Lincoln Pharmaceuticals Ltd., Ahmedabad based 40 years old, public limited having presence in 75+ countries, 1700+ registered products, own Manufacturing and R&D center and among india’s top 70 pharma company.
Post : International Regulatory Affairs Assistant Manager
Job Description
• Prepare and submit CTD / eCTD dossiers for ROW countries.
• Manage new product registrations in Asia, Africa, CIS, IATAM, and Middle East markets.
• Handle dossier compilation, review, and submission to health authorities.
• Handle regulatory activities for Rest of the World (ROW) marhets.
• Manage product registrations, renewals, and variations for international regions outside major regulated markets.
• Coordinate with local agents/distributors for regulatory submissions.
• Respond to regulatory queries, deficiency letters, and approvals from health authorities.
• Ensure compliance with country-specific regulatory requirements.
• Review labeling, packaging artwork, and product information for regulatory compliance.
• Maintain regulatory databases, submission trackers, and documentation.
• Coordinate with internal teams such as R&D, QA, QC, production, and supply chain.
• Monitor updates in regulatory guidelines for international markets.
Qualifications & Experience
• Bachelor's a Master's degree in Pharmacy / Pharmaceutical Sciences.
• 7-10 years of experience in pharmaceutical Regulatory Affairs (ROW markets).
• Experience handling Asia, Africa, CIS, IATAM, orMiddle East markets.
• Strong documentation and communication skills.
• Coordination with international regulatory partners.
Location : Ahmedabad
If your Profile match with the above requirements please Mail your CV on given Email. careers@LicolnPharma.com / ho.recruitment@LincolnPharma.com
(Only the relevant CV's will be considered to taking forward)
Address :
“LINCOLN HOUSE"
Behind Satyam Complex, Science City Road, Sola, Ahmedabad-380060.
Last Date : 31st March 2026
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