Alembic Pharma Hiring For Regulatory Affairs Dept
Regulatory Affairs Senior Executive/Assistant Manager/Deputy Manager
Location: Corporate Office, Vadodara
Key Requirements:
Qualification: B.Pharm or M.Pharm
Experience: 7-15 years in dossier filing for Mexico or ASEAN countries
Proficient in reviewing quality documents (executed batch documents, method validation, and change control)
Excellent communication skills
Roles & Responsibilities:
Compile and review product license applications, variations, and renewals for regulatory requirements in Mexico or ASEAN countries
Manage electronic documentation and submissions in CTD format
Prepare and review responses to authority questions throughout the product lifecycle
Ensure timely delivery of dossiers and track assigned projects
Design, review, and approve registration-related artwork
Conduct due diligence on dossiers for in-licensed products
Assist with the preparation of regulatory project status or submission materials
How to Apply: Please share your CV at hrd@alembic.co.in. Include the position code "RA-2025" in your email subject.
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| Alembic Pharma Hiring For Regulatory Affairs Dept |
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