Senior Regulatory Affairs Manager
Job type: Permanent
Location: Stuttgart
A well-established, leading Medical Device Manufacturer is currently looking to hire a Senior Regulatory Manager to join their growing team on their site in Stuttgart. Employees will have the chance to work in a very dynamic team and really shape the movement of the company as they continue to prepare for the MDR.
Key responsibilities of the Senior Regulatory Affairs Manager:
- Responsible for the Quality Management System within the organisation
- Develop Regulatory Strategies for the company to follow
- Responsible for Global Registration according to EU and FDA Directives
- Collaborate with various departments such as Operations, Manufacturing and Research & Development.
- Involvement in Regulatory Compliance.
- Leading and collaborating on new as well as existing projects.
Key requirements of the Senior Regulatory Affairs Manager:
- The ideal candidate should have a strong Scientific background
- + 3 years of experience in Medical Devices OR IVD
- Experience working with QMS
- Strong background in Registration according to Global directives
- University degree in a relevant area.
Benefits for the Senior Regulatory Affairs Manager:
- Flexible working hours
- Flat Hierarchy Structure
- Great healthcare and pensions schemes available
If you are interested in this position, please apply online today.