerciales : Produire des rapports de gestion nouveaux ou améliorés, incluant des prévisions à long terme et des KPI destinés à la haute direction.
Modèles de tarification : Développer et faire évoluer les stratégies et analyses de tarification afin d’améliorer la rentabilité. Mener des initiatives pour renforcer les capacités analytiques.
Analyse prix volume mix : Assumer la responsabilité de l’analyse des revenus et des marges, incluant l’analyse prix volume mix.
Amélioration de l’intégrité des données : Assurer l’uniformité et la cohérence des données à travers les systèmes et segmentations (CRM, ERP, systèmes BI, etc.) afin de soutenir un reporting fiable.
Amélioration des prévisions : Expliquer et réconcilier les fluctuations de carnet de commandes afin de dégager des tendances clients et améliorer la fiabilité des prévisions.
Évolution des prévisions clients : Soutenir les prévisions hebdomadaires, mensuelles et trimestrielles, ainsi que la planification annuelle, tout en renforçant la compréhension du comportement client au sein de l’équipe.
Partenariat commerciale : Appuyer l’analyse des opportunités, propositions et réservations dans le CRM avec l’équipe Commerciale pour favoriser la priorisation des ventes.
Analytique commerciale renforcée : Produire des rapports de gestion pertinents et bonifiés, incluant des KPI de prévision à long terme pour la haute direction.
Intégrité des données : Assurer une seule source de vérité dans les données pour un reporting constant et précis.
Rapports exécutifs : Appuyer l’analyse des écarts de prévision, les commentaires et les ponts de revue d’affaires.
Planification stratégique : Produire le plan financier à long terme et soutenir le cycle de planification stratégique avec la haute direction afin d’appuyer l’orientation commerciale et la stratégie client.

Qualifications

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Expérience : Plus de sept années d’expérience similaire dans un environnement international; une expérience en ventes commerciales ou en finance est pertinente.
Exposition FP&A/finance commerciale et responsabilité de P&L.
Éducation : Baccalauréat en administration ou discipline connexe (BA/BSc) préféré.
Comptable professionnel agréé un atout (CPA/ACCA/ICAS/ICAEW/CIMA ou équivalent).
Compétences : Capacité démontrée à gérer des initiatives analytiques rigoureuses. Excellente maîtrise d’Excel avancé et de PowerPoint.
Compréhension et expérience tangibles des systèmes ERP, entrepôts de données et systèmes de Business Intelligence, incluant reporting financier, Power BI et systèmes CRM.
Habitude de communiquer et de présenter à la haute direction.
Expérience de supervision et/ou de gestion de personnel, un atout.

Information additionnelle spécifique au poste:

Ce poste peut nécessiter des déplacements occasionnels en Amérique du Nord ou à l’international (p. ex. vers nos site des Laboratoires Charles River ou avec des clients).
Le poste est en télétravail, à partir d’un bureau à domicile situé en Amérique du Nord.

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

À propos des fonctions support

Les personnes exerçant des fonctions de gestion apportent un soutien opérationnel dans tous les domaines dans lesquels travaille Charles River, notamment dans les ressources humaines, les finances, l'informatique, les affaires juridiques, les ventes, l'assurance qualité, le marketing et le développement de l'entreprise. Elles collaborent avec leurs homologues dans toute l'entreprise pour élaborer et mettre en oeuvre des stratégies, et pour établir des normes mondiales. Ces fonctions sont essentielles dans la mesure où elles créent un lien entre la vision stratégique de l'entreprise et sa disponibilité opérationnelle afin de garantir une innovation fonctionnelle permanente et une amélioration continue de ses capacités.

Pour plus d'information, consultez www.criver.com.

Data Coordinator - Reporting Services (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Data Coordinator for our Reporting Services team at the Senneville location, you will be responsible for providing the scientists with the information necessary for them to be able to write the summary and results sections of their reports, based on individual and summary data included in the appendices, tables and graphs customized to meet client specific reporting requirements.

In this role, primary responsibilities include:

Coordination of all pertinent data and scientific interpretation information in accordance with the Study Plan to enable the correct tabulation to be included in the report;
Transcribe data from hand-written data records and/or, process computer-generated data files, into formats suitable to meet sponsors’ needs;
Prepare finished reports, tables and/or graphs, that are clear and professionally presented as per Company requirements and guidelines;
Processing of reports or tabulated data, which are accessed either electronically or from hard copy sources following specific e-file management criteria involving the use of various software;
Ensure work is compliant with applicable guidelines and regulations.

Key Elements

We are looking for the following minimum qualifications for this role:

High School diploma;
Previous experience in Sciences or Information Technology;
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above;
Knowledge of computer skills including Microsoft Office applications (e.g. Word, Access, Excel);
Ability to work under time constraints, in order to respect deadlines;
Ability to work in a team environment.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging;
Salary: 23$/hrs;
Annual bonus based on performance;
Schedule: Day shift from Monday to Friday, flexible schedule with possibility to work remotely;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Coordonnateur.trice des données (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Coordinateur.trice des données pour notre équipe de Services de rapport située au site de Senneville, vous serez responsable de fournir aux scientifiques l’information nécessaire pour qu’ils puissent écrire les sections de sommaire et résultats de leurs rapports basés sur les données individuelles et sommaires incluses dans les annexes, les tables et les graphiques adaptés afin de rencontrer les exigences spécifiques des clients.

Dans ce poste, les principales responsabilités incluront:

Coordination de toutes les données pertinentes et de l’interprétation scientifique des informations en fonction du plan d’étude pour permettre une tabulation adéquate pouvant être incluse dans un rapport;
Transcrire des données à partir d'enregistrements de données manuscrites et/ou traiter des fichiers de données générés par ordinateur dans des formats adaptés aux besoins des sponsors;
Préparer des rapports, des tableaux et/ou des graphiques finis, clairs et présentés de manière professionnelle conformément aux exigences et aux directives de l'entreprise;
Traitement des rapports ou de données tabulées, lesquels sont accessibles par sources électroniques ou par documents imprimés suivant les critères de gestion de l’e-file impliquant l’utilisation de divers logiciels;
S’assurer que le travail est conforme aux directives et réglementations applicables.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Diplôme d’études secondaire;
Expérience précédente en sciences ou en technologie de l’information;
Une combinaison équivalente d’éducation et d’expérience peut être considérée comme substitut acceptable pour l’éducation et l’expérience spécifique telle qu’énumérée ci-dessus;
Maîtrise des compétences informatiques notamment des logiciels de la suite Microsoft Office (par exemple Word, Access, Excel);
Être en mesure de gérer son temps efficacement, afin de respecter les échéanciers;
Capacité à travailler en équipe.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire: 23$/hrs;
Bonus annuel basé sur la performance;
Horaire: De jour du Lundi au Vendredi, horaire flexible et possibilité de télétravail;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Clinical Pathology Technician (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Technician for our Clinical Pathology team at the Laval location, you will carry out the analysis of biological specimens.

In this role, primary responsibilities include:

Perform the preparation and the analysis of samples;
Perform the quality control procedure and maintenances on the different instruments;
Perform the activities in a timely fashion by adhering to present schedules;
Ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), and health and safety rules.

Key Elements

We are looking for the following minimum qualifications for this role:

DEC or BSc in Biology, Biochemistry, Biotechnology, or any other related discipline;
Experience in centrifugation is mandatory;
Experience in at least one of the following areas: Biochemistry analysis, pipette handling, dilutions, hematology and/or microscopy;
Analytical and critical thinking skills;
Outstanding organizational skills and ability to adapt to changes.

Role Specific Information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Salary: Starting at 23.50$/hrs;
Annual bonus based on performance;
Schedule: Monday to Friday, daytime between 8am to 4:15pm. Depending on business needs, you may have to do overtime;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Paid development training;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career; development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technicien.ne en pathologie clinique (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Technicien.ne pour notre équipe de Pathologie clinique situé au site de Laval, vous allez effectuer l’analyse de spécimens biologiques.

Dans ce poste, les principales responsabilités incluront:

Effectuer la préparation et l’analyse des échantillons;
Effectuer la procédure de contrôle qualité et la maintenances sur les différents instruments;
Effectuer les activités en temps opportun en respectant les horaires prédéfinis;
Assurer l’intégrité des études et répondre aux exigences des agences règlementaires en exécutant les activités selon les Bonnes Pratiques de Laboratoire (BPL), les Procédures Opératoires Normalisées (PON) et les règles de santé sécurité.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

DEC ou Baccalauréat en Biologie, Biochimie, Biotechnologie ou toutes autres disciplines reliées aux sciences biologiques;
Avoir de l’expérience en centrifugation est obligatoire;
Expérience dans au minimum un de ces domaines : Analyse de biochimie, manipulation de pipettes, dilutions, hématologie et/ou microscopie;
Esprit d’analyse et esprit critique;
Bon sens de l’organisation et capacité à s’adapter aux changements.

Informations spécifiques au poste:

Localisation: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Salaire: À partir de 23.50$/hrs;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi de jour, de 8h à 16h15. Selon les besoins de l’entreprise, vous pourriez avoir à faire du temps supplémentaire;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Formations de développement payées;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Commis de plancher (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Commis de plancher pour notre équipe de Toxicologie situé au site de Laval, vous serez responsable de la gestion et du nettoyage du matériel requis pour les animaux et les études tout en respectant les procédures établies.

Dans ce poste, les principales responsabilités incluront:

Effectuer une tournée journalière pour la collection du matériel souillé;
Laver et inspecter l’équipement pour s’assurer qu’il est en bon état. Faire une requête pour la réparation au besoin;
Rapporter tout problème ou problèmes éventuels dans la conduite des activités journalières au Superviseur ou délégué;
Assurer l'intégrité des études et satisfaire les exigences des agences règlementaires en exécutant les activités et recueillant les données conformément aux Bonnes Pratiques de laboratoire (BPL), aux Procédures Normales d'Opération et aux règles du Comité de Protection des Animaux (CPA);
Faire preuve de flexibilité face à la nature du travail afin de répondre aux demandes de son groupe et de tous les autres groupes de la division.

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Diplôme d’études secondaires ou équivalence;
Capacité à gérer son temps efficacement;
Capacité à travailler de manière autonome;
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au poste:

Localisation : 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport : Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Salaire : 18.25$/hrs;
Primes : Soirée (2.50$), Fin de semaine (2.75$), Heure supplémentaire (Temps et demi), Fériés (Temps double);
Bonus annuel basé sur la performance;
Horaire : Horaire flexible, vous devez être disponible de jour, de soir, et les fins de semaine (1/2). Selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaires;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine;

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Formations de développement payées;
Programme d'aide aux employés et à leur famille;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
Des heures garanties, car le milieu de la recherche est très en demande;
3 semaines de vacances ainsi que 5 journées personnelles;
De nombreuses activités sociales !

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

À propos de l'évaluation de sécurité

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Commis de plancher (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

Dans ce poste, les principales responsabilités incluront:

Effectuer une tournée journalière pour la collection du matériel souillé;
Laver et inspecter l’équipement pour s’assurer qu’il est en bon état. Faire une requête pour la réparation au besoin;
Rapporter tout problème ou problèmes éventuels dans la conduite des activités journalières au Superviseur ou délégué;
Assurer l'intégrité des études et satisfaire les exigences des agences règlementaires en exécutant les activités et recueillant les données conformément aux Bonnes Pratiques de laboratoire (BPL), aux Procédures Normales d'Opération et aux règles du Comité de Protection des Animaux (CPA);
Faire preuve de flexibilité face à la nature du travail afin de répondre aux demandes de son groupe et de tous les autres groupes de la division.

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Diplôme d’études secondaires ou équivalence;
Capacité à gérer son temps efficacement;
Capacité à travailler de manière autonome;
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au poste:

Localisation : 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport : Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Salaire : 18.25$/hrs;
Primes : Soirée (2.50$), Fin de semaine (2.75$), Heure supplémentaire (Temps et demi), Fériés (Temps double);
Bonus annuel basé sur la performance;
Horaire : Horaire flexible, vous devez être disponible de jour, de soir, et les fins de semaine (1/2). Selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaires;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine;

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Formations de développement payées;
Programme d'aide aux employés et à leur famille;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
Des heures garanties, car le milieu de la recherche est très en demande;
3 semaines de vacances ainsi que 5 journées personnelles;
De nombreuses activités sociales !

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Floor Clerk (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Floor Clerk for our Toxicology team located in Laval, you will manage and clean the equipment required for the animals and the studies while following established procedures.

In this role, primary responsibilities include:

Make a daily round for the collection of soiled material;
Clean and inspect the equipment to ensure it is in good condition. Request repairs as needed;
Report any problem or potential problems in the conduct of daily activities to the Supervisor or delegate;
Ensure the integrity of the studies and fulfil the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP) and the Institutional Animal Care and Use Committee (IACUC) rules;
Show flexibility in regard to the nature of the work to respond to the needs of his/her group and all other groups within the division.

Key Elements

If you possess the following qualifications, we will train you in the rest:

High School diploma or equivalence;
Ability to manage time effectively;
Ability to work autonomously;
Being able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company

Role Specific Information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Salary: $18.25/hrs;
Premiums: Evening ($2.50), Weekend ($2.75), Overtime (Time and a half), Holidays (Double time);
Annual bonus based on performance plan;
Schedule: Flexible schedule, you must be available days, evening, and weekends (1/2). Depending on the needs, you may have to do overtime night, and holidays;
Permanent position as of the hiring, 37.5hrs per week;

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Paid development training;
Employee and family assistance program;
Access to a doctor and various health professionals (telemedicine);
Guaranteed hours because the research field is in high demand;
3 weeks’ Vacation & 5 Personal days;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Formateur.trice, Soins aux animaux - Toxicologie (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Formateur.trice en soins aux animaux pour notre équipe de Toxicologie située au site de Laval, vous formerez le personnel technique et vous assurerez que les dossiers de formation sont à jour et que les techniques enseignées sont réalisées d'une manière qui respecte les processus établis.

Dans ce poste, les principales responsabilités incluront:

Former sur les méthodes de nettoyage et de contention des animaux;
Former à l’enregistrement des données telles que le poids corporel, la consommation alimentaire et les signes cliniques afin de répondre aux normes de qualité et de compétence;
Évaluer le niveau de compréhension de l’employé par rapport à la formation reçue;
Assurer l’intégrité des études et répondre aux exigences des organismes réglementaires en réalisant les activités conformément aux Bonnes Pratiques de Laboratoire (BPL), aux Procédures Opératoires Standard (POS) et aux règles du Comité institutionnel de soins et d’utilisation des animaux (CICUA) ;
Assurer le suivi des différentes modifications apportées aux procédures et aux méthodes de travail et participer aux efforts d’amélioration des processus;
Assurer une bonne communication avec les superviseurs des différents départements pendant et après la formation des employés.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Diplôme d'études secondaires;
Au moins 2 à 3 ans d'expérience dans un centre de recherche en tant que Commis en soins aux animaux/Préposé.e à l’entretien des animaux;
Être une référence, un exemple et un leader en matière de bien-être animal, santé et sécurité, qualité et assiduité;
Bonnes compétences d’observation;
Capacité à inspirer confiance et assurance grâce à de solides compétences interpersonnelles et une collaboration efficace;
Capacité à travailler physiquement (soulever jusqu’à 20 kg, marcher, rester debout, se pencher, etc.).

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au poste:

Localisation: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Salaire: À partir de 22$/hrs;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi de jour;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Trainer, Animal Care - Toxicology (Laval, Quebec, CA, H7V 4B3)

Job Summary

As an Animal Care Trainer for our Toxicology team at the Laval location, you will train technical staff and ensure that the training records are up to date and that the techniques taught are done in a way that respects established processes.

In this role, primary responsibilities include:

Train animal room cleaning and restraint methods;
Train on the data recording such as body weight, food consumption and clinical signs in order to meet quality and competence standards;
Evaluate the employee's level of understanding in relation to the training received;
Ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP) and the Institutional Animal Care and Use Committee (IACUC) rules;
Ensure the follow-up of the various changes brought to the procedures and the methods of work and participate in process improvement efforts;
Ensure good communication with the supervisors of the different departments during and after completion of the employees’ training.

Key Elements

We are looking for the following minimum qualifications for this role:

High School diploma;
At least 2 to 3 years’ experience in a research center as an Animal Care Clerk/Animal Care Attendant;
Be a reference, an example and a leader for Animal Welfare, Health and Safety, Quality and attendance;
Good observation skills;
Ability to inspire trust and confidence through strong interpersonal skills and effective collaboration;
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role Specific Information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Salary: Starting at 22$/hrs;
Annual bonus based on performance;
Schedule: Monday to Friday, daytime;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Paid Animal Care Training (Laval, Quebec, CA, H7V 4B3)

Job Summary

Paid Training – AEP Animal Care (April 2026)

Have you always dreamed of working with animals in a company that participates in drug research to save lives? Good news! In partnership with Formation Korpus Laval, Charles River Laboratories is offering a paid training program as part of an Attestation of Vocational Studies (AVS) in Animal Care. This training will be given in French.

Some elements of the vocational program will be adapted to include more content related to animal care in a research environment, with the goal of being hired as a permanent employee at Charles River Laboratories upon completion of the program.

As an Animal Care Technician for our Toxicology team at the Senneville and Laval location, you will be responsible for the well-being of all our research animals. Your success will ensure the health of our animals as well as the integrity of our preclinical studies.

In this role, primary responsibilities include:

Cleaning all types of animal housing and related accessories;
Handling animals for all required activities;
Collecting data (weighing, monitoring food consumption, observing clinical signs).

Key Elements

We are looking for the following minimum qualifications for this training:

Having successfully obtained Grade 9 units;
- or the equivalent in the language of instruction, second language, and mathematics;
- or having obtained a High School Equivalency Certificate (AENS);
- or having passed the General Development Test (TDG) with or without specific prerequisites.
Having interrupted full‑time studies for at least twelve months;
- or being 18 years old at the time of entering the program;
- or having obtained a High School Diploma (DES) or a Vocational Studies Diploma (DEP) or their equivalent.
- or meeting the eligibility standards of Emploi-Québec’s Workforce Training Measure. (This AEP is eligible for the CFMS–AEP pathway.)
Being able to work physically (lift up to 20 kg, walk, stand, stoop, etc.);
Having strong attention to detail;
Ability to follow instructions and meet precise deadlines;
Ability to work independently and collaboratively within a team.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role Specific Information:

Location of Korpus Training Center: 2100, rue Cunard, Laval (QC) H7S 2G5
Location of Charles River’s sites:
- Laval - 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3 (Free parking. Near the Montmorency Subway. Electric vehicle charging station)
- Senneville - 22022 route Transcanadienne, Senneville, QC, H9X 1C1 (We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station)
Salary: 21$
Program duration: 5 months
Program Schedule: Monday to Friday from 8AM-4.15PM
Regular Work Schedule after the program : Day, Evening and nights when needed. Weekend rotation and holidays.

Why Charles River ?

Employee and family assistance program;
Excellent welcome program for new employees;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Formation rémunérée en soins aux animaux (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

Formation rémunérée – AEP Soins animaliers (Avril 2026)

Tu as toujours rêvé de travailler avec les animaux dans une compagnie qui participe à la recherche de médicament pour sauver des vies? Bonne nouvelle! En partenariat avec Formation Korpus Laval, les Laboratoires Charles River offre une formation rémunérée dans le cadre d’une Attestation d’Études Professionnelles (AEP) en soins animaliers.

Certains éléments de la formation de base seront adaptés afin d’intégrer plus d’éléments en lien avec les soins animaliers en milieu de recherche dans le but d’être embauché·e en tant qu’employé·e permanent·e chez les Laboratoires Charles River à la complétion de la formation.

En tant que Technicien·ne en soins aux animaux pour notre équipe de Toxicologie située au site de Senneville ou Laval vous serez responsable du bien-être de tous nos animaux de recherche. Votre réussite assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Nettoyer tous les types d’habitacles d’animaux et leurs accessoires.
Manipuler les animaux pour toutes activités qui le requiert;
Faire la prise de données (prise de poids, consommation de nourriture, signes cliniques).

Éléments clés

Les qualifications minimales recherchées pour cette formation sont les suivantes :

Avoir obtenu au moins les unités de 3e secondaire
- ou l’équivalent en langue d’enseignement, en langue seconde et en mathématique;
- ou avoir obtenu une attestation d’équivalence de niveau de scolarité (AENS);
- ou avoir réussi le test de développement général (TDG) avec ou sans préalable spécifique.
Avoir interrompu ses études à temps plein pendant au moins douze mois;
- ou avoir 18 ans au moment de l’entrée en formation;
- ou avoir obtenu un diplôme d’études secondaires (DES) ou un diplôme d’études professionnelles (DEP) ou leur équivalent;
- ou satisfaire aux normes d’admissibilité de la Mesure de la formation de la main-d’œuvre d’Emploi-Québec. (Cette AEP est admissible à la passerelle CFMS-AEP.)
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc,);
Bonne attention aux détails;
Capacité à suivre des instructions et des délais de temps précis;
Capacité à travailler de façon indépendante et en collaboration au sein d’une équipe.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise

Informations spécifiques à la formation:

Localisation du centre de formation Korpus: 2100, rue Cunard, Laval (QC) H7S 2G5
Localisation des sites de travail Charles River:
- Laval - 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3 (Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique)
- Senneville - 22022 route Transcanadienne, Senneville, QC, H9X 1C1 (Service de navette offert par Charles River depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique)
Salaire: 21$
Durée de la formation: 5 mois
Horaire de formation: Lundi au vendredi de 8h-16h15.
Horaire régulier suivant la formation: Jour, soir et nuit au besoin, Rotation de fin de semaine et journées fériées.

Pourquoi Charles River?

Programme d'aide aux employé·es et à leur famille;
Excellent programme d’intégration à nos nouveaux employé·es;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Inventory Clerk (Laval, Quebec, CA, H7V 4B3)

Job Summary

As an Inventory Clerk for our Lab Sciences team at the Laval location, you will manage products and supplies necessary for the proper functioning of department.

In this role, primary responsibilities include:

In charge of the reception, inventory and the distribution of products (test items, chemicals, consumable products, chromatographic columns, for example), as well as all the related documentation;
Responsible for placing the orders for the department;
Participate in maintaining inventory of products and supplies in sufficient quantity.

Key Elements

If you have the following qualifications, we'll train you for the rest:

High School Diploma;
At least 1-2 years’ experience working in a laboratory setting;
Team player with a collaborative and positive approach;
Strong observation & organizational skills;
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).

Role Specific Information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Salary: 24.75$/hrs;
Annual bonus based on performance;
Schedule: Monday to Friday daytime; Depending on the business needs, you may have to do overtime;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Commis aux inventaires (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Commis aux inventaires pour notre équipe de Science de laboratoire située au site de Laval vous serez responsable de la gestion des produits et des fournitures nécessaire au bon fonctionnement du département.

Dans ce poste, les principales responsabilités incluront:

Responsable de l’accueil, de l’inventaire et de la distribution des produits (articles de test, produits chimiques, produits consommables, colonnes chromatographiques, par exemple), ainsi que de toute la documentation associée;
Responsable de la passation des commandes pour le département;
Participer au maintien de l’inventaire des produits et fournitures en quantité suffisante.

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste :

Diplôme d’études secondaires;
Au moins 1 à 2 ans d’expérience de travail en laboratoire;
Capacité à travailler en équipe avec une approche collaborative et positive;
Solides compétences en observation et en organisation;
Capable de travailler physiquement (soulever jusqu’à 20 kg, marcher, rester debout, se pencher, etc.).

Informations spécifiques au poste:

Localisation: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Salaire: 24.75$/hrs;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi de jour. Selon les besoins de l’entreprise, vous devrez effectuer du temps supplémentaire;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Occupational Health Nurse (Laval, Quebec, CA, H7V 4B3)

Job Summary

As an Occupational Health Nurse for our team at the Laval location, you will be responsible for site clinical management and administration of occupational health services, procedures, and programs for local health & wellness operations. You will also manage medical aspects of work-related injuries/illnesses and return to work processes.

In this role, primary responsibilities include:

Provide systematic assessment and nursing diagnosis of work-related injuries/illnesses;
Advise managers/supervisors on light duty placement, ergonomics, or job modification;
Assist Human Resources and department management with planning for injured employees to return to work from leave;
Work with management, employees, medical doctors, and insurance carriers in developing proper accommodation for returning employees;
Provide health services in person and virtually, including health counseling and injury prevention education, first aid and medical treatment for minor injuries;
Develop, implement, and maintain updated procedures and programs for employee work-related medical issues aligned with Corporate Occupational Health.

Key Elements

We are looking for the following minimum qualifications for this role:

Bachelor’s degree in Nursing;
Be a member of Quebec Order of Nurse;
Minimum 3 to 5 years of relevant experience;
Able to do blood collection;
Excellent interpersonal skills, self-control, tact, diplomacy, teamwork and collaborative spirit;
Autonomy and attention to detail.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role Specific Information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Annual bonus based on performance;
Schedule: Monday to Friday, daytime;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Annual Quebec Order of Nurse membership refunded;
We offer competitive benefits and advantages from day one to support your well-being;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 10 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Infirmier.ère en Santé au travail (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant qu’Infirmier.ière en Santé au travail pour notre équipe située au site de Laval, vous serez responsable de la gestion clinique du site et de l'administration des services, procédures et programmes de santé au travail pour les opérations locales de santé et de bien-être. Vous aurez aussi à gérer les aspects médicaux des blessures/maladies liées au travail et les processus de retour au travail.

Dans ce poste, les principales responsabilités incluront:

Fournir une évaluation systématique et un diagnostic infirmier des blessures/maladies liées au travail;
Conseiller les directeurs/superviseurs sur l'affectation à des tâches légères, l'ergonomie ou la modification du travail;
Aider les ressources humaines et la direction du service à planifier le retour au travail des employés blessés après leur congé;
Collaborer avec la direction, les employés, les médecins et les compagnies d'assurance pour mettre au point des aménagements appropriés pour les employés qui reviennent au travail;
Fournir des services de santé en personne et virtuellement, y compris des conseils en matière de santé et d'éducation à la prévention des blessures, des premiers soins et des traitements médicaux pour les blessures mineures;
Élaborer, mettre en œuvre et tenir à jour des procédures et des programmes pour les problèmes médicaux liés au travail des employés, en accord avec le service de santé au travail de l'entreprise.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Baccalauréat en Sciences infirmières;
Être membre de l’Ordre des infirmiers.ères du Québec;
Minimum de 3 à 5 ans d'expérience pertinente;
Apte à effectuer des prélèvements sanguins;
Excellentes habiletés interpersonnelles, maîtrise de soi, tact, diplomatie, travail d'équipe et esprit de collaboration;
Autonomie et souci du détail.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au poste:

Localisation: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi de jour;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Cotisation annuelle à l’Ordre des infirmiers.ères du Québec remboursée;
Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 10 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Technicien.ne en histologie (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Technicien.ne en Histologie pour notre équipe située à Laval, vous serez responsable de préparer les tissus pour des fin d’évaluation microscopique. Votre réussite assurera le bon déroulement de nos recherches, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Effectuer certaines activités d’histologie telles que le rognage, la décalcification, le traitement, l’enrobage, la coupe, la coloration et le balayage;
Préparer le matériel nécessaire demandé par les procédures;
Opérer les équipements de laboratoire nécessaire;
Préparer les réactifs chimiques;
Préparer l’expédition et l’emballage des spécimens.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes:

Diplôme collégial en Science, en Biotechnologie ou toutes autres disciplines en lien avec la science;
Capable de faire preuve d’une grande minutie;
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).

Informations spécifiques au rôle:

Localisation : 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Salaire : À partir de 21.50$/hrs;
Bonus annuel basé sur la performance
Horaire : De jour & de soir. Selon les besoins de l’entreprise vous devrez être disponible de jour, de soir, de fin de semaine ainsi que les jours fériés. Les heures régulières de travail sont de 8h à 16h15, mais peuvent être appeler à changer en fonction des études en cours;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Formations de développement payées;
Programme d'aide aux employés et à leur famille;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
3 semaines de vacances & 5 jours de congé personnel/maladie par année;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Histology Technician (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Histology Technician for our team located in Laval, you will be responsible for preparing tissues for microscopic analysis. Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Perform histology activities such as trimming, decalcification, processing, embedding, cutting, scanning, and staining;
Prepare necessary material requested by procedures;
Operate necessary laboratory equipment;
Prepare chemical reagents;
Prepare shipment and packing of specimens.

Key Elements

We are looking for the following minimum qualifications for this role:

Collegial Diploma in Science, Biotechnology, or any other related field;
Able to demonstrate a high level of attention to details;
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).

Role Specific Information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Salary: Starting at $21.50/hrs;
Annual bonus based on performance plan;
Schedule: Days & Evening shifts. Depending on the needs you must be available to work during days, evening, weekends, and holidays. Regular working hours are between 8am to 4:15 pm, but may be subject to change depending on current studies;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Paid development training;
Employee and family assistance program;
Access to a doctor and various health professionals (telemedicine);
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
3 weeks’ vacation & 5 sick/personal days per year;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Stagiaire d'été - Santé Animale (Laval, Quebec, CA, H7V 4B3)

Sommaire de l’emploi

En tant que stagiaire d’été en santé animale pour notre équipe de Toxicologie à notre site de Laval, vous aurez la charge de veiller au bien-être de tous nos animaux ainsi qu’à intégrité de nos études pré-cliniques.

Dans ce rôle, les principales responsabilités incluront:

Assurer la propreté de l’environnement de vie des animaux selon les plus hauts standards de bien-être de l'industrie
Assister les techniciens dans leurs tâches quotidiennes
Manipuler les animaux;
Participer aux activités physiques/sociales des animaux

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Être étudiant.e en Technique en santé animale, Technique en Bioécologie ou Technique en Biotechnologie.
Capable de suivre des instructions précises.
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).
Bonne compréhension de l’anglais écrit.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose.

Information spécifique au poste :

Localisation:445 Boul. Armand-Frappier, Laval, QC, H7V 4B3 ;
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Salaire: 19.00 $ de l’heure
- Fin de semaine : 2.75$;
- Heure supplémentaire : Temps et demi;
- Fériés : Temps Double.

Horaire : Poste d’été (37.5HR/semaine). Possibilité de rester à l’automne à discuter. Selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaire.

Pourquoi Charles River?

Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Summer Intern - Animal Health (Laval, Quebec, CA, H7V 4B3)

Job Summary

As an Intern in Animal Care for our Toxicology team in Laval, you will be responsible of ensuring the welfare of the animals and the integrity of our pre-clinical studies.

In this role, key responsibilities include:

Ensure the cleanliness of the living environment of the animals according to the highest standards of welfare in the industry.
Assist the technicians in their daily tasks.
Handle animals.
Participate in the physical/social activities of the animals.

Key Elements

We are looking for the following minimum qualifications for this role:

Be a student in Animal Health Technology, Wildlife Management technology or Biotechnology.
Able to follow precises instructions.
Being able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).
Understanding of written English.
Passionate about animals.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Job specific information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;

Pay: $19.00 per hour.
- Weekend: $2.75;
- Overtime: Time and a half;
- Holidays: Double time;

- Schedule: During summer (37.5 hours/week), possibility to stay after school to be discuss. Depending on the needs, you may have to do overtime.

Why Charles River?

Employee and family assistance program;
Excellent welcome program for new employees;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Étudiant.e d'été - commis à l'entretien et à la sanitation (Laval, Quebec, CA, H7V 4B3)

Sommaire de l’emploi

Poste étudiant – Temporaire, temps plein. Aucune expérience requise.

En tant qu’étudiant.e d’été commis à l'entretien et à la sanitation pour notre équipe de Toxicologie situé au site de Laval, vous serez responsable du bien-être de tous nos animaux de recherche. Votre réussite assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Préparer et décontaminer les salles d’animaux selon l’échéancier prévu;
S’assurer que le matériel requis pour l’étude est disponible;
Manipuler les animaux pour toute activité qui le requiert;
Retirer les déchets domestiques et biomédicaux et en disposer dans les contenants appropriés;
Faire fonctionner le lave-cage.

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Étudiant.e au niveau collégial ou l’équivalent;
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.);
Capacité de suivre des instructions précises;
Capacité à gérer son temps efficacement;
Capacité à travailler de manière autonome;
Environnement chaud et humide dans les zones de lavage du matériel;
Présence de produits chimiques dans l’environnement de travail.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au poste:

Localisation: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique
Salaire: 18,25$/hrs
Horaire: Horaire flexible 7,5 heures/jour, de jour ou de soir (ex. de 8h à 16h15 ou de 15h à 23h15) Selon les besoins opérationnels, vous pourriez avoir à travailler les fins de semaine
Poste temporaire, temps plein à 37.5hrs par semaine

Pourquoi Charles River?

• Excellent programme d’intégration à nos nouveaux employés;
• Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Summer student - maintenance and sanitation clerk (Laval, Quebec, CA, H7V 4B3)

Job Summary

Student position – Temporary, full-time. No experience needed.

As a summer student as a maintenance and sanitation clerk for our Toxicology team located at the Laval site, you will be responsible for the welfare of all our research animals. Your success will ensure the health of our animals, as well as the integrity of our preclinical studies.

In this role, primary responsibilities include:

Prepare and decontaminate animal rooms according to the scheduled schedule;
Ensure that the materials required for the study are available;
Handle animals for any activity that requires it;
Remove household and biomedical waste and dispose of it in the appropriate containers;
Operate the cage washer.

Key Elements

If you have the following qualifications, we'll train you for the rest:

College student or equivalent;
Able to perform physical work (lifting up to 20 kg, walking, standing, squatting, etc.);
Able to follow precise instructions;
Ability to manage time effectively;
Ability to work independently;
Hot and humid environment in equipment washdown areas;
Presence of chemicals in the work environment.

Please note that upon hiring you will be required to undergo an annual tuberculosis test at the company's expense.

Informations spécifiques au poste:

- Localisation: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3
- Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique
- Salary: $18,25/hr
- Schedule: Flexible schedule of 7.5 hours/day, day or evening (e.g., 8:00 a.m. to 4:15 p.m. or 3:00 p.m. to 11:15 p.m.) Depending on operational needs, you may be required to work weekends
- Temporary position, full-time at 37.5 hours per week

Why Charles River ?

Excellent welcome program for new employees;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Étudiant.e d'été - Opérateur.trice au lave cage (Laval, Quebec, CA, H7V 4B3)

Sommaire de l’emploi

Poste étudiant – Temporaire, temps plein. Aucune expérience requise.

En tant qu’étudiant.e d’été comme commis au lavage de cages pour notre équipe de Toxicologie situé au site de Laval, vous serez responsable du bien-être de tous nos animaux de recherche. Votre réussite assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Laver le matériel nécessaire pour les études (ex : cages, jouets, bols) manuellement avec un tuyau d’arrosage et en utilisant le lave-cage industriel
Ranger le matériel une fois propre
Laver le linge nécessaire pour les études (ex : gants anti-coupures, draps) en utilisant les laveuse et sécheuse industrielles
Effectuer les tâches de nettoyage dans le vivarium (ex : passer le balai, laver le sol avec la zamboni)
Remplir les stations PPE (Équipement de Protection Individuelle)
Préparation d’enrichissement pour les animaux

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Étudiant au niveau collégial
Travail physique qui nécessite de lever, porter, déplacer des charges lourdes et d’effectuer la majorité des tâches en position debout
Mouvements répétitifs
Le niveau de bruit est habituellement élevé
Environnement chaud et humide dans les zones de lavage du matériel
Présence de produits chimiques dans l’environnement de travail
Respect des procédures
Très bonnes aptitudes à travailler en équipe

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au poste:

Localisation: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique
Salaire: 18.25$/hrs
Horaire: Semaine de 37,5h avec journée de 7,5h (ex : 8h-16h15, 10-18h15 ou 13h30-21h45), selon les besoins de l’entreprise vous pourriez faire des quarts de fin de semaine
Poste temporaire, temps plein à 37.5hrs par semaine

Pourquoi Charles River?

Excellent programme d’intégration à nos nouveaux employés;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Summer Student - Cage Washer Operator (Laval, Quebec, CA, H7V 4B3)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

Student Position – Temporary, Full-time. No experience required.

As a summer student as a cage wash clerk for our Toxicology team located at the Laval site, you will be responsible for the welfare of all our research animals. Your success will ensure the health of our animals, as well as the integrity of our preclinical studies.

In this role, primary responsibilities include:

- Wash study equipment (e.g., cages, toys, bowls) manually with a garden hose and using the industrial cage washer.
- Put away clean equipment.
- Wash study linens (e.g., cut-resistant gloves, sheets) using the industrial washer and dryer.
- Perform cleaning tasks in the vivarium (e.g., sweeping, mopping the floor with the Zamboni).
- Refill PPE (Personal Protective Equipment) stations.
- Prepare animal enrichment.

Key Elements

If you have the following qualifications, we'll train you for the rest:

College student
Physical work requiring lifting, carrying, and moving heavy loads, and performing most tasks while standing
Repetitive movements
Noise levels are usually high
Hot and humid environment in equipment wash areas
Presence of chemicals in the work environment
Compliance with procedures
Excellent teamwork skills

Please note that upon hiring you will be required to undergo an annual tuberculosis test at the company's expense.

Role Specific Information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Salary: $18.25/hr
Schedule: 37.5-hour work week with 7.5-hour days (e.g., 8 a.m. to 4:15 p.m., 10 a.m. to 6:15 p.m., or 1:30 p.m. to 9:45 p.m.). Depending on the company's needs, you may be able to work weekend shifts
Temporary position, full-time at 37.5 hours per week

Why Charles River ?

Excellent welcome program for new employees;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.