Medreich Hiring FR&D, QC, Production, IPQA
- Company Overview
- Job Role & Responsibilities
- FR&D (Solid Orals)
- Quality Control – Officer/Executive
- Production – Officer/Executive
- IPQA & Documentation
- Eligibility / Qualifications
- Location & Salary
- Application Process
- FAQs
- Summary Table
Medreich Pharma FR&D, QC, Production Vacancies – Bangalore
Hiring experienced FR&D, QC, Production, IPQA professionals in Bangalore. Apply now for formulation roles at Medreich Pharma.
Medreich Pharma, part of the Meiji Group, is expanding its formulation operations and is hiring experienced professionals across FR&D, Quality Control, Production, and IPQA. These openings focus on solid oral dosage (OSD) manufacturing and suit candidates with strong technical expertise in formulation development, analytical methods, and shop-floor operations.
Company Overview
Medreich Pharma is a Meiji Group company known for its global footprint in pharmaceutical development and contract manufacturing. The company has a strong presence in regulated markets and a reputation for delivering high‑quality formulations. Its Bangalore facility supports advanced R&D, quality operations, and large‑scale production across solid oral dosage forms.
Job Role & Responsibilities
FR&D (Solid Orals)
- Lead formulation development for solid oral dosage forms
- Design and optimize formulations for regulated markets
- Oversee scale‑up, tech transfer, and documentation
- Ensure compliance with regulatory and quality standards
Quality Control – Officer/Executive
- Perform analysis of raw materials, finished products, and stability samples
- Conduct dissolution testing, HPLC, and GC analysis
- Prepare and review analytical documentation and reports
- Support investigations, OOS/OOT, and method validation
Production – Officer/Executive
- Handle granulation, compression, and packing operations
- Monitor routine production activities and ensure batch compliance
- Coordinate with QA, engineering, and planning teams
- Maintain GMP documentation and operational SOPs
IPQA & Documentation
- Perform in‑process checks for solid oral dosage manufacturing
- Review BMRs, documentation, and compliance records
- Ensure adherence to quality systems and regulatory requirements
- Coordinate with production and QC for real‑time quality control
Eligibility / Qualifications
- FR&D: 8–15 years experience in solid orals formulation development
- QC: Experience in formulation analysis, dissolution, raw material testing, HPLC, GC
- Production: Experience in granulation, compression, packing
- IPQA & Documentation: 2–4 years experience in solid orals
- Education: B.Pharm, M.Pharm, M.Sc (Pharmaceutical Sciences, Chemistry, Industrial Chemistry, Analytical Chemistry), or related disciplines
Location & Salary
- Location: Bangalore
- Candidates who can join within 30 days are preferred
- Salary: Not disclosed (industry‑aligned compensation)
Application Process
Interested and eligible candidates can apply by sending their updated CV to:
vineeta.k@medreich.com
FAQs
1. Who can apply for these roles?
Experienced pharma candidates with solid oral dosage background in FR&D, QC, Production, or IPQA.
2. Is fresher eligibility available?
No. These openings require relevant industry experience.
3. What is the preferred location?
Bangalore‑based candidates or those willing to relocate and join within 30 days.
4. Are these full‑time positions?
Yes, all roles are full‑time.
5. What analytical skills are required for QC roles?
HPLC, GC, dissolution testing, stability studies, and raw material analysis.
Summary Table
| Category | Details |
|---|---|
| Company | Medreich Pharma (Meiji Group) |
| Vacancies | FR&D, QC, Production, IPQA |
| Required Education | B.Pharm, M.Pharm, M.Sc |
| Experience | 2–15 years depending on role |
To apply for this job email your details to vineeta.k@medreich.com