Associate Scientist - Immunology

Req ID #:  229109
Location: 

Fleurimont, Quebec, CA, J1E 0B5

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

Associate Scientist - Immunology

As an Associate Scientist for our Immunology team at the Sherbrooke location, you will support supports the Laboratory Scientists in preparing study deliverables, such as assay results tabulation and study reports, while respecting timelines and preserving a quality of work compliant with Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP), and study plans.

In this role, primary responsibilities include:

  • Contribute to the quality of the study by reviewing analytical procedures, procedure forms, or other related documentation to assigned studies.
  • Coordinate the submission of documentation and data for review and audit.
  • Interact with other departments throughout Charles River Laboratories to aid in the completion of the study.
  • Perform or review tabulation of results.
  • Participate in writing the study report and study plan.
  • Prepare or review the study summary (e.g., MQS, MVS) and the analytical procedure.
  • Collaborate with the Scientist to compile and assemble study deliverables in an audit ready state for submission to the Quality Assurance department (QA) and answer QA findings.

 

Key Elements

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

  • Minimum of a College diploma in Sciences related discipline;
  • Hands-on experience in one or some of the following areas: ELISA/ligand-binding assays, TK/ligand-binding assays, ADA/Immunogenicity, and/or multiplex assays;
  • Be able to work as part of a team. 
  • Have a positive attitude, good interpersonal relationships, and professionalism. 
  • Adapt to changes. 
  • Actively participate in departmental meetings to improve performance and quality.
  • Bilingualism is required.


Role Specific Information:

  • Location: 1580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5.
  • Transportation: Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station.
  • Salary: As per internal equity and salary scale
  • Annual bonus based on performance.
  • Schedule: Daytime between Monday to Friday. Depending on the needs and deadlines to be respected, you may have to do overtime.
  • Permanent position as of the hiring, full-time minimum 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);
  • 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 Momen

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.


About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

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

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

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 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.


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