International Regulatory Affairs Manager

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.
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