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 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.

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

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