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 an Auditor for our Quality Assurance team at the Sherbrooke location, you will perform audits of basic records, reports and inspections of routine processes to assure compliance with applicable regulatory requirements, international standards, and corporate policies and procedures.

In this role, primary responsibilities include:

• Communicate all identified compliance and quality risks to supervisor;
• Perform data audits to assess whether records are attributable, legible, contemporaneous, original, accurate, and in compliance with GLP regulations SOPs, and protocols;
• Support the review of SOPs, protocols, and reports to ensure accuracy and compliance with all applicable GLP regulations;
• Prepare written and signed records of all audits and inspections as required. These records may be countersigned by the supervisor or trainer to document the performance of audits and inspections and their reporting to management;
• Assist in the identification of deviations from regulations, protocols, and SOPs.

KEY ELEMENTS

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

• Bachelor’s degree in life science;
• Knowledge of computer skills including Microsoft Office applications (e.g. Word, Access, Excel);
• Be able to comprehend regulations and guidance documents and apply critical thinking skills to evaluate requirements;
• Be detail oriented and able to effectively communicate findings verbally and in writing.

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;

• Annual bonus based on performance;
• Schedule: Day time from Monday to Friday;
• Permanent position as of the hiring, full-time 37.5hrs per week.

In this role, primary responsibilities include:

• Communicate all identified compliance and quality risks to supervisor;
• Perform data audits to assess whether records are attributable, legible, contemporaneous, original, accurate, and in compliance with GLP regulations SOPs, and protocols;
• Support the review of SOPs, protocols, and reports to ensure accuracy and compliance with all applicable GLP regulations;
• Prepare written and signed records of all audits and inspections as required. These records may be countersigned by the supervisor or trainer to document the performance of audits and inspections and their reporting to management;
• Assist in the identification of deviations from regulations, protocols, and SOPs

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

• Bachelor’s degree in life science;
• Knowledge of computer skills including Microsoft Office applications (e.g. Word, Access, Excel);
• Be able to comprehend regulations and guidance documents and apply critical thinking skills to evaluate requirements;
• Be detail oriented and able to effectively communicate findings verbally and in writing