Lead EU and UK regulatory activities for Oral Solid Dosage products, including current registrations, variations, renewals, and lifecycle management. Prepare and review CTD/eCTD submissions, coordinate responses to regulatory queries, and develop regulatory strategies for market launches and portfolio growth.
Partner with cross-functional teams to support compliance, manufacturing changes, technology transfers, audits, and inspections. Monitor applicable EMA, MHRA, EU-GMP, ICH, and national requirements, while mentoring team members and managing relationships with European partners and affiliates.
Preferred candidate profile
📌 Regulatory Affairs Manager Europe OSD,Goa (South Goa)
🏢 Search Advisers Services ( GUJ
📍 South Goa
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