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4.0 - 9.0 years

4 - 9 Lacs

mumbai

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We are seeking an experienced and detail-oriented Executive Regulatory Affairs (ROW) to join our Regulatory team. The ideal candidate will be responsible for preparing, reviewing, and submitting dossiers for semi-regulated and non-regulated markets, ensuring compliance with global regulatory requirements, and coordinating with internal departments and external stakeholders for product registration and documentation. Key Responsibilities: Prepare and compile regulatory dossiers for semi-regulated and non-regulated markets (ROW). Respond to queries and deficiencies raised by the Ministry of Health (MOH) or buyers related to dossiers and submissions. Coordinate the arrangement and dispatch of p...

Posted 6 days ago

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5.0 - 10.0 years

12 - 15 Lacs

Mumbai

Work from Office

Regulatory Expert: Manage pharma formulations’ compliance in CIS, LATAM, Africa. Compile/review ACTD/CTD dossiers. Address MOH queries. Ensure artwork/sample compliance. Coordinate global submissions. Maintain records. Lead regulatory team. Required Candidate profile Regulatory Affairs:5 yrs in pharma formulations CIS/LATAM/Africa. Skilled in ACTD/CTD dossiers, MOH queries. Strong coordination, documentation & team leadership. Pharmacy/Regulatory degree preferred. Perks and benefits 2 & 3rd Sat off Paid leave – 21 Public Holiday- 12

Posted 3 months ago

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