30/09/2025
Immediate opportunity in Regulatory affairs with Medical devices Company .
About Co. - Orthopedic Implants manufacturing company .
Job location - Pune
Experience - 3 to 5 years relevant
Candidate should have knowledge of ISO 13485, regulations- CDSCO, CE, US FDA
2. Hands on experience in preparation and submission of regulatory documents, including applications for licenses, registrations and approvals, to the relevant authorities like CDSCO, US FDA, ISO & CE certification bodies
3. To ensure compliance with regulatory requirements- quality management systems and post-market surveillance.
For more details Pl write at jobs@mediccareers.in
www.mediccareers.in
Regulatory affairs FDA device regulatory #
We are the New kids on the block! A group of like minded professionals with an average of 20 yrs of experience in the pharma recruitment space have come together to form a new venture. We at medic careers know the pharmaceutical industry inside out and through this platform are committed to provide....