International Regulatory Affairs Manager
International Regulatory Affairs Manager
Job type: Permanent
Location: Berlin
A Leading Medical Device Consultant is looking to expand their current team to join a very diverse and friendly atmosphere.
Key responsibilities of the International Regulatory Affairs Manager:
- Develop Regulatory Strategies for the key clients to follow
- Support and training for clients through personal and online meetings
- Lead on Regulatory/QM Projects
- Collaborate with various departments such as Operations, Manufacturing and Research & Development.
Key requirements of the
International
Regulatory Affairs Manager:
- The ideal candidate should have a strong Scientific background
- knowledge and experience in quality management, ideally in the field of medical devices
- Experience working with QMS
- Hands on working experience with international standards such as ISO13485
- University degree in a relevant area.
- Fluent German and English
Benefits for the International Regulatory Affairs Manager:
- Flexible working hours
- A great chance to really develop your career for the future
- Gain in depth Technical understanding
- Flat Hierarchy Structure
- The Chance to travel and work with in many different environments
- Great healthcare and pensions schemes available
If you are interested in this position, please apply online today.
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