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  • Completed medical, scientific or technical degree
  • Min. 2 years’ experience in regulatory affairs is mandatory, preferably in medical devices industry
  • Good knowledge and understanding of the regulatory submission processes for the US and EU market
  • Communicative personality that can bring the regulatory requirements convincingly in the product development teams
  • Great interest in the technical and regulatory contexts, strong analytical skills and openness to actively participate in the ongoing changes in the regulatory environment
  • Fluent in English, German language skills are an advantage

If you are interested in this innovative position, please send your complete application documents (CV, Testimonials, Diplomas, Certificates etc.) to waltraud.bueb@nemensis.com.nemensis ag, the human factor. Your competent recruitment partner, specialized in chemistry, biology/ biotechnology, pharmaceutics, medical device/engineering or health care.nemensis agFrau Dr. Waltraud BuebKägenstrasse 184153 Reinach061 205 98 98waltraud.bueb@nemensis.comwww.nemensis.com

Job: Regulatory Affairs Specialist (m/w)


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