QA Specialist

In this position as QA Specialist you play a crucial role in ensuring quality and compliance oversight to marketed global pharmaceutical products. Do you bring QA experience in a pharmaceutical environment, would you like to be part of a global team and do you want to make a direct impact on product quality? Apply now! An international pharmaceutical company in Amsterdam. You will be part of the Third-Party Manufacturing QA department, which has a global focus. As a QA Specialist you provide quality assurance support for assigned Third-Party Manufacturers (TPM) and their quality systems to ensure that safe, effective, and compliant products are consistently supplied in accordance with global cGMP and regulatory standards. You will play a key role in ensuring product quality, compliance, and availability within an international manufacturing network. Your responsibilities: Support the TPM QA Manager in all quality-related activities for assigned third-party manufacturers Coordinate change control, deviations, CAPAs, and complaint trend follow-up to maintain compliance and product integrity. Contribute to the implementation of global quality and compliance strategies for commercialized products. Plan and support the execution of major product or material changes. Participate in QA cross-functional projects and initiatives to improve quality systems and compliance. Support inspection readiness and audit activities, ensuring third-party manufacturers meet global regulatory expectations. Maintain proactive communication with internal and external stakeholders and travel occasionally to TPM sites to assess and strengthen quality systems. For this position as QA Specialist we are looking for a candidate who recognizes him- or herself in the following profile: Bachelor’s degree (or equivalent) in a relevant scientific discipline such as Chemistry, Pharmacy, Biology, or Microbiology. Minimum of 2 years of QA experience in a Pharmaceutical manufacturing environment Solid understanding of pharmaceutical manufacturing for finished dosage forms and related quality systems. Experience with change control, deviations, CAPA, and supplier or TPM quality management. Strong communication skills, both written and verbal, with the ability to interact effectively across different cultures. Analytical mindset with experience in Quality Risk Management and data-based decision-making. Possession of a BSN (citizen service number) A contract for 12 months at CheckMark Salary indication from €4300,- gross per month based on a full-time position 13 month salary Full-time position, where 32 hours a week is negotiable Work from the office in Amsterdam with the option to work from home one day per week Neem voor meer informatie contact op met Jurjen Wilschut: 088 00 211 22 // 06 3024 7453 Vacaturenummer: 8592

Location: Weesp, 1381 CP, NL

Posted Date: 11/20/2025