V.I.E 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.