Quality Assurance Compliance Specialist

The Quality Assurance Compliance Specialist will oversee investigations related to quality systems. They will follow up and communicate introductions and modifications to regulatory and pharmacopoeia guides.

Responsibilities:

  • Investigation processing and report writing (DEV)
  • Review and approval of laboratory investigations (LIR)
  • Customer complaints program
  • Review of new projects from a regulatory point of view
  • Regulatory monitoring and Pharmacopoeia review
  • Follow-up on registration with the FDA
  • Drafting and review of Standard Operating Procedures (SOP)

Skills and experience required:

  • Bachelor’s degree in sciences (Chemistry, Biochemistry), or a discipline related
  • Minimum of five (5) years of experience in quality assurance or quality control in the pharmaceutical industry
  • Good Knowledge of Canadian Good Manufacturing Practices (GMP) (Health Canada) and American (FDA)  
  • Good technical writing
  • The ability to work in a team and good communication skills
  • Bilingual essential (French et English)
Accepted file types: pdf, doc, docx, Max. file size: 32 MB.
Accepted file types: pdf, doc, docx, Max. file size: 32 MB.

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