His responsibilities include the development of a strategy for timely filing, registration and regulation of the department of file management, the labeling guidelines of the project and the board for the European Union, the United States and international regulations. Additional tasks will be to build and maintain relationships with regulatory authorities, while keeping abreast of changes in the actors of the company worldwide regulatory requirements for medical devices ..
Candidates will usually be a degree in a relevant discipline such as natural sciences, engineering, pharmacy and medicine, with many years of experience as a professional field of regulatory affairs for medical devices.
An ideal profile should include a thorough knowledge of the rules of medical devices and procedures for registration in Europe and the United States and countries such as Africa, the Middle East and Central Asia.
Additional leadership positions are also available for specialists who want to take the next step in the management and with a corresponding increase in salary.
Business language here is English and German, other languages welcome. It is expected that the person will be proficient in Microsoft Office applications.
For more information on vacancies, medical devices or other opportunities, please contact Andrew Boroky Senior Consultant on 0044 (0) 207 940 2116 or e-mail HIM @ nonstop-a. boroky devices.com
* Expiry date
January 29, 2012
* Contact e-mail
@ A.boroky.65029.2362 nonstoppharma.aplitrak.com
* Contact the Web
http://www.nonstop-pharma.com
An EU passport or work permit is required for this position. Applicants without one of them will be automatically rejected.
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