The Quality Manager Clinical is responsible for developing, implementing, and maintaining the Quality Management System (QMS) aligned with international standards and regulations.
Requirements
- Bachelor or Master degree in biological or (para-) medical sciences, Life Science, Quality Management or equivalent by experience
- Minimum 5 years of experience in a Quality Management role within the medical device, or pharmaceutical industry.
- Proven experience with implementing and maintaining a QMS compliant with GCP.
- Experience with internal and external audits, including regulatory inspections.
- Fluent in English. Other languages are a plus
Benefits
- A fair, competitive package: tailored, transparent compensation aligned with expertise, preferences, and local market regulations
- Opportunity to contribute to shaping the future of the Life Sciences industry
- Grow within a community of experts
- Build a meaningful career in a pioneering company
- Opportunity to work on innovative projects and clients across pharma, biotech and medical devices
