Quality Expert for Medical Devices

Quality Expert for Medical Devices wanted for our Basel based client in the pharmaceutical industry.

YOUR EXPERIENCE/SKILLS:

- University degree in Chemistry, Pharmacy, Microbiology, Biotechnology or another related science
- Minimum 3 years working experience in Quality Control/Quality Assurance or in the manufacturing of pharmaceutical drug products
- Expertise in cGMP and a proven ability to analyze and evaluate GMP compliance
- Sound knowledge of medical device and product regulations, standards and guidelines along with a solid scientific, technical and regulatory background
- Languages: fluent English both written and spoken, German/French would be a plus

YOUR TASKS:

- Managing the portfolio of assigned projects, supporting a discipline and providing a service on your own or with a team of associates
- Writing, reviewing and approving deliverables and related tools to ensure GMP compliance
- Handling quality problems and technical matters to ensure they are resolved consistently and in accordance with global standards and policies
- Supporting Medical Device Risk Management through proactive risk management tools and approaches to minimize impact on global supplies and patients
- Representing MD Quality in initiatives and cross-divisional projects as well as leading project related activities

START: ASAP
DURATION: 9MM+
LOCATION: Basel, Switzerland
REF.NR.: BH12505

Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.

DUE TO WORK PERMIT RESTRICTIONS WE CAN UNFORTUNATELY ONLY CONSIDER APPLICATIONS FROM EU OR SWISS CITIZENS AS WELL AS CURRENT WORK-PERMIT HOLDERS FOR SWITZERLAND.

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In case of successful placement, we support you with:

- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more