Quality Assurance Coordinator


Quality Assurance Coordinator

Sherbrooke, QC


Our client, an innovative and growing pharmaceutical company, is currently looking for a Quality Assurance Coordinator to join their team in Sherbrooke. Under the responsibility of the Quality Director, the incumbent of the position will support the company in the implementation and maintenance of quality systems.

Main responsibilities:

  • Write and revise standard operating procedures
  • Manage the quality documentation
  • Collaborate on internal and external audits, investigations and implementation of CAPA
  • Track notifications of changes, numbering, approvals and filing
  • Track deviations, corrective and preventive actions
  • Manage the archiving and filing process
  • Revise the manufacturing documentation
  • Manage training at the documentary level
  • Establish quality indicators
  • Support production and QC in their need for documentation
  • Interact with the subcontractors when required


  • Diploma of college or university studies
  • Minimum 3 years of experience in quality assurance and documentation in the pharmaceutical industry, laboratory and/or production experience is an asset
  • Ability to apply Canadian Good Manufacturing Practice (GMP) rules (Health Canada), American (FDA) and European
  • Demonstrates good communication and technical writing skills
  • Demonstrates an intermediate level of use of the Microsoft Office and Outlook suite
  • Demonstrates knowledge of production management software
  • Autonomous, methodical and organized
  • Works well in a team
  • Ability to manage priorities
  • Ability to work in a changing environment
  • French and English bilingualism required
  • Availability and willingness to travel occasionally (Quebec, United States, Europe)

If you are interested in this opportunity, please send you C.V. to Celine Chabee at cchabee@groupelock.com

Only qualified candidates will be contacted.

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