Description
We are looking for a
Subject Matter Expert Risk Management (m/f)
Reference: -en
Start: asap
Duration: 6 MM
Place: in the Basel region
Branch: Medizintechnik
Your tasks:
- Prepare, edit and adjust existing Risk Management documentation
- Prepare, edit and adjust Design & Clinical Risk Management documentation
- Prepare, edit and adjust Risk Management Report and Risk Management Plan
- Participate in and optimise the Product Risk Management process
Your qualifications
- Profound experience in the design and development of medical devices or pharmaceuticals
- Strong background in Product Risk Management with experience in creation, review, and approval of risk management documentation (DFMEAs and PFMEAs)
- BS in engineering or science required
- Strong analytical skills, proficiency in Microsoft Office (Excel, Word etc.)
- Fluency (spoken and written) in English and German
Skills:
- Product manager
Keywords: Product Risk Management Design Clinical Risk Risk Documentation ISO 13485 Technical File and Design History File documentation DHF THF