Description
Requirements- Qualification &Validation experience (IQ,OQ,PQ)
- Expert for process and test methods validation including special processes
- Proficient with validation documentation (PFMEA, URS, VMP, VP etc)
- Sound knowledge of ISO13485 and FDA 21 part 820
- Good GMP knowledge
Languages:
- German is a must have
- English well spoken and written
If this role could be of interest to you, do not hesitate to send your CV in word to Burcu Parilti , the freelance medical devices specialist at Real Staffing in Zurich. Campaign Ref: CH