Career Opportunity: Walk-in Interviews for Experienced Pharmaceutical Professionals
A leading pharmaceutical company, part of the distinguished Meiji Group, is hosting a significant walk-in interview for experienced professionals. This recruitment drive is specifically for roles in Quality Assurance (QMS), Validation & Qualification, and In-Process Quality Assurance (IPQA) at its Unit VII manufacturing facility located near Bengaluru, Karnataka. Experienced candidates with 2-10 years in the pharmaceutical industry are encouraged to attend this event on Saturday, 25th July 2026.
About the Company
As a globally recognized pharmaceutical entity within the Meiji Group, the company specializes in the development, manufacturing, and marketing of high-quality pharmaceutical formulations. It boasts state-of-the-art manufacturing facilities that comply with stringent international regulatory standards, serving both regulated and emerging markets. The organization is renowned for its steadfast commitment to quality, innovation, and the professional development of its employees.
Available Positions and Requirements
The walk-in interview targets several key roles, each requiring specific qualifications and experience:
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Quality Assurance – QMS (2 Vacancies)
- Qualification: B.Pharm / M.Pharm
- Experience: 6–10 Years
- Key Responsibilities: Reviewing and closing OOS (Out-of-Specification), OOT (Out-of-Trend), and laboratory incident investigations; managing deviation activities; participating in Root Cause Investigation (RCI) and CAPA (Corrective and Preventive Actions) tracking; ensuring compliance with current Good Manufacturing Practices (cGMP) and quality management systems.
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Validation & Qualification (3 Vacancies)
- Qualification: B.Pharm / M.Pharm (generally expected)
- Experience: 4–7 Years
- Key Responsibilities: Managing the complete lifecycle of Equipment Qualification (Installation Qualification, Operational Qualification, Performance Qualification – IQ/OQ/PQ); performing Process Validation activities; tracking validation samples and ensuring meticulous documentation; participating in root cause investigations and CAPA implementation; ensuring adherence to global regulatory requirements.
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IPQA (In-Process Quality Assurance) (4 Vacancies)
- Qualification: B.Pharm / M.Pharm (typically required)
- Experience: 2–4 Years
- Key Responsibilities: Conducting line clearance activities before production; performing real-time monitoring of manufacturing and packing operations; carrying out in-process quality checks including weight, hardness, friability, and leak tests; reviewing Batch Manufacturing Records (BMR) and Batch Packing Records (BPR); identifying, documenting, and escalating shop-floor deviations; ensuring strict adherence to GMP and established quality procedures.
Required Skills include expertise in Quality Assurance, Quality Management Systems (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, and Pharmaceutical Manufacturing.
Walk-in Interview Details
- Date: 25th July 2026 (Saturday)
- Time: 9:00 AM – 12:30 PM
- Venue: Medreich Limited (Unit VII), Survey No. 11–15, Poojaramanahalli Village, Hosakote Taluk, Bengaluru Rural – 562114, Karnataka.
Documents to Carry
All candidates attending the interview must bring the following documents: an updated Resume/CV, all educational certificates, experience certificates, latest salary slips (if applicable), a government-issued photo ID proof, and passport-size photographs.
Contact Information
For any inquiries, prospective candidates may reach out to Mr. Nagabhushan or Madhava BC. They can be contacted via phone at 080-40487395 / 396 / 397 or by email at nagabhushan.g@medreich.com and madhava.bc@medreich.com.
Why Join This Pharmaceutical Leader?
This presents an outstanding opportunity to join a globally recognized pharmaceutical company within the Meiji Group. It offers the chance to gain invaluable experience in internationally regulated manufacturing environments and to be exposed to advanced QMS, validation, qualification, and IPQA practices. The company fosters a professional work culture with a strong emphasis on quality and regulatory compliance, providing excellent prospects for long-term career growth and continuous learning in the dynamic pharmaceutical industry.
