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Manufacturing Compliance Coordinator
Lonza
Geleen · On-siteMid level (2–5 years)Full-timePosted 24 Sep 2026
About the job
What you'll do
Support GMP inspection readiness and maintain and revise manufacturing documentation, including batch records, SOPs, protocols, and work instructions. Investigate and manage quality events, coordinate corrective actions and timely closure, support audits, resolve compliance issues with cross-functional teams, and drive continuous improvement.
What they're looking for
A bachelor's degree or equivalent in biotechnology, life sciences, or a related field is sought, ideally with a pharmaceutical background, along with up to four years of relevant experience. Candidates should understand cGMP, communicate effectively in English, and demonstrate strong planning, problem-solving, attention to detail, collaboration, and commitment to quality and safety.
Full description