Senior Specialist Medical Device
BengaluruFull-timeMid levelPosted over a month ago
Mid-level pharma role at INSC IND GBS India in Bengaluru.
About the role
Manage global regulatory product documentation, including technical files, registration dossiers, IFUs, and labeling Ensure compliance with regulatory standards and testing requirements throughout product design and development Coordinate regulatory approvals and change notifications with Notified Bodies and Authorities
What you'll do
- Manage global regulatory product documentation, including technical files, registration dossiers, IFUs, and labeling
- Ensure compliance with regulatory standards and testing requirements throughout product design and development
- Coordinate regulatory approvals and change notifications with Notified Bodies and Authorities
- Ensure global regulatory product availability aligned with commercial strategy by managing registrations, renewals, and submissions
- Coordinate regulatory product strategies
What you need
- Documentation