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Introduction
If you are aiming to build a strong career in regulatory affairs within the pharmaceutical industry, the Executive – Regulatory Affairs at Sun Pharmaceutical Industries Ltd role is a promising opportunity. This position offers hands-on exposure to global regulatory submissions, lifecycle management, and compliance activities. With a focus on international markets, this job is ideal for candidates looking to grow in regulatory science and drug approval processes.
Job Overview
| Field | Details |
|---|---|
| Job Title | Executive – Regulatory Affairs |
| Company Name | Sun Pharmaceutical Industries Ltd |
| Location | Baroda (Tandalja – R&D) |
| Employment Type | Full-Time |
| Department | R&D – Regulatory Affairs |
| Experience Required | 1–4 Years |
| Education | M.Sc / M.Pharm |
| Salary | As per company norms |
Company Overview
Sun Pharmaceutical Industries Ltd is one of India’s largest and most respected pharmaceutical companies with a global presence across multiple therapeutic segments. The company is known for its innovation-driven approach, strong R&D capabilities, and commitment to delivering high-quality medicines worldwide. Working at Sun Pharma provides professionals with global exposure and a structured environment for long-term career growth.
Job Location & Employment Type
- Location: Baroda (Vadodara), Gujarat
- Work Type: On-site (R&D facility at Tandalja)
- Employment Type: Full-Time
This role is based at the company’s R&D center, offering direct involvement in regulatory strategy and submissions.
Open Positions / Department Details
- Department: R&D1 Regulatory Affairs
- Job Grade: G12A
- Industry: Pharmaceutical & Biotechnology
- Functional Area: Regulatory Affairs
The position focuses on regulatory submissions and lifecycle management for international markets, particularly the MENA region and South Africa.
Key Roles & Responsibilities
As an Executive in Regulatory Affairs, your responsibilities will include:
- Preparing and reviewing CMC (Chemistry, Manufacturing and Controls) dossiers for new product submissions
- Managing regulatory submissions, renewals, and variations for international markets
- Reviewing development reports, scale-up data, specifications, and stability protocols
- Preparing responses to regulatory queries and deficiencies
- Supporting product approvals by coordinating with regulatory agencies
- Handling lifecycle management activities for drug formulations
- Managing changes such as API vendor updates, site changes, and test parameter modifications
- Ensuring compliance with country-specific regulatory requirements
- Maintaining product documentation and updating central regulatory databases
- Collaborating with cross-functional teams to ensure timely submissions and approvals
Eligibility Criteria
Education
- Master’s degree in Pharmacy (M.Pharm) or Science (M.Sc)
Experience
- 1 to 4 years of relevant experience in regulatory affairs
Skills Required
- Strong knowledge of regulatory guidelines and dossier preparation
- Understanding of CMC documentation and pharmaceutical processes
- Familiarity with global regulatory requirements (MENA, South Africa preferred)
- Good analytical and documentation skills
- Ability to handle multiple regulatory projects simultaneously
- Strong communication and teamwork abilities
Salary & Benefits
- Salary: As per company norms
- Opportunity to work with a leading pharmaceutical company
- Exposure to global regulatory markets
- Professional development and career advancement
- Supportive and collaborative work culture
Selection Process
The hiring process generally includes:
- Online application submission
- Resume screening
- Technical interview (Regulatory Affairs concepts)
- HR discussion
- Final selection
Candidates should be well-prepared with regulatory guidelines, dossier formats, and pharmaceutical development knowledge.
How to Apply
Interested candidates can apply through the online application method via the official careers portal of the company.
Steps:
- Visit the official careers page
- Search for “Executive – Regulatory Affairs”
- Register/login
- Submit your updated resume
- Complete the application process
Important Dates
- Application Deadline: Not specified (Apply early recommended)
Why Apply for This Job?
The Executive – Regulatory Affairs at Sun Pharmaceutical Industries Ltd role offers significant career advantages:
- Work with one of India’s top pharmaceutical companies
- Gain experience in international regulatory markets
- Develop expertise in dossier preparation and lifecycle management
- Enhance your career prospects in regulatory affairs
- Be part of a collaborative and growth-focused work culture
This position is especially beneficial for candidates aiming to progress into senior regulatory roles or global regulatory strategy positions.
FAQs
1. What is the experience required for this role?
Candidates need 1–4 years of experience in regulatory affairs.
2. What qualifications are required?
A Master’s degree in Pharmacy (M.Pharm) or Science (M.Sc) is required.
3. Where is the job located?
The job is based in Baroda (Vadodara), Gujarat.
4. What is the salary for this role?
Salary will be offered as per company norms.
5. How can I apply?
You can apply online through the official company careers portal.
Conclusion
The Executive – Regulatory Affairs at Sun Pharmaceutical Industries Ltd 2026 role is a strong opportunity for professionals seeking growth in regulatory affairs. With exposure to global markets, structured career development, and a reputable organization, this job can significantly boost your pharma career. Apply early to secure your chance.
Disclaimer
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