Description
Medical Device Technical Expert wanted for our Basel based client in the pharmaceutical sector.Your experience/skills:
- At least 8 years of experience in device development of parenteral delivery systems, e.g., drug/device combination products with main focus on medical devices for parenteral administration
- Excellent technical writing skills (e.g., Design Controls)
- Solid understanding of medical device regulations (FDA 21CFR 820, EU Medical Device Directive) paired with competency of Product Design and Design for Manufacturing
- Good technical knowledge of primary containers development and autoinjector development
- General understanding of Human Factors Engineering, Risk management, clinical trial processes and requirements and pharmaceutical development
- Languages: fluent English both written and spoken
Your tasks:
- Running and leading technical development activities for medical devices
- Preparing design controls documentation while contributing to a high-quality Design History File (DHF)
- Reviewing and changing the DHF documents while guaranteeing quality and compliance to applicable regulations of the DHF elements of the assigned projects
- Ensuring device design development in compliance with the regulations and delivered at a high quality
- Consulting the development of medical devices and combination products
Start: ASAP
Duration: 06MM+
Location: Basel, Switzerland
Ref.Nr.: BH10919
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