Exciting pharma jobs in Gujarat! RPG Life Sciences Ltd is conducting a walk-in interview on March 8, 2026, for Executive/Sr. Executive roles in Production, Packing, Quality Assurance, Quality Control, and Engineering departments at its Formulation Manufacturing Plant in Ankleshwar.
Ideal opportunity for experienced professionals in regulatory-approved pharma plants seeking pharmaceutical careers in India.
About the Company
RPG Life Sciences Limited, a part of the renowned RPG Enterprises group, is an integrated, research-based pharmaceutical company established in 1968. Headquartered in Mumbai, it specializes in branded formulations, global generics, and synthetic APIs, with a strong focus on quality, affordable medicines in therapeutic areas including immunosuppressants and general categories.
The company operates multi-location manufacturing facilities, including state-of-the-art formulation plants at Ankleshwar (Gujarat) that hold approvals such as EU GMP, WHO GMP, TGA GMP, and Schedule M. With a commitment to innovation, regulatory compliance, and global markets, RPG Life Sciences delivers trusted products domestically and internationally while fostering professional growth in a dynamic pharma environment.
Job Details
- Company Name: RPG Life Sciences Ltd
- Experience: 1–10 years (varies by role)
- Qualification: B.Sc./M.Sc. / B.Pharm / M.Pharm / B.E. (Instrumentation)
- Location: Ankleshwar, Gujarat
- Work Type: On-site (Formulation Plant)
Job Description
RPG Life Sciences is hiring experienced candidates for its Ankleshwar formulation plant, focusing on OSD (Oral Solid Dosage) operations in a regulatory-approved environment (EU GMP, WHO GMP, TGA).
These Executive/Sr. Executive positions require hands-on expertise in manufacturing, quality systems, instrumentation, and GMP documentation. Only candidates with exposure to regulatory audits and experience in approved pharma plants should apply.
Quality Control – Executive/Sr. Executive
- Department: Quality Control
- Role: Analysis and documentation in QC
- Experience: 2–10 years
- Education/Qualification: B.Sc./M.Sc.
- Vacancies: 10
Quality Assurance – Executive/Sr. Executive
- Department: Quality Assurance
- Role: IPQA, QMS, validation, and batch release
- Experience: 2–10 years
- Education/Qualification: B.Pharm / M.Pharm
- Vacancies: 6
Production – Executive/Sr. Executive
- Department: Production
- Role: Supervising OSD manufacturing processes
- Experience: 2–10 years
- Education/Qualification: B.Pharm / M.Pharm
- Vacancies: 6
Packing – Executive/Sr. Executive
- Department: Packing
- Role: Supervising blister/liquid packing operations
- Experience: 1–6 years
- Education/Qualification: B.Sc. / B.Pharm / M.Pharm
- Vacancies: 6
Engineering (Instrumentation) – Executive/Sr. Executive
- Department: Engineering
- Role: Instrumentation and plant maintenance in OSD
- Experience: 3–6 years
- Education/Qualification: B.E. Instrumentation
- Vacancies: 2
Skills / Qualifications
- Hands-on experience with instruments: HPLC, UV, Dissolution apparatus, GC, IR, AAS
- Proficiency in QMS documentation, analytical worksheets, and GMP review
- Exposure to IPQA, qualification/validation, Lab QA (AQA), vendor management, batch release
- Expertise in compression, granulation, coating, capsule filling, blister packing, liquid packing
- Troubleshooting and supervising OSD machinery (compression/granulation/coating/packing)
- Instrumentation knowledge for OSD plant equipment and GMP documentation
- Strong regulatory audit exposure in approved plants (EU GMP, WHO GMP, TGA)
- Pharma background with focus on quality, safety, and compliance
Key Responsibilities
- Analyze RM, in-process, finished, and stability samples using advanced instruments
- Review GMP documents, worksheets, and QC records
- Handle IPQA, QMS activities, qualification/validation, and vendor management
- Supervise and troubleshoot production machines (compression, granulation, coating, capsule filling)
- Manage packing operations for blister and liquid lines with documentation
- Perform instrumentation maintenance and calibration for OSD machinery
- Ensure GMP compliance and regulatory audit readiness
- Prepare and maintain batch-related documentation
Benefits / Perks
- Career growth in a reputed integrated pharma company
- Exposure to international regulatory standards and global markets
- Opportunities for skill enhancement in advanced formulation tech
- Stable work environment with focus on quality and innovation
- Competitive compensation and professional development
How to Apply
Attend the walk-in interview with:
- Copy of your resume
- Salary breakup / Last 3 months’ salary slips
- Passport-size photographs
- Copy of Aadhaar card
If unable to attend, email your resume to [email protected]. For more pharma jobs in Gujarat and updates, visit trusted platforms like Pharma Recruiter.
Walk-in Interview Details
- Date: March 8, 2026 (Sunday)
- Time: 10:00 A.M. to 04:00 P.M.
- Venue: RPG Life Sciences Ltd., Plot No. 3102/A, GIDC, Ankleshwar, Gujarat
Why You Should Join RPG Life Sciences
RPG Life Sciences offers a professional, research-driven culture with strong emphasis on quality, regulatory excellence, and employee development. As part of the established RPG Group, it provides long-term stability, exposure to global approvals, and the opportunity to contribute to high-quality, affordable medicines.
Professionals here benefit from a supportive environment, career progression, and the pride of working in a trusted pharmaceutical organization focused on innovation and patient health.
FAQs
Who is eligible for the RPG Life Sciences walk-in interview?
Experienced candidates (1–10 years) in pharma formulation plants with regulatory audit exposure; only those from approved plants (EU GMP/WHO GMP/TGA) should apply.
What documents are required for the walk-in?
Resume copy, salary breakup/last 3 months’ slips, passport photos, and Aadhaar copy.
Can I apply if I can’t attend the walk-in?
Yes—email your resume to [email protected].
What growth opportunities exist at RPG Life Sciences?
Excellent prospects in a growing integrated pharma company with international exposure, skill development, and roles in regulatory-compliant operations.