Beschreibung
We have a 3 Month Contract opportunity in canton Valais, Switzerland which is one of the few places in Europe likely to have good skiing conditions during this rather mild winter.
For the non-ski enthusiast our client is a global Medical Device company offering a very friendly and professional working atmosphere, our prior consultants have enjoyed working at this site. There is a competitive Hourly rate available and the opportunity to contribute significantly to our client's Validation Master Plan. The project is expected to begin in mid January with a one stage interview required for the role, please note that German speaking/writing is essential to an upper intermediate level (B2).
Our client searches for an experienced medical device Validation Engineer with at least 2 years experience in validating medical device manufacturing environments, you will also hold up to date knowledge in regulations for Europe and FDA (ISO/CFR/GMP). Your education will ideally be Engineering for Mechanical/Industrial/Process or life science with appropriate industrial experience.
We hope the role will be of interest to you and understand that further information may be required before making an application to the end client, please feel free to send either your full name, contact details or a complete CV via this website and I will endeavour to get back to you with further information on the role and answer any questions you may have.
Best regards,
Michael Kellitt
MBA Michael Bailey Associates AG
Job Code: 108610 (internal)/ (external)
Key words: Validation, Ingenieur, Quality Engineer, Compliance, Process Engineer, Mechanical, Black Belt, 6 Sigma, ISO 13485, Medizinprodukt, class III, FDA, 510k, GMP, GxP, Regulatory, Freelance, Consultant, Contractor, Qualitaet, Pharmaceutical, Medical Device, MedDeV, Switzerland
Michael Bailey International is acting as an Employment Business in relation to this vacancy.