Beschreibung
We have an exclusive opportunity for a Regulatory Affairs Consultant role to work with a medical device company in the Zurich region of Switzerland. The position offers a competitive Daily or Hourly rate and is until December 2014, please note that English is the only language requirement.
The role is responsible for ensuring that their medical device products are meeting FDA & European Regulatory requirements as part of an overall remediation project were Historical Changes are being made to reflect submission history (510k). The role is on a 80% FTE basis (onsite). Our client requires professionals with at least 3 years Medical Device regulatory submission/filing experience, there is a detailed job description available on request.
I hope that the role will be of interest to you and understand that further information may be required before making an application to the end client. MBA Pharmaceutical provide our consultants with fully-confidential communications, 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. Alternatively I am contactable during normal business hours (and later on request).
Kind regards,
Michael
Michael Bailey International is acting as an Employment Business in relation to this vacancy.