So… why is it free?

Employers pay when they hire through Elip. You're not the product — you're the talent it finds. No contracts, no card. Not useful? One message wipes everything. No hidden Pro tier. No “contact sales.” This is the entire pricing page.

Executive - Regulatory Affairs - EM Market at Sun Pharma — Gurgaon

Experience0–6 yrs
SalaryNot disclosed
Work modeonsite
Levelfresher
Posted21 Sept 2026

Apply for this job

About Sun Pharma

Sun Pharma is hiring in Gurgaon in pharma biotech. This role looks for around 0+ years of experience.

Skills

CMC dossiers
regulatory submissions
deficiency responses
lifecycle management
regulatory compliance
stability protocols
specifications
artworks
change controls
product information management

The role

A regulatory affairs executive at a pharmaceutical company prepares CMC dossiers for drug submissions, manages lifecycle variations, and supports regulatory compliance for emerging markets. The role reviews stability, specifications, artworks, and deficiency responses for product approvals.

Full job description

Job Summary

Regulatory submission of new products, variations, response to queries, Life cycle management for WHO Sub Sahara Africa markets through preparation of quality dossiers enabling timely approvals.

Area Of Responsibility

1 . New submissions:

a. Review prepare CMC (Chemistry, Manufacturing and Controls) dossiers for fresh submissions.

b. Review documents (Development report, scale up report, specification, stability protocol), artworks etc.

before initiation of Exhibit batches for adequacy.

2. Approval:

Review prepare response to deficiency enabling approval of products filed to regulatory agency.

3. Lifecycle management for drug formulations:

a. Prepare and review variations as per the country requirements to support approval of changes such as API

vendor changes/changes in ROS/test parameters; DF site changes; harmonization of products etc.

b. Prepare and review re-registration/PCH dossiers submit the same to regional office/ regulatory agencies

4. Regulatory compliance:

a. Prepare, Review and circulate approval package to stake holders upon receipt of approval and update the

same based on queries and variations.

b. Ensure reposition of comprehensive product information into central repository

C. Review regulatory filing impact of variations, change controls, etc.

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.