Sun Pharmaceutical Industries Ltd. has announced an Executive – Regulatory Affairs opportunity at its Panoli location in Gujarat. The position is part of the R&D1 Regulatory Affairs business unit and is intended for professionals with 4–6 years of relevant regulatory affairs experience.
Candidates with an M.Pharm or M.Sc qualification and experience in pharmaceutical regulatory documentation, GMP documentation, quality management systems, DMF submissions and international regulatory activities can consider this opportunity.
The role involves coordination of regulatory activities, document review, preparation and compilation of submission data, and interaction with plant and corporate regulatory teams for multiple international markets.
Sun Pharma’s current career listings also show Regulatory Affairs positions involving dossier preparation, regulatory submissions, lifecycle management and coordination with cross-functional teams, demonstrating the broader scope of regulatory functions within the company’s R&D organization.
Sun Pharma Regulatory Affairs Job Details
| Particular | Details |
|---|---|
| Company | Sun Pharmaceutical Industries Ltd. |
| Job Title | Executive – Regulatory Affairs |
| Business Unit | R&D1 Regulatory Affairs |
| Job Grade | G12A |
| Location | Panoli, Gujarat |
| Experience | 4–6 years |
| Qualification | M.Pharm / M.Sc |
| Employment Type | Full-time |
| Travel | Not Applicable / NA |
| Job Posted | September 22, 2026 |
Job Responsibilities
The selected candidate will be responsible for supporting regulatory affairs activities associated with pharmaceutical manufacturing and international submissions.
Key responsibilities include:
- Reviewing and maintaining GMP-related documents.
- Coordinating Quality Management System (QMS) activities, including change controls and related processes.
- Reviewing and approving regulatory and technical documents such as SOPs and STPs.
- Reviewing, following up and compiling data required for USDMF, CEP, DCP, CP and MRP submissions.
- Supporting new DMF submissions as well as DMF amendments and updates according to plans from Corporate Regulatory Affairs.
- Coordinating regulatory documentation and data for submissions involving markets such as Japan, China, Australia (TGA), Canada and other regulated markets.
- Compiling raw data required for registration and re-registration activities.
- Supporting responses to regulatory queries received from international markets.
- Preparing and compiling information for markets including China, Korea, Taiwan, Indonesia and South Africa.
- Coordinating with the plant regulatory team for planning and execution of regulatory activities.
- Tracking regulatory deliverables against agreed timelines.
- Following up with relevant stakeholders to ensure required documents and data are available for submissions.
Educational Qualification
Candidates applying for the Executive – Regulatory Affairs position should have:
- M.Pharm, or
- M.Sc
Relevant pharmaceutical, chemistry, life-science or regulatory affairs experience is particularly applicable to the responsibilities described in the vacancy.
Experience Required
The position requires 4–6 years of relevant experience.
Candidates with experience in areas such as:
- Pharmaceutical Regulatory Affairs
- DMF submissions
- Regulatory documentation
- GMP documentation
- QMS and change control
- CMC documentation
- International regulatory submissions
- Registration and re-registration
- Regulatory query responses
- Dossier compilation
- Plant Regulatory Affairs
may find their experience relevant to this position.
Skills Relevant to the Role
The following skills are particularly relevant to this Regulatory Affairs Executive job:
- Regulatory documentation review
- DMF management
- GMP documentation
- QMS coordination
- Change control management
- Regulatory submission planning
- Dossier compilation
- International regulatory requirements
- CMC documentation
- Cross-functional coordination
- Regulatory query management
- Project and timeline management
- Attention to detail
- Written and verbal communication
International Regulatory Exposure
One notable aspect of this Sun Pharma Regulatory Affairs vacancy is its exposure to multiple international regulatory markets.
The job description specifically references activities associated with markets including:
- United States
- Europe
- Japan
- China
- Australia
- Canada
- Korea
- Taiwan
- Indonesia
- South Africa
The position therefore involves regulatory documentation and submission support across multiple jurisdictions rather than being limited to domestic regulatory activities.
Salary
Salary has not been disclosed in the supplied Sun Pharma job description.
For SEO purposes, Pharmabharat should avoid presenting an estimated salary as the employer’s confirmed compensation. Google specifically states that baseSalary in JobPosting structured data should represent the actual salary provided by the employer, rather than an estimate.
Therefore, candidates should verify the compensation package directly during the recruitment process.
Benefits and Career Opportunities
The supplied vacancy states that Sun Pharma focuses on professional growth, collaboration and employee development.
Sun Pharma’s careers information also highlights training, development and career guidance opportunities for employees.
For an experienced Regulatory Affairs professional, this type of role can provide exposure to:
- International regulatory submissions
- Pharmaceutical manufacturing regulations
- DMF lifecycle activities
- GMP and QMS processes
- Cross-functional regulatory coordination
- Multiple international markets
- Regulatory documentation and compliance
Who Can Apply?
This opportunity is particularly relevant for professionals who meet the following profile:
Qualification: M.Pharm / M.Sc
Experience: 4–6 years of relevant experience
Domain: Pharmaceutical Regulatory Affairs
Location: Panoli, Gujarat
Candidates should carefully compare their experience with the responsibilities listed in the official vacancy before applying.