Laboratory Analyst
Charles River Laboratories
Date: 6 hours ago
City: Montreal, QC
Contract type: Full time

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
As a Laboratory Analyst for our Senneville site, you will perform sample analysis work in a laboratory environment, perform data analysis to determine if results meet expectations and record data in accordance with company policies and standards to meet quality and accuracy requirements. We are currently hiring for the Genetic Toxicology and the Molecular Biology teams.
In The Immunogenicity Analyst Role, Responsibilities May Include
In the Genetic Toxicology analyst role, primary responsibilities include:
We are looking for the following minimum qualifications for this role:
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 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 www.criver.com.
228065
Job Summary
As a Laboratory Analyst for our Senneville site, you will perform sample analysis work in a laboratory environment, perform data analysis to determine if results meet expectations and record data in accordance with company policies and standards to meet quality and accuracy requirements. We are currently hiring for the Genetic Toxicology and the Molecular Biology teams.
In The Immunogenicity Analyst Role, Responsibilities May Include
- Performing various immunoassays and enzyme assays on multiple platforms including antibody assay by ELISA and Electrochemiluminescence (ECL), performing cell culture as well as bioassays, protein purification, dialysis, and labelling. Various automation platforms can also be used, such as the Biomek, the Gyros and the Hamilton.
- Perform method development, validation, and sample analysis
- Document and process analytical data according to Good Laboratory Practices (GLP)
- Perform sample analysis based on a variety of immunoassays and enzyme assays such as ELISA, Luminex, radioimmunonalysis, ECL, MSC technology, Simoa technology, and Simple Protein ELLA
- Oversee method development and perform validation and data analysis to determine if results are as expected, in compliance with Good Laboratory Practice (GLP).
In the Genetic Toxicology analyst role, primary responsibilities include:
- Bacterial Mutation Test (BMT)
- Chromosome Aberration Test (CAT)
- InVitro Micronucleus (IVM)
- Mammalian Cell Mutation Test (MCM)
- Micronucleus Test (MNT), Comet Assay
- Cytotoxicity Test and Mode of Action Assay (MOA)
- Analysis of bacterial or cell cultures; manipulation of animal organs
We are looking for the following minimum qualifications for this role:
- Collegial diploma or bachelor’s in laboratory sciences;
- Ability to work under time constraints;
- Flexible and able to adapt quickly to change
- Work with precision, pay attention to detail and strive for quality work;
- Ability to work as part of a team.
- 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$/hrs;
- Annual bonus based on performance;
- Schedule: Monday to Friday, day schedule.
- Permanent position as of the hiring, full-time 37.5hrs per week.
- 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!
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 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 www.criver.com.
228065
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