Medreich Limited (A Meiji Group Company) has announced a Walk-In Interview for experienced pharmaceutical professionals in Quality Assurance (QMS), Validation & Qualification, and IPQA departments. Candidates with B.Pharm or M.Pharm qualifications and relevant pharmaceutical manufacturing experience are invited to attend the interview at the company’s Unit VII facility in Bengaluru Rural.
If you are looking for Quality Assurance jobs in Bengaluru, Pharma Walk-In Interview 2026, or B.Pharm/M.Pharm jobs in Karnataka, this is an excellent opportunity to join one of India’s leading pharmaceutical manufacturing companies.
Medreich Limited Recruitment 2026 – Overview
| Particular | Details |
|---|---|
| Company | Medreich Limited (A Meiji Group Company) |
| Department | Quality Assurance (QMS), Validation & Qualification, IPQA |
| Job Type | Full-Time |
| Qualification | B.Pharm / M.Pharm |
| Experience | 2–10 Years |
| Interview Mode | Walk-In Interview |
| Walk-In Date | 25 July 2026 (Saturday) |
| Interview Time | 09:00 AM – 12:30 PM |
| Job Location | Bengaluru Rural, Karnataka |
Vacancy Details
1. Quality Assurance – QMS
Open Positions: 02
Qualification
- B.Pharm / M.Pharm
Experience
- 6–10 Years
Key Responsibilities
- Review and closure of OOS, OOT, and laboratory incidents.
- Investigation of quality events and deviations.
- Deviation management and documentation.
- Participate in root cause analysis.
- Track and monitor CAPA implementation.
- Ensure compliance with cGMP and regulatory requirements.
2. Validation & Qualification
Open Positions: 03
Experience
- 4–7 Years
Key Responsibilities
- Execute equipment qualification (IQ/OQ/PQ).
- Perform process validation activities.
- Ensure compliance with cGMP and global regulatory standards.
- Sample tracking and documentation.
- Timely closure of validation documents.
- Participate in CAPA and root cause investigations.
3. IPQA (In-Process Quality Assurance)
Open Positions: 04
Experience
- 2–4 Years
Key Responsibilities
- Conduct line clearance activities.
- Perform real-time monitoring of manufacturing and packaging operations.
- Carry out in-process quality checks including:
- Weight variation
- Hardness testing
- Friability testing
- Leak tests
- Review Batch Manufacturing Records (BMR).
- Review Batch Packing Records (BPR).
- Identify, document, and report deviations.
- Ensure compliance with GMP standards.
Required Qualification
Candidates should possess:
- B.Pharm
- M.Pharm
Experience Required
- IPQA: 2–4 Years
- Validation & Qualification: 4–7 Years
- QA-QMS: 6–10 Years
Skills Required
- Good Manufacturing Practices (cGMP)
- OOS & OOT Investigation
- Deviation Management
- CAPA Tracking
- Root Cause Analysis
- Equipment Qualification (IQ/OQ/PQ)
- Process Validation
- Batch Record Review
- Documentation Practices
- Regulatory Compliance
Walk-In Interview Details
Interview Date
25 July 2026 (Saturday)
Time
09:00 AM – 12:30 PM
Venue
Medreich Limited (Unit VII)
Survey No. 11-15,
Poojaramanahalli Village,
Hosakote Taluk,
Bengaluru Rural – 562114, Karnataka
Contact Details
Contact Persons
- Mr. Nagabhushan
- Madhava BC
