Regulatory Affairs Manager (m/w/d)
Regulatory Affairs Manager (m/w/d)
This position is to be filled full-time (37,5 hours/week).This tasks are awaiting you:
- You prepare and submit applications for conformity assessment/clinical trials in the EU and respond to questions from Notified Bodies and Competent Authorities, in a timely and accurate manner
- You are responsible for the compilation and update of CE-dossiers for registrations/clinical trial applications (CTA), advice to concerned development departments regarding the quality, analytical methods, pre-clinical and clinical development to ensure acceptance of the data in EU and assessment of dossiers of third parties
- You prepare and update product information texts according to company core data and relevant guidelines
- You conduct the maintenance/Life-Cycle Management of the CE mark (preparation and submissions of applications for renewals, change notifications, annual updates etc.) in due time
- You assess proposed changes by the production centers, marketing departments etc. from a regulatory point of view
- You coordinate regulatory projects and interact with third parties (e.g. consultants, CROs, distribution partner) concerning regulatory issues
- You develop regulatory strategies, participate in project teams and act as contact person with regards to regulatory requirements
- You conduct Due Diligences for established products with regards to regulatory aspects
What you need to get started:
- Natural scientific background (pharmacist, biologist or chemist), approbation, diploma, master degree or PhD
- Approx. 1-3 years of experience in EU regulatory affairs for medical devices, combined with profound knowledge of the European regulatory landscape
- Experience with energy based devices is a plus
- Self-confident manner combined with strong communication skills – also fluent in Business English, further language skills would be preferable
- Your skills include strategic and analytical thinking, a highly structured way of working and networking abilities
Your contact person for this position is Mrs. Franziska Mayr
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