WALK-IN INTERVIEW – Multiple Openings in R&D & Quality Functions at Medreich Limited-12th July 2025

Medreich Limited

Website Medreich Limited

Join a leading global pharmaceutical company and accelerate your career in R&D, QC, and Manufacturing.

About Medreich Limited

Medreich Limited is a fully integrated pharmaceutical company with a strong global presence. Specializing in Contract Manufacturing (CMO) and Contract Development & Manufacturing (CDMO), we cater to diverse therapeutic categories. Our state-of-the-art Research & Development center is equipped with cutting-edge technology to develop patent non-infringing and niche generic formulations for regulated markets.

Medreich Limited, a fully integrated pharmaceutical organization with a robust global footprint, invites skilled professionals for multiple positions at its state-of-the-art facility in Bengaluru.


1. Analytical Research & Development (AR&D)

  • Qualification: M.Pharm / M.Sc

  • Experience: 2 to 6 Years

  • Key Responsibilities:

    • Analytical method development and validation

    • Stability and routine sample analysis

    • HPLC handling for Assay, Dissolution & Related Substances

    • Particle Size Distribution using particle sizer and microscopy


2. Formulation Research & Development (FR&D)

  • Qualification: M.Pharm

  • Experience: 2 to 6 Years

  • Key Responsibilities:

    • Conduct pre-formulation studies and R&D trials

    • Develop oral solid dosage forms (OSD) like tablets, capsules

    • Optimize formulations for regulatory compliance

    • Support technology transfer and collaborate with manufacturing teams


3. Pilot Plant Production

  • Qualification: B.Pharm / M.Pharm

  • Experience: 2 to 5 Years

  • Key Responsibilities:

    • Operate and manage OSD manufacturing (Granulation/Compression/Coating/Packing)

    • Ensure online documentation, calibration, and GMP compliance

    • Actively contribute to QMS and batch processing


4. Quality Control (QC)

  • Qualification: M.Pharm / M.Sc

  • Experience: 2 to 6 Years

  • Key Responsibilities:

    • Analysis of RM, PM, FP, stability samples using HPLC, GC, UV, FTIR

    • Instrument calibration and GLP/GMP compliance

    • Familiarity with regulatory audits: MHRA, TGA, PMDA Japan, Health Canada


Walk-in Interview Details

  • Date: 12th July 2025 (Saturday)

  • Time: 10:00 AM – 2:00 PM

  • Venue:
    Medreich Limited (R&D),
    Plot No. 36, Bommasandra Industrial Area,
    Anekal Taluk, Bommasandra, Bengaluru – 560099
    Landmark: Near Karnataka Bank, Jigani Road


Important Notes

  • Only candidates with 2–6 years of relevant experience will be considered.

  • Bring the following documents:

    • Updated CV

    • Highest qualification certificate

    • Latest CTC/Increment Letter

    • Last 3 months’ payslips


Step into a world of pharmaceutical innovation and be a part of Medreich’s journey to deliver excellence globally.

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