Description
Medical Device Design Control Expert - Quality engineer wanted for our Basel based client in the pharmaceutical sector.Your experience/skills:
- Master degree in Science or Engineering or equivalent academic engineering education
- Profound background in medical device quality assurance, product design or design for manufacture, DHF compilation along with Design Control process and other applicable regulatory as well as QA and GMP
- Know-how of medical device regulations FDA 21CFR 820, CFR 4 and EU Medical Device Directive
- Familiarity with mechanical engineering and good knowledge of pharmaceutical development, Human Factors Engineering and Risk management
- Languages: fluent English both written and spoken
Your tasks:
- Supporting technical activities within the development and commercialization
- Providing Life Cycle Management activities regarding changes in the DHF
- Managing product compliance for the assigned projects
- Maintaining Design Control documentation and implementing it to a high quality Design History File (DHF)
- Performing in the documentation strategy along with building applicable documents
Start:
Duration: 06MM+
Location: Basel, Switzerland
Ref.Nr.: BH12121
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