Auditor, Quality Assurance at Charles River Laboratories
Fleurimont, QC, Canada -
Full Time


Start Date

Immediate

Expiry Date

20 Nov, 25

Salary

0.0

Posted On

21 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Life Science, Thinking Skills, Regulations, Access, Computer Skills, Excel, Writing

Industry

Pharmaceuticals

Description

Req ID #: 229448enUS
Fleurimont, QC, CA
1st
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 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.

Why Charles River ?

  • Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
  • 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 & 10 Personal day policy;
  • 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.

Responsibilities

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

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
Loading...