Quality Assurance Specialist

1 week ago


SaintEustache, Quebec, Canada Groupe Parima Full time
About the Role

Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO) with a strong commitment to quality and compliance.

The Investigation and Compliance Specialist will play a key role in ensuring the quality and integrity of our products and processes.

Key Responsibilities
  • Investigation and Compliance: Manage investigations related to quality control, track and report compliance documents in the company's quality management system.
  • Quality Control: Initiate, draft, and conduct laboratory investigations and trend monitoring, as well as periodic verifications of laboratory quality documents.
  • Change Control: Initiate and monitor change control (CC) to ensure that all changes are properly documented and implemented.
  • Corrective and Preventive Actions: Initiate and monitor corrective and preventive actions (CAPA) to address quality deviations and prevent future occurrences.
  • Quality Management: Prepare documents relating to quality management meetings, draft and revise Standard Operating Procedures (SOP), and ensure compliance with Good Manufacturing Practices (GMP).
Requirements
  • Education: Bachelor of Science (Chemistry, Biochemistry), or related discipline, from a university.
  • Experience: Minimum of five (5) years of laboratory experience in the pharmaceutical industry.
  • Skills: Good knowledge of various analytical techniques, proficiency with EMPOWER software, and good technical writing skills.
  • Language: Bilingual (French and English).
What We Offer
  • Flexible Work Schedule: Flexible work schedule and telework (if applicable).
  • Benefits: Medical – dental & travel benefits, group retirement plan, recognition program & social activities, personal days, employee assistance program & online medical service.
  • Work Environment: Accessible by public transit or free parking.


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