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Regulatory Affairs Manager
This vacancy has now expired. Please see similar roles below...
Proclinical is currently looking for a Regulatory Affairs Manager for a leading biotech based in Germany.
Job Responsibilities:
- Documentation preparation (clinical) in order to gain a CE Mark for their product
- Management of team directly involved in obtaining CE Mark
- Project Management, creation of invoicing and offers
Skills and Requirements:
- 5 Years' experience within Regulatory Affairs
- Strong Medical Device background
- Experience within European markets
- CE Marking experience
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Hugh Pickerill on +44 203 854 1079 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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