International Regulatory Affairs Manager
Job type: Permanent
Location: Berlin
A Leading Orthopaedic Medical Device Manufacturer is looking to expand their current team to join a very diverse and friendly team.
Key responsibilities of the International Regulatory Affairs Manager:
- Develop Regulatory Strategies for the company to follow
- Responsible for Global Registration according to International Directives
- Lead on Regulatory Project teams
- Collaborate with various departments such as Operations, Manufacturing and Research & Development.
- Involvement in Regulatory Compliance.
Key requirements of the International Regulatory Affairs Manager:
- The ideal candidate should have a strong Scientific background
- + 2 years of experience in Medical Devices OR IVD
- 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
- Gain in depth Technical understanding
- Flat Hierarchy Structure
- Great healthcare and pensions schemes available
If you are interested in this position, please apply online today.
