Sun Pharma Recruitment Drive 2026: Openings in Quality Control, QA & Regulatory Affairs | Apply on Jobengine20
Sun Pharmaceutical Industries Ltd. is hosting a hiring drive for its flagship manufacturing and R&D facilities. They are actively seeking qualified professionals across Quality Control (QC), Quality Assurance (QA), and Regulatory Affairs (RA).
If you are looking to advance your career with India’s largest pharmaceutical company, review the position details below and submit your application.
๐ Quick Job Overview
| Parameter | Details |
|---|---|
| Company Name | Sun Pharmaceutical Industries Ltd. |
| Post Names | QC Analyst / QA Executive / RA Officer |
| Departments | Quality Control, Quality Assurance, Regulatory Affairs |
| Qualifications | B.Pharm / M.Pharm / M.Sc (Analytical / Organic Chemistry) |
| Experience | 1 to 7 Years (Freshers considered for entry-level trainees) |
| Work Location | Halol / Vadodara / Paonta Sahib / Dewas / Sikkim |
| Job Type | Full-Time, Permanent |
| Salary | Competitive (As per industry standards) |
๐ผ Department-Wise Job Requirements
1. Quality Control (QC Analyst / Executive)
- Education: M.Sc (Analytical Chemistry) / B.Pharm / M.Pharm
- Experience: 2 – 6 Years
- Key Responsibilities:
- Testing and analysis of Finished Products (FP), Raw Materials (RM), and Stability samples using HPLC, GC, UV, and IR equipment.
- Routine maintenance and calibration of analytical instruments.
- Adherence to cGMP, GLP, and electronic data integrity standards.
2. Quality Assurance (QA Executive)
- Education: B.Pharm / M.Pharm
- Experience: 2 – 5 Years
- Key Responsibilities:
- Managing Quality Risk Management (QRM), Incident handling, Deviations, CAPA, and Change Control.
- Conducting internal plant audits and ensuring line clearance across production areas.
- Reviewing electronic Batch Manufacturing Records (eBMR) and analytical data packets.
3. Regulatory Affairs (RA Officer / Executive)
- Education: M.Pharm (Regulatory Affairs / Pharmaceutics) / B.Pharm
- Experience: 1 – 4 Years
- Key Responsibilities:
- Preparation and submission of eCTD dossiers for USFDA, EMA, and ROW markets.
- Handling regulatory queries, deficiency letters, and lifecycle management of approved ANDAs/NDAs.
- Coordinating with cross-functional teams (R&D, QA, QC) to gather submission data.
๐ Required Application Documents
- Updated CV / Resume
- Educational Degrees & Transcripts
- Current Company Appointment Letter / Last Incremental Letter
- Last 3 Months' Pay Slips
- Government ID Proof (Aadhaar Card / PAN Card)
๐ฉ How to Apply via Jobengine20
- Email Application: Send your CV directly to
hr.recruitment@sunpharma.comwith the subject line: “Application for [Department] - [Total Experience] - Jobengine20”. - Official Portal: Apply online through the official careers portal at
sunpharma.com/careers.
๐จ Fraud Notice: Sun Pharma does not charge any application or recruitment fees at any stage. Beware of fraudulent emails or agents demanding payment.