Attend Medreich Limited’s walk-in interview on August 2, 2025, in Bengaluru for roles in Quality Control, Engineering, and Production. OSD manufacturing experience required. Join a global leader in pharma!
Medreich Limited Walk-In Interview for Quality Control, Engineering & Production Roles – 2nd August 2025, Bengaluru
Medreich Limited, part of the global Meiji Group, is conducting a walk-in interview on Saturday, August 2, 2025, at its Bengaluru Unit III. With approvals from UK MHRA, Australia TGA, and EU-GMP, Medreich is a trusted manufacturer of oral solid dosage (OSD) formulations for global clients including GSK, Pfizer, and Novartis. This is a great opportunity to join a company delivering healthcare excellence to 54 countries worldwide.
📅 Walk-In Interview Details
- Date: Saturday, August 2, 2025
- Time: 10:00 AM to 2:00 PM
- Venue: Medreich Limited (Unit III), Survey No. 4/3, Avalahalli, Anjanapura Post, Off Kanakapura Road, Bengaluru – 560062
- Work Location: Medreich Limited, Bengaluru
- Contact Persons: Mr. Naveena / Ms. Hemavathi
- Email: naveena.at@medreich.com, hemavathi.r@medreich.com
👨🔬 Available Departments & Requirements
| Department | Qualification | Experience | Key Skills |
|---|---|---|---|
| Quality Control | M.Sc. (Chemistry), B.Pharm | 2–6 years | HPLC, GC, UV, IR, OOS/OOT, calibration, cGLP |
| Engineering | B.E., B.Tech (Instrumentation Engg.) | 4–8 years | HMI, PLC, SCADA, cGMP, maintenance, upgrades |
| Production | B.Pharm, M.Pharm | 2–5 years | Granulation, compression, tablet coating, cGMP |
🔍 Key Responsibilities
Quality Control (QC):
- Conduct physical and wet analysis of OSD products.
- Operate HPLC, GC, UV, and IR equipment.
- Handle OOS/OOT investigations and reagent standardization.
- Ensure data integrity and cGLP compliance.
Engineering:
- Manage operation/maintenance of HMI, PLC, SCADA systems.
- Oversee equipment upgrades in OSD manufacturing.
- Lead cross-functional teams in instrumentation and software.
Production:
- Manage granulation, compression, and coating processes.
- Maintain cGMP documentation.
- Support calibration, QMS activities, and regulatory audits.
🌟 Why Join Medreich Limited?
- Global Presence: Supplying quality medicines to 54+ countries.
- Trusted Partner: Manufacturing for top pharma brands like GSK, Novartis, and Pfizer.
- Career Growth: Opportunities in a USFDA, EU-GMP certified setup.
- Employee Satisfaction: Rated 3.9/5 on AmbitionBox with positive work-life balance.
- Attractive Salaries: ₹1–₹5 LPA based on role and experience.
📝 Required Documents for Walk-In
- Updated Resume
- Aadhaar and PAN Card
- Educational Certificates
- Increment Letter
- Last 3 Months’ Payslips
- Relieving/Service Certificates from Previous Companies
✅ Application Guidelines
- Email your CV with subject line mentioning the department to naveena.at@medreich.com or hemavathi.r@medreich.com.
- Walk-in candidates must carry all required photocopies.
- Preference given to candidates with OSD formulation experience and immediate joining availability.
⚠️ Important Disclaimer
Medreich Limited does not charge fees for job applications. Communications are only sent from @medreich.com domains. Do not trust any unauthorized job offers using Gmail/Yahoo. For concerns, report to info@medreich.com.
🧪 Career in OSD Manufacturing?
With increasing global pharmaceutical demand, OSD (oral solid dosage) production and quality roles are in high demand. Professionals with experience in HPLC, PLC systems, or cGMP can expect stable and growth-oriented careers in regulated environments.
🚀 Future with Medreich
Join Medreich Limited in Bengaluru on August 2, 2025, and step into a future of pharmaceutical innovation and quality. Whether you’re in Quality Control, Engineering, or Production, Medreich offers the perfect platform to grow. Apply at the walk-in or via email. Let’s Win Together.
