Analyst, Clinical Pathology

Req ID #:  140851

Laval, Quebec, CA, H7V 4B3

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


We are seeking an Analyst for our Clinical Pathology department, site located in Laval (Greater Montreal area) in Canada.


The following are responsibilities related to the Analyst :

  • Receive, process and verify the quality of specimens for analysis in clinical pathology;
  • Carry out the analysis of samples using a range of analyzers and manual techniques;
  • Prepare standards, quality control materials and reagents for use;
  • Maintain and calibrate laboratory equipment, according to departmental and manufacturer schedules and procedures. Identify changes and trends in analyzer performance;
  • Monitor test results, ensuring that abnormal results are repeated, diluted and identified according to procedures specified by relevant SOP;
  • Review study data, including reagent and maintenance records, calculations and test results.


The following are minimum qualifications related to the Analyst position:

  • College degree in laboratory techniques, biochemistry/hematology or equivalent;
  • 1 to 3 years of experience in a multi-disciplinary analytical laboratory environment;
  • Reading of English is required. Bilingualism is preferable;
  • Strong knowledge and application of GLP (is an asset).



The advantages of working for Charles River: 

  • Minimum of 3 weeks’ vacation ; 
  • Paid sick / personal days ; 
  • Paid overtime ; 
  • Shift premiums ; 
  • Paid uniform ; 
  • Competitive benefits starting from day one (health and dental coverage) ; 
  • Access to a savings and retirement program including an employer contribution ; 
  • Free, unlimited, and confidential access to health care professionals for you and your family, through telemedicine app ; 
  • Employee Assistance Programs ; 
  • Tuition reimbursement program ; 
  • Employee Activities ; 
  • Volunteering Program (paid day) ; 
  • Employee referral bonuses ; 
  • Relocation assistance ; 
  • Career advancement opportunities and training ; 
  • A recognition program ; 
  • Positive Company Values & Culture ; 
  • Shuttle service from the Sainte-Anne-de Bellevue train station and from John Abbott College to the Senneville site ; 
  • Shuttle service from the Montmorency metro station to the Laval site; 
  • Free parking. 

Preferred Skills



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 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.


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

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 This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

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