Medreich is a mature, export‑oriented Indian pharma company offering comprehensive CMO/CDMO services, backed by strong global regulatory credentials and deep strategic partnerships. Since joining Meiji Group, it’s consistently reinforced its global manufacturing and quality capabilities—making it a reputable choice for outsourced pharma development and manufacturing.
Walk in interview details:
Date:12-07-2025 (Saturday)
Time:10.00 a.m – 02.00 p.m
Location: Medreich Limited (R&D)
Plot No. 36, Bommasandra Industrial Area, Anekal Taluk, Bommasandra, Bengaluru – 560 099
E-mail: ashithkumar.sk@medreich.com/ swathi.sr@medreich.com
Land Mark: Near Karnataka Bank, Jigani Road
Note:
1. Only 2-6 Years of expereinced candidates are eligible for selection.
2. Candidates must carry their updated CVs, certificate of their highest qualification, latest CTC /
Increment letter and the latest three months pay slips
Requirement Details:
ANALYTICAL RESEARCH & DEVELOPMENT
Qualification: M. Pharma / M.Sc
Experience: 02 to 06 Years
Job Description : • Lab experience for Analytical Method Development, regular and stability sample analysis
• Handling of HPLC for Assay, Dissolution, Related substances tests for solid orals
• Lab experience for Analytical Method Validation
• Lab experience for Particles Size Distribution Analysis using Particle sizer and microscope.
FORMULATION RESEARCH & DEVELOPMENT
Qualification : M. Pharma
Experience : 02 to 06 Years
Job Description :• Perform pre-formulation studies, R&D trials and support scale-up activities
• Conduct R&D trials for oral solid dosage forms (tablets, capsules, etc.)
• Develop and optimize formulations to meet regulatory and quality requirements
• Document and analyze trial data to improve formulations
• Collaborate with cross-functional teams for technology transfer to manufacturing.
PILOT PLANT PRODUCTION
Qualification : B.Pharma / M. Pharma
Experience : 02 to 05 Years
Job Description: • Oral solid dosage manufacturing area arrangement, operation and technical knowledge in the area of Granulation / Compression / Coating / Packing or any two area’s online documentation, Daily calibrations, QMS activity involvement.
QUALITY CONTROL
Qualification : M.Pharma / M.Sc
Experience: : 02 to 06 Years
Job Description: • Analysis of RM/PM, in process, finished product, stability samples by using HPLC, GC, UVFTIR, etc., & OC Instruments calibration, Maintain the GLP/GMP in laboratory, Compliance to regulatory requirement for MHRA, TGA, Health Canada, PDMA Japan.
