About the CompanyPharmint is a fast-growing pharmaceutical company engaged in the development, registration, and international marketing of quality pharmaceutical products across multiple global markets. The company works closely with WHO-GMP–approved manufacturers and is actively expanding its regulatory footprint in regulated and semi-regulated countries. Pharmint is driven by compliance, quality, and timely market access, offering professionals an opportunity to work in a dynamic and growth-oriented environment. Position Details • Position: Senior Regulatory Affairs • Experience: Minimum 10 years • Joining: Immediate joiner preferred • Compensation: Minimum 10% hike on current salary (based on experience and interview performance)Job SummaryWe are looking for a highly experienced Senior Regulatory Affairs professional who can independently manage regulatory activities, handle complex dossiers, and coordinate with manufacturers and regulatory authorities to ensure timely approvals and compliance.Key Responsibilities• Manage end-to-end regulatory submissions for pharmaceutical products in regulated and semi-regulated markets • Prepare, review, and submit CTD / eCTD dossiers, CoPP, CPP, WHO GMP, and related regulatory documents • Coordinate with manufacturers, QA, QC, and external consultants for dossier preparation and gap closure • Liaise with health authorities / MOH to respond to queries, deficiencies, and follow-ups • Handle post-approval changes, renewals, and lifecycle management • Ensure full compliance with WHO guidelines and country-specific regulatory requirements • Review regulatory documentation for accuracy, completeness, and consistency • Provide regulatory guidance to internal teams and support business development when required RequiredQualifications & Experience• Minimum 10 years of experience in Pharmaceutical Regulatory Affairs • Strong exposure to international product registrations • Sound knowledge of WHO guidelines, CPP, CoPP, GMP, and CTD formats • Ability to work independently and manage multiple projects • Strong communication, coordination, and documentation skills Preferred Skills • Experience handling multiple international markets • Strong follow-up, analytical, and problem-solving skills • Ability to join immediately or within a short notice period Compensation & Benefits • Minimum 10% hike on current salary (based on experience and interview performance) • Opportunity to work with a growing international pharmaceutical organization
Job Title
Senior Regulatory Affairs Professional