Quality Assurance Engineer III – Medical Devices | Maastricht, Netherlands Are you an experienced Quality Engineer / QA Specialist with a background in medical devices and ISO 13485? We are currently supporting a leading organisation within the
Senior QA Officer – Batch Record Review & Deviation Management Position Summary We are seeking an experienced Senior QA Officer to join a leading pharmaceutical manufacturing organization. The successful candidate will be responsible for batch record review, deviation
Production Team Lead – Cell & Gene Therapy Manufacturing (EU Applicants Only) Location: Geleen Contract: Permanent Start Date: ASAP Working Pattern: 24/7 rotating shift schedule (day, evening, night) On-site role (no hybrid option due to GMP