Description
Medical Device Expert - Human Factor wanted for our Basel based client in the pharmaceutical sector.Your experience/skills:
- Degree in a proper subject along with relevant working experience in the pharmaceutical or medical device industry
- Experience in planning and writing technical documentation with Medical Device Design Control for Medical Devices and product combinations
- Excellent Project Management skills
- Experince in ISO 13485, ISO14971, MDD and QMS for Medical Devices
- Ideally know-how of Auto-Injectors and Safety Devices
- Languages: fluent German and English both written and spoken
Your tasks:
- Writing, reviewing and approving deliverables (e.g. procedures) and related tools (e.g. IT) to ensure GMP compliance
- Managing quality problems and technical matters as well as ensuring global standards and policies
- Releasing of Medical Devices for clinical studies and commercial use
- Supporting Medical Device Risk Management to minimize impact on global supplies and patients as well as representing MD Quality in initiatives and cross-divisional projects
- Meeting internal and external guidelines regarding quality and safety (quality manuals, regulatory cGMP guidelines, health authority requirements, SOPs, HSE, etc.)
- Contributing to internal compliance policy and commenting to regulations
Start: ASAP
Duration: 15MM+
Location: Basel, Switzerland
Ref.Nr.: BH11622
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.
Going the extra mile…
New to Switzerland? In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more