Aurobindo Pharma Hiring Regulatory Affairs Expert

Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India. The company manufactures generic pharmaceuticals and active pharmaceutical ingredients.

Positions open for Regulatory Affairs Expert

US Market - Post Approval
Experience : 3 to 6 Years
Qualification : M.Pharm (any specialisation)
Key Skills : Handling Post-approval Activities, CB-0, CB-30, PASS, FDA Inspections
US Market - CMC
Experience : 3 to 10 Years
Qualification : M.Pharm (any specialisation)
Key Skills : Filing ANDAs, Annual Submissions, & Dossier Preparations
EU Market - Module 3
Experience : 3 to 10 Years
Qualification : M.Pharm (Pharmaceutics/RA)
Key Skills : CMC, Initial Submissions, Dossier Preparations, Pre/Post Submissions, & LCM
EU Market - Module 1
Experience : 3 to 10 Years
Qualification : M.Pharm (any specialisation)
Key Skills : Hands-on experience in Administration, Preparation & Submission of Renewals, Response to Agency Queries, RSI & RFI