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Specialist Regulatory Affairs, Medical Devices, Germany

Our client is a family owned company, and international regarded manufacturer of diagnostic instruments and devices for minimally invasive surgery.

Currently in a solid growth phase, they are advertising for a number of Regulatory Affairs professionals, at both junior and senior level to join their German headquarters.
Responsibilities will include all regulatory tasks associated with registration of advanced medical devices, resulting in the timely release of products, worldwide.
This is an autonomous role, requiring initiative and good organisation skills, managing the approval of a range of products in international markets, and including analysis of national legal requirements, development of appropriate regulatory strategies, developing relationships with international Regulatory and Health Authorities, and advising and supporting project teams on regulatory issues.

The range of products could extend to medical devices, communications and IT equipment.



Suitable candidates would typically be degree qualified in a relevant discipline (Mechanical engineering, Precision engineering and Biomedical engineering), with several years of professional experience in Regulatory Affairs / Quality Management of Medical Devices, and a thorough working knowledge of medical device regulations.
The Business languages here are English and German, with additional languages welcomed.

It is expected the person will be proficient in Microsoft Office applications.
For more information on this vacancy, or any other medical device opportunities, please contact the Senior Consultant Andrew Boroky on 0044 (0) 207 940 2116, or email him at a.boroky@nonstop-devices.com

  • Start: 20/3/2012
  • Rate: €60000 per annum + benefits
  • Location: Germany
  • Type: Permanent
  • Industry: Engineering
  • Recruiter: NonStop Recruitment
  • http://www.nonstop-pharma.com
  • Posted: 2012-02-09 07:52:39 -

 

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