Caplin Point Laboratories Ltd hiring for Regulatory Affairs department (US/ Canada / Europe Market)
WE ARE HIRING!
Key Responsibilities:
Responsible for Authoring and review of dossiers for submission to US, Canada, Europe, Australia, South Africa and other regulated markets
Review of DMF’s, technical documents and coordinate with CFT’s to ensure the submission requirements
Responsible for Change assessments and provide regulatory filling strategy for Post approval submissions
Responsible for authoring and review of PLCM submission to maintain compliance to approved MA’s
Department: Regulatory Affairs
Experience 2-6 years
No of Positions 6 No’s
Market Exposure: US/ Canada / Europe
Location Hyderabad & Chennai
Send your CVs to [email protected]
For more details please check below post
