QMS Coordinator (f/m/x)

Significant experience in preparing, coordinating, and actively participating in pharmaceutical customer audits (major role in documentation preparation, on‑site support, and follow‑up of audit findings), Practical experience supporting internal audits or external regulatory inspections, Ability to manage and maintain quality documentation in accordance with compliance requirements, Performing the function of an internal and external auditor, Bachelor’s or Master’s degree in Pharmacy, Biotechnology, Chemistry, Quality Management, or a related scientific field, Preferred 2–3 years of experience in Quality Assurance / Quality Systems within the pharmaceutical or medical device industry, Strong knowledge ISO 9001, Experience working with Quality Management Systems (Deviation Management, CAPA, Change Control, Document Control, Audits, Training)., Experience with risk management tools (e.g., FMEA), Knowledge of validation, qualification, and data integrity principles, Experience in supporting regulatory inspections and customer quality audits, knowledge of GMP, Ability to lead small quality improvement projects, Excellent analytical thinking, problem‑solving abilities, and attention to detail, Strong communication skills and ability to collaborate with cross-functional teams (QA, QC, Production, Engineering, Validation)., Fluent English (written and spoken), Experience in using the SAP system is welcome, Current, valid Driver’s License would be beneficial

sharing the costs of sports activities, private medical care, life insurance, integration events, retirement pension plan, parking space for employees, extra social benefits, charity initiatives