Supervisor, Technical Services In-Vivo

Req ID #:  221728

Laval, Quebec, CA, H7V 4B3

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.


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


As a Supervisor for our Technical Services InVivo group in Laval, you will have to coach, train, and support the technical staff. Your contribution will ensure maximum efficiency of the team and help resolve more challenging issues.



In this role, primary responsibilities include: 


  • Ensure work of departmental staff to maximize efficiency and productivity
  • Oversee the training process and developpment opportunities for all technical staff 
  • Ensure that all the resources are available, and that the working environment is safe
  • Ensure that the procedures and equipment comply with Good Laboratory Practices (GLP)

Key Elements


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


  • Collegial diploma in Science or Administration or any related discipline
  • Minimum of 3 to 5 years’ experience in a CRO (Contract Research Organisation) or in management
  • Good interpersonal and communication skills 
  • Strong problem-solving skills
  • Good listener and strategic vision
  • Bilingualism French and English is required



Role Specific Information: 


  • Location: Laval / Free parking / Near the subway Montmorency
  • Annual bonus based on performance
  • Schedule: Daytime Monday to Friday. Depending on the business needs, you may have to do overtime and weekends
  • Permanent, full-time position as of the hiring



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)
  • 4 weeks’ vacations & 10 sick/personal days per year 
  • Many social activities


If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.  

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. 


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.


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 [email protected]. 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

Job Segment: Pharmaceutical, Laboratory, Manager, Biotech, Science, Research, Management