QA Team Leader II Geleen, Netherlands – Primarily Site-Based Join a team that helps deliver life-changing therapies to patients around the world. As a QA Team Leader II, youll lead a team of Quality Assurance professionals, ensuring 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 management, and
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 management, and
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 management, and
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 management, and
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 management, and
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
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 management, and