India's DMPLOI - Jobs & Networking AppRPG Life Sciences Limited, a part of the renowned RPG Enterprises Group, has announced a major recruitment drive for its Formulation Division located at Ankleshwar, Gujarat. The company is inviting experienced pharmaceutical professionals for multiple positions across Quality Control, Quality Assurance, Production, Packaging, Engineering, Stores, Technology Transfer, Operational Excellence, and EHS departments.
This walk-in interview presents an excellent opportunity for candidates with experience in OSD (Oral Solid Dosage) manufacturing and exposure to regulatory audits to join one of India’s leading pharmaceutical organizations.
About RPG Life Sciences
RPG Life Sciences is an integrated pharmaceutical company engaged in branded formulations, global generics, and synthetic APIs. The company operates in both domestic and international markets and is known for its strong focus on quality, innovation, and regulatory compliance.
Walk-In Interview Details
Particulars Details
Company Name
RPG Life Sciences Limited
Division
Formulation Manufacturing
Walk-In Date
21 June 2026 (Sunday)
Time
9:30 AM to 5:00 PM
Venue
The Aures, Padampura Circle, Station Road, Chhatrapati Sambhaji Nagar (Aurangabad), Maharashtra – 431005
Departments Hiring
1. Quality Control (QC)
Qualification: B.Sc / M.Sc
Designation: Executive / Senior Executive
Experience: 2–10 Years
2. Quality Assurance (QA)
Qualification: B.Pharm / M.Pharm
Designation: Executive / Senior Executive
Experience: 2–10 Years
3. Production
Staff
Qualification: B.Pharm / M.Pharm
Designation: Executive / Senior Executive
Experience: 2–8 Years
Operator
Qualification: ITI / D.Pharm
Designation: Junior Executive
Experience: 2–8 Years
4. Packaging
Staff
Qualification: B.Sc / B.Pharm / M.Pharm
Designation: Executive / Senior Executive / Assistant Manager
Experience: 2–15 Years
Operator
Qualification: ITI / D.Pharm
Designation: Junior Executive
Experience: 2–8 Years
5. Engineering
Instrumentation
Qualification: B.E Instrumentation
Experience: 4–15 Years
Mechanical/Electrical
Qualification: B.E Mechanical / Electrical
Experience: 4–15 Years
Operators
Qualification: ITI/Diploma (Electrical, Fitter, RFM, Instrumentation, HVAC)
Experience: 2–6 Years
6. Stores
Qualification: ITI / Diploma / Graduate
Experience: 2–15 Years
7. Technology Transfer
Qualification: M.Pharm / B.Pharm
Designation: Assistant Manager
Experience: 8–12 Years
8. Operational Excellence
Qualification: B.Pharm / M.Pharm / M.Sc / B.Tech
Designation: Assistant Manager
Experience: 8–12 Years
9. EHS (Environment, Health & Safety)
Qualification: Diploma/B.E Environmental or Chemical, B.Sc/M.Sc Chemistry with PDIETM
Designation: Executive / Senior Executive
Experience: 4–8 Years
Required Documents
Candidates attending the interview should carry:
Updated Resume/CV
Salary Breakup
Last Increment Letter
Last 3 Months Salary Slips
Passport Size Photograph
Aadhaar Card Copy
Candidates unable to attend the walk-in may share their resumes through the email mentioned in the advertisement.
Preferred Candidate Profile
RPG Life Sciences is specifically looking for professionals who have:
Experience in OSD manufacturing facilities
Exposure to regulatory inspections and audits
Knowledge of GMP, cGMP, and data integrity practices
Strong documentation and compliance skills
Team-oriented and quality-focused mindset
Why Join RPG Life Sciences?
Opportunity to work with a reputed pharmaceutical organization
Exposure to global regulatory standards
Career growth across manufacturing and quality functions
Professional work environment with advanced manufacturing facilities
Part of the well-established RPG Group
Technical FAQs
1. What is OSD manufacturing in the pharmaceutical industry?
OSD (Oral Solid Dosage) manufacturing involves the production of tablets, capsules, granules, and other solid oral dosage forms. It includes processes such as dispensing, granulation, compression, coating, encapsulation, and packaging.
2. What is the role of Quality Assurance in pharmaceutical manufacturing?
Quality Assurance ensures compliance with GMP guidelines, validates manufacturing processes, reviews batch records, manages deviations, conducts investigations, and maintains regulatory compliance throughout the product lifecycle.
3. Why is HVAC critical in pharmaceutical facilities?
HVAC systems maintain temperature, humidity, pressure differentials, and air cleanliness levels. Proper HVAC operation helps prevent contamination and ensures compliance with regulatory requirements.
4. What is Technology Transfer in pharmaceutical operations?
Technology Transfer is the systematic process of transferring product and process knowledge from R&D or one manufacturing site to another, ensuring consistent product quality and regulatory compliance.
5. What are regulatory audits in pharmaceutical manufacturing?
Regulatory audits are inspections conducted by agencies such as USFDA, MHRA, WHO, and other authorities to verify compliance with GMP requirements, quality systems, documentation practices, and manufacturing controls.
India's DMPLOI - Jobs & Networking App
Install Now
