B.Pharm/M.Pharm QA Officer – Medreich, Bangalore
Apply for QA Officer (Formulations) at Medreich, Bangalore. B.Pharm/M.Pharm, 2–4 yrs experience in solid oral pharma manufacturing.
Medreich, a prestigious Meiji Group Company, is seeking a dedicated Officer – Quality Assurance for its Formulations OSD Plant in Bangalore. This is a remarkable opportunity for professionals with expertise in pharmaceutical solid oral dosage manufacturing to contribute to high-quality, patient-centric healthcare products. Candidates who can join within 60 days and have strong knowledge of cGMP practices, IPQA, and documentation are encouraged to apply.
Company Overview
Medreich is part of the globally recognized Meiji Group, known for its commitment to innovation, quality, and patient safety in the pharmaceutical industry. The Bangalore-based formulations facility focuses on solid oral dosage (OSD) manufacturing, producing high-standard medicines for both domestic and international markets. With robust R&D, advanced manufacturing processes, and a culture of compliance, Medreich emphasizes excellence in pharmaceutical production and quality assurance.
Why Join Medreich?
- Access to state-of-the-art OSD manufacturing and QA labs
- Hands-on experience with Laurel MES and QLMS systems
- Exposure to global cGMP-compliant processes
- Opportunities for career advancement within the Meiji Group
Job Role & Responsibilities
The QA Officer – Formulations will play a pivotal role in maintaining quality standards across the OSD manufacturing plant. The candidate will ensure all in-process activities, documentation, and dispatch processes comply with cGMP and company SOPs.
Key Responsibilities:
- Dispensing & Manufacturing Oversight
- Execute dispensing activities accurately, ensuring proper weighing and formulation.
- Monitor and carry out in-process checks and line clearances.
- In-Process Quality Assurance (IPQA)
- Conduct sampling activities: in-process samples, validation samples, cleaning validation samples, and hold-time samples.
- Perform routine checks on shop floor operations for compliance with SOPs.
- Documentation & Record Management
- Review and execute manufacturing and packing records.
- Download and analyze electronic batch records using Laurel MES.
- Ensure accurate IPQA data entry in QLMS system.
- Dispatch & Data Handling
- Supervise dispatch activities to maintain quality integrity during distribution.
- Handle data loggers for environmental monitoring and stability studies.
- Compliance & cGMP Enforcement
- Ensure all online activities adhere to cGMP compliance standards.
- Act as a key quality control resource on the shop floor.
- Support audits, inspections, and quality reviews when required.
Eligibility / Qualifications
Educational Qualification:
- B.Pharm or M.Pharm (preferred in Pharmaceutical Quality Assurance, Industrial Pharmacy, or Pharmaceutics).
- Relevant coursework: Pharmaceutical Sciences, Formulations, Quality Assurance, Analytical Chemistry, GMP Compliance, Process Validation.
Experience:
- Minimum 2–4 years in pharmaceutical manufacturing, preferably in solid oral dosage (OSD) plants.
- Hands-on experience in IPQA, batch documentation, line clearance, sampling, and cGMP compliance.
Skills & Competencies:
- Strong knowledge of cGMP guidelines and SOPs
- Familiarity with Laurel MES, QLMS, and electronic batch records
- Excellent written and verbal communication
- Detail-oriented, analytical, and proactive in problem-solving
Location & Salary
Work Location:
- Bangalore, Karnataka – OSD Formulations Plant
Compensation & Benefits:
- Competitive industry salary (based on experience)
- Exposure to global pharmaceutical manufacturing standards
- Opportunity to work in a cGMP-compliant, technologically advanced environment
- Career growth potential within Medreich/Meiji Group
Application Process
Interested candidates can apply by sharing their CV to ramanatha.n@medreich.com with the subject line: "Officer-QA Bangalore".
Walk-in / Onboarding Details:
- Candidates ready to join within 60 days are preferred.
- Bring supporting documents such as academic certificates, experience letters, and identification proof for verification.
CTA: Don’t miss this opportunity to advance your career in a world-class pharmaceutical environment! Apply before the slots fill to secure your chance at Medreich, Bangalore.
FAQs
Q1: What are the key eligibility criteria?
- B.Pharm/M.Pharm with 2–4 years of experience in OSD pharmaceutical manufacturing.
Q2: Is prior experience in solid oral dosage mandatory?
- Yes, candidates with OSD formulation experience will be preferred.
Q3: What systems will the QA Officer work on?
- Laurel MES, QLMS, electronic batch records, and data loggers.
Q4: What is the typical career path after this role?
- QA Officer → Senior QA Officer → QA Executive → QA Manager → Site/Quality Head.
Q5: What documents should be submitted during application?
- CV, academic documents, experience letters, salary slips, and identification proof.
Q6: Is immediate joining required?
- Candidates who can join within 60 days will be prioritized.
Key SEO & High CPC Keywords Included
- Pharmaceutical QA Officer jobs
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LSI/semantic keywords:
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Vertical Summary Table
| Category | Details |
|---|---|
| Company | Medreich (Meiji Group Company) |
| Vacancies | Officer – Quality Assurance (Formulations OSD Plant) |
| Required Education | B.Pharm, M.Pharm |
| Experience | 2–4 years in pharmaceutical manufacturing (OSD preferred) |
