Quality Assurance Engineer

As a Quality Assurance Coordinator in the pharmaceutical industry, you will work in the client's global QA department as a quality guarantor, ensuring compliance with GMPs, quality policies, and defined objectives. Your responsibilities may include (but are not limited to):

• Reviewing and approving operation-related documents (SOPs, protocols, reports, batch records).
• Writing risk analyses.
• Participating in deviation investigations.
• Conducting internal audits and Gemba audits if necessary.
• Ensuring correct implementation and follow-up of CAPAs.
• Reviewing SOPs, educational tools, batches, and other GMP-related documents.
• Contributing to improving the content and process of the quality system.
• Developing solutions to reduce quality-related risks.
• Assessing changes within the change control framework.

Requirements

• Master's degree in Bioengineering, Industrial Pharmacy, or related fields.
• Eligibility for the V.I.E program.
• Experience in quality systems (non-conformance, compliance, etc.) and GMPs.
• Knowledge of production processes and QA in the pharmaceutical industry.
• Proficiency in both English and French.