Medreich Limited, a Meiji Group company, has announced a Walk-in Drive for experienced pharmaceutical professionals. The company is inviting applications for Quality Control Analyst and Reviewer positions at its Unit 3, Bengaluru facility. Candidates with qualifications in B.Pharm, M.Pharm, or M.Sc Chemistry and relevant Quality Control experience are encouraged to attend the interview.

Job Overview

Particular Details

Company Name

Medreich Limited (Meiji Group)

Job Type

Walk-in Interview

Department

Quality Control (QC)

Job Location

Medreich Limited (Unit 3), Bengaluru, Karnataka

Walk-in Date

01 August 2026 (Saturday)

Interview Time

10:00 AM – 02:30 PM

Available Positions

1. Quality Control Analyst

Number of Positions: 08

Educational Qualification

M.Sc. Chemistry

B.Pharmacy (B.Pharm)

Experience

2–4 Years

Key Responsibilities

Perform analysis of raw materials, in-process samples, finished products, and stability samples.

Operate analytical instruments including HPLC, GC, Dissolution, and other QC equipment.

Ensure compliance with cGMP, GLP, and Data Integrity requirements.

Perform basic troubleshooting of analytical instruments.

Carry out calibration and verification of laboratory instruments.

2. Reviewer

Number of Positions: 03

Educational Qualification

M.Sc. Chemistry

B.Pharmacy (B.Pharm)

M.Pharmacy (M.Pharm)

Experience

5–8 Years

Key Responsibilities

Review analytical data with high accuracy.

Ensure compliance with cGMP, GLP, GDP, and Data Integrity guidelines.

Handle laboratory investigations, CAPA, analytical method validation, method transfer, and regulatory inspection activities.

Perform qualification and calibration of laboratory instruments.

Guide and monitor analysts through on-the-job training.

Lead investigations related to OOS, OOT, deviations, and laboratory incidents.

Walk-in Venue

Medreich Limited (Unit 3)

Survey No. 4/3, Avalahalli,

Anjanapura Post, Off. Kanakapura Road,

Bengaluru – 560062, Karnataka.

Contact Details

Contact Persons

Mr. Naveena

Ms. Kasturi KM

Email

naveena.at@medreich.com

kasturi.km@medreich.com

Skills Required

HPLC Operation

Gas Chromatography (GC)

Dissolution Testing

Analytical Method Validation

Laboratory Calibration

Data Integrity

cGMP Compliance

GLP & GDP Knowledge

CAPA Management

OOS & OOT Investigation

Documentation Practices

Regulatory Inspection Readiness

Documents to Carry

Candidates should carry:

Updated Resume/CV

Educational Certificates

Experience Certificates

Latest Salary Slip

Government Photo ID Proof

Passport-size Photographs

Why Join Medreich?

Opportunity to work with a reputed pharmaceutical company under the Meiji Group.

Exposure to advanced analytical laboratories.

Career growth in Quality Control and Analytical Research.

Professional work environment with regulatory compliance standards.

Opportunity to work with modern analytical instruments.

Technical FAQs

1. What analytical instruments should a QC Analyst be familiar with?

A QC Analyst should have practical knowledge of HPLC, GC, Dissolution Apparatus, UV-Visible Spectrophotometer, pH Meter, Karl Fischer Titrator, and other routine laboratory instruments.

2. What is the difference between OOS and OOT?

OOS (Out of Specification) occurs when test results fall outside predefined specifications, whereas OOT (Out of Trend) refers to results that remain within specifications but show unusual trends compared to historical data.

3. Why is Data Integrity important in pharmaceutical laboratories?

Data Integrity ensures that laboratory data is accurate, complete, consistent, attributable, legible, contemporaneous, original, and accurate (ALCOA+), meeting global regulatory requirements.

4. What is CAPA in pharmaceutical Quality Control?

CAPA (Corrective and Preventive Action) is a systematic process used to identify the root cause of quality issues, implement corrective actions, and prevent recurrence.

5. What are cGMP and GLP?

cGMP (Current Good Manufacturing Practices) ensures pharmaceutical products are consistently manufactured and controlled according to quality standards, while GLP (Good Laboratory Practices) governs laboratory testing procedures to ensure reliable and traceable results.