Befristeter Vertrag: 18 Monate -Human Resources Business Partner (m/w/d) (Sulzfeld, Bavaria (Bayern), DE, 97633)

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

An unserem Standort in Sulzfeld bieten wir eine Stelle als Human Resources Business Partner (HRBP) an. Sie verstärken unser HR-Team und unterstützen und beraten bei HR-relevanten Themen und Prozessen.

Zu den Hauptaufgaben dieser Position gehören:
- Enge Zusammenarbeit mit dem line-Management, um die korrekte Anwendung von HR-Richtlinien und -Praktiken sicherzustellen. Bei Bedarf sollen Änderungsvorschläge für Richtlinien und Praktiken unterbreitet werden.
- Coaching und Zusammenarbeit mit Führungskräften bei der Lösung komplexer Probleme im Bereich der Mitarbeiterbeziehungen; bei Bedarf soll rechtliche Beratung eingeholt werden.
- Vorbereitung von Betriebsratsinformationen und der erforderlichen Dokumente.
- Sicherstellung der zeitnahen Bearbeitung von Dokumenten und Transaktionen, Übermittlung relevanter Vertragsinformationen, zeitnahe Eingabe von Änderungen in das HR-System, Digitalisierung und Aktualisierung der Personalakten. Aktualisierung und Aufrechterhaltung der SOX-Kontrollen und Gewährleistung der vollständigen Compliance/Prüfung von HR-Daten.
- Sicherstellung der Einhaltung lokaler, staatlicher und bundesstaatlicher Vorschriften und Pflege der erforderlichen Dokumentation zu Compliance-Zwecken; Überwachung und Prüfungen der HR-Dokumentation nach Bedarf.
Unterstützung der Führungskräfte bei der Analyse ihrer Profilanforderungen zur Personalbeschaffung, Erstellung und Veröffentlichung von Stellenanzeigen; Auswahl und Durchführung von Vorstellungsgesprächen, Bewertung von Kandidaten, Beratung der Führungskräfte und Unterbreitung von Stellenangeboten.
- Analysieren und Bearbeiten von Änderungen der Vergütung und der Zusatzleistungen, Durchführung des jährlichen Lohnerhöhungsprozesses und der Bonusauszahlungen und Erstellen der entsprechenden Dokumentation.
- Unterstützen bei den Onboarding- und Offboarding-Prozessen und Sicherstellen, dass alle erforderlichen Dokumentationen und Systemaktualisierungen vollständig sind. Führen von Onboarding-Meetings und Kündigungsgesprächen.
-Sie kommunizieren aktiv vor Ort, um Führungskräfte und Mitarbeiter über HR-relevante Themen zu informieren.

Für diese Position erwarten wir folgende Mindestqualifikationen:
-Bachelor-Abschluss im Bereich Personalmanagement (People & Culture Studies);
-3 Jahre einschlägige Berufserfahrung als HR-Generalist/HRBP oder in einer ähnlichen Funktion.
-Gute Englischkenntnisse sind für die Position erforderlich.
-Proaktiver Teamplayer, sowohl abteilungsintern als auch unternehmensweit.

Rollenspezifische Informationen:
• Befristeter Vertrag: 18 Monate
• Standort: 97633 Sulzfeld; Kostenlose Parkplätze.
Arbeitszeit: Montag bis Freitagmittag, Vollzeitbeschäftigung bevorzugt, Teilzeit ist jedoch möglich.
Ein Arbeitstag zu Hause nach 6 Monaten in der Position ist möglich.

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.

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.

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.

Mitarbeiter/in in der Tierpflege (m/w/d) (Sulzfeld, Bavaria (Bayern), DE, 97633)

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.

Zum nächstmöglichen Zeitpunkt suchen wir Sie als

Tierpfleger / Mitarbeiter in der Tierbetreuung (m/w/d)

in Vollzeit

für unsere Niederlassung in 97633 Sulzfeld.

Ihre Aufgaben:

Betreuung, Zucht und Haltung unserer Labornager
Einhaltung der internen Qualitätsvorgaben und Arbeit unter sterilen Bedingungen
Dokumentationserstellung
Mitarbeit an der Verbesserung von Arbeitsabläufen

Die Anforderungen:

Freude am professionellen Umgang mit Tieren
Teamgeist
Einsatzbereitschaft und Sorgfalt
Körperliche Belastbarkeit
EDV-Kenntnisse erwünscht

Unser Angebot:

· eine ausführliche und betreute Einarbeitung im Rahmen unseres Trainingskonzepts

· ein leistungsgerechtes Einkommen

· eine interessante und verantwortungsvolle Tätigkeit in einem zukunftsorientierten Team

· Teilnahme an diversen Unternehmensveranstaltungen

· zahlreiche soziale Leistungen und Zuschüsse (z.B. zur Kinderbetreuung, Tankgutschein, VWL-Förderung u.v.m.)

Auch Bewerber ohne spezifische Vorkenntnisse/ Quereinsteiger sind uns willkommen!

Sie sind interessiert?

Dann freuen wir uns über die Zusendung Ihrer ausführlichen Bewerbungsunterlagen an:

Charles River Laboratories, Research Models and Services, Germany GmbH

Personalabteilung, Sandhofer Weg 7, 97633 Sulzfeld

Email: BewerbungenRMS@crl.com, www.criver.com

Für Vorabinformationen stehen wir Ihnen gerne unter der Telefonnummer 09761 406-11 zur Verfügung.

Über Research Models & Services

Für die Grundlagenforschung ist die Verwendung von In-vivo-Modellen zur Identifikation von Zielkrankheiten und potentieller biologischer Pfade, welche Krankheiten bestimmen, notwendig. Als eines der weltweit führenden Unternehmen für die Produktion und den Vertrieb von Versuchstieren der höchsten Qualität, welches die Hälfte aller Versuchstiermodelle weltweit für die präklinische Forschung liefert, verstehen wir, wie wichtig dieser Schritt ist. Mit sieben Jahrzehnten Erfahrung ist unser Know-how unerreicht, sodass wir das perfekte Modell liefern können, einschließlich krankheitsspezifischer und konditionierter Optionen, für die Grundlagenforschung und darüber hinaus.

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.

Veterinary Technician Assistant I (Reno, NV, US, 89511)

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

We are seeking a Veterinary Technician Assistant for our Safety Assessment site located in Reno, Nevada.

The Veterinary Technician Assistant will assist veterinary staff in the documentation and triage of all laboratory animal health cases In addition, this individual will may also perform technical in-life procedures.

Job Qualifications

MINIMUM QUALIFICATIONS:

Education: High School Diploma or G.E.D.
Experience: 1-2 years related experience in a laboratory animal facility. related experience working with animals in pre-clinical laboratory or clinical setting; experience working with 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.
Certification/Licensure: ALAT preferred
Other: None.

PREFERRED QUALIFICATIONS:

LVT license or CVT/RVT certification.
AALAS certification.

The pay range for this position starts at $20.50 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 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.

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.

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.

Veterinary Technician I - $5,000 Sign On Bonus! (Reno, NV, US, 89511)

Job Summary

***Position is eligible for a $5,000 sign on bonus!***

The Veterinary Technician 1 is responsible for assisting the veterinarians in documentation, triage, and management of laboratory animal health cases. Also responsible for daily health observations, preventive health care, environmental enrichment and handling and restraining of laboratory animals.

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 skills including the following:
Assess and follow-up on animal health concerns
Generate animal treatment records and perform, track and schedule follow-ups
Administration of various therapeutic measures by IV, IM, SQ, topical, oral routes, etc.
Bandage/wrapping techniques.
Nail/teeth clipping/trimming.
Venipuncture techniques.
Perform radiographs as required.
Daily walk through of animal rooms
Proficient animal restraint techniques.
Monitor critical care animals (i.e., place IVs, monitor fluids, etc.).
Participate in colony management (new NHP processing, TB testing, collection of biological samples, routine health monitoring, etc.)
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.
Responsible for tissue sampling, routine animal manipulations and administration of fluids or other treatments as required.

Job Qualifications

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.
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.
LVT license or CVT/RVT certification preferred. Uncertified candidates must have Vet Tech in Training (VTIT) and will be required to receive certification within 12-18 months or show that certification has been substantially completed. AALAS certification desired.

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

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

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

Research Analyst I -Bioanalytical Sciences (Reno, NV, US, 89511)

Job Summary

We are seeking a Research Analyst I for our Safety Assessment site located in Reno, NV.

This position will be responsible for handling and processing samples and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies.

Job Qualifications

The following are minimum requirements related to the Research Analyst 1 position.

Associate's degree (A.A. / A.S) or equivalent in biological science or related discipline required. Bachelor’s degree (B.A. / B.S.) preferred.
6 Months minimum 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.
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.

The pay for this position starts at $24/hr. 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 HVAC Technician (Reno, NV, US, 89511)

Job Summary

We are seeking a Senior HVAC Technician for our Safety Assessment site located in Reno, Nevada.

Perform a variety of master-level mechanical and pressure/temperature equipment repairs and maintenance requiring close interface with other trade/craft functions. Perform other semi-skilled tasks in the general maintenance of the physical plant and provide work direction to others performing HVAC projects.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Monitor and maintain HVAC systems including high/low temperature, water and electricity. Isolate and identify malfunctioning equipment for repair, adjustment, and replacement. Interpret instructions as required
•   Observe and interpret readings on gauges, meters, and charts to ensure correct functioning of systems. May calibrate equipment.
•   Perform adjustments, repairs and replacement of parts and equipment following written specifications such as blueprints, drawings and schematics.
•   Dismantle equipment fixtures and plan systematic replacement or repair of accessories and parts and return equipment to operation.
•   Oversee HVAC-related tasks being performed by other department personnel.
•   Inspect completed work for quality, safety, and proper operation.
•   Coordinate maintenance work with other departments and divisions; maintain accurate records of maintenance and repair work.
•   Periodically perform preventative maintenance programs as required.
•   Perform other semi-skilled tasks as assigned to assist in the general maintenance of the physical plant.
•   Respond to emergencies as needed. Provide 24-hour on-call maintenance coverage, as scheduled in rotation
•   May perform waste vacuum maintenance.
•   Take proper safety precautions and utilize appropriate safety gear/equipment in the performance of all duties.
•   Perform all other related duties as assigned.

Job Qualifications

•   Education: High school diploma or General Education Degree (GE.D.). Completion of trade school or formal apprenticeship program.
•   Experience: Five or more 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: Valid EPA 608 certification.
•   Other: None

The pay range for this position starts at $39.00/hr. 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

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.

Security Officer - Part Time (Reno, NV, US, 89511)

Job Summary

***This position covers weekends, Saturday - Sunday from 6:00pm to 6:00am****

We are seeking a Security Officer for our Safety Assessment site located in Reno, NV.

Ensures the protection of organizational personnel and company property against fire, theft, vandalism, illegal entry, and other hazards. Inspects credentials and facilities, and reports irregularities, alarm activation and tampering. Develops, implements and administers programs designed to protect organizational personnel and property. Ensures compliance with government and organization security policies and procedures and protects and safeguards intellectual property. Conducts investigations to identify and document instances of noncompliance and possible breaches in law.

The following are responsibilities related to the Security Officer:

•   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; conducts patrols and monitors the status of the physical security measures; and monitors 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 generates 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. Provides effective secondary communication during business hours; and primary communications during non-business hours.
•   Contact emergency personnel as required and in accordance with
•   Assist in directing appropriate emergency response efforts when required.
•   Perform all other related duties as assigned.
•   We are also seeking an individual to work on the weekends but may be available to provide coverage for others during the week, during vacation, and sick leaves

Job Qualifications

The following are minimum qualifications related to the Security Officer position:

Education: High school diploma, General Education Degree (G.E.D.) or the equivalent. Associates degree preferred.
Experience: 2 -3 years experience with at least Six to twelve months of related security experience and/or training.
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 Drivers license
Other: None

The pay for this position starts at $19/hr. 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.

Animal Care Technician - Group Housing (Reno, NV, US, 89511)

Job Summary

We are seeking a Group Housing Technician for our Safety Assessment site located in Reno, Nevada.

Responsible for performing operational, administrative and technical tasks to provide comprehensive care for all nonhuman primates at the site, including: daily health observations, feeding/watering, sanitizing primary and secondary enclosures, environmental enrichment, handling and restraint, generating and recording data and related tasks. Assist with the movement of animals and stocking of supplies.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform in-life technical procedures (e.g., handling, body weight).
Input and edit computer entries (e.g., LIMS data capture for husbandry and animal health)
Observe animals for general health and overall well being.
Clean primary enclosure and enclosure area for animals.
Sanitize group housing units, enrichment devices and other related equipment.
Measure and distribute feed to animals in accordance with established procedures.
Prepare and provide environmental enrichment.
Collect monthly animal bodyweights.
Assist with handling and restraint habituation activities.
Inspect feeding and watering devices for proper function.
Review documentation of functions performed as part of quality control requirements.
Stocking of supplies for group housing.
Retrieve and view Standard Operating Procedures using appropriate database.
Use GLPs, SOPs, processes and company policies when performing all job functions.
Handle, restrain, and provide care for all nonhuman primates at the site.
Maintain clean work areas (e.g.: laboratory area, primary enclosures, animal exam areas).
Receive animals (e.g., general health observation, sexing and identification).
May perform basic veterinary technical and husbandry tasks with guidance, including the following:
Administration of various therapeutic veterinary treatment as needed.
Assist with animal receipt processing; sedation, animal handling, and physical exam recording.
Proficient animal restraint techniques.
Veterinary Rounds and behavior treatments.

Job Qualifications

•    Education: High school diploma or General Education Degree (G.E.D.) required.
•    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.

***The pay range for this position starts at $19.75. 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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

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

Surgical Laboratory Technician I (Reno, NV, US, 89511)

Job Summary

Job Qualifications

Equal Employment Opportunity

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

Commis aux soins des animaux (St. Constant, Quebec, CA, J5A 2E7)

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

En tant que Commis aux soins des animaux pour notre site d’élevage situé à St-Constant, vous serez responsable du bien-être de nos animaux de recherche. Votre réussite assurera la santé de nos animaux.

Dans ce poste, 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 (nettoyer les salles d’animaux ainsi que les cages);
Manipuler les animaux avec soins;
Participer aux activités physiques/sociales des animaux.

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

AEP en soins animaliers (atout);
Apte à travailler physiquement (soulever jusqu’à 20-25kg, marcher, rester debout, s’accroupir, etc.);
Avoir un bon esprit d’équipe;
Passion pour les animaux.

Informations spécifiques au poste:

Localisation : 324 Rang St-Régis Nord, St-Constant, J5A 2E7;
Transport : Stationnement gratuit;
Salaire : 18$/hrs;
Horaire : Du lundi au vendredi, entre 6h00 et 14h15. Selon les besoins de l’entreprise, vous pourriez avoir à faire du temps supplémentaire ainsi que des fin de semaine;
Poste temps plein, 40 heures par semaine;
Poste temporaire à l’embauche & après la période de probation de 6 mois, poste permanent.

Pourquoi Charles River?

Aucune expérience préalable requise;
Des heures garanties, car le milieu de la recherche est très en demande;
Excellent programme de formation continue;
Opportunités de développement professionnel.

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 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 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.

Animal Care Clerk (St. Constant, Quebec, CA, J5A 2E7)

Job Summary

As an Animal Care Clerk for our Husbandry facility located in St-Constant, you will be responsible for the well-being of our laboratory animals. Your contribution will ensure the health of our animals.

In this role, primary responsibilities include:

Ensure the cleanliness of the living environment of the animals according to the highest standards of welfare in the industry (clean the animal rooms and the cages);
Handle animals with care;
Participate in the physical/social activities of the animals.

Job Qualifications

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

AEP in Animal Care (asset);
Able to work physically (lift up to 20-25 kg, walk, stand, stoop, etc.);
Have a good team spirit;
Passion for animals.

Role Specific Information:

Location: 324 Rang St-Régis Nord, St-Constant, J5A 2E7;
Transport: Free parking;
Salary: $18/hrs;
Schedule: Monday to Friday, between 6:00 am to 2:15 pm. Depending on the needs, you may have to do weekends and/or overtime;
Full-time position, 40 hours per week;
Temporary position at the hiring & after the probation period of 6 months, permanent position.

Why Charles River ?

No experience needed;
Guaranteed hours - The research field is in high demand;
Paid development training;
Professional development opportunities.

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.

Étudiant.e - Commis aux soins des animaux (St. Constant, Quebec, CA, J5A 2E7)

Sommaire de l'emploi

Emploi étudiant - 15hrs par semaine lors de la période scolaire et 40hrs par semaine cet été

Dans ce poste, les principales responsabilités incluront:

Nettoyer les salles d’animaux;
Nettoyer les cages d’animaux;
Manipuler les animaux avec soins.

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Apte à travailler physiquement (soulever jusqu’à 20-25kg, marcher, rester debout, s’accroupir, etc.);
Avoir un bon esprit d’équipe;
Passion pour les animaux.

Informations spécifiques au poste:

Localisation : 324 Rang St-Régis Nord, St-Constant, J5A 2E7;
Transport : Stationnement gratuit;
Salaire : 18$/hrs;
Horaire : Tous les samedis et dimanches, horaire entre 6h00 et 14h15;
Poste temps partiel, 15 heures par semaine – 40hrs par semaine cet été.

Pourquoi Charles River?

Aucune expérience préalable requise;
Des heures garanties, car le milieu de la recherche est très en demande;
Excellent programme de formation continue;
Opportunités de développement professionnel.

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.

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

Student - Animal Care Clerk (St. Constant, Quebec, CA, J5A 2E7)

Job Summary

Student job - 15hrs per week during school term and 40hrs per week this summer

In this role, primary responsibilities include:

Cleaning the animal rooms;
Cleaning the animal cages;
Animals handling.

Key Elements

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

Able to work physically (lift up to 20-25 kg, walk, stand, stoop, etc.);
Have a good team spirit;
Passion for animals.

Role Specific Information:

Location: 324 Rang St-Régis Nord, St-Constant, J5A 2E7;
Transport: Free parking;
Salary: $18/hrs;
Schedule: Saturday and Sunday, schedule between 6:00 am to 2:15 pm;
Part-time position, 15 hours per week – 40hrs per week this summer.

Why Charles River ?

No experience needed;
Guaranteed hours - The research field is in high demand;
Paid development training;
Professional development opportunities.

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.

Animalier.ière (Fleurimont, Quebec, CA, J1E 0B5)

Sommaire du poste

Technicien.ne en Soins aux Animaux – Formation sur place

En tant que Technicien.ne en Soins aux Animaux pour notre équipe de Toxicologie à notre site situé dans la ville de Sherbrooke (QC), 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

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

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.
Diplôme d'étude Secondaire (DES) requis - Diplôme AEP en soins animaliers est un atout.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose.

Information spécifique au poste :

Localisation : 1580 Rue Ida-Métivier, Sherbrooke (Qc), J1E 0B5.
Transport: Facilement accessible par le transport en commun (Rabais avec la Société des Transport de Sherbrooke). Stationnement gratuit. Borne de recharge pour voiture électrique.
Salaire : À partir de 18.50$/HR. Possibilité de commencer à un niveau supérieur avec un salaire plus élevé avec une expérience spécifique en recherche.
Horaire : Poste temps plein et permanent (37.5HR/semaine), selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaire. Travail de fin de semaine par rotation et Prime de quart (2.75$/HR).

Pourquoi Charles River?

3 semaines de vacances et des congés personnels.
Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire).
Accès à un programme d’épargne et de retraite qui comprend une contribution de l’employeur.
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne.
Gym gratuit sur place.
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine).

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.

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

Animal Care Technician (Fleurimont, Quebec, CA, J1E 0B5)

Job Summary

Animal Care Technician – On site training

As an Animal Care Technician for our Toxicology team for our site located in the city of Sherbrooke (QC), 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

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

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.
High School Diploma (DES) required - Having an AEP in Animal Care is an asset.

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: 1580 Ida Métivier, Sherbrooke (Qc), J1E 0B5.
Transportation: Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station.
Salary: Starting at 18.50$/hrs. Opportunity to start at higher level and higher salary with specific research experience.
Schedule: Full time, permanent position (37.5 hours/week), depending on the needs, you may have to do overtime. Weekend work (rotation) and bonus ($2.75/hour).

Why Charles River?

3 weeks’ vacation & Personal days.
Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage).
Access to a savings and retirement program that includes an employer contribution.
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).
Free gym on site.

If you want to contribute to the wellbeing of our communities across the country and around the world, join our team. 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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

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

Clinical Veterinary Surgeon (Tranent, GB, EH33 2NE)

Job Summary

An exciting opportunity has arisen for a veterinarian to join our dedicated team passionate about animal welfare. We are a growing group of 5 vets plus dedicated support staff.

At Charles River, we take a passionate approach to improving human and animal health. Our motivating force is the knowledge that our high quality of work provides people with the potential to live healthier and better lives. Scientific excellence and outstanding customer service are the hallmarks of Charles River.

As one of the world’s largest Contract Research Organisations with more than 7000 employees and a market leader in the development of novel human and veterinary medicines, Charles River can offer you the chance to build on your skills and knowledge and work with world-class experts. With more than 60 facilities in 16 countries, we have built a company uniquely designed to meet the needs of our clients in the Pharmaceutical, Biotechnology, Veterinary Medicine, and Agrochemical sectors.

At our world class preclinical facility in Elphinstone, Tranent (close to Edinburgh), our Department of Veterinary Services provides expert advice on animal health and welfare in a diverse mix of laboratory and farm animal species.

Acting as a deputy Named Veterinary Surgeon in accordance with the Animals (Scientific Procedures) Act, you will provide clinical care services to the broad range species at our site in Tranent. As a laboratory animal veterinarian, you are the advocate for the animals, you will use your clinical and interpersonal skills to ensure delivery of the highest standards of welfare, ethical consideration, and compliance in association with the Animal Welfare and Ethical Review Body.

You will assist in the conduct of clinical work across site, including medical and surgical case management, as well as supporting our studies by provision of specialist veterinary services in fields such as anaesthesia, surgery, and ophthalmology.

Due to high volume of applications we are receiving if you have not heard anything from Charles River Laboratories Edinburgh regarding the next steps of our recruitment process within 3 weeks of the closing date then please conclude you have been unsuccessful.

Job Qualifications

Eligibility for membership of the Royal College of Veterinary Surgeons and a relevant clinical work experience is essential.

You will have graduated with a Veterinary degree and have good observational and fine motor skills. You will have established skills in medicine and surgery translatable to the species you will be working with and the drive to expand your skillset. You will have the confidence and ability to communicate effectively with internal and external clients, as well as regulatory bodies. Previous experience in the laboratory animal field would be advantageous, although full training will be provided.

Participation in an out of hours on-call rota will be required although this is not onerous.

In return we offer a competitive salary and benefits package and a real commitment to your training and development needs. This includes the opportunity for undertaking, publishing and presenting relevant personal research, as we support and encourage you to develop your veterinary career.

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 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.

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.

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

Senior Data Scientist (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Senior Data Scientist, you will play a critical role in the process to help unlocking the value of data.

In this role, primary responsibilities include:

Lead and execute end to end data science projects, including problem formulation, data exploration, model development, validation, deployment and ongoing optimization for mission critical applications;
Collaborate closely with the Data Analysts team, Data Engineering team and DataOps team to automate and integrate data science solutions seamlessly into production pipelines;
Work collaboratively, in a consultative way, across the business units, advising on best approaches to leveraging data science in the most effective and efficient manner, including utilizing Generative AI technologies where applicable to develop cutting-edge 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.

Technical Expertise required:

Minimum of 5 years’ hands-on experience processing and analyzing large data sets;
Minimum of 3 years’ experience with the full Machine Learning product lifecycle process and able to take the initiative in making sure deadlines and requirements are met proactively;
Minimum of 5 years’ experience working with development toolsets such as SQL, PySpark, Python, Pandas, Scala;
Minimum of 2 years’ experience in data science projects focused on marketing, sales, or customer experience, delivering insights that drive business impact.

Role Specific Information:

Location: Remote
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 ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
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.

Equal Employment Opportunity

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

Scientifique de données sénior (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Scientifique de données sénior, vous allez jouer un rôle essentiel dans le processus visant à libérer la valeur des données.

Dans ce poste, les principales responsabilités incluront:

Diriger et exécuter des projets de science des données de bout en bout, y compris la formulation de problèmes, l'exploration de données, le développement de modèles, la validation, le déploiement et l'optimisation continue pour les applications critiques;
Collaborer étroitement avec l'équipe d'analystes de données, l'équipe d'ingénierie de données et l'équipe DataOps afin d'automatiser et d'intégrer les solutions de science des données de manière transparente dans les pipelines de production;
Travailler en collaboration, de manière consultative, avec les unités opérationnelles, en donnant des conseils sur les meilleures approches pour tirer parti de la science des données de la manière la plus efficace et la plus efficiente, y compris en utilisant les technologies d'IA générative, le cas échéant, pour développer des solutions de pointe.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Maitrise 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 autre domaine connexe;
Excellentes compétences en matière d'analyse et de 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 par le biais d'une riche visualisation des données;
Familiarité avec les méthodologies et les outils Agile;
Autonome et capable de travailler à la fois de manière indépendante et en collaboration au sein d'une équipe.

Expertise technique requise :

Au moins 5 ans d'expérience pratique dans le traitement et l'analyse de grands ensembles de données;
Au moins 3 ans d'expérience avec le processus complet du cycle de vie d'un produit d'apprentissage automatique et capacité à prendre l'initiative pour s'assurer que les délais et les exigences sont respectés de manière proactive;
Au moins 5 ans d'expérience dans l'utilisation d'outils de développement tels que SQL, PySpark, Python, Pandas, Scala;
Minimum 2 ans d’expérience dans des projets de science des données axés sur le marketing, les ventes, ou l’expérience client, fournissant des informations qui ont un impact sur les affaires.

Informations spécifiques au poste:

Localisation: Télétravail
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?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
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.

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

Animalier.ière (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Animaler.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: 18.50 $ de l’heure avec des primes de :
- Soirée : 2.50$;
- Fin de semaine : 2.75$;
- Heure supplémentaire : Temps et demi;
- Fériés : Temps Double.
Horaire: Majoritairement le jour, la fin de semaine en rotation et les 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?

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.

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: $18.50 per hour with primes of :
- Evenings: $2.50;
- Weekend: $2.75;
- Overtime: Time and a half;
- Holidays: Double time;
Schedule: Mostly days, weekend rotations and holidays with overtime on evenings or nights when needed;
Permanent position, 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.

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

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

Spécialiste de laboratoire (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que spécialiste de laboratoire pour notre site de Senneville, vous aurez à gérer les produits et fournitures nécessaires au bon fonctionnement des départements.

Dans ce poste, les principales responsabilités incluront:

Responsable de la réception, de l’inventaire et de la distribution de produits (substances d’essai, produits chimiques, consommables et colonnes chromatographiques, par exemple), ainsi que de tous les documents qui y sont reliés.
Responsable de faire les commandes du département.
Participer au maintien de l’inventaire des produits et fournitures en quantité suffisante.
Effectuer toute autre tâche connexe, telle qu’assignée.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Posséder un Diplôme d’études secondaires ;
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
Posséder un excellent sens de l’organisation et capacité à s'adapter aux changements;
Être capable de 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 : 24.25$/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 ?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Formations de développement payées;
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.

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

Laboratory Specialist (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Laboratory specialist for our Senneville site, you will manage products and supplies necessary for the proper functioning of departments.

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.
Perform all other related duties as assigned.

Key Elements

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

Possess a high school diploma;
An equivalent combination of education and experience may be considered an acceptable substitute for the specific education and experience listed above.
Flexible and able to adapt quickly to change
Ability to work as part of a team.

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: 24.25$/hrs;
Annual bonus based on performance;
Schedule: Monday to Friday, day schedule.
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);
Paid development training;
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 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

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.

Regional Biosafety Officer (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Regional Biosafety Officer for our Health and Safety team, you will be coordinating the Regional Biosafety Program to ensure our program meets federal, local and corporate requirements.

In this role, primary responsibilities include:

Coordinates the Regional Biosafety network; maintains appropriate memberships and licenses, coordinates/manages a regular meeting cadence, drives regional objectives, and maintains records.
Promotes and monitors compliance with applicable legislation, conditions of license, animal pathogen import permits, biosafety and biosecurity standards, the Biosafety Manual and standard operating procedures;
Arrange and document appropriate biosafety and biosecurity training for personnel
Develop/maintain supporting document management systems and tools to support the program including local risks assessments and inventories of regulated material.
Conduct periodic inspections and biosafety audits. Report audit findings to the license holder and animal pathogen import holder in writing of any non-compliance and drive resulting action plans to closure
Communicate with the Public Health Agency of Canada (PHAC) and the Canadian Food Inspection Agency (CFIA) on behalf of the license holder and animal pathogen import permit holder, as applicable.
Supports the review and approval of proposed work involving infectious and biological safety work conducted at site level
Collaborates with Global/ Regional EHS&S team to establish assessment and inspection tools to identify Biosafety risks associated with operations and creates solutions for gaps or opportunities for program improvement.

Key Elements

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

Technical or Bachelor’s degree in biological sciences;
3-5 years experience in biosafety work;
Experience working with NHP and asset;
Ability to inspire trust and confidence through strong interpersonal skills and effective collaboration;
Ability to effectively manage multiple projects simultaneously;
Bilingual (French & English).

Role Specific Information:

Locations (3):
- 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3(1-2x per week);
- 22022 route Transcanadienne, Senneville, QC, H9X 1C1 (3-4x per week);
- 580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5 (1x per month);
Annual bonus based on performance;
Schedule: Monday to Friday, Day schedule, On site;
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);
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.

Equal Employment Opportunity

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

Officier.e Biosécurité Régional (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant qu’ Officier.e Biosécurité Régional pour notre équipe de Santé et Sécurité, vous coordonnerez le programme régional de biosécurité pour garantir que notre programme répond aux exigences fédérales, locales et corporatives.

Dans ce poste, les principales responsabilités incluront:

Coordonner le réseau régional de biosécurité ; maintenir les adhésions et les licences appropriées, coordonner/gérer la fréquence des réunions, piloter les objectifs régionaux et tenir les dossiers à jours;
Favoriser et surveiller le respect de la législation applicable, des conditions de licence, des permis d'importation d'agents zoopathogènes, des normes de biosécurité et de biosûreté, du Manuel de biosécurité et des procédures opérationnelles normalisées;
Organiser et documenter la formation appropriée du personnel en matière de biosécurité et de biosûreté;
Élaborer et maintenir des systèmes et des outils de gestion des documents justificatifs pour soutenir le programme, notamment les évaluations des risques locaux et les inventaires de matières réglementées;
Effectuer des inspections et des audits de biosécurité périodiques. Signaler par écrit les constatations d'audit au titulaire de licence et au titulaire du permis d'importation d'agents zoopathogènes de toute non-conformité et met en œuvre les plans d'action qui en découlent jusqu'à leur résolution;
Communiquer avec l'Agence de la santé publique du Canada (ASPC) et l'Agence canadienne d'inspection des aliments (ACIA) au nom du titulaire de licence et du titulaire du permis d'importation d'agents zoopathogènes, le cas échéant.
Soutenir l'examen et l'approbation des projets de travaux de sécurité infectieuse et biologique menés sur site.
Collaborer avec l'équipe SST mondiale/régionale pour mettre en place des outils d'évaluation et d'inspection afin d'identifier les risques de biosécurité associés aux opérations et crée des solutions pour combler les lacunes ou améliorer les programmes.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

DEC ou BAC en sciences biologiques;
3-5 années d’expérience en de travail avec la biosécurité;
Experience de travail avec les NHP est un atout;
Capacité à inspirer confiance grâce à de solides compétences interpersonnelles et à une collaboration efficace ;
Capacité à gérer efficacement plusieurs projets simultanément;
Bilingue (français et anglais).

Informations spécifiques au poste:

Localisations (3):
- 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3 (1-2x par semaine);
- 22022 route Transcanadienne, Senneville, QC, H9X 1C1 (3-4 x par semaine);
- 580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5 (1x par mois);
Bonus annuel basé sur la performance;
Horaire: Lundi au vendredi de jours, sur site;
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);
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.

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

Technicien.ne en Laboratoires Cliniques (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Technicien.ne – Laboratoires cliniques

En tant que Technicien.ne pour notre équipe de Laboratoires cliniques située au site de Senneville, vous devrez accomplir les tâches techniques et suivre les directives des plans d’étude/phase et des PNO.

Dans ce poste, les principales responsabilités incluront:

Effectue les préparations ainsi que les analyses des échantillons;
Effectue le control de qualité ainsi que les maintenances sur les différents instruments;
Accomplis les activités en temps opportun en suivant les horaires établis;
Assure l’intégrité des études et satisfait les exigences des agences réglementaires en exécutant les activités et recueillant les données conformément aux Bonnes Pratiques de Laboratoires (BPL), aux Procédures Normalisées d’Opération (PNO) et aux règles de santé sécurité.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Diplôme d’études collégiales en sciences;
Une expérience connexe est un atout;
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;
Avoir la capacité de travailler sous la contrainte de temps et de s'adapter aux changements;
Lire et écrire en anglais est requis. Le bilinguisme est préférable;
Faire preuve de flexibilité et être capable de travailler de manière autonome.

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: 20$/hrs avec prime de soir et possibilité de commencer à un niveau supérieur avec un salaire plus élevé avec une expérience spécifique en recherche;
Bonus annuel basé sur la performance;
Horaire: Lundi au vendredi de 3h PM à 11h15 PM après la formation de 3 à 6 mois de 8 AM à 4h15 PM;
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.

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

Technician in Clinical Laboratories (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

Technician – Clinical Laboratories

As a Technician for our Clinical Laboratories team at the Senneville location, you will perform technical activities and follows directives from the study/phase plan and the SOP.

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 preset schedules;
Ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the GLP, SOP and health and safety rules.

Key Elements

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

College diploma in science;
Relevant experience is an asset;
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above;
Reading and writing English is required. Bilingualism is preferred;
Ability to work under time constraint and adapt to change;
Demonstrate flexibility and ability to work independently.

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: 20$/per hour, evening premiums and opportunity to start at higher level and higher salary with specific research experience;
Schedule: Monday to Friday (3h PM-11h15PM) after 3-6 months of training from (8h AM-4h15 PM);
Annual bonus based on performance;
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.

Competencies

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.

Reviseur.e de données-Immunochimie (Montreal (Senneville), Quebec, CA, H9X 3R3)

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.

Résumé du travail

En tant que Réviseur.e de données pour notre équipe de Toxicologie génétique situé au site de Ville Saint-Laurent, vous serez responsable de la vérification des données en conformité avec les Bonnes Pratiques de Laboratoire (BPL), les Procédures Opératoires Normalisées (PON), les Procédures Analytiques (PA) et les plans d’étude. 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:

Garantir l’intégrité de la révision et des corrections en conformité avec les Bonnes Pratiques de Laboratoires (BPL), les Procédures Opératoires Normalisées (PON), les Procédures Analytiques (PA) et les plans d’étude;
S’assurer que toutes les données pertinentes soient révisées;
Être en mesure de finaliser la révision et les corrections à temps, selon les dates prédéterminées;
Être proactif.ve dans ses démarches pour obtenir les réponses aux erreurs décelées;
Être responsable de documenter tout commentaire toujours en suspens à la fin du processus de révision.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Titulaire d’un DEC en sciences (biotechnologie, laboratoire médical ou l’équivalent) ou d’un BAC en sciences (immunologie, biologie, biochimie) ;
Habileté à travailler avec des contraintes de temps;
Posséder un excellent sens de l’organisation;
Travailler avec précision, faire attention aux détails et s’appliquer à réaliser un travail de qualité.

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;
Bonus annuel basé sur la performance;
Salaire: 22,50$/H
Horaire: Du lundi au vendredi, de 8h à 16h15. Selon les besoins de l’entreprise, vous pourriez avoir à effectuer du temps supplémentaire;
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);
Formations de développement payées;
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.

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.

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.

Data Reviewer - Immunochemistry (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Data Reviewer for our Genetic Toxicology team at the Ville Saint-Laurent location, you will be responsible for the verification of raw data according to Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP), and study plans.
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:

Guarantee accurate review and corrections in accordance with Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP) and study plans.
Ensure that all pertinent data is reviewed.
Ensure that the review and corrections are finalized according to established due dates.
Proactive in obtaining answers to findings.
Responsible for documenting any remaining issues at data review clearance.

Job Qualifications

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

Holder of a DEC in Science (Biotechnology, Medical Laboratory, or equivalent) or a BAC in Science (Immunology, Biology, Biochemistry);
Ability to work under time constraints;
Outstanding organizational skills;
Work with precision, pay attention to detail and strive for quality work.

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;
Annual bonus based on performance;
Salary: 22,50$/H
Schedule: Monday to Friday, 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 ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Paid development training;
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.

Reviseur.e de données-Immunochimie (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Dans ce poste, les principales responsabilités incluront:

Garantir l’intégrité de la révision et des corrections en conformité avec les Bonnes Pratiques de Laboratoires (BPL), les Procédures Opératoires Normalisées (PON), les Procédures Analytiques (PA) et les plans d’étude;
S’assurer que toutes les données pertinentes soient révisées;
Être en mesure de finaliser la révision et les corrections à temps, selon les dates prédéterminées;
Être proactif.ve dans ses démarches pour obtenir les réponses aux erreurs décelées;
Être responsable de documenter tout commentaire toujours en suspens à la fin du processus de révision.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Titulaire d’un DEC en sciences (biotechnologie, laboratoire médical ou l’équivalent) ou d’un BAC en sciences (immunologie, biologie, biochimie) ;
Habileté à travailler avec des contraintes de temps;
Posséder un excellent sens de l’organisation;
Travailler avec précision, faire attention aux détails et s’appliquer à réaliser un travail de qualité.

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;
Bonus annuel basé sur la performance;
Salaire: 22,50$/H
Horaire: Du lundi au vendredi, de 8h à 16h15. Selon les besoins de l’entreprise, vous pourriez avoir à effectuer du temps supplémentaire;
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);
Formations de développement payées;
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.

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

Reviseur.e de données (Montreal (Senneville), Quebec, CA, H9X 3R3)

Résumé du travail

En tant que Réviseur.e de données pour notre équipe de Immunologie situé au site de Senneville, vous serez responsable de la vérification des données en conformité avec les Bonnes Pratiques de Laboratoire (BPL), les Procédures Opératoires Normalisées (PON), les Procédures Analytiques (PA) et les plans d’étude. 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:

Garantir l’intégrité de la révision et des corrections en conformité avec les Bonnes Pratiques de Laboratoires (BPL), les Procédures Opératoires Normalisées (PON), les Procédures Analytiques (PA) et les plans d’étude;
S’assurer que toutes les données pertinentes soient révisées;
Être en mesure de finaliser la révision et les corrections à temps, selon les dates prédéterminées;
Être proactif.ve dans ses démarches pour obtenir les réponses aux erreurs décelées;
Être responsable de documenter tout commentaire toujours en suspens à la fin du processus de révision.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Titulaire d’un DEC en sciences (biotechnologie, laboratoire médical ou l’équivalent) ou d’un BAC en sciences (immunologie, biologie, biochimie) ;
Habileté à travailler avec des contraintes de temps;
Posséder un excellent sens de l’organisation;
Travailler avec précision, faire attention aux détails et s’appliquer à réaliser un travail de qualité.

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;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi, de 8h à 16h15. Selon les besoins de l’entreprise, vous pourriez avoir à effectuer du temps supplémentaire;
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);
Formations de développement payées;
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.

À propos de l'évaluation de sécurité

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

Reviseur.e de Données (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Dans ce poste, les principales responsabilités incluront:

Garantir l’intégrité de la révision et des corrections en conformité avec les Bonnes Pratiques de Laboratoires (BPL), les Procédures Opératoires Normalisées (PON), les Procédures Analytiques (PA) et les plans d’étude;
S’assurer que toutes les données pertinentes soient révisées;
Être en mesure de finaliser la révision et les corrections à temps, selon les dates prédéterminées;
Être proactif.ve dans ses démarches pour obtenir les réponses aux erreurs décelées;
Être responsable de documenter tout commentaire toujours en suspens à la fin du processus de révision.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Titulaire d’un DEC en sciences (biotechnologie, laboratoire médical ou l’équivalent) ou d’un BAC en sciences (immunologie, biologie, biochimie) ;
Habileté à travailler avec des contraintes de temps;
Posséder un excellent sens de l’organisation;
Travailler avec précision, faire attention aux détails et s’appliquer à réaliser un travail de qualité.

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;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi, de 8h à 16h15. Selon les besoins de l’entreprise, vous pourriez avoir à effectuer du temps supplémentaire;
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);
Formations de développement payées;
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.

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

Data Reviewer (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Data Reviewer for our Immunology team at the Senneville location, you will be responsible for the verification of raw data according to Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP), and study plans.
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:

Guarantee accurate review and corrections in accordance with Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP) and study plans.
Ensure that all pertinent data is reviewed.
Ensure that the review and corrections are finalized according to established due dates.
Proactive in obtaining answers to findings.
Responsible for documenting any remaining issues at data review clearance.

Job Qualifications

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

Holder of a DEC in Science (Biotechnology, Medical Laboratory, or equivalent) or a BAC in Science (Immunology, Biology, Biochemistry);
Ability to work under time constraints;
Outstanding organizational skills;
Work with precision, pay attention to detail and strive for quality work.

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;
Annual bonus based on performance;
Schedule: Monday to Friday, 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 ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Paid development training;
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.

Veterinary Pathology Certified (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Veterinary Pathologist for our team at the Laval location, you will mainly be responsible for tissue evaluation and interpretation of assigned studies. 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:

Perform macroscopic and microscopic tissue evaluation and interpretation of assigned studies;
Record Histopathology findings in data capturing system;
Prepare complex reports delineating pathological findings and detailing all test article effects;
Interact with clients to assure satisfaction and to market services;
Assist with necropsy supervision and may conduct necropsies, including gross pathology interpretation, sample collection and fixation;
Work with study directors to ensure data is accurately integrated into study reports;
Provide training, technical guidance and leadership to laboratory staff and to less experienced pathologists;
Provide advanced scientific expertise for experimental design and other aspects of research studies;
Collaborate with other units within the Pathology teams and other departments within the site.

Key Elements

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

Doctorate degree (D.V.M/V.M.D.) from an accredited veterinary school, or acceptable international equivalent in veterinary medicine;
Working knowledge of clinical pathology preferred;
Board certification with the American College of Veterinary Pathologists (A.C.V.P.) or European College of Veterinary Pathologists (E.C.V.P) required to enter the level grade;
Demonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought;
Ability to work on problems of diverse scope in which analysis of data requires evaluation of multiple factors;
Ability to exercise judgement within generally defined practices and policies in selecting methods or techniques for obtaining solutions;
Working knowledge of related computer applications;
Special interest in digital Pathology & Molecular Pathology as well as digital image analysis is preferred;
Bilingualism in French and English is mandatory. Good communication skills in both languages is required.

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 ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Paid ACVP / ECVP yearly license;
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.

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.

Pathologiste vétérinaire avec certification (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Pathologiste Vétérinaire pour notre équipe située au site de Laval, vous serez principalement responsable de l'évaluation des tissus et de l'interprétation des études assignées. Votre contribution assurera la santé de nos animaux ainsi que l'intégrité de nos études précliniques.

Dans ce poste, les principales responsabilités incluront:

Effectuer l'évaluation et l'interprétation macroscopes et microscopiques des tissus des études assignées;
Enregistrer les résultats d'histopathologie dans le système de capture de données;
Préparer des rapports complexes décrivant les résultats pathologiques et détaillant tous les effets des articles de test;
Interagir avec les clients pour assurer leur satisfaction et promouvoir les services;
Aider à la supervision des nécropsies et peut réaliser des nécropsies, y compris l'interprétation de la pathologie macroscopique, la collecte et la fixation des échantillons;
Travailler avec les directeurs d'études pour s'assurer que les données sont intégrées avec précision dans les rapports d'études;
Fournir formation, orientation technique et leadership au personnel de laboratoire et aux pathologistes moins expérimentés;
Apporter une expertise scientifique avancée pour la conception expérimentale et d'autres aspects des études de recherche;
Collaborer avec d'autres unités au sein des équipes de Pathologie et d'autres départements sur le site.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Diplôme de doctorat (D.V.M/V.M.D.) d'une école vétérinaire accréditée, ou équivalent international acceptable en médecine vétérinaire;
Connaissance pratique de la pathologie clinique préférée;
Certification par le American College of Veterinary Pathologists (A.C.V.P.) ou le European College of Veterinary Pathologists (E.C.V.P) requise pour accéder au grade de niveau;
Succès démontré en compétence technique, créativité scientifique, collaboration avec les autres et pensée indépendante;
Capacité à travailler sur des problèmes de portée diverse où l'analyse des données nécessite une évaluation de multiples facteurs;
Capacité à exercer un jugement dans le cadre de pratiques et politiques généralement définies lors de la sélection des méthodes ou techniques pour obtenir des solutions;
Connaissance pratique des applications informatiques connexes;
Un intérêt particulier pour la Pathologie numérique et la Pathologie moléculaire ainsi que l'analyse d'image numérique est préféré;
Le bilinguisme en français et en anglais est obligatoire. De bonnes compétences en communication dans les deux langues sont requises.

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?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Licence annuelle ACVP / ECVP payée;
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);
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.

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

Senior Formulation Scientist (Harlow, GB, CM19 5TR)

Job Summary

Are you a skilled formulator looking to take the next step in your career?

Have you got experience of working in an industrial R&D setting, developing formulations for novel small molecule API’s?

Do you want to join a global contract research organisation that improves health and lives?

Our expanding pharmaceutical development team in Harlow, Essex are recruiting for an experienced formulation scientist. In this role you will apply formulation expertise to guide formulation projects through pre-clinical development.

This leadership role in a small but far-reaching team is an excellent opportunity to help shape the future direction of the Pharmaceutical Development group at Charles River. You will have the opportunity to work on a variety of client projects spanning oral, inhaled, dermal and parenteral administration routes. This role encompasses project management and ownership of client relationships, as well as supporting lab work when required.

Main Tasks:

Advise as a subject matter expert for Integrated Drug Discovery and Development projects, guiding formulation strategy to ensure successful outcomes.
Design and execute formulation study plans, based on client needs.
Manage client formulation projects to agreed timelines and budgets.
Act as the scientific point of contact for clients, from initial discussion through to project delivery.
Mentor junior scientists in formulation techniques and strategies.

Skills and Experience

The ideal candidate has a pro-active can-do approach, pays attention to detail, and has the ability to adapt to changing demands and requirements. They use PK data and the Developability Classification System to drive formulation strategy and is comfortable communicating complex scientific data to stakeholders with varying degrees of expertise.

A working knowledge of solid form characterisations techniques, non-oral dosage routes and formulation of “Beyond Rule of 5” compounds is desirable. Experience of scientific project management would also be advantageous.

Minimum BSc. Qualification in a relevant subject (Chemistry, Pharmaceutical Sciences or related subject). Post-graduate qualifications desirable.
Extensive experience of working in an industrial R&D setting, developing formulations for novel small molecule APIs.
Strong knowledge of the drug discovery and development process.
Experience of mentoring junior colleagues.
Experience in designing and executing preformulation studies, including:- Physicochemical assessment, Solubility Assessment and Biorelevant Dissolution studies.
Expertise in at least one of the following enabling oral formulation techniques:- Spray Drying, Wet milling for particle size reduction or Emulsion development.

What We Offer You

A very comprehensive benefits package from day one, including a generous pension contribution, and flexible health benefits.
Parental leave.
Group Life Assurance and Group Income Protection.
Remote GP access 24/7.
Wellbeing support and initiatives.
Access to great discounts via our CREDS discount scheme.
Global opportunities and strong career progression.
The chance to work on several varied projects and liaise globally and nationally with other business areas.
To be able make a difference to health and wellbeing of people.
To continue your own career growth.
Cycle to work scheme and much much more!

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 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.

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.

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

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

Operaio stabularista - Categorie protette (Lg 68/99) (CALCO, IT, 23885)

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 la nostra sede di Calco/Milano 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 part-time e week-end

Buona conoscenza del pacchetto office

Essere iscritto alle categorie protette Lg 68/99

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.

Operaio stabularista - Categorie protette (Lg 68/99) (CALCO, IT, 23885)

Da quasi 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.

Riepilogo del lavoro

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.

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

Celsis Technical Support Specialist I (Charleston, SC, US, 29407)

Job Summary

The Microbial Solutions Business Located in Charleston SC, is seeking Celsis Technical Support Specialist.
The working hours for this position are Monday - Friday 830a - 5pm located in the office onsite.
The Celsis Technical Support Specialist will provide technical support to customers on Celsis instrumentation, sample preparation, and data interpretation. Assist customers regarding Celsis reagent questions, software questions and testing issues or product complaints. Process microbial samples in the laboratory utilizing various technology platforms. Perform LAL testing as needed.

ESSENTIAL DUTIES AND RESPONSIBILITIES
• Communicate with customers providing support for testing questions and resolution of issues for the Celsis and LAL product lines.
• Perform Celsis testing as needed for investigation or special studies as assigned.
• Utilizes Salesforce application for customer communication.
• Answers incoming phone calls and live chats.
• Assist with product returns and Complaints for the applicable product lines. Document product complaints as required by the SOP. Perform investigational testing for complaints.
• Assist with training to global technical staff, distributors, and customers regarding technical support issues.
• Perform laboratory activities necessary to isolate, grow and maintain cultures of bacteria.
• Perform LAL testing as needed for contract testing or special studies as assigned.
• Receipt of customer samples following applicable procedures. Contacts customer for discrepancies.
• May occasionally travel to customer site for troubleshooting assistance.
• Responsible for proficiency in all SOPs in areas of responsibility.
• Responsible for documentation as required by company policy, cGMP and FDA.
• Perform all other related duties as assigned.

Job Qualifications

• Education: Bachelor’s Degree (B.A. /B.S.) in Microbiology biology or a related discipline.
• Experience: 3+ years of customer interfacing, documentation practices.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experiencelisted above.
• Certification/Licensure: None
• Other:
•Computer literacy with Windows Office Suite programs including data entry.
• Attention to detail in all aspects of work is essential.
• Excellent interpersonal skills.
• Strong written and oral communication skills.
• Pipetting and use of basic lab equipment, microbial testing experience, making dilutions.
• Math literacy

The pay range for this position is $57,500-75,800. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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.

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 80% of the drugs approved by the FDA in the last five years.

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

Manager - Field Customer Support, Nexus (Charleston, SC, US, 29407)

For 70 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.

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

Manage activities of a team of US Nexus Field Service Technicians to provide customers (internal and external) technical service in repair, trouble shoot and training for Endosafe Brand products. Coordinate efforts with Field Service Manager(s) as well as individual contributors to meet customer expectations and company needs. Manage the development and training of team members for existing as well as new product offerings. Provide insight on customer expectations to the appropriate department management groups.

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.

• Manage team to meet customer needs (internal and external)
• Oversight of teams and on-going development to ensure growth and retention
• Identify development opportunities for team and help implement and complete career growth as you and team members agree on
• Manage customer-facing technical repair and maintenance services for endotoxin and microbial detection laboratory instruments on site at customer locations.
• Provide technical assistance and problem resolution for instrumentation to team members as well as customers via telephone, email, or on-site communication to team or customers.
• Manage all required field service activities and documentation as assigned based on specific product, customer and/or standard operating procedural requirements.
• Collaborate with leadership in identifying and developing service contract sales opportunities through up-selling; promoting the customers’ conversion from billable to contract coverage.
• Assisting field sales personnel in product demonstrations, customer training, and product validations.
• Responsible for team member training to complete all service and compliance documentation as required by company policy, cGMP and FDA.
• Responsible for resolving client testing laboratory instrument service issues.
• Oversee and maintain training documentation and global harmonization of these procedures where possible.
• Monitoring and evaluating Instrument Service department meeting customer expectation and internal metrics.
• Work with sales management to evaluate and, where applicable, improve service offerings.
• Monitor service software to ensure metrics are being met. Evaluate and improve metrics and KPIs as necessary.
• Provide feedback and collaborate with service software vendor for improvements to product and/or workflow.
• Work with internal and external teams to introduce and implement technology solutions for improving service and processes.
• Forecast service workload, carve territories and add headcount based on current and future service offerings.
• Triage urgent customer issues and provide necessary support for team to resolve issue as quickly as possible.
• Monitor team expenses.
• Perform all other related duties as assigned.

Job Qualifications

The following are the minimum qualifications related to the Field Service Supervisor:

• Education: Bachelor's degree (B.A./B.Sc.) or equivalent in Engineering or Life Sciences; Microbiology, Biology or Chemistry
• Experience: 5+ years of related experience (technical, laboratory or research); or
Equivalent combination of education and experience.

The pay for this position is $110K - $130K. 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.

With over 17,000 employees within 90 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.

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 ~85% of the drugs approved by the FDA in 2019.

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

Technicien de Laboratoire en Immunologie - H/F - CDI (Evreux, FR, 27930)

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 département Biomarkers recrute un Technicien en Immunologie pour intégrer son équipe composée de 15 techniciens.

Les missions

Au sein du Département Biomarkers, vous aurez pour principales missions sous la responsabilité du responsable du service :
•   Réaliser progressivement certaines techniques de laboratoire comme des dosages ELISA, des développements de méthode mais aussi des études de cultures cellulaires comme Elispot dans le cadre d’études dites de Cells based assays,
•   Assurer la saisie informatique des résultats et leurs conformités,
•   Transmettre au scientifique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail,
•   Lire les protocoles, avenants et notices en anglais.

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 dans le domaine scientifique et possédez au minimum 3 ans d’expérience sur un poste similaire.
Connaissances en culture cellulaire (Elispot).
Vous maitrisez l’anglais et possédez une aisance relationnelle et un sens du contact et du service.
Vous êtes organisé(e), vous appréciez de travailler 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.

Les modalités

•   Convention collective de l’industrie pharmaceutique, groupe : 3
•   Contrat : CDI Non-cadre (accord de modulation 35h)
•   Salaire : A compter de 24 500 € 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 Safety Assessment

À propos de Charles River

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.

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 2021.

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

Production Technician (m/f/d) 1 (Kaarst, DE, 41564)

Wir suchen eine Person in Vollzeit, die Teil unseres Produktionsteams für Reagenzien werden möchte.

Ihre Tätigkeit:

• Sie arbeiten direkt an den Produktionsmaschinen zur Abfüllung und Etikettierung von Reagenzien und dokumentieren die Tätigkeiten nach Vorgabe.

• Sie unterstützen beim Reinigen und Einrichten der Maschinen nach externen (GMP, ISO 9001) und internen Standards

• Sie helfen beim Reinigen von Hilfsmitteln und Vorbereiten von Rohmaterialen für die Produktion

• Sie stellen die Ausführung der übertragenen Aufgaben und Aufträge gemäß den vorliegenden Arbeitsstandards sicher.

Gerne mit einer abgeschlossenen Berufsausbildung, gleich welcher Branche, gerne Quereinsteiger (m/w/d) mit oder ohne produktionstechnische Kenntnisse.

Sie verfügen über:

• Interesse und Verständnis für technische Zusammenhänge und unsere hohen Hygieneanforderungen.

• Sichereren Umgang mit automatisierten Maschinen, handwerkliches Geschick.

• Hohes Sicherheitsempfinden und Verantwortungsbewusstsein

• Strukturiertes, zielorientiertes Arbeiten, hohe Verlässlichkeit und Flexibilität,

• Team- und Kommunikationsfähigkeit, Serviceorientierung

• Gute Deutschkenntnisse sind unerlässlich. Englischkenntnisse sind wünschenswert.

Wir bieten:

• Eine befristete Vollzeitstelle mit abwechslungsreichen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten Unternehmen

• Aktive Mitgestaltung Ihres Aufgabengebietes in einem hoch motivierten Team mit flachen Hierarchien

• Weiterentwicklung und die Möglichkeit, mehr Verantwortung zu übernehmen und innerhalb des Unternehmens zu wachsen

• Eine intensive Einarbeitung

• Flexible Arbeitszeiten

• Wettbewerbsfähige Vergütung

We are looking for a full-time person to become part of our reagent production team.

Your Tasks:

• You work directly on the production machines for filling and labelling reagents and document the activities according to specifications.

• You assist in cleaning and setting up the machines according to external (GMP, ISO 9001) and internal standards.

• You assist in cleaning auxiliary materials and preparing raw materials and for production.

• You ensure the execution of the assigned tasks and orders in accordance with the present work standards.

A completed vocational training is desirable, regardless of the industry, we welcome career changers (m/f/d) with or without technical production knowledge.

You have:

• Interest in and understanding of technical interrelationships and our high hygiene requirements.

• Confident handling of automated machines, manual dexterity.

• High sense of safety and responsibility

• Structured, goal-oriented work, high reliability and flexibility,

• Team and communication skills, service orientation

• Good German language skills are essential. Knowledge of English is desirable.

We offer:

• A full-time position (2 year fixed term contract) with varied, challenging activities in a future-oriented company

• Active participation in shaping your area of responsibility in a highly motivated team with flat hierarchies.

• Further development and the opportunity to take on more responsibility and grow within the company.

• An intensive induction

• Flexible working hours

• Competitive remuneration

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 ~85% of the drugs approved by the FDA in 2019.

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

Production Technician (m/w/d) 1 1 1 1 1 1 (Kaarst, DE, 41564)

Wir suchen eine Person in Vollzeit mit chemisch/biologischem Hintergrund (BTA,CTA,PTA, auch B.Sc. oder M.Sc.) die Teil unseres Produktions-Teams unserer Reagenzien werden möchte.

Unterstützen Sie uns bei:
•   der Bulk-Herstellung der Reagenzien (im 1-200 L Maßstab),
•   In-Prozess-Kontrollen und Freigabe-Prüfungen
•   der Aufreinigung einiger unserer Rohstoffe mittels HPLC
•   weiteren Prozessschritten (Abfüllung, Gefriertrocknung, Autoklavieren etc.)
•   der Aufrechterhaltung unseres ISO Systems und der Einhaltung der Vorgaben der Guten Herstellungspraxis (GMP)

Überzeugen Sie uns durch:
•   gute Team- und Kommunikationsfähigkeit
•   strukturiertes und auf das Ziel fokussiertes Arbeiten, Verantwortungsbewusstsein, Organisationsfähigkeit, hohe Verlässlichkeit und Flexibilität
•   Gute Deutsch- und Englisch Sprachkenntnisse

Wir bieten:
•   eine unbefristete Vollzeitstelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten Unternehmen
•   eine aktive Mitgestaltung Ihres Tätigkeitsfeldes in einem sehr motivierten Team mit flachen Hierarchien
•   Weiterentwicklung uns Spezialisierung
•   eine intensive Einarbeitung
•   flexible Arbeitszeiten
•   eine angemessene Vergütung

Haben wir Ihr Interesse geweckt?
Wenn ja, bewerben Sie sich bitte unter Angabe der Referenz „Production Technician“ mit Ihren aussagekräftigen Bewerbungsunterlagen, Ihrem frühestmöglichen Eintrittstermin sowie Ihren Gehaltsvorstellungen. Wir freuen uns auf Ihre Bewerbung.

Über Microbial Solutions

Unsere Gruppe „Microbial Solutions“ verfügt über ein umfassendes Portfolio für Endotoxin-Tests, mikrobielle Detektion sowie mikrobielle Identifikationsprodukte und -dienstleistungen, das seinesgleichen sucht und das gezielt entwickelt wurde, um die komplexen und sich ständig ändernden Anforderungen der Branche zu erfüllen. Wir helfen unseren Kunden, die Produktsicherheit und -qualität durch einfach zu verwendende und robuste Testlösungen sicherzustellen, die behördliche Anforderungen erfüllen, kritische Entscheidungsfindung ermöglichen und die operative Effizienz verbessern.

Über Charles River

Mit über 20.000 Mitarbeitern in 90 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 85% der von der FDA in 2021 zugelassenen Medikamente unterstützt haben.

Weitere Information en finden Sie unter www.criver.com.

Animal Care Technician I (Cambridge, MA, US, 02139)

Job Summary

We are looking for an Animal Care Technician I to join our Insourcing Solutions team, located in Cambridge, MA.

In the Animal Care Technician 1 role, you will use existing SOPs and quality assurance standards to monitor, observe, and record animal health and welfare daily, as well as complete various standard animal husbandry duties.

Maintain accurate records of animal breeding, health, and housing.
Follow all procedures to maintain housing areas, including room or facility personnel entry; personnel protective equipment use, spraying in all equipment and materials into controlled areas.
Receive, inspect, and put away incoming animals; and operating equipment following all safety guidelines. 
 You may also be involved in the breeding and weaning program, performing various duties from weaning and sexing, to ensuring appropriate production levels are met.
Work cooperatively with the on-site supervisor and/or facility veterinarian to assist with restraint, handling and manipulation of various animal species to include mice, rats and other rodents and possibly rabbits.

Job Qualifications

High school diploma, General Education Degree (G.E.D.) or equivalent required.
Six (6) to twelve (12) months related experience in animal husbandry.
Interest in achieving ALAT certification upon eligibility

The pay range for this position is $23-25 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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.

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.

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.

Central Services Technician I (Cambridge, MA, US, 02139)

Job Summary

We are seeking an experienced Central Services Technician I to join our Insourcing Solutions team located in Cambridge, MA.

As the Central Services Technician I, you will provide cleaning and maintenance of laboratory animal caging, equipment, and cage preparation areas, as well as cleaning of animal support areas.

Additional responsibilities include:

Transport caging and equipment between animal areas and cage washrooms.
Receive and store feed, bedding, and supplies.
Provide quality assurance to the cagewash area.
Ensure that all logbooks, checklists, and other records are completed in a timely fashion.
Conduct and collect various aseptic sampling for the monitoring of water quality, sanitized animal racks, and equipment.
Inspect enrichment devices, cages, and other items, and perform all other related duties as assigned.

Job Qualifications

The following are minimum requirements related to the Central Services Technician I position:

High school diploma, general education degree (G.E.D.) or equivalent
Minimum of six months experience working in a laboratory animal facility performing cage wash duties, or working with glassware cleaning or a commercial dishwashing operation.

The pay range for this position is $20.00-22.00 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Vaccine Mandate

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.

Animal Care Technician II (Cambridge, MA, US, 02139)

Job Summary

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

As the Animal Care Technician II, Observe, monitor, and document the health and physical environment within the client’s animal facility. Perform animal care and husbandry.

Additional responsibilities include:
• Review, comprehend and comply with all SOPs and quality assurance standards pertaining to laboratory animals for research.
• Monitor daily animal health and welfare while performing daily animal health observations. Perform animal husbandry duties to maintain quality and health of research animals, to include: perform daily water bottle /automatic water line 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.
• Perform daily cage wash duties and sanitation.
• Maintain accurate records of animal breeding, health, and housing/isolator or support areas as required by Institute and facility.
• Assist with restraint, handling and manipulation of various animal species as assigned by the on-site supervisor or facility veterinarian.
• Dispose of animal carcasses following established procedures.
• Receive, inspect and put away incoming animals; ensure and provide for sentinel animals in each rodent housing area.
• May be involved in strictly maintaining and following breeding and weaning procedures to ensure appropriate production levels.
• Operate equipment and use supplies according to safety guidelines; perform general housekeeping and adheres to safety procedures.
• Maintain required attendance level and adherence to work schedule in accordance with required staffing levels in order to ensure that assigned duties are completed.

Job Qualifications

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

• High school diploma or GED and 2 years related research husbandry experience, or Associates degree in Life Sciences or related field and 1.5 years related research husbandry experience, or Bachelor's degree in Life Sciences or related field and 1 year related research husbandry experience.
• AALAS certified as ALAT within 18 months of hire

The pay range for this position is $22-24 USD an hour. Please note that salaries vary within the range based on factors including experience, skills, education, certifications, and location.

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.

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.

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.

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

Scientific Research In Vitro - Associate (Szeged, HU)

A Charles River munkatársai 75 éve dolgoznak azon, hogy új gyógyszeres terápiák felfedezésében, fejlesztésében és biztonságos előállításában segédkezzenek. Ha csatlakozol ehhez a nagy családhoz, lehetőséged nyílik arra hogy jobbá tedd az emberek egészségét és jóllétét világszerte. Minannyiunk tudása és képessége fontos szerepet játszik a munkánkban függetlenül attól, hogy eddigi tapasztalataidat élettudományi, pénzügyi, informatikai, értékesítési vagy más területen szerezted. Cserébe segítünk egy sikeres karrier felépítésében.

Job Summary

Főbb feladatok:

- Validálásokhoz, kutatásokhoz kapcsolódó in-vitro mérések elvégzése (elsődleges feladat)
- Emlős sejtek fenntartása és kezelése, steril munkavégzés
- Laboratóriumi munka technikai előkészítése
- Oldatok, pufferek, törzsoldatok készítése
- Laboreszközök, műszerek használata, karbantartása
- Adminisztratív jellegű laboratóriumi feladatok ellátása

Job Qualifications

Az álláshoz tartozó elvárások:

- Legalább középfokú szakirányú végzettség
- Hasonló területen szerzett laboratóriumi tapasztalat - min. 2 év
- Jártasság általános laboreszközök használatában
- Önálló, precíz, felelősségteljes munkavégzés
- Dinamikus, nyitott, rugalmas, csapatjátékos személyiség
- Angol nyelvismeret
- Felhasználói szintű MS Office alkalmazások ismerete (Word, Excel)
- ISO 9001 minőségbiztosítási rendszerben való jártasság előny

A Discovery részlegről

A Charles River Discovery részlege az ipar által is bizonyítottan sikeres új terápiák fejlesztése terén. Az elmúlt 17 évben 320 új szabadalmat és 74 preklinikai gyógyszerkészítményt állítottunk elő megbízóink részére. Több mint 650 tudós által kidolgozott átfogó, integrált portfóliónk a legújabb technológiákat és platformokat alkalmazza, hogy kémiai, biológiai és farmakológiai szolgáltatásokat nyújtson, ezzel támogatva ügyfeleinket a preklinikai gyóyszerfejlesztési folyamaton át. Ügyfélközpontúak vagyunk, és együttműködéssel érjük el a valódi partnerkapcsolatok kialakulását, melyek során felmérjük az esetleges kihívásokat, legyőzzük az akadályokat és együtt haladunk azon az úton mely során új gyógyszereket juttatunk a piacra.

A Charles Riverről

A Charles River egy szolgáltató cég, mely a gyógyszerfejlesztés korai fázisára nyújt megoldásokat. Építkezve a laboratóriumi állatgyógyászati és tudományos alapjainkra egy széleskörű portfóliót hoztunk létre a gyógyszerfejlesztés preklinikai fázisaira koncentrálva (discovery és safety). Mind GLP és non-GLP rendszerben kínálunk vizsgálatokat a kezdeti lépésektől (target identification) a preklinikai fejlesztésekig. A Charles Rivernél termék- és szolgáltatáscsomagot is kínálunk, hogy segítsük ügyfeleink klinikai vizsgálatait és gyártási tevékenységüket. Ennek a széles termék- és szolgáltatás portfóliónak köszönhetően ügyfeleink egy rugalmasabb gyógyszerfejlesztési modellt hozhatnak létre, mely csökkenti a költségeiket, növeli a termelékenységüket és hatékonyságukat, hogy ezáltal gyorsabban léphessenek piacra.

A világ 20 országában, 110 telephelyen több, mint 20.000 munkavállalónkkal stratégiai helyzetben vagyunk, hogy összehangoljuk az erőforrásainkat és multidiszciplináris szempontokat alkalmazzunk ügyfeleink egyedi kihívásainak megoldásában. Ügyfélkörünk globális gyógyszergyárakból, biotechnológiai cégekből, kormányszervekből, klinikákból és akadémiai intézményekből áll szerte a világon.

A Charles Rivernél elkötelezettek vagyunk hogy javítsuk az emberek életminőségét. Küldetésünk, kitűnő tudományos hátterünk és erős céltudatosságunk vezérel minket mindenben amit teszünk, és minden napot azzal a nézettel közelítünk meg, hogy a munkánk segít az emberek egészségén és jóllétének javításán világszerte. Büszkék vagyunk arra, hogy az elmúlt öt évben az FDA által jóváhagyott gyógyszerek mintegy 80%-át mi fejlesztettük ki.

További információért látogass el a honlapra 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.

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.

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

The pay for this position is $18.47 per hour.

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.

Animal Caretaker (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 $18.47 USD 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

Cagewash Technician (Poolesville, MD, US, 20837)

Job Summary

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

Why work at Charles River?

We offer an excellent onboarding program for our new employees, internal career development, and competitive benefits.

What you will do!

In this role, you will provide cleaning and maintenance of laboratory animal caging, equipment and cage preparation areas as well as cleaning of animal support areas.

Additional responsibilities include:

Operates equipment and uses supplies according to safety guidelines; performs general housekeeping and adheres to safety procedures.
Sanitizes, maintains, and repairs caging materials as needed. Maintains cagewash and animal holding facilities in a clean and organized manner, in adherence with all SOP and facility requirements.
Disposes of waste materials in a safe and thorough manner as required.
Maintains facility equipment and performs routine preventative maintenance on cagewash and autoclaves, including routine inspection of cleaning filters and roto-arms.
Assists with the receipt, stocking and maintenance of supply inventories.
Assist with animal care activities to include, but not limited to; animal health observations, cage cleaning, water/feed checks, providing water/feed/enrichment.
Prepares and submits required written records, charts, logs and inventories.
Actively interacts with customers as required to resolve customer requests, inquiries, and complaints and to provide technical assistance.
Maintains consistent practice of general company and safety policies and procedures and MSDS guidelines, including those related to biohazards and radioactive substances. Performs all duties in compliance with local, state, and federal regulations.

Job Qualifications

The following are minimum qualifications related to the Cagewash Technician position:

Education: High school diploma or general education degree (GED) preferred.
Experience: Experience and/or training working with mechanical equipment preferred.
Certification/Licensure: none required.

The pay rate for this position is $20 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!

With over 14,000 employees within 80 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 2018, revenue increased by 22% to $2.27 billion from $1.86 billion in 2017.

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 ~85% of the drugs approved by the FDA in 2018.

Equal Employment Opportunity

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

Technical Trainer I (Poolesville, MD, US, 20837)

Job Summary

We are seeking an experienced Technical Trainer I to join our Insourcing Solutions team, located in Poolesville, Maryland.

As the Technical Trainer I, you will develop, deliver, document, and report technical skills training programs involving both small and large laboratory animal species in accordance with client’s facility SOPs, Charles River policy and applicable Federal regulations.

Additional responsibilities include:

Direct, schedule, perform and document all relevant Task-specific technical, husbandry and administrative training for all contract positions in coordination with management and supervisors.
Perform continuing education and training to maintain and enhance employee skills and capabilities, including SOP or ASP revisions, animal welfare topics, operations and maintenance, and technical advancements.
Conduct AALAS certification training, monthly health & safety training; conduct and/or coordinate ASP-directed training.
Select or develop teaching aids such as training handbooks, demonstration models, multimedia visual aids, computer tutorials, and reference works.
Conduct training sessions covering specified areas such as on-the-job training, refresher training, in laboratory animal techniques.
Test trainees to measure progress and to evaluate effectiveness of technical training.
Provide didactic and hands-on technical training on SOPs Monitor technical methods used by employees and make on the spot corrections.
Perform quality assurance responsibilities for the contract site, including:
- Inspecting procedures, reports, facilities, equipment and data for on-going administrative, husbandry and technical-related functions relevant to contract performance and research mission support for adherence to CDC protocols and SOPs.
- Scheduling and conducting phase inspections and personnel performance audits to determine compliance with internal SOPs and study protocols.
Actively interact with customers as required to solve customer requests, inquiries, and complaints and to provide technical assistance.
Occasionally provide technical support, animal husbandry, and assist with research procedures as necessary to respond to surge in work load or personnel shortages.

Job Qualifications

The following are minimum requirements related to the Technical Trainer I position.

Associate degree or bachelor’s degree in animal science, veterinary technology or equivalent college level program required.
Minimum of three (3) years related animal care and handling experience required. One (1) year technical experience performing the duties and responsibilities detailed above preferred. Previous training and successful "hands -on" performance of animal care technical procedures required. Related technical experience includes, but not limited to:
- Rodents: Handling and restraint, identification methods, sexing, tissue collection (blood, tails, various organs), administration of medications and treatment.
- Non-human Primates: Utilization of squeeze cages, transferring, TB tests, blood collection, basic injections / administration of medications, treatments and anesthesia, identification (tattoo) proper use of bite/scratch kits.
- Farm Species: Handling and restrain, identification methods, blood collection, basic injections/administration of medications and treatment.
- General techniques: Surgical pack preparation, proper scrub-in technique, proper physical/physiological observation, gas and/or autoclave sterilization (use of machines and rationale for use of each type), drug dosage calculation, pre-surgical animal prep, gestation periods of various species, proper use of anesthesia machine (portable & fixed), anesthesia monitoring, safe handling and restraint techniques, proper use of PPE, euthanasia, blood collection and injection techniques - all species, all sites.
AALAS certification at the Laboratory Animal Technologist (LATG) level preferred.

The pay range for this position is $35-38 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.

Manufacturing Specialist (Rockville, MD, US, 20850)

Job Summary

The Manufacturing Specialist is a key technical contributor responsible for process optimizations, manufacturing troubleshooting, continuous improvement initiatives to ensure Manufacturing consistently produces quality product. This role sits at the intersection of operational excellence, quality, training & development, and MSAT supporting efficient, compliant, and ever improving operations.

The ideal candidate will have a strong understanding of cGMP compliance, quality event investigation, lean production methodologies, and process technology to drive reliability in operations.

Key Responsibilities and Duties:

Process Improvement & Optimization

Identify and implement continuous improvement projects using Lean methodologies to improve and stabilize yield, efficiency, and process success.
Partner with MS&T and Process Development to monitor process performance to identify data-driven solutions and enhancements.
Support technology transfer, process scale-up, and process validation to ensure smooth transitions into manufacturing.
Partner with MS&T and Engineering to optimize equipment utilization, automation strategies, and data analytics for real time adjustments and support.

Compliance & Manufacturing Support

Conduct timely batch record reviews and deviation investigations, ensuring long term resolution of documentation/instructional issues.
Lead root cause analysis and corrective/preventive action (CAPA) for process deviations, non-conformances, and quality issues.
Work close with Quality and Manufacturing teams to ensure documentation supports data integrity & good documentation practices (GDP) incompliance with FDA, EMA, guidelines.

Training and Documentation Management

Develop and maintain SOPs, training materials, and documentation systems for manufacturing compliance and process improvements.
Partner with MS&T and Training to conduct training programs for manufacturing staff to ensure adherence to cGMP, process guidelines, and quality requirements.
Work cross-functionally to ensure employees remain qualified and up to date on process and compliance expectations.

Job Qualifications

Bachelor’s degree in relevant Science or Engineering discipline preferred.
Minimum 3 years working within industry. Strong technical writing capabilities a plus.
Experience within cell/gene therapies, biologics, and/or cGMP regulated environment preferred
Knowledge of process improvement and lean methodologies preferred.
Ability to interpret and present complex scientific data in a clear and concise manner.
Proficient in Microsoft office suite and document management systems.
Strong organizational and project management skills.

Compensation Data

The pay range for this position is $68,712 - $87,200 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 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.

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

QC Associate I - Environmental Monitoring - Shift is 1pm - 9:30pm (Rockville, MD, US, 20850)

Job Summary

At Charles River Laboratories, we are looking for a highly motivated and energetic candidate to join our growing business in the CMO industry. The QC Analyst I will perform microbiological testing, static and dynamic viable and non-viable monitoring of classified clean room areas to support planned or in process manufacturing processes. This position, as well as all positions in the Charles River team will require demonstration of Charles River DNA “Characteristics and Behaviors” (Care, Lead, Own and Collaborate).

Key Responsibilities and Duties:

Performs viable and non-viable environmental monitoring in a static and dynamic environment.
Perform water quality analysis testing such as TOC and conductivity testing
Demonstrate excellent aseptic technique and clean room gowning practices required for working in Grade C, B and A spaces
Perform bioburden testing per current cGMP guidelines to facilitate in process product development and raw material release
Perform growth promotion, microbial identification, pure colony streak plate isolation, biological indicator testing in a controlled BSL2 environment.
Complete relevant data entry requirements in accordance with current data integrity expectations and the ALCOA principals
Assist in laboratory investigations, environmental monitoring excursions and deviations.
Participate and facilitate on-going lab excellence initiatives as directed by the Senior QC Analyst or area management.
Work may be required outside of normal business hours
Additional duties as needed

Job Qualifications

B.S in Biology or related field
1-2 years working in a GMP facility is preferred, although not required.
Able to lift up to 40 pounds
Able to work in a clean room suite while wearing appropriate gowning and PPE
Excellent verbal and written communication skills
Ability to work independently or within a team setting
Team-player
Good organizational skills
General computer skills including Microsoft Office software
General lab skills or science background desired

Compensation Data

The pay range for this position is $24.00 - $26.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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.

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

Biomanufacturing Associate I - Upstream (Rockville, MD, US, 20850)

Job Summary

The Biomanufacturing Associate I will play an integral role within CRL’s gene therapy manufacturing function by understanding and applying biological, bioprocess, manufacturing, and mechanical principles, processes, procedures, inputs, and outputs, for designated production processes and handovers, within a cGMP and GLP environment. This will ensure the timely production and release of quality products, based on client specifications.

This role will perform a range of routine and semi-routine tasks, some of which are moderately difficult, requiring judgment in resolving issues or making recommendations, with guidance as needed, in order to proficiently execute manufacturing protocols in a regulated environment.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Under guidance, apply and adhere to SOPs, cGMP, GLP, Quality, and basic Safety standards and requirements when completing tasks.
Basic Upstream Activities (e.g., assist with solutions, media aliquot, and buffer preparation and autoclave materials for cell culture, staging of raw materials, seed train, bioreactor set up, fermentation monitoring and/or harvest).
Follow verbal and written instructions (e.g., SOPs), when performing planned manufacturing activities, in alignment with the batch record, and under guidance.
With guidance, use basic quality documents and apply Good Documentation Practices.
Ensure data integrity by accurately documenting, reviewing, and correcting work prior to submission.
Identify, record, and report observed process variances and deviations in real time.
Apply and adhere to SOPs, safety guidelines, and manufacturing instructions when completing process tasks and when operating equipment. Prepare, clean, maintain, and operate equipment and tools.
Recognize common safety issues and report all injuries and safety incidents immediately.
Adhere to safe working practices and comply with site-based guidelines to avoid the consequences of error by applying:
Cleanroom and aseptic behaviors and procedures.
Proper Personal Protective Equipment (PPE) and gowning requirements.
Proper preparation, disinfection, sterilization, and sanitation methods and processes for equipment, etc.
The safe handling, transport, storage, and disposal of biological specimen, chemical, and hazardous materials.
Universal precautions with respect to OSHA guidelines.
Appropriate organization, sanitizing, and stocking of work area to avoid unsafe situations.
Perform other responsibilities as required.

Job Qualifications

Education: High School Diploma or equivalent with high grades in science courses, or an Associates or Bachelors degree in biology/life sciences, bioengineering, or related discipline.
Experience: 2 years of related experience with a High School Diploma. 1 year of related experience with an Associates degree. 0-1 year of related experience with a Bachelors degree.
Related experience may include prior experience in a technical role and/or within a cGMP and/or biotech manufacturing environment or other related industry, etc.
Other:
Able to work in accordance with the Charles River Values.
Able to be a team player, have a positive attitude, professional tone and demeanor, and work effectively in a collaborative environment.
Willing and able to continuously learn and improve.
Strong attention to detail and ability to recognize deviations from accepted practices.
Good documentation and GDP skills.
Must possess good analytical, critical thinking, and problem-solving skills.
Able to hold oneself accountable by following up and doing what they say they will do.
Able to complete work accurately and on time.
Good listening, clear written, and verbal communication skills.
Working knowledge of computer software (MS Word, MS Excel, Teams, database systems, etc.).

Compensation Data

The pay range for this position is $25.00 - $27.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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.

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

Project Manager I (Cagewash Manager) (Bethesda, MD, US, 20892)

Job Summary

We are looking for a Cagewash Manager to join our Insourcing Solutions team, located in Bethesda, MD.

In the CWM role, you can do that by planning, organizing, and directing the activities of the cagewash program, which directly contributes to the integrity of the research.

Additional responsibilities include:

Use existing SOPs and quality assurance standards to provide daily direction and supervision to cagewash technicians to maintain facility operation, condition, security, and sanitation levels, as well as coordinate personnel scheduling.
Ensure staff operates and maintains equipment and supplies; develop projections for equipment, personnel
Conduct routine inspections to determine if standards are being met.
Evaluate and adjust the workflow to ensure efficiency and effectiveness of cagewash operations
Conduct/participate in training activities and ongoing learning, including improvement planning.
Develop and implement new or updated SOPs. Additional duties include coordinating and communicating special projects/procedures, supervising record maintenance, as well as generating/submitting reports to management on operations-related issues.
Coordinate preventative maintenance on all cagewash machinery, equipment, and materials; in addition to organization and up-keep of physical environments.
Troubleshooting equipment issues, performing minor repairs, and coordinating service visits would also be a responsibility of this position.
Identify, document, and/or report environmental or cagewash abnormalities.
Use of computer programs to maintain data and reporting is required; in addition to actively interacting with customers to resolve requests, inquiries, and complaints, and to provide technical assistance.

Job Qualifications

The following are minimum requirements related to the Cagewash Manager position:

A.A. in Animal Science or a related field plus 4 years lab animal experience or
B.A./B.S. degree or higher in Animal Science or related field plus 3 years lab animal experience
Minimum of 1 year supervisory experience in a multi-labor category rodent facility
AALAS certification at the Laboratory Animal Technologist level (LATG) required.

Additional requirements

Customer service experience preferred
Cagewash equipment maintenance experience preferred

The pay range for this position is $38.00 - 42.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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!

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

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.

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

Animal Care Technician II (50) (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Animal Care Technician II to join our Insourcing Solutions team located in Bethesda, MD.

As the Animal Care Technician II, you will maintain, monitor, and document the health, breeding colony production, technical support, and physical environment within the animal facility. Your role will be to maintain the quality and health of the research animals.

Additional duties:

-Perform Animal Health assessments and send notifications to clinical veterinarians and investigative lab staff
-Animal health observations across multiple species; perform basic animal husbandry
-Perform breeder set-ups, vaginal plug checks and weaning
-Perform blood collection via various routes for technical service requests
-Perform ear tag/ID placement; sample/tissue collection for genotyping and other technical service request and facility sentinel program
-Administer topical, injectable, and oral treatments
-Maintain and update all related records, logs, forms, cage cards
-Applying quality assurance/quality control standards to ensure Statement of Work expectations are fulfilled

Job Qualifications

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

High school diploma or GED required.

One or more years of related animal care and handling experience

ALAT certification, or become certified within one year of eligibility

Schedule: Monday through Friday 7AM-3:30PM. Must be available some weekends and holidays.

The hourly range for this position is $22.00- $24.00 USD per hour. Please note that salaries vary within the range based on factors including skills, certifications, and location. 

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.

Lead Cagewash Technician (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Lead Cagewash Technician to join our Insourcing Solutions team, located in Bethesda, MD.

As the Lead Cagewash Technician, you will provide quality assurance and control, in addition to coordinating preventative maintenance of equipment, as well as prioritizing workload on the assigned side to ensure daily goals are met and the integrity of the research is maintained.

Additional responsibilities include:

Maintains facility equipment and performs routine preventative maintenance on cagewash and autoclaves, including routine inspection of cleaning filters and roto-arms.
Responsible for conducting trouble shooting on the equipment and reporting any problems to the Cagewash Supervisor. If necessary, communicating directly with the manufacturers on problems with the equipment.
In the absence of the Cagewash Supervisor, is responsible for scheduling the staff, ensuring work and all related paperwork is completed.
Sanitize, maintain, and repair animal caging materials as needed and ensure cagewash facilities are kept clean and organized
Other tasks may include assisting with the receipt, stocking, and maintenance of supply inventories
Prepare and submit required written records, charts, logs, and inventories.
Assist with training and redirection of workload as necessary to ensure a cohesive team and that daily goals are met.

Qualifications

The following are minimum requirements related to the Lead Cagewash Technician position:

High school diploma or GED
Minimum six months of successful performance in cagewash facility operations

The pay range for this position is $19.00 - $19.50 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

Cagewash Technician I (Bldg 35) (Bethesda, MD, US, 20892)

Job Summary

We are looking for a Cagewash Technician I to join our Insourcing Solutions team, located in Bethesda, MD.

The duties of the Cagewash Technician I are to maintain facility equipment and perform routine preventative maintenance on cagewash and autoclaves.

You will also perform the following duties:

Sanitize, maintain, and repair animal caging materials as needed.
Ensure cagewash and animal holding facilities are kept in a clean and organized manner.
Assist with the receipt, stocking, and maintenance of supply inventories.
Prepare and submit required written records, charts, logs, and inventories.
Actively interact with customers to resolve requests, inquiries, and complaints, and to provide technical assistance.

Other duties will include general housekeeping, in addition to reviewing, comprehending and complying with all SOPs and quality assurance standards pertaining to specific areas.

Who are we looking for?

A candidate that possesses a high school diploma or general education degree is preferred. Experience and/or training working with mechanical equipment preferred.

The pay for this position is $17.50-18.47 USD 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

Sr. Supply Chain Coordinator (Hanover, MD, US, 21076)

Job Summary

As a Senior Supply Chain Coordinator for Charles River, your role involves efficiently managing materials to support testing and meet client demands. Responsible for updating the Supply Chain Database or any other Warehouse Management System, documenting raw material movements and contributing to the completion of raw material request and submission of purchase requisitions. Your attention to detail and analytical skills contribute to Charles River’s operational efficiency and success in delivering high-quality products. This position reports onsite to the facility director.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Support Receiving, Shipping & Purchasing operations as needed.
Analyze and manage current inventory needs and levels, replenishment schedules, and order quantities.
Maintain accurate records of inventory levels, track material consumption and generate reports to provide insights into material usage patterns and identify areas for improvement.
Contribute to Raw Material Request completion and Purchase requisition submission.
Coordinate physical material movements for the picking of material and supply to testing.
Issue materials to testing by completing goods issue to material requisitions in inventory database.
Coordinate physical material movements for the picking of material and supply to testing
Maintain accurate daily records of good receipts and shipments made.
Manages and maintains inventory system; facilities upgrade to related database and/or software under the direction of the purchasing or inventory manager.
Conduct cycle counts as needed.
Execute timely inventory adjustments.
Reconcile and conduct root cause analysis to determine reasons for needed inventory adjustments and transactions.
Ensure materials meet specifications, standards, cost-efficient, with adequate supply for testing.
Document inventory properly and communicate any issues with upper management immediately
Ensures adherence to Approved Supplier List for all cGMP purchases.
Manage, log, assign lot numbers (as applicable) and appropriately document all Receipt (incoming) and Shipment (outgoing) of materials, documents, testing samples and product for the facility.
Create and process purchase requisitions.
Process invoices for payment in ERP SAP for the facility.
Create and assign material part numbers.
Develops/updates facility specific standard operating procedures and internal policies for material movement and delivery flow activities and documentation requirements.
Establishes inventory categorization and storage locations within facility.
Support negotiations and problem resolution with internal and external customers to ensure all issues are addressed and countermeasures are implemented and tracked.
Optimize inbound freight routes and timing to achieve company/client expectations.
Monitor and report performance metrics including (but not limited to) misses associated with on-time deliveries, quality metrics, and cost (including overtime).

Job Qualifications

Bachelor’s degree required
Minimum 3 to 4 years of experience performing Enterprise Resource Planning (ERP) inventory transactions.
Enterprise Resource Planning (ERP) or Warehouse Management System (WMS) experience required; SAP preferred
4+ years working around manufacturing and warehousing environments including logistics, materials handling, inventory control, and shipping/receiving in a lead or senior position.
3 years working in a GMP environment including transacting inventory in ERP system preferred
Demonstrated attention to detail and accuracy
Experience with ERP cycle counting
Familiarity with inventory batch management
Experience with Quality System/Standard (ISO, TQM, Six Sigma) Good Manufacturing Practices (cGMP) preferred.
Experience with Scheduling International shipments and drafting of Pro Forma Invoices
Experience with revising or creating Standard Operating Procedures
Proficiency with office technology including Microsoft Office Applications (Outlook, Excel, Word)
Strong written and verbal communication skills
Ability to lift 35 pounds without assistance.
Ability to read, analyze, and interpret documentation.
Ability to work independently, with a team, and different departments to improve processes for improved performance.
Adaptable and able to work within a fast-paced, changing environment.

The pay range for this position is $64,700 - $71,500. 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.

Behavioral Management Technician II (Frederick, MD, US, 21701)

Job Summary

ESSENTIAL DUTIES AND RESPONSIBILITIES:

· Provide appropriate enrichments to the animals’ structural and social environments and provide opportunities for species-typical activities.

· Monitor colony behavioral health, and provide care for animals needing special attention and/or treatment.

· Observe animals and report behavioral abnormalities.

· Assist in performing behavioral assessments in response to reports of behavioral abnormalities.

· Work with other departments to coordinate animal psychological/behavioral enrichment, including the acclimation and socialization of study animals.

· Review animal approval documentation and submit approval forms to appropriate personnel.

· Work with other Behavioral staff to precondition animals for study procedures.

· Work closely with the veterinary and animal care staff to ensure proper animal care standards are maintained.

· Order fruit, enrichment foodstuffs and enrichment devices for the animals.

· Assist with evaluation of new enrichment devices and provide input on strategies for individually and socially housed animals.

· Research and review current literature regarding animal behavior and environmental enrichment as assigned.

· Assist with revisions to relevant SOPs as needed to ensure accordance with the Animal Welfare Act and accepted professional standards.

· Routinely handle animals as required for duties.

· Maintain and track data related to social housing, exemptions to social housing, and abnormal behavior.

· Maintain documentation for the Behavioral Management Program.

· Assist with training animal care staff and other site personnel on aspects of animal behavior and enrichment as needed.

· May serve as IACUC committee member.

Job Qualifications

· Education: Bachelor’s degree (B.A./B.S.) or equivalent in scientific related discipline.

· Experience: 4-6 years related experience in animal science, biology, chemistry/pharmacy, or similar lab environment or must have fully satisfied technical and experience requirements for the previous level. 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: AALAS certification at the LAT level strongly preferred.

· Other: Demonstrated advanced technical and analytical skills. Effective communication and leadership skills. Ability to handle a variety of laboratory animals. Proficient in 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 required. Understanding of basic, intermediate, and complex study design and protocols. Ability to organize and prioritize work to meet deadlines. Computer literacy including word processing, spreadsheet and database programs.

The pay range for this position is $31-$36/hour. Please note that compensation varies based on factors including, but not limited to, experience, skills, education, and certifications.

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.

Lab Coordinator I - In Vivo (Worcester, MA, US, 01608)

Job Summary

We are seeking a Lab Coordinator I for our Discovery site located in Worcester, MA.

The individual in this position will be responsible for supporting the operation of a in vivo laboratory. This position requires attention to detail and the ability to interact and communicate effectively with a wide variety of people. The position operates in a fast paced environment where the commitment to teamwork, quality, and speed is essential. This is a non-Scientific role supporting the labs and ensuring they have all equipment and materials.

Some of the responsibilities for this position include:

•   Handling of hazardous and flammable chemicals during preparation of laboratory solutions.
•   Moving, monitoring and general maintenance of temperature chambers (freezers/refrigerators) containing study samples.
•   Stocking laboratories and delivering consumables/chemicals/reagents to lab scientists.
•   Some shipping and receiving responsibilities, DOT training for hazardous materials shipping a plus.
•   Managing hazardous and biohazardous waste streams.

The pay 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

The following are minimum requirements related to the Lab Coordinator I position.

•   Education: High school diploma or General Education Degree (G.E.D.). Associate’s degree (A.A./A.S.) preferred.
•   Experience: 1 year related laboratory experience in a pharmaceutical or contract laboratory environment preferred but not required. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Ability to work effectively as a member of a team
•   Familiarity with Microsoft Office software (such as Word, Excel)
•   Ability to interact with others in a calm and professional manner
•   Ability to effectively communicate orally and in writing
•   Ability to organize and prioritize work while meeting timelines.

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.

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.

Research Technician I - In Vivo PK (Worcester, MA, US, 01608)

Job Summary

This position is working Full Time - Sunday - Thursday

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.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Perform in-life technical procedures (e.g., clipping, handling, binding, removals, body weight, dosing).
• Administer test substances by various basic methods (e.g., oral gavage).
• Input, print and edit computer entries (e.g., in life numbers, body weights, food consumption and clinical observation).
• Under supervision may act as lead/primary technician on basic studies.
• Observe animals for general health and overall well being. • Collect and record research data and biological specimens in compliance with applicable guidelines and regulations (GLPs, SOPS). • Read basic study protocols and extract pertinent information.
• Review documentation of functions performed as part of quality control requirements.
• Retrieve and view SOPs using appropriate database.
• Use applicable GLPs, SOPs, processes and company policies when performing all job functions.
• Handle, restrain, and provide care for all species of laboratory animals at the site.
• Perform study preparation activities including 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, if applicable for the site.
• Perform all other related duties as assigned.

Job Qualifications

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 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 guidelines relating to the care of laboratory animals. Basic understanding of study design and protocols.

The pay for this position is $22.50/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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

In-Vivo Scientist I - Oncology (Worcester, MA, US, 01608)

Job Summary

We are seeking an experienced Scientist I, Oncology for our Discovery site located in Worcester, MA.

We are seeking a motivated, skilled scientist to work within the Oncology team in our Worcester site. While retaining an element of hands-on responsibility, this position is also largely focused upon leveraging the individual’s scientific strengths through the mentoring of more junior staff. This position requires competency of all aspects of oncology studies including the skills and techniques necessary to satisfy the overall study objectives.

Successful candidates in this position will:

Possess strong interpersonal skills with strong scientific curiosity, initiative and resourcefulness
Possess exceptional organizational and planning skills enabling management of multiple, concurrent tasks & priorities
Careful attention to detail and the accurate, organized and timely documentation of study data and report generation
Team orientation, highly collaborative and results-oriented focus
Self-driven and enthusiastic with the ability to thrive in a dynamic environment
Design and plan projects/protocols with occasional direction from senior staff.
Follow company BOPs and guidelines.
Mentor and train technicians.

The pay range for this position is $70,000 to $74,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

The following are minimum requirements related to the Scientist I position.

Education: Bachelor’s Degree (B.S./B.A) or equivalent in a scientific related discipline. Master's degree (M.S./M.A.) or Ph.D. preferred.
Experience: Minimum of 5 years previous directly related laboratory experience in a pharmaceutical or contract laboratory environment. Animal handling in lab setting is required. Experience with cancer tumor models and imaging is preferred.
Other: Exceptional analytical and problem solving capabilities. Full understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and Good Laboratory Practices (GLPs), as appropriate. Excellent written and verbal communication skills in a team environment. Able to prioritize work and meet deadlines under minimal direction. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and with standard laboratory calculations. Proficiency in the use of analytical instrumentation software with the ability to troubleshoot for routine and non-routine work.

Compensation Data

Competencies

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.

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.

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.

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.

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

Medical Technologist I (Shrewsbury, MA, US, 01545)

Job Summary

Perform basic medical technology procedures according to protocol, SOP and GLP. Operate, maintain, and perform basic troubleshooting procedures on analyzers. Biological sample processing. Perform and review study ordered parameters and computer input of raw data.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
Perform all tasks in compliance with Standard Operating Procedures (SOP) and Good Laboratory Practice (GLP) regulations.
Read study protocols and extract pertinent information with guidance.
Maintain proficient knowledge of hematology, clinical chemistry, coagulation, urinalysis, and fecal analysis.
Operate, maintain, and troubleshoot clinical pathology analyzers with guidance.
Perform basic medical technology procedures such as blood slide differentials, reticulocyte counts and urinalysis with guidance.
Perform all specialized processing under supervision.
Prepare materials needed: labeling tubes, study books and appropriate paperwork prior to bleeding days.
Inventory and package differential and reticulocyte blood slides for each study for shipment or storage.
Manual entry of raw data into the computerized systems and review of data as needed.
Perform all other related duties as assigned.

The pay range for this position is between $30.00 - $35.00/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: Associate’s degree (A.A./A.S.) or equivalent in medical laboratory technology (MLT) or related field required. Bachelor’s degree (B.A./B.S.) or equivalent in medical technology (MT) preferred.
Experience: 0-2 years of experience in a clinical pathology laboratory.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: MT or MLT with certification or certification-eligible (ASCP or HEW) preferred.
Other: Experience with computer software programs is required. GLP environment requires attention to detail, strong organizational skills, and accurate record keeping competencies.

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.

Director, Pharmacology (Shrewsbury, MA, US, 01545)

Job Summary

Provide senior level business, scientific, and strategic leadership for Pharmacology (Oncology and Metabolism) locally with input globally:

o Manage and scale the Pharmacology (Oncology and Metabolism) business responsibly, with a balanced approach of prioritizing employees, client satisfaction, and operational efficiency while growing topline revenues and maintaining consistently high margins.

o Identify and foster science-related initiatives and capabilities.

o Provide a focal point for assessing program related needs and proposals for improvement and effect their implementation.

o Identify key science-based issues needing discussion at the appropriate meeting venue and contribute exemplary leadership in determining resolution of issues and advancement of scientific programs.

o Contribute to problem resolution of study related science-based issues.

o Provide scientists with guidance in the interpretation and reporting of data.

o Support key business financial, operational, client service, employee, quality goals and achieve targets.

o Encourage and support global collaboration across all sites involved in Pharmacology.

· Scope of work, report and protocol scientific review: Contribute to the interactions of the study directors, clients, and sponsors and provide scientific oversight for study design, preparation of protocols, interpretation of data, and preparation of reports. Interact with study directors and their supervisors to ensure reports are of high quality.

· Functional area(s) of expertise: Provide scientific oversight through both direct and indirect management of the Pharmacology (Oncology and Metabolism) functional areas including PDX, CDX, syngeneic tumor models, DIO, Type I and Type II diabetes, NASH, and new therapies. Identify and recommend innovative technologies, techniques, and/or cross-functional management of staff responsible for the specialty area. Work directly with operations staff in the functional area to resolve scientific and technical issues.

· Responsible for personnel management activities such as: macro 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.

· Work effectively with technical operations groups and direct activities of assigned group(s) to ensure optimal performance of the group/function. Identify and implement collaborative projects and synergies with other departments and sites.

· Support strategic planning in the functional area of Pharmacology (Oncology and Metabolism).

· Business development: Engage clients directly and as part of co-travel with Charles River commercial teams. Identify and evaluate new capabilities to expand the scientific base of the company. Represent Charles River at scientific meetings and support sales and marketing at local Charles River sponsored meetings on request.

· Preclinical function: Participate in cross-site initiatives related to scientific initiatives, harmonization of procedures, and standardization of Pharmacology processes, templates for protocols, and reports. Provide scientific and regulatory advice to the Pharmacology group and interact with colleagues in Laboratory Sciences and Toxicology.

The pay for this position is between $185,000 - $230,000 annually. 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: Veterinary or Medical degree (DVM/VMD, MD) and/or Ph.D. in Pharmacology- (Oncology and Metabolism) related discipline is preferred. Post-doctoral experience in a related discipline is a plus.
An equivalent combination of education and experience with documentation as a subject matter expert in the discipline of Pharmacology (Oncology and Metabolism) may be accepted as a satisfactory substitute for the requirements listed above.
Experience: Minimum of 10 years related experience in research or pharmaceutical environment. Management experience is essential.
Certification/Licensure: None required.
Other: Experience in use of desktop applications (word processing, spreadsheets, databases) and network navigation required.

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.

Research Analyst 1, Bioanalytical Chemistry (Shrewsbury, MA, US, 01545)

Job Summary

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.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   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.
•   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 pay range for this position is between $24.00 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

MINIMUM QUALIFICATIONS:
•   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
•   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 experience preferred.

WORKPLACE REQUIREMENTS:
•   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 supplies.
•   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 hold and manipulate work materials 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.
•   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 is occasionally exposed to live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
•   The noise level in the work environment ranges from low to moderate 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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

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

Research Analyst 1- Immunology (Shrewsbury, MA, US, 01545)

Job Summary

Responsible for performing basic to moderately complex laboratory work in collaboration with departmental staff.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Analyze basic to moderately complex laboratory assays based on protocols and in compliance with SOPs and GLP regulations.
Record project data in accordance with GLP regulations.
Adhere to current Health and Safety regulations.
Perform all other related duties as assigned.

Job Qualifications

QUALIFICATIONS:
Education: Bachelor's Degree (B.S./BA) or equivalent in a scientific related discipline.
Experience: Zero to two years related laboratory experience, preferably in a pharmaceutical or contract laboratory environment.
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: Demonstrated analytical and problem solving capabilities. Understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good
Laboratory Practices (GLPs), as appropriate. Written and verbal communication skills. Ability to prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft@ Excel, Word, PowerPoint, etc. and with standard laboratory calculations.
PHYSICAL DEMANDS:

While performing the duties of this job, the employee is regularly required to sit, stand and walk, work/type at computer and repetitive use of hands.
Specific vision abilities required by this job include close vision.

WORK ENVIRONMENT:

General office and lab working conditions, the noise level in the work environment is usually quiet.
While performing the duties of this job the employee is regularly required to wear protective clothing (i.e. goggles, face shield, cap, gloves, scrubs, shoe covers), work near toxic or caustic chemicals, work with biohazards.
The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors and 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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

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

Senior Director - Lab Sciences (Shrewsbury, MA, US, 01545)

Job Summary

This is a senior management position within the company with overall responsibilities for the operations and management of all Lab Sciences group within Charles River Massachusetts Shrewsbury facility. Scope includes both regulated and non-regulated work (nGLP; GLP; Clinical).
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Management
•Manage capacity, flexibility, organizational structure and scalability of assigned services including personnel, instrumentation and laboratory space
•Manage allocation of resources to satisfy and exceed client expectations and requirements while also meeting company objectives
•Identify required resources, functional roles and organizational structure necessary to meet site and enterprise objectives
Commercial
•Lead as appropriate client interactions with SHR Lab Sciences clients, consultants and CRL colleagues, Including onsite visitations.
•Responsible for establishing pricing and ensuring alignment with that of other CRL locations as appropriate. Lead person responsible for all material decisions and negotiations regarding pricing discounts as applicable
•Responsible for monitoring financial performance versus plan, including commercial revenue; intercompany revenue; and operating income. Working with CRL colleagues, provide financial forecasting information for the assigned services and communicating and collaborating with colleagues to develop plans when necessary to address material shortfalls
Regulatory
•Ensure that processes fully satisfy regulatory requirements as applicable with company policies
•Serve as Test Facility/Site management
•Serve as Lab Sciences representative in regulatory agency visits and audits
Technical
•Provide scientific direction, oversight, and guidance to staff
•Ensure that new technologies and processes, applications, software, equipment and other initiatives are evaluated to improve the quality and/or value of the service to our clients
•Lead in the evaluation of new technologies in adjacent areas to assigned responsibilities with the objective of expanding service offerings to our clients
Personnel
•Develop and maintain a positive work environment supported by effective communication to inform employees of plans and progress
•Responsible for the development of all direct reports, providing regular coaching and feedback
•Ensuring that all staff have adequate training and education to do their jobs and when necessary
•Ensure the recruitment and retention of personnel necessary to meet departmental objective

The pay range for this position is between $219,000.00 and $245,000.00. 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: Master’s degree in chemistry, biochemistry or a related scientific discipline required. PhD preferred.

Experience: 10 years relevant laboratory experience in a contract research organization (CRO), biotechnology, or pharmaceutical environment, working to Good Laboratory Practice (GLP) standards. 5 years management experience, including staff management and development, and financial responsibility including budgets.

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

Other Computer proficiency in MS Office suite. Excellent verbal and written communication and organizational skills required. Demonstrated independent analytical and problem-solving abilities. Knowledge of GLP regulations. Ability to develop and maintain productive vendor, site, and company relationships. Ability to interact appropriately with all levels of employees and work effectively as a member of a team.

Equal Employment Opportunity

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

Animal Care Associate (GEMS) - No Experience Needed - 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).

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

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
Benefits: Paid Sick Time/Volunteer Time Off and use of our gym onsite

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. 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.

Isolator Technician (Animal Housing) (Wilmington, MA, US, 01887)

JOB SUMMARY

We are seeking an Isolator Technician for our GEMS-Breed Department located in Wilmington, MA.

In this role you will be working both indoors and outdoors with our animal housing (isolators).

This is a temporary opportunity with the potential to become a full time employee.

$17.75/Hour
Paid Sick time / 401K Participation / Volunteer Time Off
Use of our onsite gym
Monday-Friday work week schedule

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Assist with isolator moves between different locations.
Remove soiled caging and other materials from isolators.
Disassemble the isolators’ component parts.
Inspect the isolator, noting any damage.
Wash, rinse, and dry the isolator box/bag.
Replace isolator gloves.
Operate industrial cage and rack washer.
Order, assemble, sterilize and manage storage of supplies.
Performs all job-related duties in accordance with company safety procedures.

MINIMUM QUALIFICATIONS:

No experience required, we will train.
Valid driver's license required.
Will be required to get certifications on personal lift, forklift and power jack (paid by CRL)

PREFERRED QUALIFICATIONS:

Mechanical experience
Forklift experience

The hourly pay rate for this position is $17.75. 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.

研究模型饲养- 支持类 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。

Animal Technician - Milano (MILANO, Milan, IT, 20122)

Job Summary

Per nostro cliente sito in Milano e Calco ricerchiamo un Animal Technician

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;
Effettuare attività e procedure tecniche sugli animali

Job Qualifications

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro full 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.

Animal Technician - Milano (MILANO, Milano, IT, 20122)

Riepilogo del lavoro

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.

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

Animal Caretaker - contratto a chiamata (Milano) (MILANO, Milan, IT, 20122)

Job Summary

Per nostro cliente sito in Milano ricerchiamo un operaio 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 full 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.

Animal Caretaker - contratto a chiamata (Milano) (MILANO, Milano, IT, 20122)

Riepilogo del lavoro

Per nostro cliente sito in Milano ricerchiamo un operaio 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

Disponibilità a lavoro nel week-end

Buona conoscenza del pacchetto office

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.

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

Operaio stabularista - Firenze (MILANO, Milan, IT, 20122)

Job Summary

Per nostro cliente sito in Firenze 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 full time e trasferta a Milano per un periodo iniziale di training

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.

Allevamento animali da ricerca - Collaboratore (MILANO, Milano, IT, 20122)

Riepilogo del lavoro

Attività aviaria

La nostra attività aviaria offre a ricercatori e produttori di vaccini la sicurezza che deriva dalla consapevolezza che i materiali impiegati per il loro processo di produzione sono esenti da agenti estranei. Charles River ha stabilito procedure per la manipolazione degli uccelli e la produzione di uova che hanno fissato lo standard d’industria a livello mondiale.

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.

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

Technician I, Animal Care Services (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, 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.

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*
Saturday - Wednesday with holiday rotations 07:00AM* – 3:30PM*
Wednesday - 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.

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.

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

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

Animal Research Technician (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 benefits.

A Technician 1 – In Vivo 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.

Equal Employment Opportunity

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

Documentation Data Reviewer 1 1 1 (Mattawan, MI, US, 49071)

Job Summary

HOURLY RATE: The pay for this position is $23.50/hr USD. 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 (must be onsite 5 days a week)

We are currently seeking a Data Analyst II for our Quality Control team located at our Mattawan, MI site.

Quality Control supports the review and archival of analysis performed and provides administrative support to the Project Scientists in Laboratory Science disciplines that may include dose formulations, large and small molecule analysis, molecular and cell-based assays, Biomarker, and flow cytometry-based lab work. Staff participate in the review of methods; equipment records and the creation of report tables. Staff participate in the tracking and managing study related materials, providing requested data/information to the Project Scientist or Sponsor as required. Staff are knowledgeable in the application of GxP’s and applicable SOPs, protocols and ensuring adherence to regulatory documents.

Essential Duties and Responsibilities

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
Accurately identify and effectively communicates any issues with data
Effectively support administrative tasks including but not limited to, filing, ordering, distribution of documents and study related materials as needed
Independently compile and archive data books and departmental records
Develop critical thinking, troubleshooting and time management skills aligned with needs of operational area
Review and issue data sets in adherence to established timelines
Accurately review departmental and study specific data to ensure adherence to SOPs, methods/protocols, industry standards, and regulatory requirements as applicable in timely manner
Oversee and maintain responsibility for one operational area with minimal oversight
Identify data discrepancies involving collection and analyses compared to study plan by working with appropriate personnel with oversight
Ensure sample analysis data collected is accurate against study plans, methods/type of analysis conducted and subjects' collection time points with oversight
Create and compile report tables with oversight
Review methods for accuracy, consistency and formatting with oversight
Review and monitor study schedules to ensure timelines are met with oversight
Ensure documents align with requirements indicated in Client Information Database (CID)
Attend study and/or department related meetings to assure understanding of assigned projects
Attain CRL personnel and Sponsor signature/approval for study documents and distribute documents when necessary
Assist in preparation, review and/or processing of specialty data shared with Sponsors
Independently generate and maintain standard and complex draft study plans/protocols/amendments and reporting templates in accordance with CRL or Sponsor specific requirements within one operational area
Review laboratory study data to provide financial information for Unit Based Invoicing
Perform all other related duties as assigned

Job Qualifications

Bachelor’s degree (BA/BS) or equivalent in a relevant field with no previous work experience
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
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

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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

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

Senior Associate Scientist - Bioanalytical Method Development 1 1 (Mattawan, MI, US, 49071)

Job Summary

We are seeking an Senior Associate Scientist for our Bioanalytical Team site located in Mattawan, MI.

The following are responsibilities related to the Senior Associate Scientist:

An Senior Associate Scientist in Laboratory Sciences is responsible for developing and validating methods to quantify chemical entities according to applicable Standard Operating Procedures (SOPs) and/or GxP regulations. The individual in this role is proficient in the use of instrumentation and laboratory techniques and in the execution of method development and validation procedures. An Senior Associate Scientist is expected to work independently, participate in process improvement initiatives, and may function as a Principal Investigator or Study Director.

Job Qualifications

The following are minimum qualifications related to the Senior Associate Scientist position:

Bachelors degree (BA/BS) with 5-7 years of relevant working experience. Master's degree (MS) with 1-2 years of relevant work experience. Doctorate degree (PhD) with some relevant experience and CRO is preferred.
LCMS Experience Required
Proficient using laboratory software applications (i.e., LIMS and data acquisition software).
Working knowledge of GxPs and industry guidance documents.
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.
Familiarity with Microsoft Office Suite.
Ability to work under specific time constraints.

The pay range for this position is $70 - 75,000 k/year. 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.

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.

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

Senior Associate Scientist, Discovery Bioanalytical 1 (Mattawan, MI, US, 49071)

Job Summary

We are seeking a Senior Associate Scientist for our Discovery Bioanalytical team at our Mattawan, MI site.

The Senior Associate Scientist in Discovery Bioanalytical is responsible for quantitative analysis of drug in body fluids and tissue from non-regulated and regulated safety evaluation, pharmacokinetic/pharmacodynamic studies. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation & reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques 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.

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 and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Actively communicate and collaborate across operational areas in order to adhere to timelines and produce quality data.
Assist with laboratory investigations, assay troubleshooting, quality observations, and problem solving of technical and/or regulatory issues with minimal oversight.
Effectively develop and validate quantitative/qualitative LC/MS-MS methods/procedures with limited complexity/scope in one operational area with minimal oversight.
Independently perform data analysis in appropriate software for at least one analytical platform with minimal oversight.
Independently operate laboratory instruments including their respective software applications for 1-2 analytical platforms with minimal oversight.
Develop critical thinking, troubleshooting and time management skills aligned with needs of operational areas.
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team.
Able to recognize method and/or data issues and communicate them to management to minimize study impact with minimal oversight.
Independently prepare summary of method development data
Write both study and non-study deviations with minimal oversight.
Full understanding of regulatory and GXP requirements, industry standards and company SOPs within one operational area
Independently lead the lab staff in the completion of method validation studies
Provide support to staff members as required by operational area as needed.
Actively participate in internal process improvements, presentations, and harmonization efforts
Performs all other related duties as assigned.

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

Job Qualifications

The following are the minimum requirements related to the Senior Associate Scientist position.

Bachelor's degree (BS) with 5-7 years of relevant working experience or Master's degree (MS) with 2-4 years of relevant work experience or Doctorate degree (PhD) with 1-2 year of relevant experience
An equivalent combination of relevant education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
LCMS 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.
This is an onsite position (no remote options) requires no travel.

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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

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

Relief Veterinarian (Stilwell, KS, US, 66085)

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

The Relief (Clinical) Veterinarian is a flexible schedule based on scope of work up to full-time. This role is meant to provide top notch and ethical veterinary health care for laboratory animals and ensure CRL’s mission of saving human and animal lives! A successful individual will also advise regarding the husbandry, care and maintenance of laboratory animals as well as facilitating training for technicians. This responsibility extends to promoting animal well-being during all phases of the animal's life as well as roles in compliance monitoring, quality management and safe work practices when working with animal models. Our goal is to save human and animal lives in the most ethical and humane way by not only adhering to regulations and guidance's such as the animal welfare act, the 3R's of ethical research, the AVMA guidance on human euthanasia, and “The Guide for the Care and Use of Lab Animals," but pursuing continuous improvement to approaches in research animal care.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Manage health care for the animals within the facility.
Perform veterinary rounds as scheduled and provide clinical care and preventive medicine support.
Perform surgical support and provide anesthesia, surgical and analgesic technical
Expertise/advice to facilitate protocol development.
Deliver training for staff. Training may include veterinary diagnostics, techniques, and minor surgical procedures.
Provide animal health care guidance for veterinary services personnel as required.
Provide support for activities of the Institutional Animal Care and Use Committee (IACUC), including protocol review, program review and facility inspections.
Perform consultation and collaboration with Researchers regarding animal care, health, welfare and treatment.
May assist in sentinel animal monitoring and other monitoring programs.
Review veterinary care and/or necropsy SOPs as required.
Perform literature searches relating to veterinary subject matters.
Ensure facility is following all applicable regulations, guidelines and standards that relate to animal care and use (E.g., USDA, FDA, AAALAC).
Make recommendations and assist in establishing and enhancing veterinary and animal care standards.
May use controlled substances and be responsible for maintaining appropriate records.
May develop new or innovative procedural improvements appropriate to research studies.
Perform special projects and assist with administrative efforts as needed.

Job Qualifications

Education: Veterinary degree (D.V.M./V.M.D.) required.
Experience: Zero plus years related experience with animal care and surgical techniques. Strong preference for experience in a research/lab animal/GLP environment.
Certification/Licensure: Licensure to practice veterinary medicine in at least one U.S. state required. Ability to practice veterinary medicine in the work state highly desirable
Other: Computer literacy in word processing, spreadsheet and database software. Ability to organize, prioritize work and meet deadlines. Good communication skills.

Compensation Data

The pay range for this position is $120/hour - $150/hour. Please note that compensation varies based on factors including, but not limited to, experience, skills, education, and certifications.

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.

Vivarium Support Technician - Cagewash (Stilwell, KS, US, 66085)

Job Summary

We are seeking a Vivarium Support Technician at our Safety Assessment site located in Stilwell. The pay for this position is $19/hour plus benefits.

A Vivarium Support Technician is responsible for assisting in vivarium operations activities which facilitate clean housing and care for laboratory animals. Also responsible for helping assist in the preparation of materials which enable study activity completion.

Essential Duties and Responsibilities:

Clean and sanitize animal cages and related environmental items.
Perform daily routine maintenance checks on the automated cage wash machines.
Prepares appropriate housing for receipt of new animals; may assist with receiving animals.
Report the need for equipment repair (cages, racks, cagewash machines, etc.) to the appropriate personnel.
Sanitize floors, walls and other surfaces in the automatic cage wash area and in other areas of the lab.
Maintain a clean cage wash area.
Maintain storage area in an organized fashion.
Complete animal care technical duties such as changing liners and sanitizing animal room walls and floors.
Receive, store, and distribute animal husbandry supplies.
Perform limited troubleshooting and calibration of instruments as appropriate for assigned area.
Prepare environmental enrichment items (edible and durable).
Operate basic lab equipment and perform routine maintenance as needed.
Prepare study and colony supplies as needed.

Job Qualifications

Education: High School diploma or General Education Degree (G.E.D) preferred.
Experience: No experience necessary
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Demonstrated ability to problem solve, make quick decisions, communicate decisions effectively.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
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.

Equal Employment Opportunity

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

Animal Care Technician I (Hamilton, MT, US, 59840)

Job Summary

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

As the Animal Care Technician I, you will be working in ABSL 2-3 facility environments to perform a variety of duties, including cleaning, sanitizing, routine preventative maintenance, and repair of caging materials and autoclaves.

Additional responsibilities include:

Maintaining cagewash and animal holding facilities in a clean and organized manner
Operating equipment and performing general housekeeping
General animal care duties
Receipt, stocking, and maintenance of supply orders
Preparing and submitting all required written records, charts, logs, and inventories
Work actively with customers to address requests, inquiries, and complaints
Provide technical assistance

Job Qualifications

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

High school diploma/GED preferred
ALAT certification, or ability to obtain certification within one year of eligibility
Experience and/or training working with mechanical equipment preferred

The pay for this position is $22.00 USD 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

Animal Care Technician I (Hamilton, MT, US, 59840)

Job Summary

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

As the Animal Care Technician I, you will be working in ABSL 4 facility environments to perform a variety of duties, including cleaning, sanitizing, routine preventative maintenance, and repair of caging materials and autoclaves.

Additional responsibilities include:

Maintaining cagewash and animal holding facilities in a clean and organized manner
Operating equipment and performing general housekeeping
General animal care duties
Receipt, stocking, and maintenance of supply orders
Preparing and submitting all required written records, charts, logs, and inventories
Work actively with customers to address requests, inquiries, and complaints
Provide technical assistance

Job Qualifications

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

High school diploma/GED preferred
ALAT certification, or ability to obtain certification within one year of eligibility
Experience and/or training working with mechanical equipment preferred

The pay for this position is $22.00 USD 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

Animal Care Technician I (Hamilton, MT, US, 59840)

Job Summary

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

Additional responsibilities include:

Maintaining cagewash and animal holding facilities in a clean and organized manner
Operating equipment and performing general housekeeping
General animal care duties
Receipt, stocking, and maintenance of supply orders
Preparing and submitting all required written records, charts, logs, and inventories
Work actively with customers to address requests, inquiries, and complaints
Provide technical assistance

Job Qualifications

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

High school diploma/GED preferred
ALAT certification, or ability to obtain certification within one year of eligibility
Experience and/or training working with mechanical equipment preferred

The pay for this position is $22.00 USD 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

Animal Care Technician I (Hamilton, MT, US, 59840)

Job Summary

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

Additional responsibilities include:

Maintaining cagewash and animal holding facilities in a clean and organized manner
Operating equipment and performing general housekeeping
General animal care duties
Receipt, stocking, and maintenance of supply orders
Preparing and submitting all required written records, charts, logs, and inventories
Work actively with customers to address requests, inquiries, and complaints
Provide technical assistance

Job Qualifications

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

High school diploma/GED preferred
ALAT certification, or ability to obtain certification within one year of eligibility
Experience and/or training working with mechanical equipment preferred

The pay for this position is $22.00 USD 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

Cagewash Technician I (Chicago, IL, US, 60637)

Job Summary

We are seeking a Cagewash Attendant for our Insourcing Solutions site located in Chicago, IL.

As the Cagewash Technician, you will use existing SOPs and quality assurance standards to perform general housekeeping, as well as maintain facility equipment and perform routine preventative maintenance on cagewash and autoclaves.

Additional responsibilities include:

Sanitize, maintain, and repair animal caging materials
Ensure cagewash and animal holding facilities are kept in a clean and organized manner
Assist with the receipt, stocking, and maintenance of supply inventories
Prepare and submit required written records, charts, logs, and inventories
Actively interact with customers to resolve requests, inquiries, and complaints, and to provide technical assistance.

Job Qualifications

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

High school diploma, General Education Degree (G.E.D.) or equivalent

Experience and/or training working with mechanical equipment preferred

The pay for this position is $17.94 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.

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.

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

Technicien(ne) Support Informatique Biomédicale - CDI (Ecully, FR, 69130)

Qui sommes-nous ?

Aux portes de Lyon, le site Charles River d'Ecully offre à ses 90 collaborateurs un environnement dynamique et une cuture d'entreprise certifiés Great Place To Work®. Nos équipes, passionnées et impliquées, contribuent aux efforts que nous accomplissons chaque jour pour améliorer la santé et le bien-être du plus grand nombre possible de personnes.

Le poste

Le Nexus est le premier système de test d'endotoxines entièrement automatisé conçu spécifiquement pour les laboratoires de contrôle qualité. Dans un contexte de ventes croissantes de notre appareil, nous souhaitons renforcer notre équipe Customer Technical Support par l’ouverture d’un poste de Technicien(ne) Support Informatique Biomédicale en CDI.

Travaillant pour un périmètre européen depuis notre site d’Ecully, vous serez l’interlocuteur privilégié des clients externes et des équipes techniques itinérantes internes pour les assister techniquement dans la mise en service, le réglage et le dépannage des appareils Nexus de nos clients. Vous serez également impliqué(e) dans la formation des utilisateurs ainsi que dans la rédaction et la mise à jour de la documentation associée aux appareils.

Missions

Qualifier le support nécessaire et les améliorations logicielles pour toutes les demandes techniques de Nexus en utilisant le logiciel approprié (par exemple, service max/TSF/Knowledge Owl, etc.)
Fournir un support technique pour les produits Nexus aux équipes techniques itinérantes ou directement aux clients
Fournir un support de test pour les mises à jour effectuées avant le déploiement pour l'automatisation et les applications logicielles
Fournir une assistance technique pour les besoins d'installation de logiciels et de technologies de l'information à distance ou sur les sites des clients.
Résoudre les plaintes des clients concernant les logiciels
Tester les produits par des essais pratiques et automatisés, et identifier les défauts potentiels des produits/logiciels
Coordonner et travailler avec notre spécialiste global des applications logicielles et les ingénieurs des logiciels/produits pour rechercher et résoudre les problèmes liés aux logiciels/systèmes en vue d'une correction immédiate, ainsi que pour documenter les problèmes en vue d'une action corrective à long terme
Créer et maintenir des guides de dépannage pour aider les équipes techniques itinérantes à résoudre rapidement et efficacement les questions des clients
Contribuer à l'élaboration et à la révision de documents contrôlés tels que les procédures opérationnelles normalisées, les documents IQOQPQ et les spécification
Aider les clients à créer et à réviser les procédures pour la gamme Nexus
Former l'assistance technique à l'utilisation et au dépannage des demandes techniques concernant Nexus
Se rendre sur les sites des clients pour les former à l'utilisation des produits Nexus et aider le service extérieur à résoudre les problèmes et à prendre des mesures correctives ou préventives à long terme pour les produits Nexus

Qualifications souhaitées

Diplômé(e) d’une formation de niveau Bac+3 minimum en informatique, en mathématiques ou dans une discipline connexe d’ingénierie, vous disposez d’une solide expérience (5 ans minimum) dans le domaine du tests logiciels et de la robotique.
Vous connaissez le matériel informatique, les bases de données SQL, le développement de requêtes simples (Visual Basic) et des logiciels de base : produits basés sur Windows et Linux et systèmes robotiques de laboratoire.
La compréhension de la microbiologie dans le domaine pharmaceutique est un atout. A défaut, l’intérêt pour ce domaine est essentiel.
Au-delà de vos compétences techniques, vous disposez d’excellentes aptitudes à la communication orale et écrite, en français comme en anglais.
Vous savez gérer un dépannage de manière autonome et efficace, et savez être force de proposition face à des problèmes logiciels ou matériels.

Enfin, ce poste ayant un rayonnement européen, vous êtes enclin à vous déplacer ponctuellement sur nos différents sites clients ou internes.

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

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

Technicien Animalier Primates - F/H - CDI (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. 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 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

Afin de renforcer notre équipe de 4 personnes, nous recherchons un Technicien Animalier en CDI (F/H) pour travailler au sein de notre zone dédiée aux Primates.

Les missions

Participer au lancement des études en préparant les cahiers dont vous aurez la charge
Vérifier l'adéquation des conditions d'hébergement avec les procédures
Assurer l'ensemble des techniques de contentions, administrations, prélèvements et examens standards sur les animaux
Assurer tout ou partie des techniques spécifiques des études de reproduction et des études de perfusion
Contrôler l'état clinique (croissance, poids, comportement) des animaux en cours d'études et remonter les anomalies
Préparer quotidienne le matériel nécessaire à l'étude et assurer sa disponibilité
Acquérir les données selon nos plans d'études, assurer leur contrôle et leur enregistrement

Conditions spécifiques du poste

Amplitude horaire : 6h/18h
Permanences de weekend (1 week-end sur 3 environ, 3h d'intervention par jour )

Qualifications souhaitées

Vous êtes titulaire a minima d'un diplôme de niveau Bac et disposez d'une première expérience dans le domaine du soin animalier, idéalement auprès de primates.

En tant que technicien(ne), vous faites du bien-être animal votre priorité. Votre investissement, votre rigueur et votre relationnel seront également des atouts pour ce poste.

Les modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : CDI non-cadre (accord de modulation 35h)
Salaire : A compter de 25 800€ 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.

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.

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.

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

Senior BI & Data Analyst (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

Senior BI & Data Analyst

We are seeking an experienced Senior Business Intelligence (BI) & Data Analyst for our Enterprise Data Analytics Team.

There’s never been a more exciting time to be on the Enterprise Data Analytics team at Charles River Labs! We are on a mission to make the Enterprise Data Analytics team the backbone of today’s business, as data-driven decision-making enables business leaders to make informed choices quickly to boost revenue, improve productivity, and stay a step ahead of the market. We have already launched our own Enterprise Data Hub, the digital backbone of this company, and we need more experts and leaders in the data analytics discipline who are forward-thinking, self-guided, and innovative to continue to build out the hub across our lines of business, integrating all of our data, mastering data and focusing on data quality to fundamentally shift the way Charles River operates through data science and advanced analytics.

You will be joining a team with an unyielding dedication to the company's purpose; Together We Create Healthier Lives. This laser focus on the patient makes the broader Global Technology Team so exciting. We are taking Charles River to a place where the Enterprise Data Analytics team will be applying the techniques of AI, Generative BI, data management, data engineering, and strategy development, as well as the use of analytics techniques that range from forecasting and simulation to linear programming and optimization and we want you to join us.

Note: It’s a fully remote home-based role for professionally qualified and experienced candidates based in India, who are willing and open to work UK shifts.

Responsibilities:

• Engage Business Stakeholders at all levels to identify requirements for current and future products through ongoing interaction
• Data Profiling, mining, and data validation to ensure data is fit for use by the business
• Ability to see the big picture and then identify key areas for deep analysis to support sound solutions
• Perform ad-hoc analysis and present results in a clear and user-friendly manner
• Perform testing, resolve issues, and work with developers to automate testing/data validation
• Design and create analytics solutions utilizing Power-BI and Copilot
• Lead requirements workshops and User Acceptance Testing for new data and analytics solutions
• Build strong business relationships that foster a collaborative and trusting approach and partnership
• Act as scrum master for the team and prepare detailed stories for developers.

Job Qualifications:

• Bachelor’s degree in Business Management, Computer Science (or related field), MBA Preferred
• 3+ years of experience with Data Visualizations tools such as Power BI, SSRS, or Tableau
• 1-2 years of experience with data analysis and profiling for Data Science Modelling
• 5+ years of experience in writing SQL queries, data mining, data profiling, and data validation/testing
• 5+ years of experience as a Business Systems Analyst / Data Analyst specializing in the Data & Analytics discipline
• Experienced in Microsoft Fabric and Copilot Power-BI components
• 5+ years of experience organizing and running User Acceptance Testing cycles and training with business users and stakeholders
• Strong business mindset with an ability to collaborate with business partners to identify needs and opportunities for improved data management and delivery

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.

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

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Job Qualifications

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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

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.

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.

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

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

工作总结

关于研究模型与服务
基础研究和发现的基本方法是使用体内模型来帮助寻找疾病靶标并确定调节相应病症的潜在生物学通路。作为世界上生产和销售最优质研究动物的领军企业，其中全球临床前研究中使用的动物模型中有一半是我们生产的，我们了解这一步的重要性。凭借七十年的经验和无与伦比的的技术专长，我们能够为您提供完美的动物模型，包括特定疾病模型和预处理模型，可用于基础研究等等。

欲了解更多信息，请访问www.criver.com。

Production Supervisor (Small Animal) (Raleigh, NC, US, 27610)

JOB SUMMARY

We are seeking a Production Supervisor to support our Breed Operation in Raleigh, NC. As the Production Supervisor, you will provide daily supervision of personnel and operations to ensure achievement of departmental goals and levels. You will independently handle routine personnel-related issues; assist in the handling of complex personnel-related issues.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

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. Schedule and prioritize workload of group members.
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.
Oversee production and shipping activities of assigned group, including SOPs and OORs. Ensure proper record-keeping and report preparation.
Review safety issues and Workers’ Compensation claims.
Actively interact with and provide technical assistance to customers as required to resolve customer requests, inquiries, and complaints.
Review customer complaints and participate in the development and implementation of any resulting procedural changes. Create and maintain complaint chart.
Audit production rooms and/or isolators.
Review and ensure appropriate inventory levels of departmental supplies.
Interview and select qualified non-exempt personnel. Recom¬mend personnel actions, including hiring, promotions and raises. Partner with Human Resources and departmental management to assist in the handling of disciplinary issues. Draft appropriate personnel action paperwork.
Identify training and development needs of direct reports. Assist in the development, implementa¬tion and delivery of depart¬mental training programs; ensure that direct reports receive departmental orien¬tation and necessary on-the-job training. Oversee main¬tenance of group training manual and training records.
Monitor performance of direct reports. Provide regular coaching and counseling. Assist in preparation and delivery of salary and performance reviews of direct reports.
Schedule overtime as authorized. Review and approve timecards. Coordinate vacation/time off schedules.
Recommend short-range operating objectives, organizational structure of direct reports and staffing requirements. Assist in the development of a departmental plan for backup and succession of key technical personnel.
May assist in development of departmental budget.
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.
Assist in the development, maintenance and communication of departmental systems and SOPs. Assist in the development and communication of job descriptions for subordinate positions.
Ensure that departmental equipment is maintained in good working condition and that departmental area(s) are maintained in a clean and orderly condition. Ensure proper recycling and setup of cages in assigned area(s).
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

Candidates must possess one of the following:

Bachelor’s degree in life sciences or related discipline and 4 years of supervisory experience of a high-performing team to deliver complex initiatives and/or support operations, and assistance in cross-functional collaboration to drive successful business outcomes.
Associates degree in life sciences or related discipline and 6 years of supervisory experience
High school diploma or GED and 8 years of supervisory experience

ADDITIONAL QUALIFICATIONS:

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

PREFERRED QUALIFICATIONS:

ALAT certification

Salary Range

The pay range for this position is $70,000 - $80,000 / annually. 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.

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 provide the highest animal welfare standards and care, in addition to maintaining vivarium cleanliness.

Additional responsibilities include:

Ensure high standards of animal welfare are met.
Provide food, water and clean housing to animals according to applicable SOPs.
Perform routine animal health observations.
Monitor temperature and humidity, reporting any issues to supervisor or manager.
Receive, unpack, and house animals according to SOP and Animal Receiving Form
Understand proper room entry order and adhere to biosafety requirements.
Maintain accurate records organize supply areas.
Maintain vivarium cleanliness and waste removal in accordance with applicable SOPs.

Job Qualifications

The following are minimum requirements related to the Animal Care Technician I position.

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 $20-22 USD per hour. Please note that salaries vary within the range based on factors including , skills, certifications, and location.

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!

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

Clinical Pathology Technician I (Reno, NV, US, 89511)

Job Summary

***Hours are from 9:30 a.m. To 6:00 p.m ***

BASIC SUMMARY:
Perform a wide variety of basic laboratory tasks. Maintain and perform record keeping. Review data recorded for others for quality control. Review, process, track, and store samples received into the laboratory.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Perform a wide variety of basic laboratory tasks.
•   Under supervision may act as lead/primary technician on routine studies.
•   Operate general laboratory equipment (i.e.: centrifuge, pipettes, water baths) used in the processing of b biological samples.
•   Perform all specialized processing under supervision
•   Read study protocols and extract pertinent information with guidance.
•   Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs).
•   Monitor, and perform tasks, related to individual study assignments.
•   Receive, process, track and store all samples received into the laboratory.
•   Observe and assist with technical/study related duties with guidance.
•   File and maintain data for department activities.
•   Maintain and perform record keeping.
•   Review data recorded by others for quality control.
•   Assist with training for less experienced staff.
•   May perform phlebotomy when appropriately certified.
•   Perform all other related duties as assigned.

Job Qualifications

•   Education: High school diploma or General Education Degree (G.E.D.).
•   Experience: Experience in a laboratory setting 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: Good keyboarding skills, proficient in utilizing personal computer, e-mail and standard office software packages (word processing, spreadsheet, presentation, database).

***The pay range for this position starts at $19.00. 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.

Validation Engineer I (Rockville, MD, US, 20850)

Job Summary

The Validation Engineer I is responsible for supporting the execution of equipment, utilities, and facility validation activities in compliance with GMP regulations and company procedures. This role involves hands-on protocol development, execution, data analysis, and documentation under the guidance of senior validation personnel.

Key Responsibilities and Duties:

Preparation, execution, and documentation of validation protocols (IQ/OQ/PQ) for manufacturing equipment, analytical equipment, utilities, and facility systems.
Coordinate and schedule system vendors with respect to the execution of Installation, Operation, and Performance Qualification (IQ/OQ/PQ) protocols, and subsequent Re-qualification (RQ) protocols, if applicable, for new and in-use equipment to ensure compliance with site procedures, Validation Master Plan, and regulatory requirements.
Participate in change control and deviation investigations related to validated systems.
Collaborated cross-functionally with Quality Assurance, Engineering, Manufacturing, and IT.
Organize an efficient method to ensure all requirements of assigned validation deliverables are completed and that validation efforts are executed in a timely manner.
Maintain accurate and complete validation documentation in compliance with data integrity principles (ALCOA++)
Participate in the development of corrective actions, as needed, for deficiencies that may be uncovered/observed during validation efforts regarding equipment, processes, test methods, facilities, computer software/systems, SOPs, and other related issues to ensure compliance with applicable regulatory requirements/guidelines, procedures, and policies.
Participate in the development of CAPA’s and assess the effectiveness of corrective action.
Participate in validation project team meetings to ensure project milestone schedules are maintained and deliverables satisfy requirements.
Assist, as needed, during client and regulatory audits and help to resolve or mitigate audit findings related to system qualification/validation.
Validation contractor oversight, as needed.
Perform all other related duties, as assigned.

Job Qualifications

Bachelor’s degree or equivalent in a scientific, Engineering, IT discipline, or related field.
Experience: 0-3 years of experience in validation, quality, or engineering roles within a regulated (GMP) environment. Internship or co-op experience in pharmaceutical, biotech, or medical device industries is a plus.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Must have excellent oral and written communication skills. Strong documentation development and technical writing skills are critical to this position.
Understanding of validation principles and regulatory requirements, (e.g., FDA 21 CFR Part 11, EU Annex 15) is a plus.
Leadership ability, project management, and facilitation skills required. Must be proficient with Microsoft Office software (Word, Excel, PowerPoint). Must have good interpersonal, organizational, and analytical skills.

Compensation Data

The pay rate for this role is $67,000 - $78,000 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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.

Senior Laboratory Analyst (Analytical Sciences) (Ballina, IE, F26D786)

Job Summary

We are seeking an experienced Senior Analytical Analyst for our Biologics Division located in Ballina, Co. Mayo, Ireland.

This role shall report to the Analytical Supervisor and the main duties & responsibilities shall be:

Carrying out analytical tests using different techniques like HPLC, Capillary Electrophoresis, UV-Vis spectroscopy, Ion Chromatography, GC, and wet chemistry.
Practical and theoretical knowledge on several analytical techniques, with capability of troubleshooting based on the specific request.
Strong knowledge of GMP regulation applied to a laboratory environment.
Assist in developing and/or verification/validation of analytical methods that use equipment like HPLC, Ion and Gas Chromatography, spectrophotometers as well as wet chemistry techniques and compendial methods.
Receipt and processing of test samples in LIMS.
Safe and compliant disposal of all laboratories generated waste.
Carry out data calculations and basic statistics.
Assist in internal, regulatory and client visits/audits and respond to findings.
Sourcing, purchasing and stocking consumables, standards and reagents required for testing.

Job Qualifications

The following are minimum requirements related to the Senior Analytical Analyst position:

BSc/MSc. in a relevant science discipline (e.g. chemistry, biochemistry, pharmacy, and biotechnology)
A minimum of 3 years relevant experience in Laboratory preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO, CMO, CDMO Industry.
Analytical techniques (HPLC, GC, MS and similar) experience essential.
Experience in development and validation of analytical methods according to ICH guideline required but not essential.
Experience in analytical techniques/immunoassays desirable but not essential.

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 characterzation, 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 supported the development of 80% of the drugs approved by the FDA in the last 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.

Animalier contrôle de production - F/H - CDI Week-end (Paris, FR)

Rejoignez une équipe passionnée par les animaux où chaque jour fait avancer la recherche scientifique !

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.

Nous recherchons un Animalier contrôle de production (F/H) pour un contrat en CDI week-end et jours fériés pour un contrat de 8h/semaine à raison de 4h par jour (samedi, dimanche et jours fériés) sur l'un de nos site client basé à Paris 13ème.
Vous contribuerez au respect du bien-être animal et au maintien des meilleures conditions d'hébergement pour les animaux (poissons).

Missions principales

Contrôle du bien-être des animaux selon les consignes préalablement transmises
Vérifier l'abreuvement, l'alimentation et l'enrichissement
Vérification et relevé des paramètres d'ambiance
Respect des consignes transmises
Garantir la mise à jour des registres de suivi.

Profil recherché

Vous êtes étudiant dans des études scientifiques, motivé, rigoureux, passionné par le travail des animaux et vous voulez acquérir une expérience en contact avec les animaux de laboratoire:

Formation initiale: étudiant en étude vétérinaire, biologie ou en cours d'obtention d'un diplôme dans un domaine scientifique ou animalier.
Expérience: une première expérience en contact avec les animaux et/ou en animalerie de laboratoire est un atout
Esprit d'équipe et capacité à collaborer avec les différents interlocuteurs
Organisation et rigueur au quotidien
Sens de l'observation et capacité à identifier des anomalies
Autonomie et proactivité

Modalités contractuelles

   • Convention collective de l’industrie pharmaceutique
   • Nous vous proposons un CDI avec le rythme de travail suivant : samedi, dimanche matin (4h/jour) et jours fériés
   • Prime de transport, 13e et 14e mois, Intéressement, participation, mutuelle et prévoyance, CE

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.

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

Environmental Health, Safety and Sustainability Manager (Hollister, CA, US, 95023)

JOB SUMMARY

We are seeking an experienced Environment, Health, Safety, and Sustainability (EHS&S) Manager to lead the integration of safety and sustainability practices across multiple operational sites. This role will be based at our Hollister, CA facility and will also support several CRADL locations in South San Francisco and San Diego. The position requires a minimum of 2.5 days per week on-site in Hollister, with the remaining 2.5 days dedicated to CRADL site support, either on-site or remote, as agreed upon with your manager and in alignment with each location’s needs. Time allocation may vary based on project priorities and operational requirements. In this role, you will be responsible for developing, implementing, and promoting EHS&S procedures and programs that align with our organizational framework, and embedding a culture of safety to ensure a safe and sustainable workplace.

ESSENTIAL DUTIES AND RESPONSIBILITIES

Develop and implement policies and procedures targeted toward increasing the safety and protection of the environment for the businesses.
Ensure facility compliance with applicable environment health and safety regulations.
Implement site audit program of the EHS&S compliance of the site, track and report status of corrective actions, and alerting senior management to developing problems where intervention or oversight is required.
Participate in site leadership as a member of the site Leadership Team and conduct reviews at appropriate intervals with facility senior management.
Consult with site management and employees on Federal, State, and Local regulatory compliance related issues. Work with site facility management to ensure proper training programs are established with regards to environmental and health and safety compliance.
Responsible for timely submission of environmental reports and permits to local, state and federal regulatory agencies.
Work with site Leadership and Site/Global Procurement to develop cost savings initiatives to ensure business continuity and best in class service pricing.
Provide lead support and formal response to EHS agency inspections conducted by local, state and federal regulatory bodies.
Manage moderate size capital infrastructure projects from inception to completion including regulated areas.
Develop program budgets and schedules in support of EHS&S initiatives including platform tools (e.g. Enablon).
Monitor and drive progress of EHS&S projects and programs, maintaining budgets and schedules.
Lead the selection process for hiring third party service firms, evaluating proposals, conducting interviews and making recommendations to senior management, in partnership with site Procurement and Management
Provide supervision and development of EHS Site staff. Ensure appropriate communication takes place around EHS issues.
Consult with Corporate Engineering, Company management and workplace staff to identify and resolve potential EHS&S issues through engineering design changes or other means necessary, such as Facilities controls, risk assessments.
Clarify, define, and assist in enforcement and application of Agency and Company policies and practices.
Support and affirm the Company policy of Equal Opportunity through Affirmative Action.
Partner with site leadership to address audit findings from clients, regulatory agencies, or internal CRL audits.
Develop and provide EHS&S training to staff and contractors including SOP and EHS&S policy training.
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

- Candidate will possess one of the following:
  - Master's degree (M.A. / M.S.) in life science (biology, chemistry), environmental engineering, or environmental health and safety with 5 years of related experience
  - Bachelor’s degree (B.A. / B.S.) in a life science (biology, chemistry), environmental engineering, or environmental health and safety with 7 years of related experience
  - Associate degree (A.A. / A.S.) in life science (biology, chemistry), environmental engineering, or environmental health and safety with 10 years of related experience
- Sound working knowledge of Good Laboratory Practices (GLPs), Good Manufacturing Practices (GMPs) and government regulatory requirements and guidelines, including California OSHA regulations. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in MS Office suite including Excel, Word, Power point and Project. In- depth knowledge of environment, health and safety regulations required.
- Ability to communicate and influence senior management on EHS compliance initiatives.

Compensation Data

The pay range for this position is $125,000 - $155,000. 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.

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 provide the highest animal welfare standards and care, in addition to maintaining vivarium cleanliness.

Additional responsibilities include:

Ensure high standards of animal welfare are met.
Provide food, water and clean housing to animals according to applicable SOPs.
Perform routine animal health observations.
Monitor temperature and humidity, reporting any issues to supervisor or manager.
Receive, unpack, and house animals according to SOP and Animal Receiving Form
Understand proper room entry order and adhere to biosafety requirements.
Maintain accurate records organize supply areas.
Maintain vivarium cleanliness and waste removal in accordance with applicable SOPs.

Job Qualifications

The following are minimum requirements related to the Animal Care Technician I position.

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 $20-22 USD per hour. Please note that salaries vary within the range based on factors including skills, certifications, and location.

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!

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

Senior Associate Scientist- Manual Ion Channel Testing (Cleveland, OH, US, 44128)

Job Summary

We are seeking a Senior Associate Scientist for our Manual Ion Channel Testing team at our Safety Assessment site located in Cleveland, Ohio.

The Manual Ion Channel Testing group is responsible for evaluating test article effects on ion channels in vitro. Personnel are responsible for operating and maintaining manual patch clamp electrophysiology workstations. Validated hardware and software systems are used to collect and analyze data under regulated (GLP) or non-regulated conditions. The group prepares, collects and transfers test article formulation samples to the CLE analytical chemistry unit (or other appropriate laboratory) for concentration verification and homogeneity analyses, and is responsible for interpretation and reporting of data outcomes

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:

Effectively manage a portfolio of sample analysis projects while ensuring timelines are met in a single operational area with oversight
Execute review and approval of data with oversight for final scientific/technical decisions within a single operational area
Develop understanding of compliance expectations to respond to quality assurance audit observations in appropriate software with oversight
Assist with oversight the completion of laboratory investigations, assay troubleshooting and quality observations
Assist in problem solving for technical and/or regulatory issues with oversight
Responsible for writing and preparing study plans/protocols/amendments with minimal oversight
Participate in Sponsor visits/tours with minimal oversight
Develop expertise in developing and validating quantitative/qualitative methods/procedures with limited complexity/scope in one operational area with minimal oversight
Perform data analysis using appropriate software with minimal oversight
Develop critical thinking, troubleshooting and time management skills aligned with needs of operational areas
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team
Function as a liaison, maintaining timely and frequent communication between CRL and Sponsor/Client/SD with minimal oversight
Ensure scientific integrity of studies with minimal oversight
Function as a Principal Investigator, Individual Scientist and/or Study Director as assigned with minimal oversight
Actively communicate and collaborate across operational areas in order to adhere to timelines and produce quality data
Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Write, review and approve deviations with oversight
Develop knowledge of regulatory and GXP requirements, industry standards and company SOPs within one operational area
Effectively manage a small portfolio of research projects including assay development and validation while ensuring timelines are met in a single operational area with oversight
Perform all other related duties as assigned

The pay range for this role is $75-78K. 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:

Bachelor’s degree (BA/BS) with 5-7 years of relevant working experience. Master’s degree (MS) with 1-2 years of relevant work experience. Doctorate degree (PhD) with no experience
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
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

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

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

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.

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.

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

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

Research Support Specialist I -Veterinary Technicians encouraged to apply (Poolesville) (Poolesville, MD, US, 20837)

Job Summary

We are seeking a Research Support Specialist I for our Insourcing Solutions site located in Poolesville, MD.

Prepare and administer research treatments; collect and record physiological data (weight, temperature, pulse, respiration)
Perform technical procedures as needed associated with the Animal Study Proposals in relation to NHP retroviral, human respiratory and flavivirus studies to include but not limited to blood collection, IV catheterization, intubation, broncho-alveolar lavage, tracheal and nasal lavages, documented research observations, and administration of research treatments
Must have a basic understanding of aseptic technique, anesthesia induction, monitoring, and recovery as well as drug dosage calculations and administration
Assist Veterinarian & Sr. RSS staff with surgeries and specialized procedures
Perform daily animal health observations and report any abnormal findings to veterinarian
Maintain electronic medical records, send daily emails regarding animal health information to vet staff
Collect, preserve, and prepare blood, urine, stool, and tissue samples
Participate in study related necropsies/tissue harvest
Set-up for procedures and prepare supplies and equipment
Ability to maintain freezer organization and sample inventory
Practice universal precautions appropriate to different levels of ABSL. Work safely with animal / human pathogen biohazards and help to maintain the research animal facility as a safe work environment / operation
Report any animal health, care, and / or wellbeing concerns to the appropriate facility management staff
Report any facility infrastructure issues, relative to the animal care and support areas to the appropriate facility management

Job Qualifications

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

- High school diploma or general education degree (GED) required. BS degree in Animal Science, Biology, or similar discipline, or A.A. in Veterinary Technology is preferred.

- 2-3 years’ experience working with non-human primates in biomedical research or 2-3 years Veterinary Hospital technical experience preferred.

- Must have computer program proficiency such as MS Word / Access / Excel. Must have a proficient technical vocabulary.

- RVT/CVT/LVT or LAT certification preferred

The hourly range for this position is between $28/hour and $30/hour. Please note that salaries vary within the range based on factors including, but not limited to skills, certifications and locations.

Equal Employment Opportunity

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

Senior HVAC Technician (Wayne, PA, US, 19087)

Job Summary

The Senior HVAC Technician is responsible to perform a variety of master-level mechanical and pressure/temperature equipment repairs and maintenance requiring close interface with other trade/craft functions. Perform other semi-skilled tasks in the general maintenance of the physical plant and provide work direction to others performing HVAC projects.

This position will work on-site at the Wayne, PA Charles River site. Position will also be responsible to travel to additional CRL sites located in Malvern and Philadelphia.

Position is scheduled to work Monday - Friday, from 9am - 5pm.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Monitor and maintain HVAC systems including high/low temperature, water and electricity. Isolate and identify malfunctioning equipment for repair, adjustment, and replacement. Interpret instructions as required.
• Observe and interpret readings on gauges, meters, and charts to ensure correct functioning of systems. May calibrate equipment.
• Perform adjustments, repairs and replacement of parts and equipment following written specifications such as blueprints, drawings and schematics.
• Dismantle equipment/fixtures and plan systematic replacement or repair of accessories and parts and return equipment to operation.
• Oversee HVAC-related tasks being performed by other department personnel.
• Inspect completed work for quality, safety, and proper operation.
• Coordinate maintenance work with other departments and divisions; maintain accurate records of maintenance and repair work.
• Periodically perform preventative maintenance programs as required.
• Perform other semi-skilled tasks as assigned to assist in the general maintenance of the physical plant.
• Respond to emergencies as needed. Provide 24-hour on-call maintenance coverage, as scheduled in rotation.
• May perform waste vacuum maintenance.
• Take proper safety precautions and utilize appropriate safety gear/equipment in the performance of all duties.
• Perform all other related duties as assigned.

Job Qualifications

QUALIFICATIONS:
• Education: High school diploma or General Education Degree (G.E.D.) and trade school diploma.
• Experience: Four to six 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: Valid HVAC license (where required by state).
• Valid Driver's License.

PHYSICAL DEMANDS:
• While performing the duties of this job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel objects, tools, or controls; and reach with hands and arms. The employee is occasionally required to stoop, kneel, crouch, or crawl and talk or hear.
• The employee must frequently lift and/or move up to 25 pounds and occasionally lift and/or move more than 100 pounds.
• Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, and depth perception.

WORK ENVIRONMENT:
• While performing the duties of this job, the employee frequently works near moving mechanical parts and in outside weather conditions.
• While performing the duties of this job, the employee occasionally works in high, precarious places and is occasionally exposed to wet and/or humid conditions, fumes or airborne particles, toxic or caustic chemicals, risk of electrical shock, risk of radiation, and vibration.
• The noise level in the work environment is usually moderate.

Compensation Data

The pay range for this position is $35.63/hr. USD. 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.

Directeur des Productions - F/H - CDI (L'Arbresle, FR, 69592)

Qui sommes-nous ?

Le poste

Nous recherchons notre nouveau Directeur des productions F/H en CDI en charge de définir et piloter la stratégie pour l'ensemble des activités de production des modèles animaux, des services supports afférents (pré-zone, conditionnement et logistique) et des activités soumises au BPF et/ou cGMP sur les sites de l'Arbresle (69) et Châtillon sur Chalaronne (01) dans un contexte évolutif pour ces activités.

En tant que membre de Comité de direction, vous impulsez la définition d’actions garantissant l’intégration de votre département dans les objectifs et politiques générales de l’entreprise et du Groupe, en alignement avec la réglementation et nos standards exigeants.
Directement rattaché à notre Directeur Général, vous êtes responsable d’un département d'une centaine de personnes.

Vous jouez ainsi un rôle déterminant en assurant le bon déroulement, la conformité et la performance de l'ensemble des opérations de votre périmètre dans un environnement multisites, dans le respect des budgets, des procédures de l'entreprise et ce en vue d'obtenir le meilleur niveau de qualité possible.

Responsabilités principales

Garantir le développement de la culture, de la maturité et de la performance des activités de votre périmètre autour de 7 piliers majeurs : HSE, biosécurité, bien-être animal, sûreté, qualité, productivité et service client.

Sécuriser les activités en anticipant les risques, renforçant la culture sécurité et développant des actions de prévention en matière de sécurité, biosécurité et sûreté en lien avec les objectifs site
Assurer la productivité de votre département via le pilotage d’indicateurs clés de performance, en maîtrisant les coûts et garantissant l’efficacité de l’organisation
Être garant du respect des exigences réglementaires et de l’application des directives du groupe, proportionnellement aux réalités terrain et enjeux des activités.
Organiser et animer les équipes de votre département par un management structurant, engageant et orienté résultats. Assurer le développement des compétences et des talents en impulsant au quotidien une culture de transparence et de progrès.
Identifier et conduire des projets significatifs d'amélioration continue, de transformation ou d'investissement, dans un souci constant d'efficience.
Proposer aussi souvent que nécessaire les évolutions d'organisation permettant d'accomplir l'ensemble des missions ci-dessus de manière efficace
Tenir le rôle de représentant de l'entreprise auprès des clients, autorités, sociétés du groupe et autres partenaires extérieurs dans le périmètre de votre responsabilité.
Participer activement à la vie du Comité de direction, en apportant une vision opérationnelle, transverse et stratégique afin de faire progresser l’ensemble de l’organisation.

Profil recherché

Formation : Diplôme de niveau bac+5 minimum (Ingénieur, master ou équivalent)
Expérience d’au moins 7 ans dans des postes de management de production en environnement industriel structuré à forte exigence qualité et réglementaire
Appétence démontrée pour le pilotage en environnement multisites et la conduite de projets transverse
Leadership, capacité à fédérer vos équipes et à incarner au quotidien les valeurs fondamentales de l'entreprise.
Sens poussé de l'analyse et de la résolution de problèmes, avec une forte orientation résultat.
Capacités confirmées de communication, de présentation et de collaboration avec des publics très variés, en interne comme en externe.
Enfin, notre groupe international requiert un niveau d’anglais courant (lu, écrit et parlé).

Modalités

Convention collective de l’industrie pharmaceutique
Contrat : Poste cadre
Localisation : Basé à l'Arbresle (69) et déplacements réguliers à prévoir à Châtillon sur Chalaronne (01)
Salaire : A discuter selon profil, sur 14 mois + bonus + intéressement et participation
Indemnités de transport, accord de télétravail, prise en charge de la mutuelle à 60%, restaurant d’entreprise, CSE
Site non accessible en transport en commun : moyen de locomotion indispensable

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

Customer Service Team Lead (Charleston, SC, US, 29407)

Job Summary

The Customer Service Team Leader oversees and provides direction to the Microbial Solutions, North American, Customer Service team.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Supervisory Duties
⦁ Oversee daily operational activities and training for a group of non-exempt employees. Ensure optimum group performance.
⦁ Coordinate activities of customer service department to ensure efficient and timely availability of product.
⦁ Resolve all customer disputes, including counseling Customer Service staff in dispute resolution, complaint memos, and Trackwise cases.
⦁ Establishes and maintains close working relationships with the customer, Account Managers, Key Account Managers, Customer Service Representatives, and other support resources
⦁ Supports management activities such as: scheduling, personnel actions (hiring, promotions, transfers, etc.), training and development, providing feedback and coaching on performance, preparing reports and KPIs for annual performance reviews.
⦁ May assist in development of departmental budget.
⦁ Ensure adherence to pertinent regulatory requirements and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols].
⦁ Coordinate vacation/time off schedules.
⦁ 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.

Functional SME Duties
⦁ Maintain records in SAP and generate reports. Work with Global Supply Chain team to provide sales forecast. Interact with accounting to provide sales reporting information required for SOX compliance.
⦁ Act as backup for sign off requirements
⦁ Work with Accounts Receivable to resolve discrepancies in billing and customer accounts
⦁ Perform UAT, Integration, and Regression testing prior to implementation of new processes within platforms
⦁ Provide post go-live production support in Salesforce and SAP
⦁ Assist with inter and intra-company orders

These responsibilities are in addition to the basic requirements of a Customer Service Representative.
⦁ Perform customer service functions, including processing orders, providing documentation (e.g., health certificates), and communicating availability of product to customers, telephoning/emailing/faxing quotes/delivery/product information, and order confirmations.
⦁ Ensure coordination between Customer Service, freight forwarders and domestic carries to ensure efficient and timely delivery of product.
⦁ Work closely with global distributers for accurate and timely allocation of products.
⦁ Perform all other related duties as assigned.

Job Qualifications

⦁ Education: Bachelor’s degree (B.A./B.S.) or equivalent in Business or related discipline.
⦁ Experience: 2-3 years related experience with a Bachelor’s degree or 4-6 years related experience in customer service or business.
⦁ Experience using SAP ECC Order Management and Salesforce Service Cloud and/or ServiceMax
⦁ 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: Supervisory and dispute resolution skills; excellent verbal and written communication skills; computer skills.

PHYSICAL DEMANDS:
⦁ Regularly operates a computer and other office productivity machinery, such as a calculator, copy machine, and computer printer.
⦁ Must occasionally move about inside the office to access file cabinets, office machinery, etc.
⦁ Regularly provides information to and receives information from/through various technologies, media, sources and contacts. Must be able to accurately exchange accurate information in these situations.

WORK ENVIRONMENT:
⦁ General office working conditions
⦁ The noise level in the work environment is usually quiet.

Comments:
⦁ This position requires occasional domestic travel.

Compensation Data

The pay range for this position is $55,000 to $58,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

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 supported the development of 80% of the drugs approved by the FDA in the last five years.

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

Alternance : Technicien de Toxicologie - F/H (Evreux, FR, 27930)

Qui sommes-nous ?

Choisir Charles River Evreux, c’est intégrer un site unique de 500 personnes dans la province Normande, dans un environnement scientifique en constante évolution, ayant pour objectifs l'avancée de la recherche et le bien-être animal.

L’équipe

L’équipe de Toxicologie regroupe environ une vingtaine de personnes. Elle assure les techniques demandées dans le cadre des études scientifiques et est garante du bon report des tâches réalisées, dans le suivi des Bonnes Pratiques de Laboratoire (BPL).

Votre quotidien

•   Effectuer les opérations nécessaires à la conduite des tâches ou des études dont vous êtes responsables, conformément aux bonnes pratiques de laboratoire, aux procédures standards, à la charte éthique, aux protocoles d’études et au règlement intérieur,
•   Réaliser les traitements, assurer le suivi de l’état clinique et l’évolution pondérale des animaux,
•   Procéder à des prélèvements sanguins, d’urine ou de fèces,
•   Saisir l’intégralité des actes réalisés sur informatique,
•   Assurer la qualité des données recueillies et de résultats,
•   Transmettre à votre supérieur hiérarchique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail.

Pourquoi nous rejoindre ?

Vous êtes étudiant en Bac+2 dans le domaine de la biologie médicale (BTS BMB, Anabiotech...) et vous recherchez un contrat d’apprentissage avec des missions opérationnelles et polyvalentes.
Vous êtes dynamique, et êtes reconnu pour vos capacités d’organisation et votre proactivité.
Vous voulez obtenir une expérience enrichissante au sein d’un groupe International, leader dans le domaine de la santé.

Vous voulez bénéficier d'un véritable parcours d'intégration et formation dispensé par des experts techniques et scientifiques au sein de notre environnement BPL.

Les Modalités

•   Rémunération : Selon convention
•   13ème mois, Indemnités de transport, intéressement/ participation, Accord d’ancienneté,
•   Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
•   Accord de modulation 35h,
•   Convention collective de l’industrie pharmaceutique, groupe : 2
•   Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

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 85 % des médicaments approuvés par la FDA en 2021.

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

Operaio addetto gestione animali (PERUGIA) - ven/sab/dom (MILANO, Milano, IT, 20122)

Riepilogo del lavoro

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.

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

Operaio addetto gestione animali (PERUGIA) - ven/sab/dom (MILANO, Milan, IT, 20122)

Job Summary

Per cliente sito in Perugia ricerchiamo un operaio stabularista

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

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 nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature e carrelli

Job Qualifications

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro part-time nelle giornate di venerdì - sabato e domenica

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.

Scientific Support - Associate (Ashland, OH, US, 44805)

Job Summary

Perform QC review of study data and perform room inspections. Monitor and track common errors and assist with document medication to reduce error and deviations. Assist with implementing and monitoring quality control (QC) standards, methods, and procedures.

Essential Duties & Responsibilities:

Assist in monitoring quality control standards, methods, and procedures.
Monitor and track common deviations and problem documentation.
Perform general QC practices.
Assist in recommending form and SOP modifications, and changes to standard protocol wording to avoid deviations.
Assist in maintaining and revising QC documents, processes and manuals.
Assist in reviewing deviations.
Perform QC reviews of study data.
Perform room inspections.
Perform other duties as assigned.

Job Qualifications

Education:

High school diploma, or General Education Degree (GED) required.
Associate’s Degree in scientific discipline preferred.

Experience:

No previous experience required.
One- or two-years related experience in GLP environment preferred.
Previous and broad QC or QA experience preferred.
Knowledge and/or background in preclinical technical functions also 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:

Demonstrated leadership and word processing skills.
Effective written, verbal and communication skills.

Physical Demands:

While performing the duties of this job, the employee is regularly required to talk, hear and work/type at a computer.
Walking and standing for periods of up to 1 hour.
Specific vision abilities required by this job include close vision and the ability to adjust focus.
Must be able to communicate with other personnel regarding all aspects of a study.
Regularly provides information to and receives information from/through various technologies, media, sources and contracts.
Must be able to accurately exchange accurate information in these situations.

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 occasionally is required to ear protective clothing (lab coat, shoe covers, safety glasses) when entering laboratory areas.

The pay range for this position is $19-22/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.

Veterinary Technician Assistant I (Worcester, MA, US, 01608)

Job Summary

We are seeking a Veterinary Technician Assistant for our Discovery site located in Worcester.

The Veterinary Technician Assistant will assist veterinary staff in the documentation and triage of all laboratory animal health cases. Also responsible for daily health observations, preventative health care, environment enrichment and handling and restrain of laboratory animals. In addition, this individual will may also perform technical in-life procedures.

ESSENTIAL DUTIES:

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:
- Generate animal treatment records and perform treatment distribution
- Administration of various therapeutic measures by IM, SQ, topical, oral routes, etc. o Proficient animal restraint techniques.
- Observe basic care animals o Daily walk through of animal rooms
- Participate in colony management (new NHP processing, TB testing, collection of biological samples, routine health monitoring, etc.)
- Animal observations, reporting abnormalities
- Perform animal follow-ups as needed
Monitor animal heath, visually and by following detailed schedules.
Maintain accurate record keeping procedures for the veterinary department May perform routine technical and husbandry functions (general housekeeping) on studies and must adhere to safety procedures.
May assist in surgical pack preparation and cleaning of surgical instruments. Assistance in acclimation and behavior management of animals in our care.
Provide environmental enrichment for laboratory animals according to facility and Federal guidelines.
Assist in keeping inventory and stocking the vet rooms (i.e. drugs and supplies).
Assist in organizing and maintaining the vet exam rooms.
Record keeping of required logs.
Triage and recheck non-USDA covered species.

The pay range for this position starts at $22 to $24 per 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

MINIMUM QUALIFICATIONS:

Education: High School Diploma or G.E.D.
Experience: 1-2 years related experience in a laboratory animal facility. related experience working with animals in pre-clinical laboratory or clinical setting; experience working with 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.
Certification/Licensure: ALAT preferred
Other: None.

PREFERRED QUALIFICATIONS:

LVT license or CVT/RVT certification.
AALAS certification.

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.

Animal Care Technician I (Chicago, IL, US, 60637)

Job Summary

We are seeking an Animal Care Technician I for our Insourcing Solutions site in Chicago, IL

In the Animal Care Technician role, you will perform daily animal health observations, as well as animal husbandry duties to include water bottle/line and cage checks, provide food/water, and perform cage changes and/or clean cages all to maintain the quality and health of research animals.

Additional responsibilities include:

Maintain accurate records of things like animal breeding, as well as housing or support areas, and you may also be tasked with receiving, inspection, and housing of incoming animals.
Assist with restraint, handling, and manipulation of animal species, and you may become involved in the animal breeding and weaning procedures.
Other duties may include monitoring personnel and equipment entry into various rooms, operating required equipment and general housekeeping, when required.

Job Qualifications

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

Bachelor’s degree or high school diploma with 1 year of animal care/handling required. Interest in achieving ALAT certification upon eligibility.

The pay range for this position is $17.00 - $19.80 per hour. 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

Facilities Technician I (Rockville, MD, US, 20850)

Job Summary

The Facilities Technician I is responsible for maintaining the facility in good operating and physical condition, as well as responding to normal and emergency service calls, and taking corrective action via diagnosis and repairs. As directed, conducts/oversees preventive maintenance. The Facilities Technician I will be required to perform a wide range of repair, maintenance, and escorting tasks.

Key Responsibilities and Duties:

· Perform routine GMP spaces cleaning

· Maintain stock of consumables (HVAC filters, cleaning supplies, etc)

· Perform routine simple maintenance and repair throughout the facilities, such as repairing cosmetic damage

· Oversee building utility systems equipment maintenance to ensure expected conditions in the facility. This may include HVAC, electrical, water (domestic and DI), compressed gasses, and controlled temperature storage systems.

· Recognize and correct potential safety hazards to avoid injuries

· Support building personnel by insuring the availability of water, gasses, and electrical, as well as furniture requests, office relocations, and general accommodations to assist employees with their work duties

· Paint & caulk small areas when paint or wall surface has become damaged

· Support general cleaning & housekeeping efforts as required. Pallet removal as needed from building

· Maintain relationship and coordination with janitorial contractor for non-lab domestic cleaning of facility

· Process/Manufacturing equipment support, ensuring written record keeping, and forms are completed as required

· Conduct systems rounds as required

· Check and confirm process gasses are at service pressure daily

· Move/relocate laboratory equipment as directed

· Work with the engineering personnel to handle process equipment needs

· Required to review relevant documentation for accuracy and completeness i.e., suite cleaning documentation

· Replace light bulbs as required

· Employ safe work practices

· Engage and inspire others

· Comprehends all duties assigned and performs responsibilities in absence of Manager when needed

· Other responsibilities as needed

Job Qualifications

· Associate degree in science preferred, or High School Diploma or GED with 0-3 years of prior work experience in the Biotechnology Industry in a GMP Facilities setting

· Proficiency with Microsoft Office including Word, Excel, PowerPoint, and Teams. Maintain Calendar(s)

· Possess the willingness to learn new concepts to fully understand aseptic techniques and demonstrate proper clean-room behavior

· Excellent interpersonal and communication skills

· Detail-oriented and demonstrate the ability to perform highly detailed work

· Excellent organizational, multitasking, and problem-solving skills

· Able to accurately perform basic math calculations, including time conversion, fractions, decimals, and percentages

· Availability - Overtime work and schedule changes are required to meet business needs. Holiday, weekend, and night work will also be required based on manufacturing schedule. On-call as business needs arise

· Reliable mode of transportation to travel between sites in the Rockville area

· Able to work standing, bending, stooping, pulling, pushing, sitting, and reaching overhead for long periods of time

· Able to work around various cleaning chemicals that produce non-hazardous odors like bleach and vinegar

· Able to wear appropriate gowning covering most parts of the body and face. (Gowning Qualification)

· Able to lift, push, and pull 50 lbs.

· Use of basic hand tools

· Use multimeter

· Work from height not to exceed 10’

· Confined spaces could be encountered

· Work in heat and cold as required

· Climb ladders

Compensation Data

The pay range for this position is $22.00 - $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.

For more information, please visit 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 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.

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 (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.

Manager Virology Scientific Support (Wayne, PA, US, 19087)

Job Summary

Responsible for the management of a team dedicated to scientific development and assay optimization as it pertains to the Virology laboratory. Will provide operational supervision, technical support and professional and scientific expertise, as needed, to ensure operational excellence.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Planning and ensuring on-time delivery of client projects.
Lead the development, qualification and validation of new assays that meet industry expectations and current regulatory guidelines. As Virology Subject Matter Expert, provide guidance for resolution of technical problems affecting Virology assays.
Oversees the optimization of existing Virology assays and their life cycle management, which will include monitoring to assess the need for subsequent requalification.
Support and manage the technical transfer of in vitro Virology assays.
Work with Sales to identify and fill gaps in Virology testing.
Partner with Business Development in providing and reviewing pricing and proposals, and provide excellent service to clients.
Act as a liaison with other departments to ensure that any method development appropriately aligns with Virology processes and subsequent routine testing.
Supports other operational areas in relation to virus based work, as needed, by providing guidance for R&D.
Participate in client technical calls to assist with Virology assay development or trouble shooting.
Supervise technical staff and perform personnel management activities such as: scheduling, personnel actions (hiring, promotions, transfers, etc.), training and development, providing regular direction and feedback on performance, disciplinary actions, time and vacation approval and preparing and delivering annual performance and salary reviews.
Develop and maintain departmental systems and SOPs. Maintain compliance of operating documents through review and revision as required by SOPs. Assist in the development and communication of departmental policies and procedures.
Participate in and support cross-functional communication and laboratory activities, as necessary.
Assist in the development of the departmental budget, including resource allocations and needs, and authorize expenditures.
Ensure adherence to pertinent regulatory requirements and to departmental policies.
Perform all other related duties as assigned.
With respect to all Virology assays and tests, the manager assures that:
Study or assay protocols are approved as provided by applicable regulatory requirements and that the protocols are followed.
All experimental data, including unanticipated observations, are accurately recorded and verified.
Unforeseen circumstances that may affect the quality and integrity of the study are noted when they occur, and corrective action is taken and documented.
Test systems, including reagents, live cells, equipment or other materials are as specified in the protocol.
All applicable good laboratory or manufacturing practice regulations are followed, as applicable.
All raw data, documentation, protocols, specimens, and final reports are transferred for archiving during or at the close of the study.

Job Qualifications

Education: Bachelor's degree or equivalent in biology or a related discipline. Master's degree preferred.
Experience: Minimum of 4-5 years related laboratory experience in Virology or related field.
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: Demonstrated leadership skills required. Working knowledge of cGMPs or regulatory requirements pertaining to the pharmaceutical and biotechnology industries required.

PHYSICAL DEMANDS:

May have exposure to potential chemical, electrical, biological and waste-handling hazards.
Must regularly operate a computer and other office machinery (i.e., calculator, copy machine, and computer printer).
Regularly moves about to access file cabinets, equipment, and personnel.
Ability to observe laboratory test results using a microscope to differentiate shapes, colors and other qualitative properties.

WORKING ENVIRONMENT:

General office and laboratory working conditions.
Laboratory working conditions may occasionally require wearing personal protective equipment, including but not limited to: goggles, face shield, surgical mask, cap, gloves, scrubs and/or shoe covers.
Work with or near toxic or caustic chemicals and biological agents including potential biohazards. Possible exposure to fumes or airborne particles.

Compensation Data

The pay range for this position is $105,000-$110,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

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.

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

Alternance : Technicien de Toxicologie Non-Rongeurs - F/H (Evreux, FR, 27930)

Qui sommes-nous ?

L’équipe

Votre quotidien

Pourquoi nous rejoindre ?

Vous voulez bénéficier d'un véritable parcours d'intégration et formation dispensé par des experts techniques et scientifiques au sein de notre environnement BPL.

Les Modalités

•   Rémunération : Selon convention
•   13ème mois, Indemnités de transport, intéressement/ participation, Accord d’ancienneté,
•   Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
•   Accord de modulation 35h,
•   Convention collective de l’industrie pharmaceutique, groupe : 2
•   Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

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 85 % des médicaments approuvés par la FDA en 2021.

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

Alternance : Technicien de Laboratoire en Immunologie - F/H (Evreux, FR, 27930)

Qui sommes-nous ?

L’équipe

L’équipe d'Immunologie regroupe environ 15 personnes. Elle assure la réalisation des techniques d’Immunologie, dans le respect des normes des Bonnes Pratiques de Laboratoire (BPL).

Votre quotidien

•   Réaliser progressivement certaines techniques de laboratoire comme des dosages ELISA, des développements de méthode mais aussi des études de cultures cellulaires comme Elispot dans le cadre d’études dites de Cells based assays,
•   Assurer la saisie informatique des résultats et leurs conformités,
•   Transmettre au scientifique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail,
•   Lire les protocoles, avenants et notices en anglais.

Pourquoi nous rejoindre ?

Vous êtes étudiant en Bac+2/3 dans le domaine de la Biologie et vous recherchez un contrat d’apprentissage avec des missions opérationnelles et polyvalentes.
Vous êtes dynamique et proactif et recherchez une expérience avec beaucoup de technique.
Vous voulez obtenir une expérience enrichissante au sein d’un groupe International, leader dans le domaine de la santé.
Vous voulez bénéficier d'un véritable parcours d'intégration et formation dispensé par des experts techniques et scientifiques au sein de notre environnement BPL.

Les Modalités

•   Rémunération : Selon convention
•   13ème mois, Indemnités de transport, intéressement/ participation, Accord d’ancienneté,
•   Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
•   Accord de modulation 35h,
•   Convention collective de l’industrie pharmaceutique, groupe : 2
•   Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

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 85 % des médicaments approuvés par la FDA en 2021.

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

Alternance : Technicien de Laboratoire en Analyses Physico-Chimiques - F/H (Evreux, FR, 27930)

Qui sommes-nous ?

L’équipe

L’équipe d'Analyse Physico-Chimique regroupe environ 7 personnes. Elle assure la réalisation des techniques d’Analyses Physico-Chimiques, dans le respect des normes des Bonnes Pratiques de Laboratoire (BPL).

Votre quotidien

•   Recherches bibliographiques pour l'établissement du protocole d'étude,
•   Formations aux différentes techniques d'analyses (SEC-UV, UHPLC-UV, UV,etc....),
•   Développement et mise en place des méthodes génériques,
•   Réalisation d'une étude (test du protocole d'étude et des méthodes génériques).

Pourquoi nous rejoindre ?

Vous êtes étudiant en Bac+2/3 dans le domaine de la chimie Analytique et vous recherchez un contrat d’apprentissage avec des missions opérationnelles et polyvalentes.
Vous êtes dynamique, et êtes reconnu pour vos capacités d’organisation et votre proactivité.
Vous voulez obtenir une expérience enrichissante au sein d’un groupe International, leader dans le domaine de la santé.
Vous voulez bénéficier d'un véritable parcours d'intégration et formation dispensé par des experts techniques et scientifiques au sein de notre environnement BPL.

Les Modalités

À propos de Safety Assessment

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 85 % des médicaments approuvés par la FDA en 2021.

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

Scheduler I (Reno, NV, US, 89511)

Job Summary

The pay range for this position is $20.50 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

We are seeking an experienced Scheduler (Technical Operations) for our Safety Assessment site located in Reno, Nevada.

The Scheduler schedules all protocol-required tasks for in-life studies, ensuring proper placement of employees into specific study activities based on competency and responsibilities. Additionally, schedule employee department and global trainings, and manage the department level study schedule and resources.

The following are minimum requirements related to the Scheduler position.

Associate’s degree (A.A./A.S.) or equivalent in scientific support/administrative or related discipline.
2 years of related experience in a laboratory or research environment. Previous experience in a GLP environment preferred.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Ability to interact with all levels of staff and sponsors. Strong communication and interpersonal skills and attention to detail. Proficient in the use of word processing, spreadsheet and database desktop applications.

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 supported the development of ~85% of the drugs approved by the FDA in 2019.

Equal Employment Opportunity

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

Head of CSD (Sulzfeld, Bavaria (Bayern), DE, 97633)

Wir suchen ab sofort eine/n

Head of CSD (kaufmännische/r Angestelle/r) (m/w/d)

in Vollzeit

für unsere Niederlassung in 97633 Sulzfeld

DAS SIND IHRE AUFGABEN:

Planung und Koordination von Kundenprojekten
- - Leitung des Customer-Service-Department-Teams am Standort Sulzfeld
  - Spezialwissen zur Logistik in Deutschland und EU-weit
  - Aufbereitung, Informationssammlung und Analyse über europäische Logistik
  - Effiziente Fehlerbehebung und Optimierungen in SAP und anderen angewandten unterstützenden IT-Tools

DAS BRINGEN SIE MIT:

Abgeschlossene kaufmännische Ausbildung
Sie verfügen über mindestens 5 Jahre Berufserfahrung im Bereich Customer Service

Sie haben Spaß an der Kundenbetreuung
Sie bringen Erfahrung in SFDC und E-Commerce-Plattformen mit sowie im Bereich Zoll und Logistik
Sie sind offen für Arbeiten in großen Netzwerken auf internationaler Ebene
Sie sind zuverlässig, belastbar, flexibel, verantwortungsbewusst und teamfähig
Sie beherrschen die englische Sprache in Wort und Schrift
Der versierte Umgang mit Microsoft Office (Excel, PowerPoint, Word) sowie mit SAP und Inventarmanagementsystemen wird vorausgesetzt
Hohe Resilienz
Wünschenswert wären Personalführungserfahrung und Versiertheit bei Behördenkontakten

DAS BIETEN WIR:

eine ausführliche und betreute Einarbeitung
eine interessante und verantwortungsvolle Tätigkeit in einem zukunftsorientierten Team mit Raum für Kreativität
ein internationales Arbeitsumfeld
attraktive Fort-/Weiterbildungsangebote
ein wettbewerbsfähiges Vergütungspaket
zahlreiche soziale Leistungen und Zuschüsse

Sie sind interessiert?

Dann freuen wir uns über die Zusendung Ihrer ausführlichen Bewerbungsunterlagen an:

Charles River Laboratories, Research Models and Services, Germany GmbH

Personalabteilung, Sandhofer Weg 7, 97633 Sulzfeld

Email: BewerbungenRMS@crl.com , www.criver.com

Vorabinfos unter: 09761-40611

Über Research Models & Services

Über Charles River

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 rund 80% der von der FDA in den letzten fünf Jahren zugelassenen Arzneimittel unterstützt haben.

Weitere Informationen finden Sie unter www.criver.com.

Supervisor, InVivo Operations (Stilwell, KS, US, 66085)

Job Summary

We are seeking an supervisor to join our Integrated Toxicology (ITox) team at the Kansas 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. This role will be responsible for the oversight of in-vivo operations staff and all daily functions to support animal care and study execution. They will provide, coordinate, document, and schedule routine and highly complex training activities for In-Life, Animal Care, and Cage Wash personnel. This individual will also be responsible for defining a new technical training plan, in alignment with the global program, that includes developing, revising, and implementing the use of training documents and processes. They will also provide leadership and/or support of new hire orientation.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Provide guidance in the day-to-day activities of assigned departmental employees to ensure accurate, high-quality work, and adherence to pertinent departmental policies, practices, and procedures (SOPs, safety procedures and biosafety protocols). Ensure schedule is prepared daily, accurately reflecting required tasks and workload. Serve as a model as it relates to effective time management, communication, and utilization of resources.
Perform technical tasks to support completion of study tasks (as needed).
Lead and mentor less experienced training personnel.
Work with department management to coordinate and facilitate multi-species technical training at all levels of complexity for department personnel.
Maintain and update all documents and databases used for the support and conduct of training tasks, including but not limited to training standards, training records, training timelines, and proficiency standards.
Provide oversight, scheduling, and coordination of training animal use to enable optimal learning while prioritizing animal care and welfare.
Practice/maintain advanced technical skills and procedures, work independently, and follow operating procedures and processes.
May conduct sponsor/visitor tours and interact with clients.
Provide input/review of new, and/or revised processes, operating procedures, training standards, quizzes, proficiency standards, and other training documents.
Assist in facilitating, coordinating, and scheduling new hire orientation and on-the-job training for personnel.
Participate in recruiting efforts by assisting in interviews and selecting qualified non-exempt level departmental personnel.
Assist in the scheduling, coordination, and execution of study procedures.
24/7 emergency duty coverage as assigned.
Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor’s degree (B.A./B.S.) or equivalent in scientific related discipline.
Experience: 4-6 years related experience in animal science, biology, chemistry/pharmacy, or similar lab environment.
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 ALAT/LAT level strongly preferred; or other applicable certification/licensure.
Other: Demonstrated advanced technical and analytical skills. Effective communication and leadership skills. Ability to handle a variety of laboratory animals. Proficient in 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 required. Understanding of basic, intermediate, and complex study design and protocols. Ability to organize and prioritize work to meet deadlines. Computer literacy including word processing, spreadsheet, and database programs.

PHYSICAL DEMANDS:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 25 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.

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

The pay range for this position is $70-75k/year. 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

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.

Technicien de laboratoire en Histologie - F/H - CDD 9 mois (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Le département de Pathologie recrute un Technicien en Histologie pour intégrer son équipe composée de 33 techniciens.

Les missions 

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

Réaliser les techniques de laboratoire en Histologie (colorations histologiques, techniques de fabrication de lames de routine ou d’immunohistochimie…),
Assurer la réalisation des autopsies pour toutes les espèces utilisées dans le cadre de nos études,
S’assurer de la conformité des résultats obtenus,
Assurer la saisie informatique des résultats,
Transmettre au scientifique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail.

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 type DUT/BUT dans le domaine scientifique.

Vous maitrisez l’anglais scientifique (compréhension écrite)

Vous savez faire preuve d’autonomie mais vous appréciez également 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.

Les modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
CDD de 09 mois
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 25 400 € 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 Safety Assessment

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 85 % des médicaments approuvés par la FDA en 2021.

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

Technicien de Laboratoire en Génomique - H/F - CDD 9 mois (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Le département de Biologie Moléculaire recrute un Technicien de Laboratoire en Génomique pour intégrer son équipe composée de 17 techniciens.

Les missions 

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

Réaliser progressivement certaines techniques de laboratoire : extractions d’acides nucléiques, dosages quantitatifs et qualitatifs, réalisation de PCR,
Assurer la saisie informatique des résultats et leurs conformités,
Lire les protocoles, avenants et notices en anglais,
Transmettre au scientifique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail.

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 type DUT/BUT dans le domaine de la Biologie Moléculaire.

Vous maitrisez l’anglais scientifique (compréhension écrite).

Vous savez faire preuve d’autonomie mais vous appréciez également 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.

Les modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 24 000 € 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 85 % des médicaments approuvés par la FDA en 2019.

Electronic Technician - Hybrid (Charleston, SC, US, 29407)

Job Summary

We are seeking an experienced Electronic Technician, for our Microbial Solutions site located in Charleston, SC.

The Electronic Technician’s primary role is testing, troubleshooting, repairing, performing preventative maintenance, and calibrating Microbial Solutions instruments. The Electronic Technician must be able to troubleshoot to the component level. Support of our Field Technicians and production staff is included in this position. They must be able to operate test equipment including DVM’s, oscilloscopes, and soldering irons. All associated paperwork as required by cGMP and FDA, along with updates to our database are also part of the responsibilities. We are seeking a motivated individual with good communication skills and attention to detail. Your ability to handle these tasks in a timely manner will be a major part of meeting the service needs of our customers.

The following are the job duties & responsibilities related to the Electronic Technician:

Administer test, trouble shoot and repair electronics to the component level.
Understand and read schematics.
Mechanically assembly and disassemble new and existing equipment
Perform and operate on test equipment and solder equipment when needed.
Create, develop and continuously improve SOP’s pertaining to the PTS and MCS machines.
Able to analyze situations and apply own judgment when accessing mechanical problems, independently.
Coordinate scheduling and support department personnel in the absence of the PTS Engineer.
Responsible for proficiency in all SOPs in areas of responsibility.
Responsible for documentation as required by company policy, cGMP and FDA.
Support and serve as second back-up to Technical Services by loading software, calibration of new equipment and ensuring proper packaging of new equipment.
Perform and assess data entry in software program in order to track machine repairs.
Interpret past repairs on PTS and MCS machines, historically, in order to resolve and diagnosis new machine issues.
Perform all other related duties as assigned.

Job Qualifications

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

Education: Associates Degree(A.S) in Electronic Engineering Technology, or related discipline
Experience: 0-1 years related experience in a regulated environment.
Computer literacy with Windows Office Suite programs including data entry and tracking.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

The pay range for this position is $25.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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 ~85% of the drugs approved by the FDA in 2019.

Equal Employment Opportunity

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

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

Senior Project Manager CMC (Rockville, MD, US, 20850)

Job Summary

The Senior CMC Project Manager leads project execution after deal closure. Responsible for directing, leading, and motivating multi-disciplinary project teams, project managers, and hold team members accountable to deliver results within an agreed project governance structure to ensure customer satisfaction throughout the life of the projects. Holistically plans all projects at any stage through mapping resource across projects.

In this role, the Senior CMC Project Manager is the key interface between Business Development and Operations organizations and the customer. The Senior CMC Project Manager manages multiple projects, either within one technology or within multiple technologies, and oversees the complete life cycle of all the projects while managing a team of project managers.

Key Responsibilities and Duties:

Direct project manager and project's scope, timelines, budget, and Project profitability
Raise and prepare scope changes and communicate them to a customer in close collaboration with Business Development
In collaboration with Business Development, create mid-long-term Project strategies
Define, organize and be responsible for all customer communication (using an open communication model), agreeing on milestones and conducting "lessons learned" with the customer, as well as executing decommissioning at the end of contractual activities
Ensure the right and effective internal and external governance are in place and are effective. Also ensure very clear alignment of internal stakeholders
Responsible to ensure flawless and smooth execution of assigned contracted Projects according to defined timelines and cost, via leading multidisciplinary project teams
During execution, key focus is on the customer centricity and internally on quality, cost, profitability, timelines, and risk management
Manage Project budgets and material cost
Additional duties as requested

Job Qualifications

Bachelor's degree (B.A./B.S.) or equivalent in project management, business, biological sciences, or related discipline with Life Sciences technical background, or equivalent experience. Master's Degree preferred
Minimum of 5 years of experience in project management
Experience in biologics manufacturing, preferably in viral vector production
PMP Certification required and experience in a CRO/CMO preferred
Previous technical competency in the areas of the Biologics Industry e.g., process development, cGMP manufacturing, process registration, analytical science, Quality Assurance etc.
Strategic, operational, and technical project management experience
Proven business awareness and commercial acumen
Record of accomplishment of successfully managed projects and personnel
Leadership and motivational skills to maintain naturally high moral within the Project management team
Ability to communicate effectively at all levels across the organization. Has strength of character to have difficult conversations with senior stakeholders including customers, internal team members and senior management; excellent written, verbal, and presentation skills
Pragmatic, organized, and results-oriented and with ability to manage multiple priorities
Excellent planning, organizational, and controlling skills
Problem solving skills - ability to analyze using critical thinking and solve complex issues that do not have routine solutions
Skilled with Microsoft Project, Teams, and other automated presentations

Compensation Data

The pay rate for this role is $100,000 - $140,000 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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.

Data Coordinator - Reporting Services 1 (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: 18.50$/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.

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: 18.50$/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.

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

Technicien de laboratoire en Pharmacie - F/H - CDD 9 mois (Evreux, FR, 27930)

Résumé du travail

Qui sommes-nous ?

Le poste

Au sein du département Pharmacie et dans une équipe composée de 22 collaborateurs, vous aurez pour objectif de vous assurer de la préparation des produits pour nos études.

Les missions

Etudes :

Réaliser tous les types de préparations galéniques (solutions, suspensions, remplissage de gélules, etc…) suivant les spécifications des dossiers d’études, des procédures et des BPL pour tous types d’études,
Réaliser les prélèvements d’échantillons de préparations galéniques et leur stockage, pour la réalisation d’analyses,
Mesurer les densités des substances d’essai, véhicule et formulation,
Livrer les substances d’essai ou les préparations galéniques aux services demandeurs sur notre site, selon le planning de livraison,
Assurer l’enregistrement des nouveaux lots de véhicules dans le système informatique,
Maintenir le matériel et les locaux propres à son poste de travail.

Documentation/Données :

Assurer l’acquisition des données d’études dans un environnement BPL,
Créer et /ou contrôler les conditions de préparations des études en cours dans le système informatique.

Conditions spécifiques du poste 

Prise de poste le matin (aux environ de 7h30)

Travail le week-end et jours fériés

Qualifications souhaitées

Vous êtes titulaire d’un Bac +2/Bac +3 idéalement spécialisé dans la formulation scientifique.

Vous maitrisez l’anglais, à l’écrit comme à l’oral.

Vous êtes rigoureux, ponctuel et assidu.

Vous possédez un bon esprit d’équipe.

Modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 25 415 € 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, accord de télétravail,...
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

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 85 % des médicaments approuvés par la FDA en 2021.

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

Expert en Pharmacologie de Sécurité - F/H- CDI (Evreux, FR, 27930)

Qui sommes-nous ?

Au sein du Département de Toxicologie, agir en tant qu’Expert de la pharmacologie de sécurité auprès de nos équipes et de nos clients, auprès du site d’Evreux et de Lyon.

Les missions

En tant qu’Expert Scientifique :

-   Agir comme un mentor auprès de l’équipe de Directeurs d’études, et assurer de la formation,
-   Participer à la rédaction d’articles, de posters, intervenir lors de congrès,
-   Conseiller nos clients sur les aspects scientifiques.

En tant que Directeur d’Etudes :

- Être responsable de la rédaction des plans d’études et modifications qui peuvent y être apportées,
-   Assurer le suivi, le respect du plan, en lien avec les services qui sont concernés. Apporter des corrections sur certaines procédures si besoin,
-   Veiller à la bonne réception et enregistrement des données d’études,
-   Réaliser l’interprétation des résultats et rédiger le rapport d’études,
-   Maintenir le lien avec le client pendant tout le suivi de l’étude,
-   Dans le cas d’études multisites, assurer le lien avec les différents services et responsables impactés (Pourra être nommé Responsable Principal d’Essai dans le cas d’études multisites).

Qualifications souhaitées

Vous êtes titulaire d’un Doctorat en Pharmacologie et avez idéalement 5 années d’expérience en pharmacologie de sécurité ou en toxicologie.
Avoir travaillé sur des études cardiovasculaires serait un atout pour ce poste.
Vous êtes bilingue en anglais, à l’écrit comme à l’oral.
Vous êtes reconnu pour votre relationnel, notamment clients ainsi que votre capacité de gestion de crises.

Modalités

•   Convention collective de l’industrie pharmaceutique, groupe : 7
•   Contrat : Cadre forfait jours
•   Salaire : A compter de 50 000 € bruts / an sur 13 mois
•   Prise en charge de la mutuelle à 100%, restaurant d’entreprise, CSE
•   Primes de transport, d’intéressement/participation, accord de télétravail,...
•   Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

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 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.
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 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.

Research Scientist LC-MS/MS - F/H - CDI (Saint-Nazaire, FR, 44600)

Le poste

Notre Laboratoire de chromatographie recrute un Research Scientist LC-MS/MS - H/F en CDI, 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.

Vous ferez partie d’une équipe dans laquelle votre rôle sera la réalisation technique et la responsabilité de conduite d'études de développements de méthode de bioanalyse sur de nouveaux médicaments.

Les missions

Réaliser techniquement des développements de méthode de bioanalyse pour tout type de matrices biologiques (plasma, sang,tissus,…) de façon autonome et efficace
Assumer la responsabilité générale de la conduite d'étude de développement et y apporter son expertise technique et scientifique
S’assurer de la disponibilité du matériel et des réactifs pour respecter le planning établi
Interpréter les données avec précision et faire preuve de minutie dans la vérification et la validité des informations
Produire des documents analytiques précis et de haute qualité pour transférer efficacement les méthodes développées aux collègues chargés de la partie réglementaire (validation)
Travailler en étroite collaboration avec l’ensemble des personnes du laboratoire (techniciens de laboratoire, responsables d’études, responsables d’équipe) et des services supports (planification, Archiviste, Publisher et coordinateur scientifique, Magasin et achats, etc…)
Communiquer régulièrement avec les clients, fournisseurs, auditeurs, etc…

Qualifications recherchées

De formation Bac + 2 minimum, vous disposez idéalement d'une expérience technique d'au moins 5 ans en bioanalyse (préparation d’échantillons biologiques, LC-MS/MS).

Vous avez de bonnes connaissances des normes BPL/BPC ou du travail en contexte qualité/réglementaire (suivi et respect de procédures et consignes).

Rigoureux et autonome, vous êtes reconnu(e) pour votre bon sens du relationnel et êtes à l’aise avec les outils informatiques.

Enfin, notre environnement est international et un anglais professionnel (oral et écrit, B2 minimum) est attendu.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique : groupe 6
Contrat : CDI cadre (forfait jours, RTT)
Salaire : Environ 34 000 € bruts/an, sur 12 mois, selon expérience
Prise en charge de la mutuelle à 60% et tickets restaurants

À propos de Safety Assessment

À propos de Charles River

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

Assistant vétérinaire - F/H - CDI (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Au sein du département Vétérinaires, vous aurez pour objectif d'assurer le support aux Vétérinaires Cliniciens, dans le respect des réglementations.

Les missions

Agir en tant qu'accueil du service et hierarchiser les demandes pour optimiser les visites vétérinaires, en fonction des urgences,
Assurer les soins des animaux aux côtés du vétérinaire,
Réaliser les visites de suivis,
Participer à différents projets en soutien de l'équipe vétérinaire (amélioration des process, commandes, gestion des salles d'opérations),
Gérer la pharmacie des médicaments vétérinaires,
Maintenir le respect de la documentation et des données acquises, en appliquant rigouresement les procédures réglementaires.

Qualifications souhaitées

Vous êtes titulaire d’un Bac +2/Bac +3 dans le domaine des soins vétérinaires.

Vous possédez une première expérience sur ce type de poste, idéalement en CRO.

Vous êtes reconnu(e) pour votre organisation, votre assiduité et votre esprit d'équipe.

Modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 25 415 € 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, accord de télétravail,...
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

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 85 % des médicaments approuvés par la FDA en 2021.

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

Cagewash Technician I (Bldg 35) 1 (Bethesda, MD, US, 20892)

Job Summary

We are looking for a Cagewash Technician I to join our Insourcing Solutions team, located in Bethesda, MD.

The duties of the Cagewash Technician I are to maintain facility equipment and perform routine preventative maintenance on cagewash and autoclaves.

You will also perform the following duties:

Sanitize, maintain, and repair animal caging materials as needed.
Ensure cagewash and animal holding facilities are kept in a clean and organized manner.
Assist with the receipt, stocking, and maintenance of supply inventories.
Prepare and submit required written records, charts, logs, and inventories.
Actively interact with customers to resolve requests, inquiries, and complaints, and to provide technical assistance.

Other duties will include general housekeeping, in addition to reviewing, comprehending and complying with all SOPs and quality assurance standards pertaining to specific areas.

Qualifications

Experience and/or training working with mechanical equipment preferred.

Obtain ALAT certification within 1 year of employment with HS Diploma/GED or within 2 years of employment if no HS Diploma/GED.

The pay for this position is $17.50-18.47 USD 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

Technicien animalier - F/H - CDI (Paris, FR)

Rejoignez une équipe passionnée par les animaux où chaque jour fait avancer la recherche scientifique !

Dans le cadre de cette activité, nous recherchons un Technicien animalier F/H en CDI pour travailler au sein d'animaleries de recherche au sein de nos sites client basés à Paris.

A ce titre, vous intégrerez une équipe de zootechniciens engagés au cœur du bien-être animal et travaillerez en interface directe avec les équipes de recherche.

Missions principales

Gestion d'élevage (rongeurs)

Gestion les animaux selon les instructions données par équipes de recherche via un logiciel de gestion d'animalerie
- Contrôle de l'état de gestation, suivi des animaux, sexage et sevrage
- Réalisation des accouplements contrôlés
Identification des animaux
Réalisation de prélèvements à des fins de génotypage/phénotypage
Mise à jour et suivi des données d'élevages sur le logiciel d'animalerie
Travail en lien avec les équipes de recherche

Entretien, soin et surveillance des animaux

Assurer le bien-être des animaux au quotidien : observation, abreuvement, alimentation, enrichissement et la vérification des paramètres d'ambiance
Assurer l'hébergement des animaux: change des cages sous hotte de change
Nettoyage et désinfection des locaux en respectant les règles de prophylaxie et de biosécurité
Gestion des stocks de consommables, déclenchement des commandes et suivi des réceptions

Profil recherché

Idéalement niveau 2/Fonction A en Expérimentation animale
Expérience requises: expérience dans la gestion d'élevage de rongeurs
Savoir travailler en milieu confiné ou en zone protégée avec des équipements de protection individuelles (EPI)
Respect des procédures et de la réglementation en expérimentation animale
Esprit d'équipe et capacité à collaborer avec différents interlocuteurs
A l'aise avec les outils informatiques

Modalités

Convention collective pharmaceutique
Permanences ponctuelles les week-ends et/ou jours fériés
Rémunération à partir 30 K€ brut annuel sur 14 mois, selon profil.
Indemnité de transport, prime d’Intéressement et participation, accord d’ancienneté
Prise en charge de la mutuelle à 60%, tickets restaurants, comité d'entreprise

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

Medical Technologist I (Reno, NV, US, 89511)

Job Summary

BASIC SUMMARY:
Perform basic medical technology procedures according to protocol, SOP and GLP. Operate, maintain and perform basic troubleshooting procedures on analyzers. Process additional study samples. Perform and review study ordered parameters and computer input of raw data.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Assist in the preparation of appropriate paperwork and materials prior to clinical pathology blood collection days. Assist with the computer protocol work schedule for each study, as needed.
•   Perform basic medical technology procedures such as record blood slide differentials, reticulocyte counts, and urinalysis with minimal supervision; prepare blood and cytology slide smears.
•   Inventory and package differential and reticulocyte blood slides for each study for shipment or storage.
•   Maintain proficient knowledge of hematology, clinical chemistry, coagulation, and urinalysis.
•   Analyze proficiency survey samples.
•   Review documentation of functions performed as part of quality requirements.
•   Input raw data into the computer system and review data.
•   Operate, maintain, and troubleshoot clinical pathology analyzers.
•   Perform daily maintenance and quality control of instruments.
•   Perform all other related duties as assigned.

Job Qualifications

Education: Associate’s degree (A.A./A.S.) or equivalent in medical laboratory technology (MLT) or related field required. Bachelor’s degree (B.A./B.S.) or equivalent in medical technology (MT) desired.
Experience: 2-3 years of experience in a clinical pathology laboratory.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: MT or MLT with certification or certification-eligible (ASCP or HEW) preferred.
Other: Experience with computer software programs is desirable. Effective organizational and leadership skills desired.

The pay range for this position is $30.00-32.00 an hour.

Equal Employment Opportunity

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

Environmental Health and Safety Specialist (Cambridge, MA, US, 02142)

Job Summary

Responsible for implementing/maintaining the Environmental, Health, Safety & Sustainability (EHS&S) Program(s) for adherence to local, state, and federal regulations. Identify and mitigate potential hazards to reduce/eliminate risk exposure.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Establish, administer, and update specific EHS&S programs for compliance with state and federal Occupational Safety and Health Administration (OSHA), Environmental Protection Agency (EPA), Department of Transportation (DOT) and other regulations as necessary.
Manage OSHA and EPA records and maintain reporting and documentation standards.
Provide initial and periodic safety and environmental training to all employees as required and advise management on safety and environmental issues.
Review new regulatory standards and make compliance recommendations.
Inspect the facility for compliance with OSHA and EPA regulations as applicable. Recommend solutions to management that address deficiencies in EHS&S compliance. Submit work orders for facility corrective action on EHS&S concerns.
Assist in the development of EHS&S programs and metrics.
Manage the hazardous waste (RCRA) and medical waste disposal function including waste profiling, permitting, manifesting, and record keeping and reporting.
Assist management team in emergency response and function as EHS&S Emergency Coordinator for 24-hour incident response.
Serve or Co-chair as a member of the Safety Committee(s)
Assist in the investigation of injuries resulting in lost time claims and/or safety violations and property damage. Make recommendations for corrective action.
Provide regulatory guidance on EHS&S issues to all staff.
Available to clients and federal and state investigators to explain procedures and produce written documentation as proof of compliance.
Request and maintain necessary facility permits, licenses and compliance reports to federal, local and state regulatory authorities.
Obtain necessary licenses to function as wastewater and underground storage tank operator.
Coordinate communications to regulatory agencies and client inspections on EHS&S related matters.
Provide initial and periodic safety and environmental training to all employees as required by regulation and as needed for ‘best practice’.
Liaise with Document Control team to ensure SOPs and BOPs are properly formatted, updated, and entered.
Recommend and implement changes to facility SOPs, Global Operating Framework (GOFs) and Business Operating Procedures (BOPs) relating to EHS&S.
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.

Job Qualifications

Education: Bachelor’s degree (B.A./B.S.) or equivalent in Environmental Science, Occupational Health and Safety, Environmental Engineering or related discipline.
Experience: 3 – 5 years related experience in Environmental Health, Safety.& Sustainability.
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 interpret federal and state regulation and apply them to address compliance solutions as required. Effective writing, organizational and time management skills. Computer skills including MS Office and database management. Ability to speak Spanish is a plus.

Compensation Data

The pay range for this position is $95,000 - $105,000. 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.

QC Officer (Ballina, IE, F26D786)

We are seeking an experienced QC Officer for our Biologics Division located in Ballina, Co. Mayo, Ireland.

This role shall report to the Biosafety and Cell Based Assay Department Manager and the main duties & responsibilities shall be:

Project Management of routine batch release testing in the Biosafety and Cell Based Assay Department (client correspondence,/weekly calls, management of subcontractors, ensuring samples are released within the required timelines i.e. scheduling of tests, review of basic data, liaising with QA, generation of CoA etc.)
Generation and updating of GMP compliant SOPs, Protocols and reports.
Sourcing, purchasing and stocking consumables, standards and reagents required for testing.
Receipt and processing of test samples in LIMS
Carry out data calculations ,basic statistics and trending. Provide additional information at the clients request as required.
Assist in internal, regulatory and client visits/audits and respond to findings.

The following are minimum requirements related to this Position;

A minimum of 2 years relevant experience in Scientific Research preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry.
Experience in project management essential.
BSc/M.Sc. in a relevant science discipline (e.g. cell biology / Molecular Biology / Biomedical Science)
Experience in cell-based assays / molecular techniques desirable but not essential.

Job Summary

Job Qualifications

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 characterzation, 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 supported the development of 80% of the drugs approved by the FDA in the last 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.

Veterinary Technician I (Horsham, PA, US, 19044)

Job 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 which may include administration of various therapeutic measures by IV, IM, SQ, topical, oral routes, etc., bandage/wrapping techniques, venipuncture techniques and other techniques.
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.
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.

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.. 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.

Data Engineer (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

There has never been a more exciting time to be part of the Enterprise Data Analytics team at Charles River Labs. We are on a mission to position data as the core driver of our business, empowering leaders to make informed, data-driven decisions that accelerate revenue, enhance productivity, and keep us ahead of the competition. Our recently launched Enterprise Data Hub serves as the company's digital backbone, and we are looking for visionary people in data analytics to help us further expand and refine this hub.

Your role will be key in integrating, mastering, and ensuring the quality of our data across all business functions, ultimately transforming how Charles River operates through data science and advanced analytics. You will be joining a team that is deeply committed to our purpose: Together We Create Healthier Lives. This unwavering focus on patients makes our global technology team uniquely inspiring. As we look to the future, we reimagine how we do business through our Digital Journey.

Note: It’s a fully remote home-based role for professionally qualified and experienced candidates based in India, who are willing and open to work UK shifts.

Essential Qualifications:

•    Bachelor’s degree in computer engineering, Computer Science, or a related discipline (Master’s degree preferred)
•    3+ years of experience in ETL design, development, and performance tuning using the Microsoft BI Stack in a multi-dimensional data warehousing environment.
•    3+ years of advanced SQL programming expertise (PL/SQL, T-SQL)
•    1+ years of experience in Enterprise Data & Analytics solution architecture
•    1+ years of experience in Python Programming
•    1+ years of hands-on experience with Azure, especially for data-heavy/analytics applications leveraging relational and NoSQL databases, Data Warehousing, and Big Data solutions.
•    1+ 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.

Preferred Skills:

•    Experience with Big Data technologies, such as Hadoop, Sqoop, Hive, Kafka, Spark, Pyspark, Python, Scala, or Pig
•    Experience managing both relational and non-relational data using Big Data Management (BDM) techniques (formats like JSON, XML, Avro, Parquet, etc.)
•    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
•    Familiarity with stream-processing systems (e.g., Event Hubs, Storm, Spark-Streaming)
•    Experience in data and analytics within the Life Sciences industry is a plus.

Equal Employment Opportunity

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

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

Laboratory cook (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a laboratory cook for our formulation team located at the Senneville site, you will be responsible of preparing different formulations required for dosing, in solution, suspension or powder mix , for our research teams.

In this role, primary responsibilities include:

Prepare formulations for dosing, in solution, suspension or powder mix using various techniques while adhering to GLP regulations;
Operate various computer programs and equipment such as PH meter, homogenizer, balance, osmometer, densimeter and glove box;
Handle samples in a fume hood using aseptic method;
Prepare study materials according to protocol.

Key Elements

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

AEC/DEC in Laboratory Sciences;
Comfortable following strict procedures;
Motivated, autonomous, and meticulous person;
Positive attitude and good team spirit.

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: 23$/hour;
Annual bonus based on performance;
Schedule:
- Monday to Friday & 1 weekend out of 2 in rotation;
- Start time between 6AM and 9AM;
- Holidays;
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.

Equal Employment Opportunity

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

Cuisinier.ère de laboratoire (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant que Cuisinier.ère de laboratoire pour notre équipe de Formulation située au site de Senneville, serez responsable de préparer les différentes formulations requises pour le dosage, en solution, suspension ou mélange de poudre, pour nos équipes de recherche.

Dans ce poste, les principales responsabilités incluront:

Préparer des formulations pour le dosage, en solution, suspension ou mélange de poudre en utilisant différentes techniques tout en respectant les règles des BPL;
Utiliser différents programmes informatiques et équipements tels que PH mètre, appareil d’homogénéisation, balance, osmomètre, densimètre et boîte à gants;
Manipuler des échantillons sous la hotte en utilisant une méthode aseptique;
Préparer le matériel de l’étude selon le protocole.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

AEC/DEC en sciences de laboratoire;
À l’aise de suivre des procédures strictes ;
Personne motivée, autonome et minutieuse ;
Attitude positive et un bon esprit d’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$ de l’heure;
Bonus annuel basé sur la performance;
Horaire:
- Lundi au vendredi avec 1 fin de semaine sur 2 en rotation;
- Heure de début entre 6 et 9 heures du matin;
- Journées fériées;
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.

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

Research Scientist I - Method Development, Bioanalytical Chemistry (Cleveland, OH, US, 44128)

Job Summary

We are seeking a Research Scientist I - Method Development for our Bioanalytical Chemistry team for our Safety Assessment site located in Cleveland, Ohio.

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.

Effectively manage a portfolio of sample analysis projects while ensuring timelines are met in a single operational area with minimal oversight
Execute review and approval of data with minimal oversight for final scientific/technical decisions within a single operational area
Develop understanding of compliance expectations to respond to quality assurance audit observations in appropriate software with minimal oversight
Assist with minimal oversight the completion of laboratory investigations, assay troubleshooting and quality observations
Independently assist in problem solving for technical and/or regulatory issues
Responsible for review of study plans/protocols/amendments
Participate in Sponsor visits/tours with minimal oversight
Provide expertise in developing and validating quantitative/qualitative methods/procedures with limited complexity/scope in one operational area
Independently perform data analysis using appropriate software
Develop critical thinking, troubleshooting and time management skills aligned with needs of operational areas
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team
Independently function as a liaison, maintaining timely and frequent communication between CRL and Sponsor/Client/SD
Independently ensure scientific integrity of studies
Independently function as a Principal Investigator, Individual Scientist and/or Study Director

Essential Duties and Responsibilities: continued

Actively communicate and collaborate across operational areas in order to adhere to timelines and produce quality data
Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Write, review and approve deviations with minimal oversight
Full understanding of regulatory and GXP requirements, industry standards and company SOPs within one operational area
Effectively manage a small portfolio of research projects including method development and validation while ensuring timelines are met in a single operational area with minimal oversight
Able to recognize method and/or data issues and communicate them to management to minimize study impact with minimal oversight
Provide support to staff members as required by operational area as needed
Actively participate in internal process improvements, presentations and harmonization efforts
Performs all other related duties as assigned

The pay range for this position is $85-90K. 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:

Bachelor’s degree (BA/BS) with 7-9 years of relevant working experience. Master’s degree (MS) with 3-4 years of relevant working experience. Doctorate degree (PhD) with 1-2 years of experience.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
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.

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.

Technician II, Formulations (Ashland, OH, US, 44805)

Job Summary

We are seeking an experienced Formulations Tech II for our Formulations Team at our Safety Assessment site located in Ashland, OH.

Basic Summary:

A Technician II will prepare basic to complex dosing material and samples for vehicles, solutions, suspensions, diets, and dispensations independently with some oversight.

Prepare basic to complex dosing material and samples for solutions, suspensions, diets, and dispensations.
Efficiently perform and document all procedures, materials, and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.).
Independently sterilize laboratory equipment using autoclave or other methods.
Assist in washing and maintenance of glassware and lab cleanliness.
Assist with the disposal of residual dosing material.
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team.
Independently be able to identify equipment issues for troubleshooting and notify proper personnel.
Actively participate in process improvement initiatives.
Be able to provide feedback on laboratory investigations and quality observations.
Utilize various mixing methods and apparatuses to prepare formulations.
Prepare aseptic and glovebox formulations with oversight.
Prepare formulations under observation of Study Directors.
Performs all other related duties and functions as assigned.

The pay for this position is $20.00. 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 & Experience: Associate’s degree (A.A./A.S.) or equivalent with a minimum of 1-2 years of relevant experience and CPhT with 1-2 years of compounding experience recommended. Bachelor’s degree (B.A./B.S.) in a relevant field with no experience strongly recommended. 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.
Good 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, and extended shifts sometimes with short notice or unscheduled.
Ability to work under specific time constraints.

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 supplies.
Must be able to perform procedures, standing or sitting, for long periods of time, 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 hold and manipulate work materials while utilizing fine motor skills.
Must be able to regularly provide information to and receive information from/through various technologies, media, sources, and contacts. Must be able to accurately exchange information in these situations.
Regularly operates a computer and other office productivity machinery, such as a calculator, copy machine, and computer printer.
Move about inside the work area to access file cabinets, office machinery, etc.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

Work Environment:

General office and lab working conditions, the noise level in the work environment is usually moderate.
While performing the duties of this job the employee is regularly required to wear protective clothing (i.e., goggles, face shield, cap, gloves, scrubs, shoe covers), work near toxic or caustic chemicals, work with biohazards.
The employee may occasionally be exposed to live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors, and extreme temperature conditions.
The noise level in the work environment ranges from moderate to high depending upon the task being performed.

Equal Employment Opportunity

For more information, please visit 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.

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

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

Histology Technician II (Shrewsbury, MA, US, 01545)

Job Summary

BASIC SUMMARY:
Independently perform basic histology laboratory procedures. Assist with specialized histology procedures. Review data for quality control.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Perform basic histology procedures independently (trimming, processing, embedding, microtomy, staining, coverslipping).
•   Assist with and perform advanced histology procedures (slide QC, special stains, thin/thick sections, IHC, serial/step sectioning).
•   Review laboratory documents for accuracy, completeness and compliance with Standard Operating Procedures (SOPs), Good Laboratory Practices (GLPs), and study specific requirements.
•   Assist in training of staff junior to this position.
•   Assist in the preparation of responses, deviations and other documentation resulting from internal and external reviews and/or audits.
•   May assist with basic necropsy procedures (basic dissection, tissue collection/preservation, fresh tissue trimming).
•   May cross-train in other areas of pathology and/or other laboratory departments (flow cytometry, clinical pathology, special pathology, bioanalytical, reproductive toxicology, etc.).
•   Perform all other related duties as assigned.

The pay rate for this position is between $29.00 and $30.00 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.) required. Bachelor’s degree (B.A./B.S.) or equivalent in a biological science preferred.
•   Experience: Minimum 2 years of pathology laboratory 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: HT (ASCP) or HLT (ASCP) preferred.
Other: Placement at this level requires successful completion/competency of the required tasks of the position preceding this level and continued ability to perform those tasks are required. Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, maintain a positive work atmosphere, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors. Experience with computer software programs is required.

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.

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

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

Spécialiste Senior en Santé et Sécurité (Laval, Quebec, CA, H7V 4B3)

Sommaire du Poste

Nous sommes à la recherche d'un.e Spécialiste en Santé et Sécurité d'expérience pour notre site de Laval (QC).

Dans ce poste, les principales responsabilités incluront:

Être un agent mobilisateur de changement, assurer un leadership interactif et pratique pour assurer la transformation de la culture S&S;
Participer à la standardisation des programmes et procédures en s'assurant du respect des lois, normes et standards des autorités gouvernementales locales et des directives corporatives ;
Collaborer à l'élaboration et à la présentation de formations S&S pour le personnel de la région;
Aider au développement des communications et des présentations S&S;
Soutenir le processus d'enquête et d'analyse des incidents afin d'identifier les causes profondes, les actions correctives et les suivis;
Réaliser/participer à des analyses de risques, recommander des mesures d'atténuation des risques appropriées et assurer la mise en place de méthodes de travail sécuritaires (approche pratique/à la base);
Participer aux comités/gouvernances Santé & Sécurité;
Classer les différents rapports et fournir des statistiques et des résultats de performance en santé et sécurité;
Améliorer le niveau d'excellence et de performance des programmes S&S du site.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Un minimum de 5 à 10 ans d'expérience en tant que spécialiste en santé et sécurité ;
Baccalauréat ou certificat en santé et sécurité;
Excellentes habiletés interpersonnelles, diplomatie, travail d'équipe et esprit de collaboration;
Autonomie et souci du détail;
Bilingue (anglais et français, écrit et parlé).

Informations spécifiques au poste:

Localisation: 445 Boul.Armand-Frappier,Laval, Québec H7V 4B3
Horaire: Lundi au Vendredi

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
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);
3 semaines de vacances et 10 jours 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.

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

Senior Health & Safety Specialist (Laval, Quebec, CA, H7V 4B3)

Job Summary

We are seeking an experienced Health and Safety Specialist for our Laval (QC) location.

In this role, primary responsibilities include:

Be a mobilizing agent of change, provide interactive and practical leadership to ensure the transformation of the H & S culture;
Participate in the standardization of programs and procedures by ensuring compliance with the laws, norms and standards of local government authorities and corporate directives;
Collaborate in the development and delivery of H & S training for staff in the region;
Assist in the development of H & S communications and presentations;
Support the incident investigation and analysis process in order to identify root causes, corrective actions and follow-ups;
Carry out / participate in risk analyses, recommend appropriate risk mitigation measures and ensure the implementation of safe work methods (hands-on / ground-up approach);
Participate in the Health & Safety committees/governances;
File the different reports and provide statistics and performance results on health and safety;
Improve the level of excellence and performance of the site's H & S programs;
Perform any other related tasks, as assigned.

Key Elements

We are looking for the following minimum qualifications for this role

A minimum 5-10 years experience as a Health and Safety Specialist;
Bachelor’s degree or Certificate in Health and Safety;
Excellent interpersonal skills, diplomacy, teamwork and collaborative spirit;
Autonomy and attention to detail;
Bilingual (English & French, Written & Spoken).

Role Specific Information:

Location: 445 Boul.Armand-Frappier, Laval, Québec H7V 4B3
Schedule: Monday to Friday

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Paid development training;
Employee and family assistance program;
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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

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

Occupational Health Nurse - Part-time (24 hrs/wk; 7:30am - 3:30pm) (Mattawan, MI, US, 49071)

Job Summary

An Occupational Health Nurse is responsible for emergent/non-emergent medical procedures and triage within certification/licensure; respiratory fit testing, recordkeeping, and injury prevention.

Position will work 3 days per week (benefit eligible), from 7:30am - 3:30pm on-site at the Mattawan, MI Charles River Site.

Essential Duties and Responsibilities

Performs and reviews medical and respiratory assessments.
Performs other medical procedures allowed under standing orders.
Assists in all medical emergencies.
Assists in preparation of departmental reports.
Manage OSHA Logs
Support for Return to work, Restricted work
Maintain and safeguard confidentiality of employee health and workers compensation records, Understanding of HIPAA
Maintain records of incidents, injuries, first aids and near misses (KPI’s)
Attend departmental meetings, safety meetings

Job Qualifications

Education/Experience:
- Licensed Practical Nurse (LPN) and 1-2 years of relevant experience;
- or, Certified Medical Assistant (CMA) and 3 or more years of relevant experience;
- or Registered Medical Assistant (RMA)
- or Medical Assistant (MA) and 5 or more years of relevant experience.
- Must be licensed in the state of Michigan. Experience in Care/Case management

An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Ability to make critical health decisions in emergency situations and daily decisions regarding employee health
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system. Basic familiarity with Microsoft Office Suite.
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.
Working knowledge of Michigan Workers Comp Law
Understanding of OSHA standards as they apply to work related care and injuries, Including Bloodborne Pathogens, Hearing Conservation, PPE, Respiratory Protection
CPR Certification

Compensation Data

The pay range for this position is $43.50/hr - 48.00/hr 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 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.

Medical Technologist II - Clinical Pathology (Horsham, PA, US, 19044)

Job Summary

A Medical Technologist II is responsible for performing and maintaining proficient knowledge of basic medical technology techniques on primary benches. Performs basic operation, daily maintenance, quality control, and basic troubleshooting on all clinical pathology analyzers. Performs manual urine microscopy, cell counting, and manual differentials.

Essential Duties and Responsibilities:
Performs basic medical technology techniques on primary benches (urinalysis, coagulation, hematology, and chemistry).
Performs urine microscopy, cell counting, and manual differentials.
Maintains proficient knowledge of hematology, coagulation, chemistry, and urinalysis.
Performs basic operation, daily maintenance, quality control, and basic troubleshooting on all analyzers.
Records and reviews hand recorded or computer generated raw data.
Trains in MVP training (System Administrator role)
Trains and gains proficiency in Medical Technologist II core skills and values.
Perform all other related duties as assigned.

The pay range for this position is between $32-$34 . 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: Associate degree (A.A./A.S.) or Bachelor’s degree (B.A./B.S.) or equivalent in medical technology certification (MT) preferred.
Experience: 1-4 years of experience in a clinical pathology laboratory 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: MLT, MT, or MLS with certification or certification eligible (ASCP or HEW) required.

Demonstrated ability to learn and perform clinical laboratory procedures, both manually and using instrumentation.
Excellent written and verbal communication skills inside and outside the organization.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office), 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.
GLP environment requires attention to detail, strong organizational skills, and accurate record keeping competencies.
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.

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.

Facility Manager II (33) (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Facility Manager II to join our Insourcing Solutions team, located in Bethesda, MD.

As the Facility Manager II, you will be the primary point of contact for the facility, utilizing existing SOPs and quality assurance standards to oversee and coordinate the daily activities of the facility within varied animal care environments, including scheduling of staff.

Additional responsibilities include:

Oversee the animal surveillance program and all aspects of husbandry, including technical and cage wash support.
Provide quality assurance to include animal health surveillance; monitoring of the effectiveness of facility sanitation, cage washing and autoclaving procedures; monitoring of incoming animal shipments for container integrity and animal health; monitor the heating, ventilation, and air conditioning (HVAC); internal facility reports for monitoring deviations from pre-established parameters; and other quality assurance services as deemed necessary (e.g., water cultures).
Participate in interviewing applicants for open positions, developing performance improvement plans, and writing employee performance evaluations.
Assist in assessing, developing, and presenting training for staff and investigators.
Participate in QC/QA, and ensure CAPA development, implementation, and adherence.
Occasionally provide technical support (e.g., restraining animals, collecting blood, collecting tissues, performing injections, treatments, surgical preparation, assisting with research procedures).
Occasionally provide animal husbandry and environmental enrichment.
Provide data entry/data base report generation for computerized systems which monitor facility internal environmental parameters, security, or other animal facility monitoring and management requirements.
Prepare and submit written records, charts, logs, and inventories.
Actively interact with Project Officers, facility veterinarian(s) and investigators to solve customer requests, inquiries, and complaints.

Job Qualifications

The following are minimum requirements related to the Facility Manager II position:

High school diploma or GED required.
Bachelor’s degree in animal science or related preferred
Minimum of 6 years’ experience in a research vivarium facility, with at least 2 years’ experience in an ABSL3 environment, and 3 years of supervisory experience
AALAS certification at the Laboratory Animal Technologist level (LATG) required.

The pay range for this position is $45.00 to $50.00 USD per hour. Please note that salaries vary within the range based on factors including, skills, certifications, and location.

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

Research Scientist 1 - Immunochemistry (Shrewsbury, MA, US, 01545)

Job Summary

Charles River Laboratories is seeking a Research Scientist to join our Laboratory Sciences group within our Safety Assessment site located in Shrewsbury, MA. The incumbent will serve as a scientific team member in the conduct of preclinical and clinical research studies at all levels of complexity. Responsibilities include study management, interpretation, and reporting of study data and assuring the regulatory compliance of these projects, as appropriate. Additional responsibilities include serving as a Principal Investigator for the development and validation of biomarker, PK and ADA assays (eg: ligand binding assays, enzymatic assays, Luminex, Bioplex, MSD, Quanterix, ProteinSimple). This individual would be responsible for the composition and execution of validation and sample analysis protocols/plan in accordance with company standard operating procedures and industry regulatory guidelines. This position will serve as the primary scientific contact for key clients and the on-site support of their programs.

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.

Equal Employment Opportunity

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

Supervisor - Animal Care/Husbandry (GEMS) (Wilmington, MA, US, 01887)

Job Summary

We are seeking an Animal Care/Husbandry Supervisor for our GEMS: Breed Department located in Wilmington, MA. The Animal Care/Husbandry Supervisor directs day-to-day operations.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Develops production/service (or operations) and resource plans that meet goals in terms of safety, quality, output and cost.
Oversees the management for site operations and ensures continuous process improvement.
Ensures effective management of site operations, finances and budgets in close collaboration with the functional area directors within the company’s matrixed organization.
Develops/supports best practices for managing, allocating and accruing project and trial level resources.
Selects, develops and evaluates personnel to ensure efficient operations. Provides general direction to and review of managers in various functional areas, groups and/or operations, etc.
Develops/supports corporate and/or organizational policies and authorizes the implementation of these policies.
Provides daily supervision of personnel and operations to maintain and monitor the health, production, and physical environment of Charles River or external customer animals within isolators, micro-isolator caging and/or ventilated cage systems, to ensure achievement of departmental goals and levels.
Independently handles routine personnel-related issues; assists in the handling of complex personnel-related issues.
Performs all other related duties as assigned

MINIMUM QUALIFICATIONS

Candidates must possess one of the following:

Bachelor’s degree in animal science or a related field plus 2 years’ experience.
Associate’s degree in animal science or a related field plus 4 years’ experience.
High school diploma plus 6 years' experience.

Also required:

Effective communication and interpersonal skills.
Proficient in computers (MS Office Suite).

PREFERRED QUALIFICATIONS:

One (1) year experience in a Supervisor or Lead position.
ALAT certification.

The pay range for this position is $67,000 - $72,000 annually. 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.

Assembler - Associate (Charleston, SC, US, 29407)

Job Summary

An essential member of the larger production team, responsible for mechanical assembly, rework, documentation, instrument release, and installation of software for automation equipment, as well as support instrument production deliverables. Reports to the production supervisor.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Test and release instrumentation, and robotics systems
• Perform rework on instrumentation and robotics systems as necessary
• Perform onsite service and instrumentation of robotics systems as required in support of the Field Service Team
• Draft/Edit MPIs (Manufacturing Process Instructions)
• Draft/Edit SOPs (Standard Operating Procedures) related to primary job function
• Mechanically assemble and disassemble new and existing equipment
• Receive, sort, inspect and stock components in a warehouse area
• Identify and report defects, including potential defects to aid in product improvement
• Operate hand and power tools such as torque drivers, screw drivers, wire cutters and other tools for instrument assembly
• Perform rework including but not limited to soldering, crimping, separating, cutting etc.
• Read and understand CAD drawings, BOM etc.
• Assist in:
   Perform general housekeeping and adhere to safety procedures.
   Production process development
   Continuous improvement
Product improvements
Manufacturing processes
Testing processes
• Perform SAP operations to facilitate the processing of components and instruments
• Set up instruments in Service Max, track defects and RMAs.
• Work with PLM system and work instructions
• Perform general housekeeping and adhere to safety procedures.
• Proficient in all SOPs in areas of responsibility
• Perform all other related duties as assigned.
• Responsible for adhering to all documentation as required by company policy, cGMP and FDA.
• Cross train as required for all other roles within the department
   Periodically assist in those roles with direction as needed
LEADERSHIP:
• Onboard and train new team members, cross train other team members
ADDITIONAL RESPONSIBILITIES:
• Equipment safety / manuals etc.
• Trained by Hamilton in the service of the nexus instrument.
• Capable of traveling internationally. 10% travel as necessary.

Job Qualifications

Education: High school diploma or General Education Degree (G.E.D.)
Experience: 2 years+ experience working in assembly with basic mechanical knowledge.

PHYSICAL DEMANDS:

Specific vision abilities required by this job include close vision and the ability to adjust focus..
Sitting and standing for periods of time.
Specific vision abilities required by this job include close vision and the ability to adjust focus.

WORK ENVIRONMENT:

General production working conditions, the noise level in the work environment is usually quiet.

COMMENTS:

Employee is responsible to verify and validate his or her job output as specified through verbal and/or written instructions. Verbal and written instructions may include training, policy statements, work instructions, Standard Operating Procedures, or workmanship standards.

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 80% of the drugs approved by the FDA in the last five years.

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

Medical Technologist I - Clinical Pathology (Horsham, PA, US, 19044)

Job Summary

A Medical Technologist I is responsible for performing specimen analyses and administrative duties, required by protocols, Business Operating Procedures (BOPs), and Standard Operating Procedures (SOPs), on biological specimens from all species to produce sound, accurate, and reliable data. The individual in this role must use good communication and interpersonal skills in a collaborative team environment.

Essential Duties and Responsibilities:
Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train on all Good Laboratory Practices (GLPs).
Train in on-boarding tasks which may include reading protocols, SOPs, and BOPs.
Performs basic medical technology techniques on primary benches (urinalysis, coagulation, hematology, and chemistry).
Processes specimens: checking for clots, making blood smears and pipetting of serum/plasma.
Trains and gains proficiency in Medical Technologist I core skills and values.
Perform all other related duties as assigned.

The pay for this position is between $30.00 and $33.00 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: Associate degree (A.A./A.S.) or equivalent in medical laboratory technology (MLT) or related field desired. Bachelor’s degree (B.A./B.S.) or equivalent in medical technology (MT) preferred.
Experience: 0-1 year of experience in a clinical pathology laboratory.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: MLT, MT, or MLS with certification or certification eligible (ASCP or HEW) preferred.
Demonstrated ability to learn and perform clinical laboratory procedures, both manually and using instrumentation.
Excellent written and verbal communication skills inside and outside the organization.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office), 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.
GLP environment requires attention to detail, strong organizational skills, and accurate record keeping competencies.
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.

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.

Laboratory Assistant (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Laboratory Assistant for our Formulations team located at the Senneville site, you will ensure the cleanliness and orderliness of all work areas, maintenance and calibration of laboratory equipment, and ensure that the laboratory and preparation rooms have sufficient product inventory.

In this role, responsibilities may include

Maintain laboratory facilities, clean glassware and manage waste in accordance with Good Laboratory Practices (GLP), Standard Operating Procedures (SOPs).
Maintain supply of commonly used materials (gloves, masks, tubes, etc.).
Maintain, check and calibrate certain laboratory equipment (e.g. baths, pipettes, pH meters, etc.)
Help technical staff according to operational needs

Key Elements

If you have the following qualifications, we will train you for the rest:

Have a high school diploma
Be comfortable with physical work and be able to move a load of up to 11.5 kg (25 lbs)
be motivated and autonomous
Understanding of English is mandatory. Bilingualism in French and English is preferred.

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: 17$/hr
- Premiums: weekends (2.75$/hrs)
Schedule: Weekday schedule, Monday to Friday, be flexible in work schedule and available to work weekends.
Permanent position as of the hiring, full time 37.5hrs per week

Why Charles River?

Competitive hiring benefits. We pay up to 85% of premiums (medical and dental coverage).
Paid developmental training
Employee and family assistance program
24/7 access to a physician 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 also around the world, join the team, This is Your Moment.

Equal Employment Opportunity

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

Assistante de laboratoire (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant qu'Assistant.e de laboratoire pour notre équipe de Formulations située sur le site de Senneville, vous veillerez à la propreté et à l'ordre de toutes les zones de travail, à l'entretien et à l'étalonnage des équipements de laboratoire, et vous vous assurerez que le laboratoire et les salles de préparation disposent d'un stock de produits suffisant.

Dans ce poste, les principales responsabilités incluront:

Entretenir les installations de laboratoire, nettoyer la verrerie et gérer les déchets conformément aux bonnes pratiques de laboratoire (BPL), aux procédures opérationnelles standard (POS).
Maintenir l'approvisionnement en matériel d'usage courant (gants, masques, tubes, etc.).
Entretenir, vérifier et calibrer certains équipements de laboratoire (par exemple, bains, pipettes, pH-mètres, etc.)
Assister le personnel technique selon les besoins operationnels

Éléments Clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste :

Avoir un diplôme d'études secondaires
Etre à l'aise avec le travail physique et être capable de déplacer une charge allant jusqu'à 11,5 kg (25 lbs)
Etre motivé(e) et autonome
La compréhension de l'anglais est obligatoire. Le bilinguisme en français et en anglais est préférable.

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 : 17$/hr
- Prime de fin de semaine : 2.75$/hrs
Horaire : Horaire en semaine, du lundi au vendredi, être flexible dans l'horaire de travail et disponible pour travailler les fins de semaine.
Poste permanent des l'embauche, temps plein a 37.5hrs semaine

Pourquoi Charles River ?

Des avantages compétitifs à l'embauche. Nous payons jusqu'à 85 % des primes (couverture médicale et dentaire).
Formation de développement payée
Programme d'aide aux employés et aux familles
Accès 24h/24 et 7j/7 à un médecin et à divers professionnels de la santé (télémédecine).
3 semaines de vacances et 5 jours de congé personnel
Nombreuses activités sociales organisées

Si vous voulez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais aussi dans le monde entier, rejoignez l'équipe, C’est Votre Moment.

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

Supervisor - Bioanalytical (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Supervisor for our Bioanalytical & Analytical Chemistry group in Laval, you will be responsible for the management of technical staff, services, and standards, qualify and cost-effectiveness of all relevant activities. Your contribution will ensure maximum efficiency of the team and help resolve more challenging issues.

In this role, primary responsibilities include:

Coach, train and support employees to ensure maximum efficiency of teams and resolve more challenging issues;
Schedule work of departmental staff to maximize efficiency and productivity;
Oversee the training process of all staff;
Provide performance appraisal and development opportunities for staff members.

Key Elements

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

Bachelor’s degree in Chemistry, Biochemistry, Biology or any related scientific field;
Minimum of 2 years’ experience in a management role;
Good interpersonal and communication skills;
Strong problem-solving skills;
Good listener and strategic vision;
Bilingualism in French and English is mandatory. However, the level of English can be intermediate to advanced.

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: Daytime Monday to Friday;
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);
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;
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.

Clinical Pathology Lab Assistant (Reno, NV, US, 89511)

Job Summary

We are seeking a Clinical Pathology Assistant for our Safety Assessment site located in Reno, NV.

The following are responsibilities related to the Clinical Pathology Assistant:

*Perform a wide variety of basic laboratory tasks.
*Maintain and perform recordkeeping.
*Review data recorded for others for quality control.
*Prepare all materials required for sample receipt and processing.
*Maintain data files for department.
*Perform all tasks in compliance with Good Laboratory Practice (GLP) regulations and with Standard Operating Procedures (SOPs).

Job Qualifications

Education: High school diploma or General Education Degree (GED)
Experience: None
Certification/Licensure: None
Other: Good keyboarding skills, proficient in utilizing personal computer, email, and standard office software packages.

The pay range for this position starts at $18.00 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.

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

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

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

Superviseur.e - Bioanalyse (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Superviseur.e pour notre équipe de Bioanalyse & Chimie Analytique à notre site de Laval, vous serez responsable de la gestion du personnel technique, des services et des normes, de la qualité et de la rentabilité de toutes les activités concernées. Votre contribution assurera une efficacité maximale de l’équipe et aidera à résoudre les problèmes les plus difficiles.

Dans ce poste, les principales responsabilités incluront:

Encadrer, former et soutenir les employés pour assurer une efficacité maximale des équipes et résoudre les problèmes les plus difficiles;
Planifier le travail du personnel du département afin de maximiser l’efficacité et la productivité;
Superviser le processus de formation de tout le personnel;
Offrir des opportunités d’évaluation des performances et de développement aux membres du personnel.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Baccalauréat en Chimie, Biochimie, Biologie ou toutes autres disciplines reliées à un domaine scientifique;
Au minimum de 2 ans d’expérience dans un poste en gestion de personnel;
Bonnes aptitudes interpersonnelles et de communication;
Bonnes compétences en résolution de problème;
Bon sens de l’écoute et vision stratégique.
Le bilinguisme français & anglais est obligatoire. Toutefois, le niveau d'anglais peut être de niveau intermédiaire à avancé.

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: De jour en semaine, du lundi au vendredi
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);
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;
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.

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

Regional Environmental Specialist (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Regional Environmental Specialist for our Health & Safety team at the Senneville location, you will be responsible for managing environmental programs in compliance with local, provincial, and federal regulations for our regional sites: Senneville, Ville St-Laurent, Laval, and Sherbrooke.

In this role, primary responsibilities include:

Establish, manage, and update specific environmental programs to ensure compliance with municipal, provincial, and federal administrations and organizations;
Help sites conduct environmental audits as well as establish and implement an action plan to address the gaps identified during the audits (internal and external);
Inspect the facilities to ensure they comply with local regulations, where applicable. Advise management on environmental issues and recommend solutions to address gaps;
Manage the disposal function for hazardous and medical waste, including permits, reporting, releases, record keeping, and establishing disposal profiles related to this waste;
Explain the procedures and produce written documents as evidence of compliance for clients and municipal, provincial, and federal investigators. Coordinate communications with regulatory bodies and clients on environmental issues;
Promote sustainable development on the sites by keeping updated and communicating monthly the data and key performance indicators (KPIs) related to the environment and sustainable development.

Key Elements

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

Bachelor's degree or equivalent in environmental sciences or sustainable environmental engineering;
Minimum 5 years of related experience in environmental and sustainable development work;
Experience in a laboratory or a scientific organization is an asset;
Bilingual (French & English).
Ability to inspire trust and confidence through strong interpersonal skills and effective collaboration;
Ability to effectively manage multiple projects simultaneously;
Commitment to excellence and attention to detail, ability to work within a complex and fast-moving 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 station;
Annual bonus based on performance;
Schedule: Day schedule from Monday to Friday;
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);
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.

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.

Spécialiste régional.e en environnement et développement durable (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant que Spécialiste Régional.e, Environnement et développement durable pour notre équipe de Santé et Sécurité située au site de Senneville, vous gérerez les programmes environnementaux dans le respect des réglementations locales, provinciales et fédérales de nos sites régionaux :Senneville, Ville St-Laurent, Laval et Sherbrooke.

Dans ce poste, les principales responsabilités incluront:

Établir, administrer et mettre à jour des programmes environnementaux particuliers afin d’assurer la conformité avec les administrations et les organismes municipaux, provinciaux et fédéraux;
Aider à réaliser les audits environnementaux ainsi qu’établir et mettre en œuvre un plan d’action pour combler les lacunes décelées lors des audits (internes et externes);
Inspecter les installations pour s’assurer qu’elles sont conformes aux réglementations locales, le cas échéant. Conseiller la direction sur les questions environnementales et recommander des solutions pour remédier aux lacunes;
Gérer la fonction d’élimination des déchets dangereux et des déchets médicaux, notamment les autorisations, la production de rapports, les communiqués, la tenue de registres et l’établissement des profils d’élimination relatifs à ces déchets;
Expliquer les procédures et produire des documents écrits comme preuve de conformité à la clientèle et aux enquêteur.trices de niveau municipal, provincial et fédéral. Coordonner les communications avec les organismes de réglementation et la clientèle sur les questions liées à l’environnement;
Promouvoir le développement durable sur les sites, en tenant à jour et en communiquant mensuellement les données et les indicateurs de rendement clés (IRC) en matière d’environnement et de développement durable.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Baccalauréat ou équivalent en sciences de l’environnement ou en ingénierie de l’environnement durable;
Minimum de 5 ans d’expérience en environnement et développement durable;
Expérience dans un laboratoire ou une organisation scientifique est un atout;
Bilingue (français et anglais).
Capacité à inspirer confiance grâce à de solides compétences interpersonnelles et à une collaboration efficace ;
Capacité à gérer efficacement plusieurs projets simultanément ;
Engagement envers l'excellence et le souci du détail, tout en ayant la capacité à travailler dans un environnement complexe et en évolution rapide.

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;
Bonus annuel basé sur la performance;
Horaire: De jour du Lundi au Vendredi;
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);
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.

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

Director, Human Resources (Mattawan, MI, US, 49071)

Job Summary

The Human Resources Director will serve as the strategic HR partner and site HR leader for the Safety Assessment business at the Mattawan, Michigan site. As the HR Director, you understand that in today’s market, innovative and forward-thinking people strategy is essential to short and long-term business success. To achieve this, you will collaborate with business leaders to turn strategy into action, resolving talent gaps and seizing opportunities that support our goals of hiring, engaging, developing, and retaining outstanding talent.

Essential Duties & Responsibilities:

Provides high-level consultation to senior leaders in areas such as organizational assessment, compensation, succession planning, organizational structure, work force planning and change management in order to strengthen overall organizational capability.
Lead, develop and coach a team of HR Professionals, ensuring they deliver exceptional HR services.
Acts as a senior trusted advisor and strategic partner to leadership by gathering and analyzing HR and client information to drive the development and implementation of solutions.
Understands the site business model and drivers. Partners closely with the site leader and other senior leaders to anticipate and address issues impacting the business as it relates to talent and organizational issues.
Undertakes diagnostics and analysis of complex data, to facilitate HR Leadership decision making.
Collaborates with internal process experts to execute and implement large scale HR initiatives (i.e., roll out of annual programs, new programs, policies, etc.).
Provides consultation and leadership on the handling and resolution of complex employee relations issues ensuring consistency with corporate policies and practices.
Directs annual HR processes such as performance reviews, succession planning, bonus and merit programs.
Bring solutions to continuously improve HR support to the business around efficiency, process and performance.

Job Qualifications

Education: Bachelor’s degree (B.A. /B.S.) or equivalent in Human Resources, or related discipline.
Experience: 8+ years related Human Resources experience serving in a business partnership oriented role for executive leaders.
Must have demonstrated skills in change management and organizational development. Must possess excellent interpersonal communication and influencing skills.
Key skills and abilities include coaching, influencing, facilitation, process development, project management, analysis, presentation, written & verbal communication and problem solving.
Working knowledge of EEO, Federal & State employment laws, Worker’s Comp, STD and LTD issues.
Proficient in collaborating effectively and utilizing networks.
High degree of autonomy and strong decision-making skills.
Ability to analyze and interpret relevant data to inform business decisions.
Keeps commitments; exhibits candor and courage – is not afraid to establish a visible presence and point of view, to engage in spirited and constructive debate, to hold others accountable.
Demonstrated experience in HR strategy development and fostering continuous improvement.

Compensation Data

The pay range for this position is $140,000-$190,000/yr. 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

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.

Animal Care Specialist I - In Vivo PK 1 (Worcester, MA, US, 01608)

Job Summary

We are seeking Animal Care Specialist I's for our Discovery site located in Worcester, MA.

Schedule is Tuesday- Saturday or Thursday-Sunday (Day Shift)

As an Animal Care Specialist you will be responsible for the following:

Care of animals at our Discovery site
Feeding/watering, sanitizing enclosures
Environmental enrichment
Handling and restraint
Other related tasks including assisting with the movement of animals and stocking of supplies

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

•   You have a great sense of team spirit and responsibility.
•   You have a positive attitude and love to bring that energy into the lab every day to support your colleagues.
•   You have the ability to work in a fast-paced environment both independently and in a team setting
•   You concentrate on the details and can work reliably and precisely
•   You are dependable

The pay range 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 equivalent

Experience: None

Certifications: None

Other:
•    Ability to communicate and follow direction
•    Local to the area (no relocation assistance provided for this position)
•    Ability to lift 50 pounds

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.

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

Technicien animalier en élevages rongeurs (F/H) - Mission temporaire (Paris, FR, 75012)

Rejoignez une équipe passionnée par les animaux où chaque jour fait avancer la recherche scientifique !

Dans le cadre de cette activité, nous recherchons un Technicien animalier en élevages rongeurs (F/H) en pour une mission temporaire de plusieurs mois pour travailler au sein d'une animalerie sur l'un de nos site client à Paris. A ce titre, vous intégrerez une équipe de zootechniciens engagés au cœur du bien-être animal et travaillerez en interface directe avec les équipes du client.

Missions principales

En tant que Technicien animalier en élevages rongeurs (F/H), vous serez directement impliqué dans la gestion des élevages transgéniques destinés à des projets de recherche. Vos responsabilités incluront :

Gestion d'élevage transgénique (rongeurs)

Gestion des colonies murines transgéniques via un logiciel de gestion d'animalerie :
Accouplement, suivi des gestations et naissances
Identification des animaux
Sevrage
Saisies des données d'élevages sur le logiciel Anibio et sur des fichiers Excel

Participation aux suivis des projets expérimentaux

Pesées des animaux
Mise en place d'accouplements contrôlés
Injections intra-péritonéales ou sous-cutanées

Entretien, soin et surveillance des animaux

Assurer le bien-être des animaux au quotidien : observation, abreuvement, alimentation, enrichissement et vérification des paramètres d'ambiance
Assurer l'hébergement des animaux : change des cages sous hotte ou PSM
Contrôle des équipements et des installations
Entretien des zones de stabulation et des parties communes de l'animalerie
Participation aux activités de laverie

Profil recherché

Vous êtes idéalement expérimenté en gestion d'élevage de rongeurs transgéniques, rigoureux, passionné par le travail des animaux et vous avez à cœur de contribuer à la progression des projets scientifiques.
Niveau 2/Fonction A en Expérimentation animale
Savoir travailler en milieu confiné ou en zone protégée avec des équipements de protection individuelles (EPI)
A l'aise avec les outils informatiques
Esprit d'équipe et capacité à collaborer avec différents interlocuteurs
Organisation et rigueur au quotidien, sens de l'observation et capacité à identifier des anomalies
Autonomie et proactivité

Modalités

•   Convention collective pharmaceutique
•   Permanences ponctuelles les week-ends et/ou jours fériés : (1 à 2 fois par mois) pour contrôler le bien-être des animaux et vérifier les paramètres d'ambiance
•   Indemnité de transport, prime d'Intéressement et participation, accord d'ancienneté
•   Prise en charge de la mutuelle à 60%, tickets restaurants, comité d'entreprise

À propos des modèles et services de rechercheIndispensable 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 RiverCharles 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 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.

Senior Infosec Analyst (Vulnerability Management) (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

As an Infosec vulnerability analyst, you will be a hands-on practitioner and representative of the vulnerability management practice in cyber security defence. This is a technical role, and candidates must possess a solid understanding of information security, applications, operating systems, networking, cloud infrastructure, and attacker tactics, techniques, and procedures (TTPs). Responsibilities of this position include vulnerability management, reporting, remediation and continuous assessment, penetration testing, and red teaming.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Manage vulnerabilities across applications, endpoints, databases, networking devices, and mobile, cloud, and third-party assets.
•   Conduct continuous discovery and vulnerability assessment of enterprise-wide assets.
•   Support auditors in their duties that focus on compliance and risk reduction.
•   Perform penetration tests against company-owned assets, including internal and cloud-based assets, as well as web applications and APIs.
•   Perform other duties as assigned.

QUALIFICATIONS:

•   Education: Bachelor’s degree (B.A./B.S.) or equivalent in computer science, information technology, or related discipline.
• Very strong experience in information security operations, vulnerability management, or related disciplines.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Understanding of OWASP, CVSS, the MITRE ATT&CK framework, and the software development lifecycle.
•   Capable of scripting in Python, Bash, Perl, or PowerShell.
•   Certification/Licensure: IT security-related certification desired (e.g., Security +, CISSP, CISA, GCED, GPEN, GCIH, or similar professional certification).
•   Other:
   Must have strong interpersonal, teamwork, and self-initiative skills.

WORK ENVIRONMENT:
• This position has been designated as permanently remote.

Comments:
• May require occasional domestic or international travel.

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.

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

Environmental Health & Safety - Management (Charleston, SC, US, 29407)

Job Summary

Responsible for the development and implementation of policies, procedures and programs to ensure the Environment Health, Safety, and Sustainability (EHS&S) compliance of the. facility

Collaborate on the development and support rollout of corporate programs as related to implementation at the facility. Lead and manage site EHS&S audits in collaboration with site management.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Develop and implement policies and procedures targeted toward increasing the safety and protection of the environment for the businesses.
Ensure facility compliance with applicable environment health and safety regulations.
Implement site audit program of the EHS&S compliance of the site, track and report status of corrective actions, and alerting senior management to developing problems where intervention or oversight is required.
Participate in site leadership as a member of the site Leadership Team and conduct reviews at appropriate intervals with facility senior management.
Consult with site management and employees on Federal, State, and Local regulatory compliance related issues. Work with site facility management to ensure proper training programs are established with regards to environmental and health and safety compliance.
Responsible for timely submission of environmental reports and permits to local, state and federal regulatory agencies.
Work with site Leadership and Site/Global Procurement to develop cost savings initiatives to ensure business continuity and best in class service pricing.
Provide lead support and formal response to EHS agency inspections conducted by local, state and federal regulatory bodies.
Manage moderate size capital infrastructure projects from inception to completion including regulated areas.
Develop program budgets and schedules in support of EHS&S initiatives including platform tools (e.g. Enablon).
Monitor and drive progress of EHS&S projects and programs, maintaining budgets and schedules.
Lead the selection process for hiring third party service firms, evaluating proposals, conducting interviews and making recommendations to senior management, in partnership with site Procurement and Management
Provide supervision and development of EHS Site staff. Ensure appropriate communication takes place around EHS issues.
Consult with Corporate Engineering, Company management and workplace staff to identify and resolve potential EHS&S issues through engineering design changes or other means necessary, such as Facilities controls, JHA job hazard analysis.
Clarify, define, and assist in enforcement and application of Agency and Company policies and practices.
Support and affirm the Company policy of Equal Opportunity through Affirmative Action.

Partner with site leadership to address audit findings from clients, regulatory agencies, or internal CRL audits.
Provide EHS&S training to staff and contractors including OEB, SOP, and EHS&S policy training.
Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor’s degree (B.A./B.S.) or equivalent in a life science (biology, chemistry), environmental engineering, or related discipline.
Experience: Seven to ten 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.
Other: Sound working knowledge of Good Laboratory Practices (GLPs), Good Manufacturing Practices (GMPs) and government regulatory requirements and guidelines. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in MS Office suite including Excel, Word, Powerpoint and Project. In- depth knowledge of environment, health and safety regulations required. Ability to communicate and influence senior management on EHS compliance initiatives.

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.

WORK ENVIRONMENT:

While performing the duties of this job, the employee is occasionally exposed to fumes or airborne particles and toxic or caustic chemicals.
General office working conditions, the noise level in the work environment is usually quiet.

COMMENTS:

This position requires occasional domestic and international travel.

Compensation Data

The pay range for this position is $100,000 to $120,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

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 supported the development of 80% of the drugs approved by the FDA in the last five years.

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

Data Review Analyst I (Reno, NV, US, 89511)

Job Summary

This is not a Remote role. Candidate must reside in Reno, NV

We are seeking a Data Analyst I for our site located in Reno, NV.

The Data Analyst I is responsible for QC reviewing all tabulated study data to ensure it is accurate and complete. Ensure that all data received for review follows SOP guidelines that apply to the recording of study data.

•   Complete QC for tabulated study data produced in operational departments.
•   Ensure all report table corrections are completed by the appropriate staff members and that they are completed correctly.
•   Demonstrate comprehension of applicable regulatory driving documents, including protocols/phase plans, Analytical Procedures, Data Transfer Agreements, SOPs/BOPs, etc. as they relate to reported study data.
•   Ensure sample analysis data collected is appropriate and in scope with driving documents (protocol/phase plans, Analytical Procedures, Data Transfer Agreements, SOPs/BOPs, etc.) for what is intended to be reported.
•   Develop effective communication skills through informal discussions with peers, supervisor, and team.
•   Develop critical thinking, troubleshooting, and time management skills to ensure data quality and study timelines are maintained.
•   Identify process improvement initiatives based on observed trends and errors.
•   Support data review assistants with data review on all paper and electronic data produced in operational departments as needed.
•   Support with archiving, collating, and organizing all completed and reviewed data and/or file as needed.
•   Perform all other related duties as assigned.

Job Qualifications

The following are minimum qualifications related to the Data Analyst 1 position:

•   Education: High school diploma or General Education Degree (G.E.D.) required.
•   Experience: Minimum of 2-4 years related experience, including GLP and/or GCP experience required, or must have demonstrated full knowledge of competencies and positive performance at 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: None
•   Other: Strong organizational skills and acute attention to detail. Proficient in utilizing personal computer, e-mail, and standard office software packages (word processing, spreadsheet, presentation, database). Basic understanding of processes used for study data collection. Basic understanding of SOPs, GLPs, and other applicable regulatory guidelines governing the recording and review of study data.

The pay range for this position is $22.00 USD 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.

Head of Continuous Improvement (Charleston, SC, US, 29407)

Job Summary

We are looking for a hands-on Continuous Improvement Lead to drive improvement projects by working directly with all stakeholders including Operators on the plant floor. The ideal candidate will have a background in lean manufacturing and Six Sigma, with experience coaching and mentoring teams to solve problems and implement process improvements. This role is a member of the Production team, collaborating cross functionally with manufacturing teams, manufacturing support teams, and site leadership.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
⦁ Lead and manage continuous improvement projects in the manufacturing areas. Will also plan a key leadership role in CI projects in other areas across the site.
⦁ Strong communication, influencing and stakeholder management skills, with the ability to engage and present recommendations to senior leadership
⦁ Oversight for training, introduction and optimization of lean tools and processes across the site such as 6S, Standard Work, Visual Management, Meeting Effectiveness, Gemba and Kaizen.
⦁ Lead value stream mapping workshop in order to identify and drive improvement projects
⦁ Excellent strategic thinking and problem-solving skills
⦁ Develop 3-5 Year C.I. Strategic Plan in conjunction
⦁ Strong analytical skills and data-driven decision-making capabilities
⦁ Ability to work collaboratively and build strong relationships across the organization
⦁ Demonstrated ability to drive change and foster a culture of continuous improvement
⦁ A strong sense of prioritization and time management
⦁ Ability to prioritize work, influence team members to execute, and measure success
⦁ Overall success leads to annual P&L financial savings target and execution of plans for process improvement
⦁ Work with Operators and area leaders to implement Lean and Six Sigma tools
⦁ Coach and train plant floor teams to improve processes
⦁ Identify and eliminate inefficiencies to drive operational excellence

Job Qualifications

⦁ Education: B.S./B.A./M.S. or equivalent in engineering and/or related discipline. Formal Black Belt Qualification or experience of oversight of signification continuous improvement change programs is desired.
⦁ Experience:
⦁ 6+ 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:
⦁ PMP or project management experience.
⦁ Six Sigma green belt or black belt certification a plus.
⦁ Other:
⦁ Effective communication and interpersonal skills required.
⦁ Demonstrated computer skills (data input, word processing) required.
⦁ Experience with project management software and tools such as Microsoft project, smart sheet or similar.
⦁ Extensive experience in biotech industry in process development, process scale up, tech transfer and manufacturing.
⦁ Experience in the design, installation, and operations of GMP processes and equipment.

PHYSICAL DEMANDS:
⦁ Must regularly operate a computer and occasionally operate other office productivity machinery such as a calculator, copy machine, and computer printer.
⦁ Regularly provides information to and receives information from/through various technologies, media, sources and contacts. Must be able to accurately exchange accurate information in these situations.
⦁ Ability to move about the manufacturing environment, including operating within clean rooms and other controlled areas

WORK ENVIRONMENT:

⦁ The employee must be able to follow site safety procedures as they will occasionally work near moving mechanical parts; in high, precarious places; and is occasionally exposed to wet and/or humid conditions, fumes or airborne particles, toxic or caustic chemicals, and risk of electrical shock.
⦁ The noise level in the work environment is moderate.

Compensation Data

The pay range for this position is $130,000 - $145,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

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.

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.

System Engineering (Charleston, SC, US, 29407)

Job Summary

We are seeking a highly motivated and detail-oriented Systems Engineer to support our Research & Development (R&D) team throughout the product development lifecycle. This role will focus on facilitating cross-functional collaboration, documenting system requirements and workflows, and ensuring serviceability and risk mitigation are addressed from concept to launch.

Key Responsibilities:

· Lead Product Requirements Document (PRD) review sessions with R&D subject matter experts (SMEs) and managers.

· Collaborate with Product Management (PM) to clarify product requirements and expectations.

· Document System Requirements and Technical Specifications (SRTS) by translating PRD items into actionable technical tasks (“how” responses).

· Provide ongoing technical and documentation support to R&D throughout development.

· Ensure cross-functional team members (R&D SMEs, PMs, Technical Services) have the information they need.

· Lead cross-functional technical discussions as needed.

· Gather and integrate input from internal stakeholders (Field Service, Production, Service Depots, etc.) to ensure products are designed with serviceability in mind.

· Capture and document user workflows with input from SMEs to ensure user needs are clearly understood and incorporated into design.

· Lead Failure Modes, Effects, and Criticality Analysis (FMECA) work sessions to ensure risks are documented, mitigated, and validated through testing.

Job Qualifications

· Bachelor’s degree in engineering, or related technical field.

· 3–5 years of experience in systems engineering, product development, or technical project coordination.

· Proven ability to translate business and user needs into detailed technical requirements.

· Experience working with cross-functional teams in an R&D environment.

· Familiarity with FMECA, risk analysis methodologies, and serviceability planning.

· Excellent communication, facilitation, and documentation skills.

· Detail-oriented, proactive, and comfortable managing multiple tasks in a fast-paced environment.

Preferred Skills:

· Experience in laboratory analytical devices.

· Understanding of product lifecycle processes, from concept through manufacturing.

· Azure DevOps.

· Strong analytical thinking and systems-level problem-solving skills.

Compensation Data

The pay range for this position is $85,000 to $95,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

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.

Technicien en Chimie Analytique - F/H - CDI (Saint Germain Nuelles, FR, 69210)

Qui-sommes-nous ?

Le poste

Intégré(e) au département Formulations & Contrôle du site, nous recrutons un Technicien en Chimie Analytique (F/H) en CDI pour rejoindre notre laboratoire dès que possible.
Rattaché(e) à la manager d'équipe, le technicien en chimie pratique les analyses de routine (prinpalement UPLC) et participe activement à la vie du laboratoire. Il sait identifier les anomalies, problèmes et difficultés rencontrés dans son quotidien.

Les missions

Participer au développement et à la validation de méthodes analytiques en apportant une expertise technique
Réaliser toutes les étapes d’une analyse de routine (méthode validée) jusqu’à la constitution des dossiers
Utiliser des logiciels assurant le pilotage des équipements analytiques (chromatographie et spectrophotométrie)
Réaliser l’acquisition et le traitement des données analytique
Transmettre les résultats d’analyse en interne
Effectuer le contrôle interne des dossiers des analyses de routine
Préparer les rapports et les transmettre aux Directeurs d’étude
Transférer des données aux Directeurs d’Etude (compilation des dossiers, fichiers Excel transférés sur réseau…)

Conditions spécifiques du poste

Amplitude horaire : 7h30/18h avec planning à la semaine

Qualifications souhaitées

Vous êtes titulaire d'un diplôme de niveau Bac +2/3 en chimie et disposez d'une première expérience professionnelle concluante en chimie analytique (UPLC).
Vous appréciez le travail en équipe, mais savez évoluer en autonomie.
Organisé(e), vous êtes capable de vous adapter à des changements de planning avec flexibilité et rigueur.
Vous avez de bonnes bases de compréhension en anglais, écrit et lu.

Modalités

Convention collective de l’industrie pharmaceutique : groupe 3
Contrat : CDI non-cadre (accord de modulation 35h)
Salaire : A partir 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
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.

Research Scientist Biomarker - F/H - CDI (Saint Germain Nuelles, FR, 69210)

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

Afin de renforcer notre équipe de 15 scientifiques impliquée dans la gestion d'études de type immunoessais pour la détection d’anticorps ou protéines, nous recherchons un Reseach Scientist en Immunologie (F/H) en CDI sur notre site de Saint-Germain-Nuelles (69), à 30 minutes de Lyon. Vous interviendrez plus spécifiquement pour nos études liées aux biomarqueurs (plate-based assays et cell-based assays).

Vous travaillerez ainsi en support analytique afin de démontrer l'efficacité et la potentielle toxicologie de produits lors d’études animales ou d’essais cliniques humains. Pour cela, vous démontrez une connaissance approfondie du développement d’immunoessais sur les plateformes suivantes : ELISA, MSD, Gyrolab, cytométrie en flux et ELISpot.

Vous aimez également les défis techniques et l’opportunité de travailler sur plusieurs projets variés en parallèle est stimulante pour vous afin de faire avancer concrètement les projets clients préclinique et clinique.

Les missions

1/ Assurer un rôle de Directeur d'Etudes dans la gestion scientifique de développement, validation et analyse d'échantillons sur des études de toxicologie animale ou bien cliniques (80%) :

Etablir la faisabilité technique et scientifique des projets
Assurer un rôle de chef de projet (supervision des résultats générés, rédaction de rapports en anglais)
Prendre en charge l'analyse des données générées et leur acceptation sur Watson (LIMS)
Interpréter les données générées et être garant de leur fiabilité
Construire les procédures analytiques et plans expérimentaux préalable aux études (plan de plaque, détail de l'annexe technique)
Conseiller et orienter le client dans le design de l'essai et les démarches analytiques associées entreprises
Communiquer les informations clés aux équipes techniques de manière à faciliter les changes et travailler de manière efficiente

2/ Assurer également un rôle d’expert technique lors des phases de développement et validation (20%) :

Assurer de manière autonome la réalisation des essais ou bien s'assurer de leur réalisation, leur analyse, la vérification des données générées et leur communication dans le respect des délais et des procédures en vigueur.
Participer activement à la gestion opérationnelle de l'activité et des études (planification des essais, suivi des stocks de réactifs critiques, rédaction et vérification des annexes techniques)
Dispenser des formations ciblées aux techniciens et les développer en cas de besoin identifié
Être force de propositions pour améliorer les process et les méthodes analytiques

Qualifications souhaitées

Titulaire d'un Doctorat dans les domaines de l'immunologie, l'hématologie ou des biotechnologies, vous bénéficiez d’une expérience minimale de 5 ans en CRO, en développement et validation d’immunoessais en biomarqueurs et/ou cytométrie en flux.
Vous appréciez le travail en équipe dans un environnement collaboratif et évolutif.
Vous êtes reconnu(e) pour votre côté pédagogue, votre capacité à transmettre votre savoir aux collègues avec qui vous travaillez.
Vous êtes à même de convaincre des clients que votre approche analytique est pertinente et permettra d’atteindre les objectifs souhaités.
Une connaissance des exigences BPL serait un atout supplémentaire ; de même que la connaissance des logiciels suivants : Watson, Softmax, Gyrolab, sector S600, DIVA, FCS Express,...
Enfin, un niveau d’anglais confirmé (C1 minimum) est indispensable en vue des interactions avec nos clients ou avec les autres entités du groupe réparties à travers le monde.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique : groupe 6
Contrat : CDI Cadre (forfait jours + 12 RTT)
Salaire : A partir de 48 000€ bruts/an, sur 13 mois
Indemnités de transports (site non accessible en transport en commun : moyen de locomotion indispensable)
Accord de télétravail (jusqu'à 3 jours/semaine), prise en charge de la mutuelle à hauteur de 60%, restaurant d’entreprise, CSE, primes de participation et d’intéressement, ...

À propos de Safety Assessment

À propos de Charles River

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.

Animal Care Specialist I - In Vivo PK (Worcester, MA, US, 01608)

Job Summary

Schedule: Full Time. Tuesday - Saturday (Day Shift)

We are seeking a Animal Care Specialist I for our Discovery site located in Worcester, MA.

As an Animal Care Specialist you will be responsible for the care of animals at our Discovery site, having responsibilities that include, feeding/watering, sanitizing enclosures, environmental enrichment, handling and restraint and other related tasks including assisting with the movement of animals and stocking of supplies.

Job Qualifications

Qualifications:

Education: High School Diploma or equivalent

Experience: None

Certifications: None

Other:
•    Ability to communicate and follow direction
•    Local to the area (no relocation assistance provided for this position)
•    Ability to lift 50 pounds

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.

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

Assistant Facility Manager (14DNR) (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Assistant Facility Manager to join our Insourcing Solutions team, located in Bethesda, MD.As the Assistant Facility Manager, you will use existing SOPs and quality assurance standards to oversee and coordinate the daily activities of the animal facility, to include scheduling of staff.

Operates and maintains equipment and supplies
Oversees all aspects of husbandry support, to include related paperwork, cage change scheduling, and supplies
Actively interacts with Project Officers, facility veterinarian(s) and investigators to solve customer requests, inquiries, and complaints
Ensure that all work is performed according to the task Statement of Work
Participates in interviewing applicants for open positions, developing performance improvement plans, and writing employee performance evaluations
Assist in assessing, developing, and presenting training for staff and investigators
Performs daily clinical observations, preliminary health exam of sick animals prior to reporting to the Clinical Veterinarian.
Oversees the animal surveillance program related to the husbandry staff.
Occasionally provides technical support (e.g., restraining animals, collecting blood, collecting tissues, performing injections, treatments, surgical preparation, assisting with research procedures).
Occasionally provides animal husbandry and environmental enrichment for colony animals
Provides quality assurance to include animal health surveillance, monitoring of the effectiveness of facility sanitation, cage washing and autoclaving procedures, monitoring of incoming animal shipments for container integrity and animal health, monitor the HVAC, internal facility reports for monitoring deviations from pre-established parameters, other quality assurance services
Provides data entry/data base report generation for computerized systems which monitor facility internal environmental parameters, security, or other animal facility monitoring and management requirements
Prepares and submits written records, charts, logs, and inventories

Job Qualifications

The following are minimum requirements related to the Assistant Facility Manager position:

High school diploma or GED
A minimum four years’ experience working in an animal facility, two (2) of which in a supervisory capacity, must have experience with rodents and rabbits
Current AALAS certification at the LAT level; successful achievement of LATG within one year of eligibility

The pay range for this position is $40.00 to $43.00 USD per hour. Please note that salaries vary within the range based on factors including, skills, certifications, and location.

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.

Commis de laboratoire - Gestion des échantillons (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Commis de laboratoire pour notre équipe de Gestion des échantillons située au site de Laval, vous assisterez les Techniciens.nes et fournirez un soutien technique général.

Dans ce poste, les principales responsabilités incluront:

Recevoir ou ramasser les échantillons de l'installation;
Préparer le matériel nécessaire à la conduite de l'étude;
Vous êtes responsable de l'organisation des échantillons dans les congélateurs et veillez à ce qu'ils soient correctement documentés;
Effectuer l'entretien et le nettoyage des réfrigérateurs et des congélateurs;
Veiller à la propreté et à l'organisation de l'espace de travail.

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Au minimum, 3ème secondaire complété;
Bonnes compétences en matière d'organisation, de relations interpersonnelles et de communication;
Souci du détail et méticulosité;
Capacité à travailler dans des délais serrés et à s'adapter au changement;
Capacité à travailler en équipe.

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: 17$/hrs;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi de 8h à 16h15. Selon les besoins de l’entreprise, vous pourriez avoir à faire du temps supplémentaires;
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);
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.

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

Technicien de Laboratoire en Pathologie Technique - F/H - CDI (Saint Germain Nuelles, FR, 69210)

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 900 personnes travaillent chaque jour dans l'objectif commun de participer au développement de pharmacothérapies, dans le respect du bien-être animal.

Le poste

Suite à une évolution interne, nous recherchons un Technicien de Laboratoire (F/H) en CDI pour rejoindre notre département de Pathologie Technique.
Sous la responsabilité de votre manager d'équipe (10-15 personnes), vous pratiquerez les autopsies et préparerez les lames histologiques pour interprétation par nos vétérinaires pathologistes.
Vous participerez également à la vie du laboratoire, en apportant un regard critique sur votre travail.
Vous savez identifier les anomalies, problèmes ou difficultés rencontrés dans votre quotidien.

Les missions

1. Histologie

Assurer la préparation des échantillons pour toutes les espèces
Réaliser l'inclusion des organes en blocs de paraffine
Réaliser la coupe des lames histologiques au microtome
Effectuer la coloration standard des lames et le montage
Utiliser en routine les automates à déshydrater, de coloration et les colleuses de lamelles

2. Autopsie

Assurer la réalisation des autopsies de toutes les espèces utilisées en toxicologie
Réaliser la saisie des données manuscrites ou à l'aide de système informatique
Contribuer à la qualité des études en assurant sans erreur les techniques de prélèvement et de fixation des organes

Conditions spécifiques du poste

Amplitude horaire : 7h/19h avec planning à la semaine
Astreintes (week-ends, jours féries)

Qualifications souhaitées

Vous êtes titulaire d'un diplôme de niveau Bac+2 dans le domaine de la biologie, et avez un attrait pour le domaine de la physiologie et l'anatomie.
Vous êtes à l'aise avec le travail en équipe mais également capable d'évoluer en autonomie. Vous êtes observateur, minutieux et rigoureux.
Vous avez des bases en anglais écrit et lu.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 25500 € bruts / an, sur 13 mois
Prise en charge de la mutuelle à 60%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement, de participation, accord d’ancienneté,...
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.

Laboratory Clerk - Sample Management (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Laboratory Clerk for our Sample Management team at the Laval location, you will assist the Technicians and provide general technical support.

In this role, primary responsibilities include:

Receive or pick up samples from the facility;
Prepare the required materials for the study conduct;
Keep the samples well organized within the freezers and ensure proper documentation;
Perform maintenance/cleaning of the fridges and freezers;
Keep the working area clean and organized.

Key Elements

If you have the following qualifications, we'll train you for the rest:

At least secondary 3 completed;
Good organizational, interpersonal and communication skills;
Detail oriented and meticulous;
Ability to work under time constraints and to adapt to change;
Ability to work in a team environment.

Role Specific Information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Salary: $17/hrs;
Annual bonus based on performance;
Schedule: Monday to Friday, 8am to 4:15pm. 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 ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
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.

Research Analyst I - Immunology (Ashland, OH, US, 44805)

Job Summary

We are seeking a Research Analyst 1- for our Immunology team at our Safety Assessment site located in Ashland, OH.

Basic Summary:

Perform laboratory tasks by various basic methods. 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.

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:

Perform assays such as ELISA, multiplex, immunophenotyping, comet, and micronucleus.
Perform density gradient cell separations.
May act a lead/primary technician on basic studies.
Utilize micropipettes for all assays.
Perform study preparation activities including ordering supplies, preparing/verifying paperwork, and tube labeling.
Receive and log in reagents, solutions, and samples.
Prepare simple to complex lab solutions.
Assist in method development studies, method validation studies, and equipment validations as needed.
Operate, perform quality control and maintenance procedures on equipment such as microplate readers, plate washers, cell counters, multiplex instruments, flow cytometers, freezers, liquid scintillation counter, gamma counter, and eyewash stations.
Maintain clean work areas by cleaning dishes/glassware, wiping down countertops, and sweeping/mopping floor as needed.
Collect and record data in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), protocols, and study plans.
Input, print, and edit basic to complex data.
Prepare materials for shipment and archival.
Review documentation for quality control.
Perform all other related duties as assigned.

The pay for this position is $21 USD 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: Bachelor’s degree (B.A/B.S.) in scientific field 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 4 years related experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None
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 experience preferred.

Equal Employment Opportunity

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

Senior Staff Veterinarian (Reno, NV, US, 89511)

Job Summary

Oversee and perform veterinary procedures that support all studies. Assist the Director in oversight of the animal care and use program. May supervise or oversee veterinary staff and manage the activities of assigned section to ensure effective performance. Assist the Director in department management functions as required and serve as acting department head in Director's absence.

ESSENTIAL DUTIES AND RESPONSIBILITES:

Oversee daily animal health assessment program
Perform veterinary rounds as scheduled, and provide clinical care and preventive medicine support
May perform surgical support and provide anesthesia, surgical and analgesic technical expertise/advice to facilitate protocol development
May assist in sentinel animal monitoring and other monitoring programs
Responsible for the overall training program for veterinary technicians/staff. Ensure that training is properly documented and regularly updated as necessary
Provide animal health care guidance for veterinary services personnel as required
Ensure that internal and external applications, reports and other materials are prepared and submitted as required
Oversee responses to internal/external inspections and quality assurance audits of veterinary or animal welfare type content
Participate in the design and implementation of programs to assess vendors for animals and critical animal related suppliers. Monitor a Biosecurity program appropriate to the sites needs.
Serve as advisor to management in technical matters as they relate to the site including application of new technology, the use of alternatives, new animal models, and any changes in national policies, procedures, guidelines or regulations affecting animal care and use
Assist Director in oversight of quarantine and conditioning program which includes participation in vendor management, e.g. conducting site visits, reviewing vendor health information, communicating specific issues related to shipments to them, and tracking overall vendor performance
May serve as a full or ad-hoc member of the Institutional Animal Care and Use Committee (IACUC), assisting in protocol review and other efforts as identified
Assist Director as a consultant to Study Directors and/or sponsors regarding study design prior to IACUC submission and as part of the veterinarian review and IACUC monitoring
Ensure all study related in-life procedures and processes are accomplished in accordance with the study protocol as it relates to animal welfare and veterinary issues
Oversee long-term improvement projects such as redesign of SOPs and basic research procedures
Perform expert veterinary research support to Study Directors and Sponsors
Maintain compliance with all applicable laws and regulations including the Animal Welfare Act
Ensure that all animal care related activities are conducted in accordance with Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Association for Assessment and Accreditation of Laboratory Animal Care (AAALAC), United States Department of Agriculture (USDA), and Food and Drug Administration (FDA) standards and regulations
Oversee and administer the Veterinary Care Program as outlined in the AAALAC Program Description. Write updated Program for the Veterinary Care section of the AAALAC re-certification.
May use controlled substances and be responsible for maintaining appropriate records
May develop new or innovative surgical techniques or other procedural improvements appropriate to research studies
May assist in management of the activities of assigned section, including supervising employees, scheduling, personnel actions (hiring, promotions, raises), discipline, personnel development and performance monitoring

Job Qualifications

MINIMUM QUALIFICATIONS:

Education: Veterinary degree (D.V.M./V.M.D.) or international equivalent.
Experience: Minimum of 6 years related experience in research/lab animal/GLP environment.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: Licensure to practice veterinary medicine in at least one U.S. state required.
Other: Computer literacy (Windows PC) WordPerfect and Excel. Good communication, interpersonal, and organizational skills. Knowledge of laws, regulations, policies and guidelines that govern animal research, research conduct principles (GLP) and current methodology of laboratory animal medicine and management is important.

PREFERRED QUALIFICATIONS:

Experience: Two years supervisory/ management experience preferred.
Certification/Licensure: Ability to practice veterinary medicine in the work state highly desirable. ACLAM eligibility or accreditation is highly desired.

Compensation Data

The pay range for this position is $180,000 - $200,000 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 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.

Research Technician I - In Vivo PK (Worcester, MA, US, 01608)

Job Summary

This position is working Full Time - Tuesday - Saturday 6:00 a.m. to 2:30 p.m.

Job Qualifications

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 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 guidelines relating to the care of laboratory animals. Basic understanding of study design and protocols.

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.

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

Technicien Animalier - F/H - CDI (Saint Germain Nuelles, FR, 69210)

Qui sommes-nous ?

Le poste :

Afin de renforcer nos animaleries en charge de la bonne conduite de nos études de toxicologie, nous recherchons 3 techniciens animaliers (F/H) en CDI.

Vous rejoindrez un département d'environ 160 personnes, comportant une zone protégée (hébergeant souris, rats, lapins) et une zone conventionnelle (hébergeant chiens, porcs et primates).

En fonction de la charge fluctuante de notre activité, et après une formation dispensée en interne, vous serez amené(e) à réaliser les interventions techniques auprès de toutes nos différentes espèces.

Missions :

Participer au lancement des études en préparant les cahiers dont vous aurez la charge
Vérifier l'adéquation des conditions d'hébergement avec les procédures
Assurer l'ensemble des techniques de contentions, administrations, prélèvements et examens standards sur les animaux
Assurer tout ou partie des techniques spécifiques des études de reproduction et des études de perfusion
Contrôler l'état clinique (croissance, poids, comportement) des animaux en cours d'études et remonter les anomalies
Préparer quotidienne le matériel nécessaire à l'étude et assurer sa disponibilité
Acquérir les données selon nos plans d'études, assurer leur contrôle et leur enregistrement

Conditions spécifiques du poste :

Amplitude horaire hebdomadaire du département : 6h/18h
Permanences de weekend: 1 par mois environ

Qualifications souhaitées :

Titulaire d'un diplôme de niveau Bac (général ou professionnel), vous disposez d'une première expérience en tant que technicien de laboratoire ou technicien animalier.

Passionné(e) par les animaux, vous avez à coeur de réaliser les actes techniques dans le respect des procédures et de leur bien-être.

Votre première expérience ou votre formation vous a idéalement permis d'être titulaire de la formation à l’Expérimentation Animale de niveau A/II.

Vous savez prioriser, organiser vos tâches et communiquer auprès de vos coéquipiers.

Modalités contractuelles :

Convention collective de l'industrie pharmaceutique, groupe : 3
Contrat : CDI non-cadre (accord de modulation - 35h)
Salaire : A compter de 25 800€ 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.

Technicien de Toxicologie Rongeurs - F/H - CDI (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Le service Toxicologie recrute un Technicien en Toxicologie pour intégrer son équipe composée de 30 techniciens (rongeurs).

Les missions 

Au sein des services de Toxicologie In Vivo, vous aurez pour principales missions sous la responsabilité de votre supérieur :

Effectuer les opérations nécessaires à la conduite des tâches ou des études dont vous êtes responsables, conformément aux bonnes pratiques de laboratoire, aux procédures standards, à la charte éthique, aux protocoles d’études et au règlement intérieur,
Réaliser les traitements, assurer le suivi de l’état clinique et l’évolution pondérale des animaux,
Procéder à des prélèvements sanguins, d’urine ou de fécès,
Saisir l’intégralité des actes réalisés sur informatique,
Assurer la qualité des données recueillies et de résultats,
Transmettre à votre supérieur hiérarchique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail.

Conditions spécifiques du poste

Travail en milieu confiné avec port obligatoire d’équipements de protection individuelle.

Travail le WE.

Retours et horaires décalés possibles (Discutés en amont avec le Responsable).

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 dans le domaine scientifique.

Vous êtes à l’aise au contact des animaux, notamment des rongeurs.

Vous maitrisez l’anglais

Vous possédez une aisance relationnelle et un sens du contact et du service, vous êtes organisé(e), vous appréciez de travailler en équipe.

Vous êtes rigoureux(se), vous respectez les délais, les procédures et les consignes.

Les modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : Non-cadre (accord de modulation 35h) - CDI
Salaire : A compter de 25 400 € 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 Safety Assessment

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 85 % des médicaments approuvés par la FDA en 2021.

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

Behavioral Technician I (Reno, NV, US, 89511)

Job Summary

We are seeking a Behavioral Technician for our Safety Assessment site located Reno, Nevada.

The following are responsibilities related to the Behavioral Technician:

Assist with providing appropriate enrichments to the animals’ structural and social environments and provide opportunities for species-typical activities. Monitor colony behavioral health and provide care to animals needing special attention and/or treatments as directed.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Assist with providing appropriate enrichments to the animals’ structural and social environments and provide opportunities for species-typical activities.
•   Monitor colony behavioral health, and provide care for animals needing special attention and/or treatment as directed.
•   Observe animals and report behavioral abnormalities.
•   Assist in performing behavioral assessments in response to reports of behavioral abnormalities.
•   Assist with coordinating animal psychological/behavioral enrichment, including the acclimation and socialization of study animals.
•   Review animal approval documentation and submit approval forms to appropriate personnel.
•   Work with other Behavioral staff to precondition animals for study procedures.
•   Work closely with the veterinary and animal care staff to ensure proper animal care standards are maintained.
•   Assist with evaluation of new enrichment devices and provide input on strategies for individually and socially housed animals.
•   Assist with revisions to relevant SOPs as needed to ensure accordance with the Animal Welfare Act and accepted professional standards.
•   Routinely handle animals as required for duties.
•   Maintain and track data related to social housing, exemptions to social housing, and abnormal behavior.
•   Maintain documentation for the Behavioral Management Program.
•   Assist with training animal care staff and other site personnel on aspects of animal behavior and enrichment as needed.
•   May serve as IACUC committee member.
•   Perform all other related duties as assigned.

Job Qualifications

•   Education: Bachelor’s degree (B.A./B.S.) or equivalent in animal or life sciences or related discipline.
•   Experience: 1-3 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.
•   Certification/Licensure: AALAS certification at the LAT 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.

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

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

Veterinary Pathologist (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Veterinary Pathologist 2, for our team located in Senneville, Quebec, Canada, you will mainly be responsible for tissue evaluation and interpretation of assigned studies. 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:

Perform macroscopic and microscopic tissue evaluation and interpretation of assigned studies.
Record pathology findings in data capturing system(s).
Prepare complex reports delineating pathological findings and detailing all test article effects.
Interact with clients to assure satisfaction and to market services.
May assist with necropsy supervision and may conduct necropsies, including gross pathology interpretation, sample collection and fixation.
As needed, work with study directors to ensure data is accurately integrated into study reports.
Provide training, technical guidance and leadership to laboratory staff and to less experienced pathologists, as needed.
Provide advanced scientific expertise for experimental design and other aspects of research studies as needed.
Perform all other related duties as assigned.

Key Elements

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

Open to new graduates, eligible for ACVP/ECVP board exam.
Doctorate degree (D.V.M/V.M.D.) from an accredited veterinary school, or acceptable international equivalent in veterinary medicine.
Working knowledge of clinical pathology preferred; specialized training and/or experience in medical device pathology preferred.
Board certification with the American College of Veterinary Pathologists (A.C.V.P.) or European College of Veterinary Pathologists (E.C.V.P) required to enter the level grade.
Demonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought.
Ability to work on problems of diverse scope in which analysis of data requires evaluation of multiple factors.
Ability to exercise judgement within generally defined practices and policies in selecting methods or techniques for obtaining solutions.
Working knowledge of related computer applications.

Role Specific Information:

Place of work: Senneville.
Schedule: Onsite, Monday to Friday.

Why Charles River?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage)
Relocation amount and assistance.
Retention Bonus.
Paid development training.
Paid ACVP / ECVP yearly license.
Employee and family assistance program.
Access to a doctor and various health professionals (telemedicine).
4 weeks’ vacation & 10 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!

Equal Employment Opportunity

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

Senior Financial Analyst, Gene Therapy (Hybrid-Rockville, MD) (Rockville, MD, US, 20850)

Job Summary

Charles River Labs is seeking an experienced financial analyst to help support their growing Gene Therapy site in Rockville, Maryland. This position will be hybrid.

The Senior Financial Analyst will be responsible for supporting the Senior Finance Manager with activities related to monthly/quarterly financial close, forecasting & reporting, as well as participating in the preparation of the annual operating plan and any site improvement initiatives. The ideal candidate will have experience in a finance function in the life sciences or biotech industry and be comfortable working and building business relationships with both local and corporate business partners.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Partner with client project management and client services on Statements of Work and relevant SAP workflow as needed, including cost analysis used to develop pricing.
•   Analyze client unbilled and aging receivables and partner with CRL Credit and Collections, Project Coordination, Client Project Management, Business Development, and Site Operations to drive resolution.
•   Partner with site Operations and Quality to develop KPI’s and reporting to allow for relevant business decision making and measurement of the business operations and efficiency.
•   Utilize SAP, AFO and SAC applications to develop routine financial reporting tools for variance analysis and reporting.
•   Analyzes financial and operational performance, provides concise, relevant explanations, observations and/or recommendations to leadership and executive management.
•   Contribute to the development of monthly/quarterly forecasts, Annual Operating Plan, Strategic Plan, and analyze the variances.
•   Support monthly business reviews with senior management discussing operational and financial results, challenges, opportunities, strengths, and weaknesses.
•   Proactively partner with site leadership (Manufacturing, Operations, Quality, Sales, Human Resources, etc.) to address organizational needs and identify financial risk and opportunities to improve financial reporting.
•   Perform all other related duties as assigned.

Job Qualifications

•    Education: Bachelor’s degree (B.A./B.S.) or equivalent business or science degree.
•   Experience: 5 - 7+ years experience in financial analysis or business. Experience in Life Science industry strongly preferred.
•    Strong attention to detail, excellent analytical skills with recommendations grounded in data.
•    High proficiency in Microsoft Office applications.
•    Must be able to work with minimal supervision
•    An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. 10 yrs experience as a Financial Analyst will be accepted in lieu of Bachelor's degree.

Compensation Data

The pay range for this position is $90,000 - $100,000K USD annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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

Pathologiste Vétérinaire (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant que Pathologiste Vétérinaire 2, pour notre équipe située à Senneville, Québec, Canada, vous serez principalement responsable de l'évaluation des tissus et de l'interprétation des études assignées. Votre contribution assurera la santé de nos animaux ainsi que l'intégrité de nos études précliniques.

Dans ce rôle, les principales responsabilités sont les suivantes:

Effectuer l'évaluation et l'interprétation macroscopique et microscopique de tissus.
Entrer les observations microscopiques dans le(s) système(s) de capture de données.
Rédiger des rapports narratifs exhaustifs détaillant tous les effets de la substance évaluée.
Interagir avec les clients pour assurer leur satisfaction.
Supervision de nécropsie, possible de participer directement à des nécropsies, incluant la collecte et la fixation des échantillons et la description des observations macroscopiques.
Au besoin, collabore avec les directeurs d'étude pour s'assurer que les données de pathologie sont intégrées avec précision dans les rapports d'étude.
Effectuer toutes les autres tâches connexes assignées.

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Diplôme de doctorat (D.V.M./V.M.D.) d'une école vétérinaire accréditée ou équivalent international acceptable en médecine vétérinaire.
Certification du Collège américain ou européen des pathologistes vétérinaires (A.C.V.P ou E.C.V.P).
Capable de travailler sur des problèmes complexes dans lesquels l'analyse de situations ou de données nécessite une évaluation approfondie de divers facteurs. Il a fait preuve de compétence technique, de créativité scientifique, de collaboration avec d'autres personnes et d'indépendance d’esprit; il a la réputation d'être un leader émergent avec des performances et des réalisations soutenues.
Maîtrise des logiciels de traitement de texte, de feuilles de calcul et de bases de données.

Informations spécifiques au poste:

Lieu de travail: Senneville.
Horaire: Du lundi au vendredi

Pourquoi Charles River?

Avantages compétitifs dès l'embauche. Nous payons jusqu'à 85% des primes (santé et dentaire).
Montant et aide à la relocalisation.
Prime de rétention.
Formation de développement payée.
Licence annuelle ACVP / ECVP payée.
Programme d'aide aux employés et aux familles.
Accès à un médecin et à divers professionnels de la santé (télémédecine).
4 semaines de vacances et 10 jours personnels par an.
Nombreuses activités sociales.

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais partout dans le monde, joignez-vous à nous, C’EST VOTRE MOMENT.

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

Junior Technical Service (Hyderabad, IN)

Job Summary

Responsible for technical support for Endosafe® (including automated NEXUS system) and/or Celsis™ and their associated systems. Support customers on Endosafe® and/or Celsis™ instrument installation, qualifications and product validation. Provide on-site training, sample testing or troubleshooting for continued customer satisfaction of our clients. Manage activities to help meet revenue targets and goals for the business.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Understanding and application of one or more of the product lines under the Microbial portfolio (Endosafe® and/or Celsis™)
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.
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.
Responsible for the initial training and validation/application development support for customers, ensuring full and continued utilization of Microbial Solutions products.
Recommends or performs remedial actions to troubleshoot customer issues related to application, reagents and software for the assigned product line.
Performs instrument qualification and installation for new customers.
Establishes regular interface and communication with the Account Management and Field Services 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 Microbial portfolio.
Input, manage and monitor cases on Service Cloud or SFDC.Ensures activities of the Technical Services team are continuously compliant to ISO 9001, Company local & global SOPs and data integrity principles and requirements, where appropriate.

GENERAL REQUIRMENTS

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, 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.
Must be willing to travel domestically and internationally to customers’ sites.
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 M.Sc. or equivalent in Biology, Microbiology, Life Sciences, Biotechnology or any other related scientific discipline.
Experience: 0-5 years of relevant industry experience, preferably involving customer-facing responsibilities.
Salary range : 4 to 7 LPA.
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.

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.

Director Regulatory Compliance (Wayne, PA, US, 19087)

Job Summary

Responsible for managing the Quality Assurance program(s) at one or more Charles River operations and serves as a member of the Regulatory Affairs and Compliance management team. Provides direction in implementing the Charles River Compliance Program and may lead corporate quality initiatives to improve the program.

Essential Duties

⦁ Communicate all identified compliance and quality risks to his/her supervisor.
⦁ Develop departmental policies and procedures and assure their consistency with Quality Assurance programs at other Charles River sites/operations.
⦁ Identify the need for Corporate Quality and Compliance Policies and lead development and implementation efforts.
⦁ Direct site/operation Quality Assurance program to assure inspections and audits are accurate, thorough, timely, and provide the correct interpretation of regulatory requirements and corporate policies.
⦁ Maintain a close working relationship with site/operation management to assure a cohesive approach to regulatory compliance.
⦁ Assure staff receives appropriate regulatory and management training, and mentoring to enable the execution of regulatory and management responsibilities.
⦁ Assume a lead role in the development and presentation of regulatory training for Quality Assurance and operations staff.
⦁ Manage site/operation Quality Assurance inspection and audit programs and schedule resources to assure efficient and effective operation of the site/operation Quality Assurance organization. Align Quality Assurance staffing level and expertise with identified business needs.
⦁ Monitor the effectiveness of subordinate Quality Assurance managers in reviewing Quality Assurance reports of audits and inspections to assure proper and consistent interpretation of regulatory requirements and corporate policies. Identify and resolve inconsistencies between Quality Assurance audit teams should they occur.
⦁ Assure that all records and reports are prepared, communicated, and retained in accordance with applicable regulatory requirements.
⦁ Serves as the principal liaison with site operations managers to identify regulatory deficiencies, explain audit findings, resolve escalated conflicts, and consult on corrective and preventative actions.
⦁ Assemble, evaluate, and report site metrics measuring compliance and quality key performance indicators.
⦁ Serve as the principal site representative for scheduling and management of regulatory and client inspections/audits.
⦁ Interact, as appropriate, with regulatory agencies in developing a positive working relationship.

Responsibilities:

⦁ Train site/operation personnel and management on interacting with client and regulatory auditors prepare appropriate summaries and reports of such audits.
⦁ Review and endorse regulatory and client audit responses and corrective action commitments.
⦁ Monitor site/operation corrective actions commitments and communicate “at risk” commitments to management with recommendations for their timely resolution.
⦁ Identify practices, methods, and processes for improvement and assist other operations on related compliance issues.
⦁ Provide regulatory guidance to internal departments for the development of new products, test methodology, new facility construction, and new processes.
⦁ Participate in development and revision of regulatory submissions, e.g., license applications, supplements, annual reports, and master files.
⦁ Participate in the review and development of quality agreements with clients and contract service providers.
⦁ Assure vendors and suppliers identified/designated by Charles River are assessed for the compliance with applicable regulatory requirements.
⦁ Assume a key role in designated Regulatory Affairs and Compliance projects and programs.
⦁ Participate in Corporate Quality Meetings, Regulatory Affairs and Compliance meetings, intranet communications, and relevant strategic planning sessions.
⦁ Assure that Corporate Quality and Compliance Policies are implemented and administered at the site/operation.
⦁ Direct 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.
⦁ Develop short- and long-range operating objectives, organizational structure, staffing requirements and succession plans.
⦁ Integrate activities with those of other major organizational units (e.g. segments, departments, functions).
⦁ Develop and recommend 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 and biosafety protocols].
⦁ Communicate all identified compliance and quality risks to his/her supervisor.
⦁ Perform all other related duties as assigned.

Job Qualifications

⦁ Education: Bachelor's degree (B.A. /B.S.) or equivalent. Advanced degree in biological sciences, pharmaceutical sciences, or computer sciences preferred.
⦁ Experience: Ten to twelve years related experience in the pharmaceutical, and/or biotechnology based industry.
⦁ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
⦁ Other: Strong experience and direct responsibility for management of Quality Assurance programs. Extensive experience with management of government regulatory inspections and preparing/reviewing responses to any inspectional findings. Excellent knowledge of pertinent national and international regulations pertaining to the pharmaceutical and biotechnology industries. Excellent leadership 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.

WORK ENVIRONMENT:
⦁ General office working conditions; the noise level is usually quiet.

COMMENTS:
⦁ Requires regular domestic and international travel.

Compensation Data

The pay range for this position is 170K-190K Base and equity eligible (RSUs). 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 supported the development of 80% of the drugs approved by the FDA in the last five years.

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

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

Job Summary

Full Time - 40 Hours/Week - Tuesday-Saturday 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.

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

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

Clinical Veterinarian (Ashland, OH, US, 44805)

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

The Clinical Veterinarian is a full-time role meant to provide top notch and ethical veterinary health care for laboratory animals and ensure CRL’s mission of saving human and animal lives! A successful individual will also advise regarding the husbandry, care and maintenance of laboratory animals as well as facilitating training for technicians. This responsibility extends to promoting animal well-being during all phases of the animal's life as well as roles in compliance monitoring, quality management and safe work practices when working with animal models. Our goal is to save human and animal lives in the most ethical and humane way by not only adhering to regulations and guidance's such as the animal welfare act, the 3R's of ethical research, the AVMA guidance on human euthanasia, and “The Guide for the Care and Use of Lab Animals," but pursuing continuous improvement to approaches in research animal care.

Note: This posting is for networking purposes for future opportunities.

For successful hires we offer:

PAID TIME OFF TO STUDY FOR BOARDS AND TUITION ASSISTANCE FOR CONTINUING EDUCATION
STRONG BONUS INCENTIVES AS WELL AS RETENTION BONUSES FOR 3 YEARS
SUPPORT FOR ANNUAL CONFERENCE ATTENDANCE, CONTINUING EDUCATION AND JOURNAL PUBLICATIONS IF DESIRED
THE SATISFACTION OF BEING PART OF A TEAM THAT IS COMMITED TO ANIMAL WELFARE AND ON THE CUTTING EDGE OF DRUG DISCOVERY

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Manage health care for the animals within the facility.
Perform veterinary rounds as scheduled and provide clinical care and preventive medicine support.
Perform surgical support and provide anesthesia, surgical and analgesic technical
expertise/advice to facilitate protocol development.
Develop and deliver training for staff. Training may include veterinary diagnostics, techniques, and minor surgical procedures.
Provide animal health care guidance for veterinary services personnel as required.
participate in the response to internal/external inspections and quality assurance audits of veterinary or animal welfare type content.
Provide support for activities of the Institutional Animal Care and Use Committee (IACUC), including protocol review, program review and facility inspections. May serve on the IACUC committee.
Perform consultation and collaboration with Researchers regarding animal care, health, welfare and treatment. May also consult on the planning, conduct, and reporting of studies.
May assist in sentinel animal monitoring and other monitoring programs.
Write, review and update veterinary care and/or necropsy SOPs as required.
Perform literature searches relating to veterinary subject matters.
Ensure facility is following all applicable regulations, guidelines and standards that relate to animal care and use (E.g., USDA, FDA, AAALAC).
Make recommendations and assist in establishing and enhancing veterinary and animal care standards.
May use controlled substances and be responsible for maintaining appropriate records.
May develop new or innovative procedural improvements appropriate to research studies.
May assist in management of the activities of assigned section, including supervising
employees, scheduling, personnel actions (hiring, promotions, raises), discipline, personnel development and performance monitoring.
Perform special projects and assist with administrative efforts as needed.

Job Qualifications

QUALIFICATIONS:

Education: Veterinary degree (D.V.M./V.M.D.) or international equivalent.
Experience: 0 to 2 years related experience with animal care. Preferred but not required as we have a training program to assist with joining the CRL team.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: Licensure to practice veterinary medicine in at least one U.S. state required. Ability to practice veterinary medicine in the work state highly desirable.
Other: Computer literacy in word processing, spreadsheet and database software. Ability to organize, prioritize work and meet deadlines. Good communication skills.

Compensation Information:

Base salary + short-term and long-term incentive plans
Professional development and continuing education (e.g., CE (national/local meetings, virtual & in-person), leadership development, cross-site and international collaboration within CRL)
Other academic and credentialed pursuits (e.g., ACLAM Boards, Toxicology specialty boards). 
Enhanced flexibility/consistency of hours, valued support for work/life balance
Comprehensive onboarding, mentorship during transition, and training opportunities
Access to a global network of veterinarians across Safety Assessment and other business units.

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 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.

Staff Veterinarian (Reno, NV, US, 89511)

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

We are seeking an experienced Staff Veterinarian for our Safety Assessment site located in Reno, Nevada, or Houston, Texas

Note: This posting is for networking purposes for future opportunities.

Job Summary

This position is responsible for overseeing and performing veterinary procedures that support all studies. This position will also oversee all aspects of the animal care and use program.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Manage health care for the animals within the facility.
Perform veterinary rounds as scheduled and provide clinical care and preventive medicine support.
Perform surgical support and provide anesthesia, surgical and analgesic technical
expertise/advice to facilitate protocol development.
Develop and deliver training for staff. Training may include veterinary diagnostics, techniques, and minor surgical procedures.
Provide animal health care guidance for veterinary services personnel as required.
participate in the response to internal/external inspections and quality assurance audits of veterinary or animal welfare type content.
Provide support for activities of the Institutional Animal Care and Use Committee (IACUC), including protocol review, program review and facility inspections. May serve on the IACUC committee.
Perform consultation and collaboration with Researchers regarding animal care, health, welfare and treatment. May also consult on the planning, conduct, and reporting of studies.
May assist in sentinel animal monitoring and other monitoring programs.
Write, review and update veterinary care and/or necropsy SOPs as required.
Perform literature searches relating to veterinary subject matters.
Ensure facility is following all applicable regulations, guidelines and standards that relate to animal care and use (E.g., USDA, FDA, AAALAC).
Make recommendations and assist in establishing and enhancing veterinary and animal care standards.
May use controlled substances and be responsible for maintaining appropriate records.
May develop new or innovative procedural improvements appropriate to research studies.
May assist in management of the activities of assigned section, including supervising
employees, scheduling, personnel actions (hiring, promotions, raises), discipline, personnel development and performance monitoring.
Perform special projects and assist with administrative efforts as needed.

Qualifications

The following are minimum requirements related to the Staff Veterinarian position:

Veterinary degree (D.V.M./V.M.D.) or international equivalent required
Licensure to practice veterinary medicine in at least 1 U.S. state required
Computer literacy, good communication, interpersonal, and organizational skills

Preferred:

Ability to practice veterinary medicine in the work state highly desirable
ACLAM eligibility or accreditation preferred
Minimum 3 years experience in laboratory animal medicine preferred
2 years management experience preferred
Knowledge of laws, regulations, policies and guidelines that govern animal research, research conduct principles (GLP) and current methodology of laboratory animal medicine and management is important

Compensation information:

Base salary + short-term and long-term incentive plans
Professional development and continuing education (e.g., CE (national/local meetings, virtual & in-person), leadership development, cross-site and international collaboration within CRL)
Other academic and credentialed pursuits (e.g., ACLAM Boards, Toxicology specialty boards). 
Enhanced flexibility/consistency of hours, valued support for work/life balance
Comprehensive onboarding, mentorship during transition, and training opportunities
Access to a global network of veterinarians across Safety Assessment and other business units.

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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

Associate Director, Laboratory Support & Logistics, Lab Sciences (Reno, NV, US, 89511)

Job Summary

The Associate Director of Laboratory and Logistics position at Charles River Laboratories in Reno, NV is responsible for overseeing the laboratory logistics and support functions (e.g., Sample Management, Data Management, Scientific Coordination, and Scientific Writing teams) in the Laboratory Sciences department. This leadership role drives operational excellence by ensuring clinical and non-clinical study samples, data, and reports are managed in a compliant, secure, efficient, and timely manner, in accordance with sponsor and regulatory specifications.

· Sample Management Oversight: Oversee the Sample Management team to ensure biological specimens (e.g., plasma, whole blood, tissues, etc.) are properly received, labeled, stored, tracked, and dispositioned for clinical and non-clinical studies.

· Data Management Leadership: Oversee the Data Management team to ensure efficient review of laboratory data and study reports according to CRL Standard Operating Procedures (SOPs), Business Operating Procedures (BOPs), study documentation (e.g., Plans, Protocols, and Methods), relevant regulations, and sponsor specifications.

· Scientific Coordination and Scientific Writing Oversight: Oversee Scientific Coordinators and Scientific Writers to ensure study data and reports progress through the process and are delivered to the sponsor within the agreed timelines, according to their specifications. Ensure adequate support of scientific staff is maintained. Ensure study progress is appropriately tracked and communicated to all stakeholders.

· Stakeholder Collaboration: Liaise with sponsors, clinical project managers, scientific and operational staff, and other internal teams to align on deliverables, timelines, and quality expectations.

· Staff Management: Lead, train, and mentor a multidisciplinary team, fostering a culture of accountability and continuous improvement. Develop and oversee study macro scheduling at time of study award and liaise with Operations and Scientific management to adjust the schedule as necessary on an ongoing basis. Ensure appropriate systems are kept up to date with accurate delivery dates.

· Regulatory Compliance: Ensure all processes adhere to the relevant regulatory guidelines, maintaining audit-ready documentation and addressing discrepancies promptly.

· Ensure appropriate resources are provided for the conduct of non-clinical and clinical studies by monitoring the daily macro level scheduling through supervisors and making recommendations to management for expected additional staffing needs based on review of projected workload.

· Resolve technical and operational issues inter- and intra-departmentally (e.g., troubleshooting procedural and technique issues).

· Continuously review and improve departmental processes and procedures to uphold the highest industry standards and sponsor requirements while also implementing efficiencies.

Job Qualifications

· Education: Bachelor’s degree (B.A./B.S.) or equivalent in a biological science or related field

· Experience: Minimum 10 years’ experience working in a hospital, contract research/manufacturing, or biotech/pharmaceutical industry conducting scientific research. Experience working in a regulated (GMP, CAP, CLIA, GLP, etc.) laboratory environment required. Management experience required. At least 3 years’ experience in a supervisory/management role.

· 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 verbal and written communication, and organizational skills. Demonstrated independent analytical and problem-solving abilities. Demonstrated proficiency in managing a team supporting or working in a laboratory environment

Note: The pay range for this position is $105,000 - $115,000 anually. 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

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.

Senior Business Development Executive - Cell Solutions (West Coast Territory) (Northridge, CA, US, 91325)

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 Senior 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, located in the West Coast of the USA.

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: Six to nine 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 $130K - 140K USD + 50% commission. 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 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.

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.

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.
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

QUALIFICATIONS:

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.
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 (SOPS).

Equal Employment Opportunity

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

Technician I, Animal Care (Cage Wash) (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. *This role will primarly work within our Cage Wash discipline within the Animal Care department*

A Technician 1 – 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 changes, 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.

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.

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

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

Study Coordinator I (Reno, NV, US, 89511)

Job Summary

We are seeking a Study Coordinator for our Safety Assessment site located in Reno, NV.

The following are responsibilities related to the Study Coordinator:

*Coordinate shipping or study related activities to ensure compliance with the protocol, applicable study documentation and applicable SOPs.
*Serve as lead/primary technician on assigned studies to assure activities are performed in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), study protocols or Sponsor guidance documents and company policies/practices.
*Read study protocols or Sponsor guidance documents and extract pertinent information related to required action items.
*Assist the various stakeholders in the execution of study-related activities required.
*Perform all tasks related to preparation and documentation of materials in support of sample collection, processing, management, and shipping. Includes entry of relevant information into LIMS systems or current database and may include scheduling shipments in the shipping database.
*Review study protocols and provide recommendations to study director/supervisor on technical and logistical aspects of protocol design.
*May work in conjunction with other departments to coordinate assignments to facilitate scheduling of study-related processes on assigned studies to ensure protocol or study requirements are met.
*Prepare and review department calendars using protocols and other study documents to ensure all activities are appropriately scheduled.
*May communicate with Sponsor representatives on protocol-driven, study-related activities conducted by Pathology Services (e.g., shipment of biological samples in support of assigned studies).
*Assist in preparing responses to both internal and external quality assurance audits.
*Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs).

Job Qualifications

The following are minimum qualifications related to the Study Coordnator position:

Education: High school diploma or General Education Degree (G.E.D.) required. Associate’s (A.A./A.S.) degree in a scientific field preferred.
Experience: Minimum of 3-5 years related experience, including GLP experience required, or must have demonstrated full knowledge of competencies and positive performance at 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: None.
Other: Good keyboarding skills, proficient in utilizing personal computer, e-mail and standard office software packages (word processing, spreadsheet, presentation, database). Ability to work on assignments that are extremely complex in nature where independent action and a high degree of initiative are required in resolving problems and developing recommendations. Acts independently to determine processes and procedures on new assignments and may provide guidance and oversee the activities of other support personnel.

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.

Necropsy Technician I (Horsham, PA, US, 19044)

Job Summary

Full Time - 40 hours/week. Day Shift

As a Necropsy Tech I, you will have the opportunity to learn and perform necropsy functions and generate data on various types of studies. You will prepare and review documentation and perform quality control review of study data. You will contribute to department operations improvement in areas such as process development, SOP revisions, department inspections and equipment maintenance.

Essential Duties:
-Perform necropsies/autopsies on rodents and rabbits
-Collect/evaluate organs/tissues from rodents and rabbits
-Perform c-sections and related maternal/pup evaluations on rodents and rabbits
-Perform blood collections via vena cava, aorta, etc. on laboratory animals
-Perform specialized techniques such as whole body perfusions, neuro-dissections, etc on laboratory animals

The training and development offered to our Technicians is state of the art and designed to help you succeed. The work you will be doing will impact the lives of patients and animals across the world.

The pay rate for this position is $21.70 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

Education: Bachelor’s degree B.S. or equivalent in a biological science or a High School diploma or G.E.D.
Experience: Minimum of 1-year laboratory experience strongly preferred

Charles River, offers a comprehensive benefit package including
-Group insurance (medical, dental, vision, disability, Life insurance and employee assistance program)
-3 weeks Paid vacation
-Tuition Reimbursement
-401k with employer match
-Opportunity for career advancement

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

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

Apheresis Registered Nurse - $5000 Sign on bonus included (Northridge, CA, US, 91325)

For over 40 years, HemaCare, a Charles River company, 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 HemaCare a rewarding and valuable place to work. We believe in making a difference, and at HemaCare, you will make a difference every day.

Job Summary

The Registered Nurse will assume responsibility for the daily activities involved in the collection of plateletpheresis, leukapheresis, and whole blood. Partner with other donor room staff to ensure a smooth operation and efficient production of blood products. Must be able to interact with various departments to ensure integrity and quality of daily processes.

Essential Responsibilities

Utilize applicable aseptic techniques to plan, perform, and chart the following procedures in accordance with Hema Care Donor Center policies and procedures.
Automated plateletpheresis and leukapheresis including set-up, run, quality control, troubleshooting and routine maintenance.
White blood cell collections and other special procedures as required.
Whole blood procedures.
Make appropriate adjustments to apheresis machines based on product integrity and physical status of donor
Expertise in venous access, identification and treatment of donor reactions.
Expertise in blood donor medical history.
Expertise in assessment of laboratory reports.
Appropriate handling of information regarding positive test results.
Work cohesively as a team member and at times in a non-verbal manner while under pressure and time constraints.
Consistently manage self in ways that express professionalism.
Demonstrate warmth and compassion in a meaningful manner.
Understand and correctly use the Blood Establishment Computer Software (BECS).
Responsible for the evaluation, management, and documentation of donor reactions, post donation reports, risk management reports and customer complaint forms.
Provide technical and clinical guidance to staff as needed.
Preparation of all paperwork related to daily production.
Maintain positive communication with interacting departments.
Ensure satisfactory completion of all donor records.
Rigid adherence to all safety and quality protocols and regulation.
Other duties as assigned.

Job Qualifications

Minimum of 2 years acute care nursing experience.
3 years previous blood banking, apheresis and phlebotomy experience preferred.
Associates degree in healthcare required, BSN preferred.
Must have current state RN licensure.
Current BLS certification.

Compensation Data

The pay range for this position is $41.35 - $51.06 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 HemaCare

HemaCare, a Charles River company, 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. HemaCare’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 HemaCare, 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 and www.hemacare.com.

Clinical Pathology Technician I (Shrewsbury, MA, US, 01545)

Job Summary

Perform a variety of basic laboratory tasks. Prepare, process and store samples received into the laboratory. Maintain and perform record keeping. Review raw data for quality control.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Perform all task in compliance within Standard Operating Procedures (SOPS) and Good Laboratory Practice (GLP) regulations.
•   Read study protocols and extract pertinent information (with guidance).
•   Prepare materials needed: labeling tubes, study books and appropriate paperwork prior to bleeding days (with supervision).
•   Operate general laboratory equipment (centrifuges, pipettes, water baths) used in the processing of biological samples.
•   Receive and process BA/TK samples.
•   Manual entry of raw data into computerized systems and review of data as needed.
•   File and maintain data for department activities.
•   Sample and biohazard waste management.
•   Perform all other related duties as assigned.

The pay for this position is between $23.00 and $25.00/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 Equivalent Degree (G.E.D.) required. Associates degree (A.A) or college level courses in a science or health-related discipline preferred.
•   Experience: 0-1 year of experience in a laboratory setting.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Other: Experience with computer software programs is required. GLP environment requires attention to detail, strong organizational skills, and accurate record keeping competencies.

PHYSICAL DEMANDS:
•   Must be able to perform procedures, which require, talking, hearing, walking or standing for long periods of time (75% of the work day), 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.
•   Must be able to frequently hold and manipulate work materials while utilizing fine motor skills.
•   Must be able to lift, move, manipulate, and/or hold heavy objects up to and including 30 pounds.

WORK ENVIRONMENT:
•   General laboratory working conditions. While performing the duties of this job, the employee regularly wears protective clothing (lab coats, safety glasses and gloves).
•   Regularly works with biohazards.
•   Occasionally works with sharp objects (e.g. needles).
•   Occasionally works with chemicals or preclinical research compounds with known or unknown levels of toxicity.
•   The noise level in the work environment is usually moderate.

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.

Research Analyst I - Bioanalytical Chemistry (Mattawan, MI, US, 49071)

Job Summary

We are seeking an experienced Research Analyst for our Safety Assessment site located in Mattawan, MI.

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:

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

Job Qualifications

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
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Experience with LC/MS/MS preferred
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
Ability to wear proper PPE for the duration of the shift; which includes and is not limited to the following: Gloves, safety glasses, laboratory coat, cartridge respirator, dust/mist respirator, supplied air respirator, Tyvek suit, sleeve protectors.

The pay for this position is $23.50. 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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

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

Business Development Director - Biologics Testing (New England territory) (Wilmington, MA, US, 01887)

Job Summary

The Business Development Director will support the Biologics Testing Commercial team in the New England region.

Position will work from home office and ideally live within Boston or the New England area.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Lead sales program in assigned territory applying technical/scientific skills to compete for customers.
Develop and qualify leads through customer contact and prospecting. Communicate available Charles River products and services and inform customers of new products and services in a timely manner.
Fulfill subject matter expertise role, working with marketing to assure design, development and implementation of marketing tools and programs that support company goals.
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.
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.
Build relationships with customers to influence the acceptance and use of company products and services.
Work with other specialists within Biologics and across the organization to generate major account specific sales strategies to close opportunities.
Assist Global Account Management with presenting global capabilities, qualifying leads, demonstrating added value and closing new business opportunities by providing scientific support during sponsor teleconference calls, field visits and at scientific trade shows.
As required, give overview of assigned product line and services to internal and external contacts. Share portfolio opportunities with Account Manager from other divisions withing Charles River.
As required gather data on market trends and competitive products and pricing. Gather data on potential competitors in the designated geographic region.
Share customer problems/concerns with relevant departments for quality resolution.
Participate and assume support role in national and international tradeshows and aid in the coordination of tradeshow events and or presentations.
Participate in sales meetings as required.
Complete all required sales documentation and training in a timely manner.
Utilize CRM to capture customer information and maintain all communications within the CRM system with routine status reporting.
Perform as organizational lead for CRM system monitoring and reporting. Specifically, ensuring all proposals are followed up on in a timely manner.
Develop and maintain reports for tracking and reporting on Sales Initiatives within CRM and/or other tools.
Assist Sales Specialists and Management with specific assigned customer projects as needed.
Perform all other related duties as assigned.
Responsible for ensuring that a safe working environment is maintained for him/herself and his/her colleagues 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 to him/her.
To participate in overtime as is reasonably required for the successful completion of your role.

Job Qualifications

Education: Bachelor's degree (B.A. /B.S.) or equivalent in business or related discipline.
Experience: Three to Five 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: Valid driver's license required.
Other: Fluent in verbal and written English and German. Must possess excellent communication 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 $110,000 - $125,000K USD annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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.

Commis aux soins des animaux (Laval, Quebec, CA, H7V 4B3)

En tant que Commis aux soins des animaux pour notre site de quarantaine situé à 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 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:

AEP en soins animalier (atout);
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.);
À l’aise pour suivre des instructions précises;
Passion pour 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 : 531 Boul. des Prairies, Laval, QC, H7V 1B7;
Transport: Stationnement gratuit. Près du métro Montmorency;
Salaire : 18.50$/hrs;
Bonus annuel basé sur la performance;
Primes: Fin de semaine ($2.75), temps supplémentaires (temps et demi), jours fériés (temps double);
Horaire : De jour en semaine du lundi au vendredi, 7h00 à 15h15. Selon les besoins de l’entreprise vous pourriez avoir à effectuer des rotations de fin de semaine ainsi que du temps supplémentaire;
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);
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 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.

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

Animal Care Clerk (Laval, Quebec, CA, H7V 4B3)

As an Animal Care Clerk for our Quarantine facility located in Laval, 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;
Animals handling.

Key Elements

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

AEP in Animal Care (asset);
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.);
Able to follow precises instructions;
Passion for 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: 531 Boul. des Prairies, Laval, QC, H7V 1B7;
Transportation: Free parking. Near the Montmorency Subway;
Salary: $18.50/hrs;
Annual bonus based on performance;
Premiums: Weekends ($2.75), Overtime (time and a half), Holidays (double time);
Schedule: Weekdays, between Monday to Friday 7am to 3:15pm. Depending on the needs, you will have to do overtime and weekend rotations;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive health and dental benefits as of day 1. We pay up to 85% of premiums;
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 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.

Equal Employment Opportunity

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

Senior Data Engineer (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

This journey is central to advancing our position in the market, unlocking new growth opportunities, and positioning us as a leading, digitally powered Contract Research Organization (CRO) that enables our clients to deliver innovative, safe, and effective treatments to patients faster and more efficiently than ever before.

Note: It’s a fully remote home-based role for professionally qualified and experienced candidates based in India, who are willing and open to work UK shifts.

Essential Qualifications:

•   Bachelor’s degree in computer engineering, Computer Science, or a related discipline (Master’s degree preferred)
•   7+ years of experience in ETL design, development, and performance tuning using the Microsoft BI 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.

Preferred Skills:

•   2+ years of experience with Big Data technologies, such as Hadoop, Sqoop, Hive, Kafka, Spark, Pyspark, Python, Scala, or Pig
•   2+ years of experience managing both relational and non-relational data using Big Data Management (BDM) techniques (formats like JSON, XML, Avro, Parquet, etc.)
•   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
•   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 in data and analytics within the Life Sciences industry is a plus.

Equal Employment Opportunity

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

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

Veterinary Technician I (Poolesville, MD, US, 20837)

Job Summary

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

What you will do!

In the Veterinary Technician I, II, and III role, you will assist will 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.

You will perform the following duties:

Prepare and distribute animal diets, enrichment, and clinical treatments; collect and record physiological data (pulse, respiration, heart rate, body temperature, etc.).
Perform technical procedures including femoral blood collection, IV catheterization, aseptic tissue collection and processing, anesthesia, food or liquid consumption, drug dosage calculation and administration (Topical, PO, IM, SQ, IV and ID), TB testing, weighing, physical examinations, restraint and handling of animals, radiographs, and other technical procedures as needed.
Understand basic animal behavior for training techniques; including positive reinforcement and cognitive testing; assist in on-going behavioral testing and data collection.
Assist veterinarian or investigators with surgeries or specialized procedures.
Perform animal health surveillance checks and report any abnormal findings.
Maintain electronic medical records, update treatment plans, send daily emails regarding clinical and experimental information vet staff and client.
Collect, preserve, and prepare blood, urine, stool, and tissue samples.
Participate in study related necropsies and tissue harvest.
Perform weekly mid-day health checks and daily pm health checks of all animals in the colony (including geriatric rhesus monkeys).
Daily, weekly, and monthly cleaning and sanitization of prep areas and procedure rooms. Set-up procedure areas and prepare supplies and equipment for procedures.
Ability to maintain freezer organization and sample inventory.
Participate in all required training (topics may include animal specific information and technical procedures, medical care, OSHA, regulatory, ASP support, and standard operating procedures).

Job Qualifications

Education: All levels- a high school diploma or GED is required; a BS degree in Animal Science, Biology, or similar discipline, or A.A. in Veterinary Technology is preferred.

Experience: Level I – 2-3 years’ experience working with animals in biomedical research is required, of which 1 year must be with non-human primates. Veterinary Hospital technical experience will be considered.

Level II-III a minimum of 5 years’ experience of same. Supervisory experience preferred for Level III.

Certification: Level I- Eligibility to take the AALAS certification at the LAT level required. Level II-III LATG eligibility required.

The pay range for this position is $27.00 to $33.00 USD per hour.  Please note the range covers level I-III, salary will depend on level, in addition to factors such as experience, skills, and certification.

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.

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

BTA / Biologielaborant / BSc als Technical Officer (m/w/d) - Virology (Erkrath, NW, DE, 40699)

Für die Abteilung Virologie am Standort Erkrath suchen wir ab sofort unbefristet in Vollzeit eine/n

Biologisch-Technischen Assistenten (BTA) /

Biologielaboranten / B.Sc. Biologie-Biotechnologie

als Technical Officer (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 228532 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

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.

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

Supervisor (Boston, MA, US, 02115)

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.

JOB SUMMARY

We are seeking a Supervisor to join our Insourcing Solutions team, located at Boston’s Children’s Hospital.  You will be working with multiple animal species.

Under the direction of the Manager, Animal Care, this position provides direction and leadership for the daily operations of Boston Children’s Hospital animal facilities and program. Maintains performance levels consistent with and according to Animal Resources Children’s Hospital (ARCH) standards and requirements. Collaborates with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines and regulations. Responsible for providing back up and assistance for the Manager, Animal Care.

ESSENTIAL DUTIES AND RESPONSIBILTIES

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 assisting in the training of animal care staff in the following: cage changing, microisolator cage changing techniques, room sanitation, autoclave operation, cagewash operations, waste disposal and other husbandry duties as required.
Outlines the job responsibilities of animal care staff, including Children's Hospital policies, procedures and the daily husbandry assignments of the animal care staff.
Collaborates with Animal Facility Manager and maintains necessary supply and equipment inventory to operate the day-to-day operation of the animal care program, including feed/bedding, sanitation supplies, office supplies, cage equipment, autoclave supplies and other supplies and equipment as needed.
Responsible for developing and maintaining animal records including, room logs, health reports, cage card labels, autoclave records, cagewash records, animal census and other records as required.
Ensures that all animal rooms are observed on a daily basis to monitor for sick, or dead animals, and reports findings to the veterinary staff or alternatively to the Animal Facility Manager.
Interviews and recommends selection of candidates for employment to the Animal Facility Manager. In consultation with the Animal Facility Manager and Human Resources Manager, this position performs personnel actions including but not limited to hiring, transferring, suspending, counseling, disciplining, discharging, assigning, rewarding or addressing employee concerns.
Supervises direct reports in their efforts to maintain quality performance of departmental and client objectives, including meeting/exceeding departmental standards with respect to animal health and welfare, facilities condition, sanitation levels.
Build competence among employees through conducting appropriate training activities and through appropriate supervision related activities (e.g. recruitment, separation, performance appraisal, disciplinary actions, etc.).
Supports and affirms the company policy of Equal Opportunity through Affirmative Action.
Conducts daily inspections of animal holding and support facilities to determine the degree to which established levels of animal health, facilities condition, sanitation levels, environmental parameters and security are being met/exceeded.
Participates in the development and implementation of site-specific standard operating procedures (SOP's), in compliance with all state, federal and industry requirements. Oversee adherence to site SOP's and all required documentation related to department. Coordinate operations with the assistance of staff support departments and personnel.
Coordinates repair and general up-keep of physical environment in areas of responsibility. Is available on site for assistance, coordinating during upkeep and repairs.
Participates as required in the development of projections for equipment, supplies and personnel needed to effectively operate the research facilities in a manner consistent with the Guide for the Care and Use of Laboratory Animals and all local, state and federal requirements.

.

Actively interacts with customers as required to solve customer requests, inquiries, and complaints and to provide technical assistance. Act as liaison between scientific staff and support personnel.
Trains and oversees consistent practice of general Children's Hospital safety policies and procedures, including those related to biohazards and radioactive substances. Supervises in compliance with local, state, and federal regulations.
In coordination with Human Resources Manager, investigates personnel problems and to employees in accordance with company policies and procedures.
Maintains required attendance level and adherence to work schedule in accordance with required staffing levels in order to ensure that assigned duties are completed.
Assists in any contract related activity, as assigned by Supervisor, to complete the required work.
Performs all other related duties as assigned.

MINIMUM QUALIFICATIONS

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

- High school diploma/General education development plus six plus years husbandry experience in a laboratory animal facility of which six to twelve months is leadership experience.
- Bachelor or Associate degree plus two-four years husbandry experience in a laboratory animal facility of which six to twelve months is leadership experience.

Certification/Licensure: AALAS Certification at the LAT level required LATG preferred.

The pay range for this position is $90,000-$95,000 annually. 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

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.

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 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.

Les modalités

Convention collective de l’industrie pharmaceutique, groupe : 2
Contrat : CDD de 09 mois - Non-cadre (accord de modulation 35h)
Salaire : A compter de 23 946€ 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 Safety Assessment

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 85 % des médicaments approuvés par la FDA en 2021.

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

Animalier en Toxicologie Non-Rongeurs - F/H - CDD 09 mois 1 (Evreux, FR, 27930)

Résumé du travail

À propos de Safety Assessment

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 85 % des médicaments approuvés par la FDA en 2021.

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

DIRECT LABOR - 饲养技术员 (Pudong New Area, SH, CN)

重要信息：应聘此职位，必须在申请过程中上传并提交简历，请确保正确添加工作履历和教育背景。

工作总结

重要信息：此职位需要上传简历，如您尚未在候选人简介中上传简历，请返回至上传字段并附上简历。

关于安全评估
Charles River致力于帮助我们的合作伙伴加快临床前药物开发，我们提供卓越的安全评估服务、先进的设施和专家监管指导。从单独的专业毒理学研究和试验性新药（IND）相关研究，到定制的服务组合和全套实验室支持，我们经验丰富的团队可以设计和执行相应计划，能够预期可能遇到的挑战并避免问题，以协助您顺利、高效地将药物推向市场。我们的安全评估设施每年都开展大约300项试验性新药（IND）计划。

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18个国家和地区拥有70家设施及11000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。2016年，公司收入增长23.3％，达到16.8亿美元，而2015年收入是13.6亿美元。

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2016年FDA批准的所有药物中约70％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

Auditeur Qualité - F/H - CDI (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Nous recherchons un Auditeur en AQ pour rejoindre une équipe d’environ 15 personnes sur le site.
Rattaché(e) au Directeur du service Qualité et affaires réglementaires, vous aurez la responsabilité de garantir la bonne application des Bonnes Pratiques de Laboratoire (BPL) et des procédures par le biais des audits que vous réaliserez sur les études précliniques.
 

Les missions

Effectuer en autonomie des inspections et audits d’évaluation (processus, installations, équipements, personnel, matériaux, méthodes, pratiques, les enregistrements et les contrôles),
Assurer la conformité des activités de recherche à la réglementation internationale (GxP, BPL),
Contrôler l’exactitude, la clarté et la précision des plans d’étude et des rapports finaux,
Participer aux audits des sous-traitants, des vendeurs et des fournisseurs de produits et services,
Participer à la formation réglementaire du personnel assurance qualité et des opérations,
Participer à la planification et au suivi des audits, inspections et activités AQ,
Participer à la collecte et à la communication d’indicateurs concernant la qualité,
Conseiller les équipes scientifiques et la direction, être force de proposition.

Conditions spécifiques du poste 

Amplitude horaire : 8h/18h avec planning partiel à la semaine
Interventions de week-end ponctuelles sur la base du volontariat
Interventions en animaleries dans le cadre des audits
 

Qualifications souhaitées

Vous êtes titulaire d'un diplôme Bac+3 dans le domaine de la biologie, ou gestion de la qualité.
Vous avez une première expérience en gestion de la qualité dans l’industrie pharmaceutique.
Vous avez le sens de l’écoute, le souci du détail et travaillez avec rigueur et organisation.
Des connaissances des techniques d'audits dans un environnement (GxP BPL) sont un atout.
Vous êtes à l’aise avec l’anglais écrit et oral.

Modalités

Convention collective de l’industrie pharmaceutique, groupe : 4
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 28 184 € 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, accord de télétravail,...
Site non-accessible en transport en commun – Moyen de locomotion indispensable.

À propos de Safety Assessment

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 85 % des médicaments approuvés par la FDA en 2021.

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

Technicien.ne en Santé Animale (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Technicien.ne en santé animale pour notre équipe de Toxicologie située au site de Senneville, 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-cliniques.

Dans ce poste, les principales responsabilités incluront:

Administrer les éléments de test et/ou médicament (Gavage, injection intramusculaire, sous-cutanée et intraveineuse);
Effectuer les prélèvements d’échantillons (sang, urine, etc.);
Faire la prise de données (prise de poids, consommation de nourriture, signes cliniques, etc.);
Manipuler les animaux pour toutes activités qui le requiert;
Nettoyer tous les types d’habitacles d’animaux et leurs accessoires.

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Bon sens de l’observation;
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.);
Bonne compréhension de l’anglais écrit;
Diplôme collégial en Santé animale ou en Bioécologie;
Baccalauréat en Biologie ou toutes autres disciplines en lien avec la Science animale.

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: 23.00$ de l’heure avec des primes de:
o Soirée: 2.50$;
o Fin de semaine: $2.75;
o Heure supplémentaire: Temps et demi;
o Fériés: Temps double;
Bonus annuel basé sur la performance;
Horaire: Poste à temps plein standard : Majoritairement le jour, la fin de semaine en rotation et les jours fériés. Selon les besoins, il pourrait y avoir du temps supplémentaire de soir ou de nuit;
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.

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

Trade Show Manager (Life Sciences), DSA (Wilmington, MA, US, 01887)

Job Summary

The Events Manager is responsible for the planning, execution, and review of conference / tradeshow participation and customer-focused events within the Discovery & Safety Assessment (DSA) division globally.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Manage, plan, and execute a section of conferences, tradeshows and CRL hosted events assigned for the DSA division.
• Understand the strategic business objectives and collaborate with both commercial and operational stakeholders to build and execute on a comprehensive plan of events that results in visible impact on revenue.
• Oversee and build on the successful range of CRL hosted scientific summit events across the manufacturing portfolio.
• Perform extensive research on each potential event; strategize on key initiatives to drive success, enforce a culture of continuous evaluation, and implement change to drive improvement.
• Establish and communicate out KPI’s (leads, pre-set meetings, attendees, survey results) for each event. Provide KPI metrics to the wider team and stakeholders, provide suggestions on improvements.
• Perform pre-event planning strategies to provide historical, demographic, and statistical analysis and return on investment.
• Provide advice and guidance to senior management regarding event budget requirements, ROI, suggested level of participation and recommendations for future event involvement.
• Select, manage, and build relationships with a selection of third-party vendors associated with event execution. Where possible provide expertise and advice to enhance ROI and the overall CRL experience at events.
• Manage the global event schedule, including all aspects of negotiation, contracting, preparation and logistics for CRL’s event involvement.
• Provide clear and concise information for stakeholders and attendees on participation, roles & responsibilities and expectations.
• Assist in the development and recommendation of departmental budget. Authorize expenditures in accordance with budget. Manage event expenses, including negotiation whilst striving to provide maximum value on investment by means of bundling, value adding and discount discussions.
• Evaluate event involvement, including effectiveness of activities, content, and messaging, and make changes and improvements as needed.
• Identify and research potential new events that meet the objective for growing new CRL business or acquisition.
• Ensure adequate staffing at all events and provide appropriate selection of marketing literature and materials.
• Organize, chair and record pre and post event planning meetings for each event. Develop event strategy from group discussion, assign tasks to complete strategy, and manage completion of all tasks to ensure prominent presence for CRL at the event.
• Identify and take advantage of all promotional opportunities available for each event.
• Determine 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.
• Experience: 5-10 years related experience, ideally working within the life sciences tradeshow arena.
• 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: Negotiation, organization, statistical analysis, problem solving and strong communication skills required.

This position requires regular domestic travel.

Compensation Data

The pay range for this position is $75,000 - $100,000K USD annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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.

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

Qui sommes-nous ?

Le poste

Le département de Toxicologie recrute un Animalier 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.
Travail de Week-End.
Contact avec les animaux (rongeurs).

Les modalités

Convention collective de l’industrie pharmaceutique, groupe : 2
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 23 940 € 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 Safety Assessment

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 85 % des médicaments approuvés par la FDA en 2021.

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

Chargé(e) HSE - H/F - CDI (Ecully, FR, 69130)

Qui sommes-nous ?

Aux portes de Lyon, le site Charles River d'Ecully offre à ses 90 collaborateurs un environnement dynamique et une cuture d'entreprise certifiés Great Place To Work® pour la 4ème année consécutive. Nos équipes, passionnées et impliquées, contribuent aux efforts que nous accomplissons chaque jour pour améliorer la santé et le bien-être du plus grand nombre possible de personnes.

Le poste

Dans le cadre d'une création de poste et afin de répondre à l'intégralité de nos enjeux dans le domaine, nous recherchons un(e) Chargé(e) HSE en CDI.
Votre rôle sera de participer à la définition de la politique HSE et à sa mise en œuvre afin d’assurer la prévention des risques pour le personnel, les prestataires et l’environnement, par le développement et le maintien d’une dynamique et d’une culture HSE.
Il s'agit d'un poste polyvalent et autonome, en interface avec de nombreuses parties prenantes internes et externes. Sur ce poste, vous rapporterez directement au Responsable des Services Généraux du site, et indirectement au pôle HSE du groupe.

Missions :

1/ Responsabilités générales :

Participer à la définition de la politique HSE, en lien avec la stratégie globale et locale, en étant force de proposition
Veiller et participer au bon avancement et mise en œuvre de la politique HSE
Conduire et coordonner des projets et des initiatives et surveiller leur avancement
Faire le lien avec les équipes HSE globales et des autres sites, notamment pour déployer la politique HSE globale et échanger sur les bonnes pratiques
Assurer la veille réglementaire en matière HSE et anticiper les évolutions afin de garantir la conformité HSE du site
Proposer et suivre des indicateurs HSE et en dégager une analyse
Contrôler la bonne application des réglementations et préconisations HSE
Planifier et suivre les audits HSE
Communiquer sur les bonnes pratiques et les réalisations du site en matière HSE

2/ Hygiène et Sécurité :

Identifier, analyser et hiérarchiser les risques professionnels en observant les conditions de travail des salariés, et proposer des actions d’amélioration
Assurer la mise en place et/ou la mise à jour de la documentation HSE et des moyens nécessaires pour garantir le travail en toute sécurité de l’ensemble du personnel
Informer et sensibiliser les différents acteurs et le personnel de l’entreprise aux enjeux HSE, et être moteur dans le développement de la culture sécurité
Superviser et animer le comité PRAP (Prévention des Risques liés à l’Activité Physique)
Analyser les accidents et mettre en place des plans d’actions correctives et préventives
Proposer, concevoir et animer des formations sur les modalités, les règles et les consignes de sécurité et environnement
Veiller à la bonne qualité de services des prestataires, et notamment la prestation de ménage

3/ Environnement :

Gérer les dossiers réglementaires sécurité et environnement de la société (DUERP, assurances, etc.)
Superviser les flux de déchets générés par les activités et proposer des actions d’amélioration
Piloter la maintenance des infrastructures, principalement liée aux contrôles règlementaires réguliers
Participer aux projets de travaux et au suivi de leur réalisation sur le site

Qualifications requises :

Vous êtes issu(e) d'une formation de niveau bac+5 spécialisée en management HSE, ou vous disposez d'une expérience équivalente de 5 ans minimum sur un poste similaire.

Au-delà de vos connaissances techniques et de votre savoir-faire, vos qualités relationnelles seront vos principaux atouts : empathie et écoute, excellent niveau de communication, aisance relationnelle, capacité à animer en transversale et à fédérer.

Notre entreprise ayant un rayonnement international, une bonne maîtrise de l’anglais est indispensable à l’oral comme à l’écrit.

Modalités contractuelles :

Convention collective de l’industrie pharmaceutique : groupe 6
Contrat CDI cadre, forfait 217 jours par an
Salaire annuel à partir de 39 663 € bruts sur 14 mois + variable
Primes de transport et titres restaurant
Prime d’intéressement

Dans le cadre de sa politique en faveur de la diversité et de l’inclusion, Charles River s’engage à respecter les principes d’égalité des chances et de non-discrimination tout au long du process de recrutement.

À propos de Microbial Solutions

À propos de Charles River

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

Bioanalytical Chemistry - Director (Mattawan, MI, US, 49071)

Job Summary

Job Functions:

Efficiently perform supervisory responsibilities in accordance with organizational policies and applicable laws to include interviewing, hiring, training and developing employees
Develop organizational strength by hiring, identifying and developing personnel who are scientifically and/or technically strong
Establish culture and atmosphere to maintain good retention and low turnover using available tools and metrics
Assist with providing costing estimates for components of applicable studies
Provide short- and long-term solutions that support continuous improvement
Maintain critical thinking, troubleshooting and time management skills aligned with needs of operational areas
Demonstrate effective communication skills through informal discussions with peers, supervisor, team, cross-site, and externally with collaborators and sponsors
Ensure laboratory tasks and operations are executed in compliance with SOPs, protocols, regulatory requirements as needed
Review and approve Standard Operating Procedures (SOPs), protocols, policies, best practices and study procedures
Maintain contemporaneous knowledge of regulatory requirements
Effectively plan, assign and direct work within one or more operational areas
Establish and monitor performance metrics for one or more operational areas
Skillfully oversee the design, conduct, interpretation and reporting of studies as needed
Lead implementation of new procedures and refinement of existing procedures to meet current and future business needs
Align operational resources with the current needs in one or more operational area
Manage cross-service line interdependencies in collaboration with organizational leadership
Collaborate with multiple departments within and outside of site
Lead planning (resource management, budgets and study coordination) as well as track budgets and spend vs. revenue for one or more operational areas
Collaborate and consult with prospective Sponsors, providing scientific expertise and developing ongoing Sponsor relationships
Provide leadership, expert consultation and mentorship to cross-functional company teams
Provide vision and determines business priorities for one or more operational areas
Performs all other related duties as assigned

Job Qualifications

Bachelor’s degree or equivalent with 15+ years of relevant experience. Greater than 8 years of management experience required
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
LCMS/MS Experience Preferred
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

The pay range for this position is $165-175k/year. 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

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.