Sun Pharma Hiring 2026: Executive – Regulatory Affairs – EM Market in Gurgaon
Sun Pharmaceutical Industries Ltd. is hiring for an Executive – Regulatory Affairs – EM Market position at its Gurgaon R&D location. The role is focused on regulatory submissions, CMC dossier preparation, variations, deficiency responses and lifecycle management activities for WHO and Sub-Saharan Africa markets.
The official Sun Pharma careers listing is dated September 18, 2026 and confirms the position as Executive – Regulatory Affairs – EM Market at Gurgaon – R&D.
For professionals working in Regulatory Affairs, CMC documentation and pharmaceutical product registration, this opportunity involves coordinating regulatory activities across emerging markets and supporting submissions through different stages of the product lifecycle.
Sun Pharma Regulatory Affairs Job 2026 – Highlights
| Particular | Details |
|---|---|
| Company | Sun Pharmaceutical Industries Ltd. |
| Position | Executive – Regulatory Affairs – EM Market |
| Department | Regulatory Affairs |
| Location | Gurgaon – R&D, India |
| Market | WHO & Sub-Saharan Africa |
| Job Type | Full Time |
| Experience | Not specified in the official listing |
| Qualification | Not specified in the official listing |
| Job Posted | September 18, 2026 |
About Sun Pharmaceutical Industries
Sun Pharmaceutical Industries Ltd. is a global pharmaceutical company with operations spanning specialty medicines, generics, branded generics, APIs and other pharmaceutical products. The company says its medicines reach more than 100 countries and that it has more than 40 manufacturing facilities globally.
Sun Pharma also has a significant presence in emerging markets, including countries in Africa and other regions. Its global operations make regulatory compliance and market-specific product registration an important part of its pharmaceutical business.
Visit Sun Pharma Official Website
About the Executive – Regulatory Affairs – EM Market Role
The selected professional will support regulatory submissions for new products, variations, responses to regulatory queries and lifecycle management activities for WHO and Sub-Saharan Africa markets.
According to the official job description, the position involves preparation and review of quality dossiers, CMC documentation, deficiency responses, variations and re-registration/PCH dossiers.
The role also requires regulatory assessment of changes such as API vendor changes, manufacturing-site changes, testing parameters and product harmonization activities.
Key Responsibilities
1. New Product Submissions
The Executive will be involved in reviewing and preparing CMC dossiers for new product submissions.
The role also includes reviewing supporting documents before exhibit batches are initiated, including:
- Development reports
- Scale-up reports
- Specifications
- Stability protocols
- Product artworks
- Other relevant regulatory documents
The objective is to ensure that the documentation is adequate before moving forward with regulatory and development activities.
2. Regulatory Approval Support
The position includes preparing and reviewing responses to regulatory deficiencies and queries received during the approval process.
This requires careful assessment of regulatory comments and coordination with relevant internal stakeholders to prepare appropriate responses.
3. Product Lifecycle Management
A major part of the position involves regulatory support for post-approval product changes.
Responsibilities include preparing and reviewing variations related to:
- API vendor changes
- Changes in regulatory or testing parameters
- Drug product manufacturing-site changes
- Product harmonization
- Other lifecycle changes
The official listing also mentions preparation and review of re-registration and PCH dossiers for submission to regional offices or regulatory agencies.
4. Regulatory Compliance
The role also covers activities after regulatory approvals are received.
This includes:
- Preparing approval packages
- Reviewing approval documentation
- Circulating approval packages to stakeholders
- Updating information based on queries and variations
- Maintaining comprehensive product information in the central repository
- Reviewing the regulatory impact of variations and change controls
Skills Relevant to This Role
Candidates targeting this type of Regulatory Affairs position should be comfortable working with pharmaceutical regulatory documentation and CMC information.
Important skills include:
- CMC documentation knowledge
- Regulatory submission preparation
- Understanding of pharmaceutical product registration
- Variation filing knowledge
- Lifecycle management
- Dossier preparation and review
- Regulatory deficiency response
- Document review
- Change-control assessment
- Attention to detail
- Stakeholder coordination
- Regulatory timeline management
- Strong documentation and organizational skills
What Candidates Should Know About the Role
This position is particularly centered on emerging-market regulatory activities rather than a general administrative Regulatory Affairs function.
The official job description specifically references WHO and Sub-Saharan Africa markets, new submissions, variations, regulatory queries and lifecycle management.
Professionals applying should therefore make sure their resumes clearly highlight relevant experience in areas such as CMC dossiers, pharmaceutical registrations, variations, regulatory submissions and post-approval activities, where applicable.
Qualification and Experience
The official Sun Pharma listing currently available for this position does not specify a qualification or experience requirement in the job description published on the careers portal.
Candidates should therefore carefully review the official application page for any eligibility information requested during the application process.
Location
Job Location: Gurgaon – R&D, India
The position is associated with Sun Pharma’s R&D operations in Gurgaon.
Salary
The official job listing does not provide a salary figure for this position.
Candidates should not rely on unofficial salary estimates when applying and should refer to the employment terms provided during the recruitment process.
How to Apply for Sun Pharma Regulatory Affairs Job
Interested candidates should apply through the official Sun Pharma careers portal.
Apply for Executive – Regulatory Affairs – EM Market
When applying, candidates should ensure that their resume accurately reflects relevant Regulatory Affairs experience and technical skills, particularly where they have worked on:
- CMC documentation
- Regulatory submissions
- Variations
- Product registrations
- Deficiency responses
- Lifecycle management
- Change controls
- Emerging-market submissions
Resume Tips for Regulatory Affairs Candidates
A targeted resume can make it easier for recruiters to identify relevant experience.
Consider highlighting:
Regulatory Expertise
- CMC dossier preparation
- New product submissions
- Variations
- Re-registration
- Lifecycle management
Technical Knowledge
- Development reports
- Stability documentation
- Specifications
- Scale-up documentation
- API and manufacturing-site changes
Compliance Experience
- Regulatory queries
- Deficiency responses
- Change-control assessments
- Approval documentation
Professional Skills
- Cross-functional coordination
- Documentation
- Deadline management
- Attention to detail
- Regulatory communication
Quick Summary
| Job Detail | Information |
|---|---|
| Company | Sun Pharmaceutical Industries Ltd. |
| Job Title | Executive – Regulatory Affairs – EM Market |
| Department | Regulatory Affairs |
| Location | Gurgaon – R&D |
| Markets | WHO & Sub-Saharan Africa |
| Core Area | Regulatory Submissions & Lifecycle Management |
| Key Technical Area | CMC |
| Job Type | Full Time |
| Posted | September 18, 2026 |
| Application | Official Sun Pharma Careers Portal |
Frequently Asked Questions
Q1. What is the position available at Sun Pharma?
Sun Pharma is recruiting for an Executive – Regulatory Affairs – EM Market position at its Gurgaon – R&D location.
Q2. Where is the Sun Pharma Regulatory Affairs job located?
The position is based at Gurgaon – R&D, India.
Q3. Which markets are covered by this Regulatory Affairs role?
The official job description identifies WHO and Sub-Saharan Africa markets as the focus of the role.
Q4. What are the main responsibilities?
The position covers new product submissions, CMC dossier preparation, regulatory deficiency responses, variations, re-registration/PCH dossiers and lifecycle management activities.
Q5. Does the role involve CMC documentation?
Yes. Reviewing and preparing CMC dossiers for new product submissions is specifically mentioned in the official job description.
Q6. Does the position involve variation filings?
Yes. The role includes preparing and reviewing variations related to API vendors, manufacturing sites, testing parameters, product harmonization and other lifecycle changes.
Q7. Is regulatory query handling part of the job?
Yes. The Executive will support the preparation and review of responses to regulatory deficiencies and queries associated with product approvals.
Q8. Is salary mentioned in the official posting?
No salary amount is stated in the official job listing currently available.
Q9. Where can candidates apply?
Applications should be submitted through the official Sun Pharma careers portal.
Q10. What should applicants highlight on their resumes?
Candidates should highlight relevant experience with regulatory submissions, CMC documentation, variations, lifecycle management, deficiency responses, product registration and regulatory compliance, where applicable.
Final Note
The Sun Pharma Executive – Regulatory Affairs – EM Market opening in Gurgaon focuses on regulatory submissions and lifecycle activities for WHO and Sub-Saharan Africa markets. The position covers CMC dossiers, regulatory responses, variations, re-registration and regulatory impact assessments.
Candidates interested in this opportunity should review the official job description carefully and submit their application through the Sun Pharma careers portal.
Official Sun Pharma Job Listing – Executive Regulatory Affairs – EM Market
