Sun Pharma Hiring for Executive Regulatory Affairs RD Baroda location with M.Pharm qualification and 2–5 years experience required.
Key Highlights – Sun Pharma Executive RA Vacancy 2025
- Company Name: Sun Pharmaceutical Industries Ltd
- Job Title: Executive – Regulatory and Business Continuity
- Business Unit: R&D1 – Regulatory Affairs
- Job Grade: G12A
- Location: Baroda (Vadodara), Gujarat
- Facility Location: Tandalja – R&D
- Qualification Required: M.Pharm
- Experience Required: 2 to 5 Years
- Functional Area: Regulatory Affairs – Drug Products
- Hiring Type: Experienced Professionals
- Industry: Pharmaceutical Research & Development
- Travel Requirement: Not Applicable
- Job Posting Date: 7th December 2025
Sun Pharma Executive – Regulatory Affairs Job Opening 2025
Sun Pharmaceutical Industries Ltd, India’s largest pharmaceutical company and a globally respected specialty generics organization, is hiring for the position of Executive – Regulatory and Business Continuity in its R&D1 Regulatory Affairs division at the Tandalja R&D facility in Baroda (Vadodara), Gujarat. Sun Pharma Hiring for Executive Regulatory Affairs RD
This opportunity is ideal for M.Pharm professionals with 2 to 5 years of experience in Regulatory Affairs who are looking to establish a long-term career in global regulatory submissions, approvals, and life-cycle management of drug products.
At Sun Pharma, professionals are empowered to grow continuously, lead with responsibility, and collaborate in an environment that promotes learning, ownership, and innovation. Sun Pharma Hiring for Executive Regulatory Affairs RD
About Sun Pharmaceutical Industries Ltd
Sun Pharmaceutical Industries Ltd is a globally recognized pharmaceutical organization with operations across more than 100 countries, offering high-quality generic and specialty medicines. With a strong commitment to innovation, compliance, and quality excellence, Sun Pharma is considered one of the most respected pharmaceutical companies in regulated markets like the US, Europe, and Japan. Sun Pharma Hiring for Executive Regulatory Affairs RD
The R&D facilities play a critical role in product development, regulatory strategy, and global dossier submissions, making this Executive – Regulatory Affairs role strategically important for new product approvals and life-cycle sustainability. Sun Pharma Hiring for Executive Regulatory Affairs RD
Organizational Philosophy – “Create Your Own Sunshine”
Sun Pharma follows a unique philosophy that encourages every employee to:
- Grow continuously and become better every day
- Take ownership of personal and professional development
- Work with confidence and accountability
- Thrive together through collaboration and teamwork
The organization strongly believes in nurturing talent through training, leadership development, and employee wellness programs, ensuring long-term professional success. Sun Pharma Hiring for Executive Regulatory Affairs RD
Position Overview – Executive – Regulatory and Business Continuity
The Executive – Regulatory Affairs will be responsible for managing new product regulatory submissions, approvals, and life-cycle management activities for drug products. The candidate will work closely with product development teams, cross-functional teams (CFTs), manufacturing units, and global regulatory authorities. Sun Pharma Hiring for Executive Regulatory Affairs RD
This role demands strong regulatory knowledge, dossier preparation expertise, and the ability to manage regulatory communications effectively. Sun Pharma Hiring for Executive Regulatory Affairs RD
Primary Job Responsibilities
The role broadly covers four critical regulatory areas:
1. New Submissions – Regulatory Strategy & Global Filings
The selected candidate will: Sun Pharma Hiring for Executive Regulatory Affairs RD
- Work closely with Product Development teams for Drug Products and other cross-functional teams within and outside R&D
- Ensure that sufficient and timely regulatory information, documentation, and controls are implemented during product design and development
- Provide early-stage feedback related to:
- Country-specific regulatory requirements
- Document expectations
- Filing strategies for new Drug Formulations (DF)
- Review and approve development documents on behalf of Regulatory Affairs
- Prepare, review, and submit high-quality dossiers to ensure:
- Faster regulatory approvals
- Timely commercial product launches
- Prepare and submit:
- Meeting packages
- Scientific discussion documents
- Regulatory briefing materials for agency interactions
- Anticipate expected regulatory deficiencies and proactively develop risk mitigation strategies
2. Approval Stage – Deficiency Response Management
The candidate will be responsible for:
- Preparing and submitting timely and scientifically sound responses to regulatory authority queries
- Coordinating with internal teams to collect required technical data
- Ensuring that deficiency responses are:
- Complete
- Accurate
- Submitted within regulatory timelines
- Supporting faster product approvals and regulatory clearances
3. Regulatory Life-Cycle Management for Approved Drug Products
The Executive will also manage the post-approval regulatory maintenance of products, including: Sun Pharma Hiring for Executive Regulatory Affairs RD
a. Annual Reports & Renewals
- Timely preparation and submission of:
- Annual regulatory reports
- Product renewals
- Post-marketing updates
b. Variations, Supplements & Change Management
- Evaluation, preparation, and submission of:
- Manufacturing changes
- Formulation updates
- Specification revisions
- Site transfers
- Handling:
- Variations
- Supplements
- Amendments that impact product supply
c. Regulatory Compliance
- Ensure that regulatory decisions related to:
- Change implementation
- Manufacturing updates
- Documentation changes
are implemented on time at Drug Formulation plants
d. Central Repository Management
- Ensure proper repositioning and maintenance of:
- Comprehensive product regulatory information
- Approved dossiers
- Commitment tracking documentation
into the central regulatory database
4. Self Development & Knowledge Enhancement
Sun Pharma strongly encourages continuous learning. The selected candidate will:
- Stay updated with:
- Global regulatory guidelines
- Emerging regulatory trends
- Changes in international regulatory frameworks
- Participate in:
- Internal technical discussions
- Training programs
- Regulatory knowledge-sharing sessions
- Deliver presentations to enhance organizational regulatory awareness
Educational Qualification Requirement
- Mandatory Qualification: Master of Pharmacy (M.Pharm)
- Specialization in Regulatory Affairs, Pharmaceutics, or related pharmaceutical disciplines is preferred.
Experience Requirement
- Minimum Experience: 2 Years
- Maximum Experience: 5 Years
- Candidates must have hands-on experience in regulatory submissions, approvals, and lifecycle management for drug products.
Key Skills Required
To succeed in this role, the candidate should possess:
- Strong understanding of:
- Global regulatory guidelines
- Drug product registration requirements
- Experience in:
- Dossier preparation and review
- eCTD / CTD formats
- Global submissions
- Ability to handle:
- Regulatory deficiencies
- Variations and supplements
- Strong documentation accuracy
- Excellent coordination with cross-functional teams
- Good written and verbal communication skills
- High level of attention to detail and compliance orientation
Job Location & Work Environment
- Location: Baroda (Vadodara), Gujarat
- Facility: Tandalja – R&D
- This facility is a high-end research environment focused on:
- Product development
- Regulatory submissions
- Global product support
- Offers professional exposure in:
- International regulatory affairs
- Global submission standards
- Data integrity systems
Travel Requirement
- Travel: Not Applicable
- This is a location-stable R&D and regulatory documentation role.
Career Growth Opportunities at Sun Pharma
Joining Sun Pharma as an Executive – Regulatory Affairs opens doors to:
- Senior Regulatory Affairs Executive
- Regulatory Manager
- Global Regulatory Strategy Lead
- Project Regulatory Head
- Regulatory Compliance & Intelligence Specialist
Sun Pharma provides structured career advancement through:
- Leadership development programs
- Functional skill enhancement
- International project exposure
- Long-term professional stability
Employee Benefits & Work Culture
Sun Pharma places employee well-being and growth at the center of its workplace strategy. Employees receive: Sun Pharma Hiring for Executive Regulatory Affairs RD
- Competitive compensation
- Performance-linked growth opportunities
- Professional training programs
- Leadership mentoring
- Collaborative and inclusive work culture
- Work-life balance in professional R&D environments
Employees are encouraged to grow not only professionally, but also personally through a supportive organizational ecosystem. Sun Pharma Hiring for Executive Regulatory Affairs RD
Who Should Apply for This Role
This position is best suited for:
- Regulatory professionals with 2–5 years experience
- M.Pharm graduates specializing in regulatory affairs
- Candidates experienced in:
- New submissions
- Post-approval regulatory management
- Professionals seeking long-term stability in a top pharmaceutical organization
Who Should Not Apply
- Freshers without regulatory experience
- Candidates without M.Pharm qualification
- Candidates from non-pharmaceutical regulatory backgrounds
- Professionals unwilling to work in a corporate R&D environment
Important Disclaimer
The above job description outlines the general nature and responsibilities of the role. The organization reserves the right to modify duties and responsibilities as per business requirements and organizational policies. Sun Pharma Hiring for Executive Regulatory Affairs RD
Why This Opportunity Is Valuable
This role provides:
- Direct exposure to global regulatory markets
- Involvement in new drug product approvals
- Participation in end-to-end product life-cycle management
- Opportunity to work with one of India’s top pharmaceutical R&D organizations
- Long-term career security in regulatory affairs
Regulatory Affairs professionals play a critical role in the pharmaceutical industry by ensuring that safe, high-quality, and compliant medicines reach patients worldwide. Sun Pharma Hiring for Executive Regulatory Affairs RD
How to Apply
Interested and eligible candidates can apply through the official Sun Pharmaceutical Industries Ltd career portal. Candidates are advised to: Sun Pharma Hiring for Executive Regulatory Affairs RD
- Apply only through authorized official platforms
- Upload updated resume with complete regulatory experience details
- Ensure accurate qualification and experience information
- Keep all academic and employment documents ready for verification
Applicants shortlisted by the recruitment team will be contacted for further interview and assessment rounds. Sun Pharma Hiring for Executive Regulatory Affairs RD
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