Support regulatory submissions and product registrations across ROW markets for pharmaceutical, API and formulation products.
Responsibilities
Prepare and coordinate CTD/eCTD dossiers, renewals and variations.
Coordinate health-authority queries with internal teams.
Track regulatory requirements, compliance, approvals and response timelines.
Maintain submission records and support product lifecycle activities and timely market registrations.
Qualifications
Experience: 7 years
Education: B.Pharm / M.Pharm / Life Sciences / Chemistry or related discipline