QA Officer

QA Officer Geleen, Netherlands – Full-time Company Description For a global Cell Therapy CDMO, operating across five continents. We combine cutting-edge science with the power of collaboration to create technologies that help customers deliver breakthrough therapies to patients. In Geleen, our work supports the production of advanced therapies in a state-of-the-art GMP manufacturing environment. Job Description As QA Officer, you will support the daily execution of GMP-compliant operations by providing oversight and guidance in quality assurance processes. You will partner with internal teams to ensure documentation, batch records, and quality-related events meet regulatory standards. This is an ideal role for a QA professional with 2–3 years of experience looking to deepen their expertise within a fast-paced, highly regulated manufacturing setting. You will report into the QA team and receive ongoing mentorship from senior QA staff to expand your knowledge of sterile operations, quality systems, and regulatory frameworks. Key Responsibilities: Review and prepare batch records for QP release and ensure timely resolution of related deviations, CAPAs, and change requests Participate in QA on-the-floor activities, including witnessing and supporting GMP operations in production, QC, and warehouse areas Review and approve GMP documents including SOPs, forms, master batch records, and protocols Support QA metrics tracking and preparation of quality reports Assist in the coordination of QA-related meetings and project updates Ensure accurate documentation and closure of batch-related records Flexibility to work in shifts when necessary to support timely batch disposition Essential Requirements: BSc or MSc degree in life sciences, biotechnology, or a related field 2–3 years of experience in a GMP-regulated QA role Familiarity with batch record review and deviation/CAPA management Experience working in a sterile environment is highly desirable Strong attention to detail and ability to work cross-functionally Fluent in English Must hold a valid Dutch work permit Additional Insights: Location: Geleen, The Netherlands Contract Type: Permanent Start Date: ASAP Sound interesting? Send your CV to Khanyi Mabena at k.mabena@panda-int.com or reach out directly at 31 2020 44502.

Location: Geleen, Limburg, NL

Posted Date: 7/15/2025