Medreich Limited (A Meiji Group Company) is conducting a Walk-in Interview for experienced professionals in Quality Assurance (QMS), Validation & Qualification, and IPQA at its Unit VII manufacturing facility near Bengaluru. This recruitment drive is open to candidates with 2–10 years of pharmaceutical experience. The walk-in interview will be held on 25th July 2026.
About Medreich Limited
Medreich Limited, a part of the Meiji Group, is a globally recognized pharmaceutical company specializing in the development, manufacturing, and marketing of high-quality pharmaceutical formulations. The company operates state-of-the-art manufacturing facilities compliant with international regulatory standards and serves regulated as well as emerging markets. Medreich is known for its strong focus on quality, innovation, and employee development.
Job Overview
| Particulars | Details |
|---|---|
| Company | Medreich Limited (A Meiji Group Company) |
| Departments | Quality Assurance (QMS), Validation & Qualification, IPQA |
| Employment Type | Full-Time |
| Industry | Pharmaceuticals |
| Job Location | Bengaluru Rural, Karnataka |
Open Positions
| Department | Qualification | Experience | Vacancies |
|---|---|---|---|
| Quality Assurance – QMS | B.Pharm / M.Pharm | 6–10 Years | 2 |
| Validation & Qualification | B.Pharm / M.Pharm* | 4–7 Years | 3 |
| IPQA | B.Pharm / M.Pharm* | 2–4 Years | 4 |
*The poster explicitly mentions B.Pharm/M.Pharm under QA-QMS. Validation and IPQA experience requirements are specified, and pharmaceutical qualifications are generally expected for these roles.
Key Responsibilities
Quality Assurance – QMS
- Review and close OOS, OOT, and laboratory incident investigations.
- Handle Deviation Management activities.
- Participate in Root Cause Investigation (RCI) and CAPA tracking.
- Ensure compliance with cGMP and quality management systems.
Validation & Qualification
- Manage the complete lifecycle of Equipment Qualification (IQ/OQ/PQ).
- Perform Process Validation activities.
- Track validation samples and ensure error-free documentation.
- Participate in root cause investigations and CAPA implementation.
- Ensure compliance with global regulatory requirements.
IPQA
- Conduct line clearance activities before production.
- Perform real-time monitoring of manufacturing and packing operations.
- Carry out in-process quality checks, including weight, hardness, friability, and leak tests.
- Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
- Identify, document, and escalate shop-floor deviations.
- Ensure adherence to GMP and established quality procedures.
Required Skills
- Quality Assurance
- Quality Management System (QMS)
- OOS & OOT Investigation
- Deviation Management
- Root Cause Analysis (RCA)
- CAPA
- Equipment Qualification (IQ/OQ/PQ)
- Process Validation
- IPQA
- Line Clearance
- BMR & BPR Review
- In-Process Quality Checks
- Documentation Compliance
- cGMP
- Pharmaceutical Manufacturing
Walk-in Interview Details
| Particulars | Information |
|---|---|
| Interview Date | 25th July 2026 (Saturday) |
| Interview Time | 9:00 AM – 12:30 PM |
| Interview Venue | Medreich Limited (Unit VII), Survey No. 11–15, Poojaramanahalli Village, Hosakote Taluk, Bengaluru Rural – 562114, Karnataka |
Documents to Carry
Candidates should bring:
- Updated Resume/CV
- Educational Certificates
- Experience Certificates
- Latest Salary Slips (if applicable)
- Government-issued Photo ID Proof
- Passport-size Photographs
Contact Details
| Details | Information |
|---|---|
| Contact Persons | Mr. Nagabhushan / Madhava BC |
| Phone | 080-40487395 / 396 / 397 |
| nagabhushan.g@medreich.com | |
| madhava.bc@medreich.com |
Why Join Medreich Limited?
- Work with a globally recognized Meiji Group pharmaceutical company.
- Gain experience in internationally regulated manufacturing and quality systems.
- Exposure to advanced QMS, validation, qualification, and IPQA practices.
- Professional work environment with strong emphasis on quality and regulatory compliance.
- Excellent opportunities for long-term career growth and continuous learning in the pharmaceutical industry.
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