Quality Assurance Specialist

2 days ago

Montreal, Quebec, Canada Groupe PARIMA Full time
Quality Assurance Specialist - CSV & Conformity

Groupe PARIMA is seeking a highly skilled Quality Assurance Specialist to join our team. As a Quality Assurance Specialist, you will be responsible for ensuring the quality and integrity of our CSV and conformity processes.

Key Responsibilities:
  • Manage the data integrity program, ensuring that all data is accurate, complete, and reliable.
  • Oversee the validation of IT systems, ensuring that they operate in compliance with cGMP, 21CFR11, and GAMP5 requirements.
  • Manage the audit program, including client and internal audits, and CAPA Program.
  • Develop and maintain procedures related to data integrity and ethical code of conduct for Groupe PARIMA employees.
  • Provide training to employees on data integrity principles and ensure that they are consistently followed.
  • Oversee the conformity of the quality system and adherence to procedures and working instructions.
  • Work with the senior CSV Manager to provide guidance on CSV documentation requirements and approaches.
  • Generate lifecycle CSV deliverables for each electronic system, including validation assessments and plans, risk assessments, software and configuration testing, reporting, and change management.
  • Review and approve CSV documentation.
  • Act as the principal host during client audits and actively participate in regulatory inspections.
  • Manage the internal audit program, including the internal audit of the IT Department.
  • Manage the CAPA program, monitoring and following up on deadlines and contacting departments to implement CAPA.
Requirements:
  • BSc (Chemistry, Biochemistry, Microbiology), or a related discipline, from a Canadian university or diploma recognized by a Canadian university or accreditation body as equivalent in a scientific field.
  • Minimum of five (5) years of experience in Quality Assurance in the pharmaceutical industry, with experience in IT system validation, audits, and quality systems.
  • Minimum of 5 years of applied CSV experience in the pharmaceutical or medical device industry.
  • Expertise in the application of Health Canada and FDA GMP requirements, including 21CFR11, GAMP5 guidance pertaining to highly complex automated electronic systems for Quality and manufacturing/packaging and engineering operations.
  • Expertise in electronic quality management systems (QMS), QMS product management, and systems validation.
  • Excellent knowledge in system integration methodologies and tools.
  • Thorough knowledge and understanding of Canadian (Health Canada), American (FDA), and European Good Manufacturing Practices (GMP).
  • Knowledge and thorough understanding of data integrity principles and computer system validation (21CFR11, GAMP5).
  • Technical and regulatory expertise in information technology systems supporting GxP activities.
  • Good knowledge of ICH Q9 and Q10 (Risk Management and Quality System).
  • Excellent communication skills, with the ability to interact with auditors, clients, employees, and managers.
  • Excellent technical writing skills.
  • Bilingual (French and English).
  • Able to work in a demanding environment and meet deadlines.
  • Team player.
What We Offer:
  • Medical, dental, and travel benefits.
  • Group retirement plan.
  • Recognition program and social activities.
  • Personal days.
  • Employee assistance program and online medical service.
  • Hot beverages (hot chocolate, coffee, Mokaccino).
  • Accessible by public transit or free parking.
  • Referral program.
  • Subsidized meal program.

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