Job Description

Eligibility Criteria:

Candidate must be a

Science graduate

with

B.Pharm or M.Pharm

Experience:

Minimum

3 to 5 years

Gender:

Female candidates only

Location Preference:

Candidates must reside on the

Western Railway line (Churchgate to Nallasopara)

Key Responsibilities:

Dossier Preparation & Review

Prepare, compile, and critically review regulatory dossiers (CTD/eCTD format) for submission in compliance with country-specific regulatory guidelines.

Ensure completeness, accuracy, and quality of all submission documents.

Query Management:

Handle and respond to regulatory queries in a timely and efficient manner.

Coordinate with cross-functional teams to gather required clarifications and documentation.

Lifecycle & Project Management:

Manage the end-to-end lifecycle of product registrations including new submissions, renewals, and variations.

Track project timelines, regulatory milestones, and ensure on-time delivery of submissions.

Regulatory Intelligence & Guideline Updates:

Regularly monitor and interpret updates in country-specific regulatory guidelines.

Ensure internal processes and documentation are aligned with the latest regulatory expectations.

Countries of Regulatory Responsibility:

Nigeria*

Zimbabwe*

Ukraine*

French West Africa (FWA) - Additional updates applicable*

Cross-Functional & External Coordination:

Liaise with third-party manufacturers to gather technical documents and compliance-related data.

Collaborate with internal departments such as QA, QC, R&D, and Supply Chain for seamless documentation and query resolution.

Job Type: Full-time

Pay: ₹450,000.00 - ₹1,200,000.00 per year

Benefits:

Leave encashment Life insurance Provident Fund
Work Location: In person