The Regulatory Affairs Manager will lead and manage regulatory submissions, approvals, and compliance activities for medical devices
Job Summary
The Regulatory Affairs Manager will lead and manage regulatory submissions, approvals, and compliance activities for medical devices.
This role ensures that products meet all national and international regulatory requirements, facilitating timely market access and maintaining post-market compliance.
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry.
Matching Summary
The Regulatory Affairs Manager will lead and manage regulatory submissions, approvals, and compliance activities for medical devices.
Skills & Requirements
Must-have
Medical device regulatory strategy
Regulatory submissions and approvals
Global regulatory requirements
Quality system regulations
Cross-functional team guidance
Nice-to-have
Fosters creativity and innovation
Culture of excellence and flexibility
Purpose-driven work environment
Continuous learning and growth
Key Requirements
Bachelor's degree in scientific/engineering field
5-7 years medical device regulatory affairs experience