Quality Assurance Compliance Specialist - Montréal, Canada - Groupe Parima
Description
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
- Followup 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)
What we offer:
- Flexible work schedule and telework
- Medical dental & travel benefits
- Group retirement plan
- Recognition program & social activities
- Personal days
- Employee assistance program & online medical service
- Hot Beverages (Hot chocolate, Coffee, Mokaccino)
- Accessible by public transit or free parking
- Referral program
Schedule:
- Day shift
- Monday to Friday
Education:
- Bachelor's Degree (required)
Work Location:
Hybrid remote in Montréal, QC H4S 1X6
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