Sun Pharma Walk-in Drive for Quality Control, Quality Assurance, Production, and Engineering Roles on 25th May

Sun Pharmaceutical Industries Ltd., the world’s fourth-largest specialty generic pharmaceutical company and India’s largest pharmaceutical enterprise, is renowned for delivering high-quality medicines trusted in over 150 countries. With multiple state-of-the-art manufacturing facilities and R&D centers, we are committed to innovation and excellence.

We are hosting a walk-in interview on May 25, 2025, in Rangpo, Sikkim, for roles at our advanced Guwahati, Assam formulation plant. Join our team to contribute to our mission of enhancing global healthcare!

Note: Candidates must have experience in pharmaceutical formulations (OSD or sterile injectables). API-only experience is not eligible. Sun Pharma does not charge any fees for job applications. Beware of fraudulent invitations requesting payment; contact AKASH.GOGOI@SUNPHARMA.COM for verification.

Interview Details

• Date: Sunday, May 25, 2025
• Time: 9:30 AM to 4:30 PM
• Venue: Eco Paradise Resort, Rangpo, Sikkim
• Requirements: Bring updated resume, last 3 months’ salary slips, appointment letter/last increment letter, qualification documents, PAN card, and Aadhar card.
• Unable to Attend? Email your CV to AKASH.GOGOI@SUNPHARMA.COM. Mention the position and department in the subject line (e.g., “QC Officer Application”).
• Contact: +91 8473959757
• Website: Sun Pharma

Available Positions

1. Quality Control (QC)

• Position: Officer / Sr. Officer / Executive / Sr. Executive
• Qualification: B.Sc / M.Sc (Chemistry) / B.Pharm / M.Pharm
• Experience: 2-12 Years

Desired Exposure:

• Expertise in HPLC, GC, stability studies, and finished product analysis.
• Proficiency in analytical instruments (e.g., UV, FTIR, dissolution, KF titrator) and software like Empower.
• Conduct method validation, method transfer, and stability sample analysis per ICH guidelines.
• Manage OOS, OOT, deviations, CAPA, and QMS documentation.
• Ensure compliance with cGMP, USFDA (21 CFR Part 210, 211), and WHO-GMP standards.
• Support regulatory audits and instrument calibrations (IQ, OQ, PQ).

2. Quality Assurance (QA)

• Position: Officer / Sr. Officer / Executive / Sr. Executive
• Qualification: B.Pharm / M.Pharm
• Experience: 2-12 Years

Desired Exposure:

• Perform IPQA activities, including line clearance, in-process checks, and batch record reviews.
• Handle QMS, deviations, CAPA, market complaints, and APQR preparation.
• Support process validation, cleaning validation, and regulatory audits (USFDA, WHO).
• Ensure compliance with cGMP and SOPs for OSD and sterile formulations.

3. Production (Injectable)

• Position: Technician / Officer / Sr. Officer / Executive / Sr. Executive
• Qualification: ITI / Diploma / D.Pharm / B.Pharm / M.Pharm
• Experience: 2-10 Years

Desired Exposure:

• Manage manufacturing activities for sterile formulations (e.g., ampoules, vials, PFS).
• Operate equipment like autoclaves, filling machines, and lyophilizers.
• Handle BMR/BPR documentation, media fills, and aseptic process validations.
• Ensure compliance with cGMP and sterile manufacturing standards.

4. OSD Production (Manufacturing/Packing/Warehouse)

• Position: Technician / Officer / Sr. Officer / Executive
• Qualification: ITI / Diploma / D.Pharm / B.Pharm / M.Pharm
• Experience: 2-10 Years

Desired Exposure:

• Operate tablet/capsule manufacturing equipment (e.g., FBD, RMG, compression, coating machines like Fette, Sejong).
• Manage packing processes using strip/blister/BQS/cartonator/Ullman machines.
• Handle raw material dispensing, inventory control, and PPIC activities in the warehouse.
• Ensure compliance with cGMP, SOPs, and batch documentation.

5. Engineering (OSD/Sterile)

• Position: Technician / Officer / Sr. Officer / Executive / Sr. Executive
• Qualification: ITI / Diploma / B.Tech / M.Tech
• Experience: 2-10 Years

Desired Exposure:

• Maintain and troubleshoot process engineering systems for OSD and sterile (non-OSD) facilities.
• Manage water systems, HVAC, electrical systems, and utility equipment.
• Perform equipment qualifications (DQ, IQ, OQ, PQ) and preventive maintenance.
• Ensure compliance with cGMP and safety standards during regulatory audits.

Why Join Sun Pharma?

• Global Leader: Work with the world’s fourth-largest generic pharmaceutical company, trusted in 150+ countries.
• Innovative Environment: Contribute to cutting-edge OSD and sterile formulation manufacturing in a state-of-the-art Guwahati facility.
• Career Growth: Access world-class training, mentorship, and career advancement opportunities.
• Benefits: Competitive salary, health insurance, performance incentives, and a supportive work culture (rated 3.7/5 for job security on AmbitionBox).

Learn more about our mission at Sun Pharma and industry standards at USFDA or WHO.

How to Apply

• Attend the Walk-in: Bring all required documents to Eco Paradise Resort, Rangpo, Sikkim, on May 25, 2025.
• Email Application: If unable to attend, send your CV to AKASH.GOGOI@SUNPHARMA.COM.
• Stay Updated: Follow #PharmaJobs and #GuwahatiJobs on X.com for the latest pharmaceutical career opportunities.

Join Sun Pharma to drive innovation and quality in global healthcare!