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Tablets Medopharm Pvt. Ltd., a reputed pharmaceutical company, has announced exciting job openings in the Regulatory Affairs Department. The company is seeking qualified and experienced professionals to join its team in Chennai.
Position: Regulatory Affairs – Finished Formulations
Location: Chennai
Qualification: B.Pharm / M.Pharm / M.Sc
Experience: 2 to 8 years
Key Responsibilities:
Manage Regulatory Affairs activities for finished formulations in export or merchant-exporter environments.
Compile, review, and format CTD / ACTD / eCTD dossiers for various global markets such as Africa, Asia, CIS, and LATAM.
Coordinate with contract manufacturing partners to gather all necessary technical and regulatory documentation.
Review and approve artworks, labels, and cartons as per regulatory guidelines and client specifications.
Maintain a regulatory submission tracker for dossiers, samples, and artworks.
Provide regulatory insights for new product feasibility and market expansion initiatives.
This opportunity is ideal for professionals with strong regulatory knowledge, dossier preparation experience, and a keen interest in international pharmaceutical compliance.
Interested candidates can share their resumes at hr@medopharm.com.
Join Tablets Medopharm Pvt. Ltd. and contribute to regulatory excellence in global pharmaceutical markets!
