About the Company

Pharmint 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-GMPapproved 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 Summary

We 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 Required

Qualifications & 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

Senior Regulatory Affairs Professional