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.

AD