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Published on: November 8, 2026
Sun Pharmaceutical Industries Ltd. has listed an opening for Executive – Regulatory Compliance at its Dewas manufacturing facility in Madhya Pradesh. The position requires 3+ years of experience, and a master’s degree is preferred.
The selected candidate will handle regulatory compliance activities for pharmaceutical products manufactured at the plant for export markets. The responsibilities include reviewing manufacturing and quality documents, monitoring regulatory approvals, managing change controls and deviations, and coordinating with different departments to fulfil regulatory commitments.
This opportunity may be relevant to professionals working in Regulatory Affairs, Regulatory Compliance and pharmaceutical Quality Assurance.
Looking for similar opportunities? Explore the latest Regulatory Affairs Jobs and QA/QC Jobs on Pharma Career Updates. Candidates preparing for regulatory roles can also practice using our Free Regulatory Affairs Mock Test with Certificate.
| Particulars | Details |
|---|---|
| Company | Sun Pharmaceutical Industries Ltd. |
| Position | Executive – Regulatory Compliance |
| Business Unit | RBC |
| Job Grade | G12A |
| Department | Regulatory Compliance |
| Location | Dewas, Madhya Pradesh |
| Work Location | Dewas SGO – Plant |
| Qualification | Master’s degree preferred |
| Experience | 3+ years |
| Application Mode | Online |
| Apply Link | Executive – Regulatory Compliance – Apply Online |
Search for More Jobs at Sun Pharma: Candidates interested in other openings can visit the official Sun Pharma Careers website and search for vacancies across different departments and locations.
The Executive – Regulatory Compliance position focuses on maintaining regulatory compliance at Sun Pharma’s Dewas manufacturing facility.
The selected professional will coordinate with relevant departments to ensure that manufacturing activities, product documentation and quality-related processes remain consistent with regulatory requirements and commitments made for export markets.
The work also involves reviewing operational documents, supporting regulatory submissions, monitoring approval implementation and providing regulatory inputs when changes are proposed in manufacturing processes, equipment, materials or quality systems.
According to the official job description, the selected candidate will handle the following activities:
| Area | Key Responsibilities |
|---|---|
| Plant Compliance | Manage regulatory compliance activities at the Dewas manufacturing facility. |
| Document Review | Review and approve manufacturing, packaging, stability and product specification documents. |
| Regulatory Samples | Arrange registration samples, placebos and working standards required for regulatory filings. |
| Vendor Compliance | Verify regulatory compliance requirements and vendor commitments. |
| RFC Review | Review RFCs to confirm regulatory compliance and supply continuation requirements. |
| Change Controls and Deviations | Review and approve change controls and deviations. |
| Regulatory Submissions | Support filings, deficiency responses, variations and annual updates. |
| Approval Tracking | Monitor regulatory approvals and ensure their implementation at the plant. |
| Quality Coordination | Participate in Quality Review Board meetings at manufacturing locations. |
| Regulatory Commitments | Coordinate with departments to fulfil regulatory commitments. |
| Business Continuity | Provide regulatory inputs for renewals, variations and changes involving manufacturing processes, equipment, materials and quality systems. |
The position involves reviewing manufacturing, packaging, stability and quality-related documentation. The company has specifically mentioned the following documents and activities:
| Document / Activity | Description |
|---|---|
| Formulation Order | Formulation-related manufacturing documentation. |
| Manufacturing Instructions | Instructions governing manufacturing operations. |
| Packaging Order and Instructions | Documents covering approved packaging operations. |
| PPQ Protocols and Reports | Process Performance Qualification documentation. |
| Stability Protocols | Documents describing stability study requirements. |
| Stability Termination Notes | Records related to the termination of stability studies. |
| API Specifications | Active Pharmaceutical Ingredient specifications. |
| Finished Product Specifications | Quality requirements for finished pharmaceutical products. |
| Raw Material Specifications | Specifications for materials used in manufacturing. |
| Packaging Material Specifications | Quality requirements for packaging materials. |
| Annual Product Review (APR) | Periodic review of product quality and manufacturing performance. |
| OOS and Trend Investigations | Out of Specification and trend investigation documentation. |
| Equipment Equivalence Certificates | Documents supporting equipment equivalence assessments. |
| Change Controls and Deviations | Records used to assess and document changes and deviations. |
Other activities include reviewing market diversion requests, material code transfers, exhibit batch destruction reports and conditional release documentation.
Why is this knowledge important?
Regulatory compliance at a pharmaceutical manufacturing site requires more than preparing registration dossiers. Manufacturing processes, product specifications, equipment, raw materials and quality systems must remain aligned with applicable regulatory approvals and commitments. This requires coordination between Regulatory Affairs, Quality Assurance and manufacturing teams.
The educational preference mentioned in the official job description is:
The published description does not specify a compulsory specialization or provide a complete list of eligible degree programmes. Candidates should check the official job page for any additional eligibility requirements.
This is an experienced-level opportunity rather than an entry-level position.
Candidates with relevant experience in Regulatory Affairs, plant-level regulatory compliance, pharmaceutical documentation or Quality Assurance may consider applying, subject to the company’s eligibility requirements.
This opening may be relevant to professionals with experience in the following areas:
| Relevant Experience | How It Relates to the Role |
|---|---|
| Regulatory Affairs | Understanding regulatory approvals, variations and commitments. |
| Regulatory Compliance | Monitoring compliance requirements at manufacturing sites. |
| Quality Assurance | Familiarity with GMP documentation, change controls and deviations. |
| Manufacturing Documentation | Reviewing manufacturing and packaging instructions. |
| Stability and Specifications | Understanding stability protocols and product specifications. |
| Quality Systems | Experience with investigations, documentation and compliance processes. |
Practical experience in pharmaceutical manufacturing documentation and regulatory coordination can be particularly useful for this position.
Interested and eligible candidates can apply online through the official Sun Pharma careers portal.
Follow these steps:
Read the complete job description and eligibility requirements.
Check whether your qualifications and experience match the position.
Update your resume with relevant regulatory and pharmaceutical industry experience.
Complete the online application process.
Direct Application Link: Apply Online – Executive – Regulatory Compliance, Dewas
Sun Pharma Careers Portal: Visit the Official Sun Pharma Careers Website
1. What position is available at Sun Pharma?
Sun Pharma has listed an opening for Executive – Regulatory Compliance at its Dewas manufacturing facility.
2. Where is this job located?
The position is based at Dewas SGO – Plant, Dewas, Madhya Pradesh.
3. How much experience is required?
The company has specified 3+ years of experience.
4. Is a master’s degree compulsory?
A master’s degree is preferred according to the published job description. No mandatory specialization is specified in the description.
5. Can freshers apply for this position?
The position requires 3+ years of experience, so it is not a fresher-level opportunity.
6. What are the main responsibilities of this role?
The major responsibilities include regulatory document review, plant compliance, change control approvals, deviation management, regulatory filing support and tracking the implementation of regulatory approvals.
7. Where can candidates find other Sun Pharma vacancies?
Candidates can visit the official Sun Pharma Careers portal to search for other available positions.
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