Job Description
About Our Client
A leading multinational in the minimally invasive medical technology space. Known for combining cutting-edge robotics with digital health solutions, this company values innovation, inclusion, and professional development, and has a strong global presence in the surgical device market.
Job Description
- Handle full product registration lifecycle, amendments, renewals, and local labeling
- Liaise with TFDA and internal global teams for submission strategies
- Maintain compliance databases (SAP, Veeva-RIM)
- Review promotional materials from a regulatory standpoint
- Participate in QMS audits, regulatory intelligence, and association-driven advocacy
- Provide RA input to cross-functional...
Apply for this Position
Ready to join Michael Page? Click the button below to submit your application.
Submit Application