Group Lead Regulatory Affairs Manager
Job type: Permanent
Location: Munich
For this opportunity we have partnered with one of the world's Leading Diagnostic Device Manufacturer. They are looking to expand their Regulatory team in there fantastic Munich office.
Key responsibilities of the Group Lead 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 Group Lead Regulatory Affairs Manager:
- The ideal candidate should have a strong Scientific background
- + 2 years of experience in Medical Devices, Preferably 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 Group Lead Regulatory Affairs Manager:
- Flexible working hours
- A great chance to really develop your career
- Work for one the World's leading Diagnostic Device Manufacture's
- Flat Hierarchy Structure
- Great healthcare and pensions schemes available
If you are interested in this position, please apply online today.
