Company: Caplin Point Laboratories Ltd.
Location: Hyderabad & Chennai
Department: Regulatory Affairs
Experience: 2-6 years
Number of Positions: 6
Key Responsibilities:
- Author and review dossiers for submission to the US, Canada, Europe, Australia, South Africa, and other regulated markets.
- Review DMFs, technical documents, and coordinate with cross-functional teams to ensure submission requirements are met.
- Conduct change assessments and provide regulatory filing strategies for post-approval submissions.
- Author and review PLCM submissions to maintain compliance with approved MAs.
Market Exposure: US, Canada, Europe
How to Apply:
Send your CV to careers@caplinpoint.net
For more details, please check the post below.