Sun Pharma Senior Officer RA Job in Pithampur

Published on: October 11, 2026

Last updated: October 25, 2026

Sun Pharmaceutical Industries Ltd. previously advertised a Senior Officer – Team Member, MSTG position at Pithampur, Madhya Pradesh. The role was associated with R&D II, Regulatory Affairs and Global Pharmacovigilance and involved regulatory documentation, post-approval product lifecycle activities, regulatory submissions, and labelling review.

The advertised requirements included an M.Pharm qualification and 2–4 years of experience.

Job Status: Closed. The recruitment status for this vacancy is marked closed, and candidates should not consider the original listing an active application opportunity. Interested candidates can search for other openings on the official Sun Pharma Careers portal and check the status and eligibility requirements of each vacancy before applying.

Preparing for Regulatory Affairs opportunities? Explore our guide to Career in Regulatory Affairs After B.Pharm and practise with our Free Pharma Mock Tests.

1. Sun Pharma Job Overview

The details above refer to the previously advertised vacancy. Its original application link is retained for reference, but candidates should use the official careers portal to find other available opportunities.

2. Eligibility Criteria

The previously available job description specified the following requirements:

• Educational qualification: M.Pharm.
• Required experience: 2–4 years.
• Job location: Pithampur, Madhya Pradesh.

The supplied description did not specify a mandatory M.Pharm specialisation or confirm whether all the required experience had to be in Regulatory Affairs.

This vacancy was not advertised as a fresher-level position because the stated experience requirement was 2–4 years.

Candidates interested in this career path can read our guide to Career in Regulatory Affairs After B.Pharm.

3. Roles and Responsibilities

The previously advertised position involved regulatory activities related to sterile injectable products. The responsibilities described in the available job information included:

• Regulatory documentation: Reviewing, compiling, and maintaining accurate regulatory documents.
• Post-approval lifecycle management: Supporting variations, renewals, amendments, supplements, notifications, and annual updates.
• Regulatory submissions: Coordinating submissions and assisting with responses to health authority queries.
• Registration management: Maintaining product registration records, approval status, regulatory commitments, databases, and submission trackers.
• Regulatory change assessment: Evaluating the regulatory impact of changes to manufacturing processes, equipment, specifications, analytical methods, packaging materials, and manufacturing sites.
• Artwork and labelling review: Reviewing labels, cartons, package inserts, and other packaging components for regulatory compliance.
• Cross-functional coordination: Working with Quality Assurance, Quality Control, Manufacturing, R&D, Packaging Development, Supply Chain, and regional regulatory teams.

These responsibilities are included for career reference and do not indicate that the position remains available.

4. Regulatory Affairs for Sterile Injectable Products

Regulatory Affairs teams help maintain the documentation and approvals required for pharmaceutical products. For sterile injectable products, changes to manufacturing processes, specifications, analytical methods, or packaging may require regulatory assessment.

The team evaluates proposed changes, coordinates supporting documentation, and determines the applicable submission or notification requirements for the relevant market.

5. Skills Relevant to This Position

Candidates preparing for similar Regulatory Affairs roles should understand the following skill areas:

When updating your resume, highlight tasks you have actually performed and distinguish professional experience from academic knowledge or training.

Explore other opportunities on our Regulatory Affairs Jobs page.

6. How to Find Other Sun Pharma Job Openings

The Senior Officer – Team Member, MSTG vacancy is marked closed. To explore other opportunities:

1. Visit the official Sun Pharma Careers portal.
2. Search for relevant positions using terms such as Regulatory Affairs, R&D, or Global Pharmacovigilance.
3. Review the location, qualifications, and experience requirements for each listing.
4. Confirm that the vacancy is active and accepting applications.
5. Follow the instructions on the official portal to submit your application.

Important: Other available Sun Pharma vacancies do not mean that this particular position has reopened.

7. Frequently Asked Questions

1. Which company previously advertised this position?

Sun Pharmaceutical Industries Ltd.

2. What was the job title?

Senior Officer – Team Member, MSTG.

3. Where was the job located?

Pithampur, Madhya Pradesh.

4. What qualification was required?

The available job description specified an M.Pharm qualification.

5. How much experience was required?

The listed experience requirement was 2–4 years.

6. Is this vacancy currently open?

The vacancy is marked closed. Candidates can check the official Sun Pharma Careers portal for other openings.

7. What was the salary?

A verified salary figure was not specified in the available job information.

8. What was the application deadline?

The deadline was not specified in the supplied listing.

9. Where can candidates find other Sun Pharma jobs?

Visit the official Sun Pharma Careers portal to search for other opportunities.

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• Regulatory Affairs Jobs in Pharma
• QA/QC Jobs in Pharma
• Career in Regulatory Affairs After B.Pharm
• Free Pharma Mock Tests

Important Notice: This article is for informational purposes only. PharmaCareerUpdates.com is not a recruitment agency and is not affiliated with Sun Pharmaceutical Industries Ltd. Vacancy information may change; verify current opportunities through the official company careers portal. Never pay money in exchange for a job offer.