Medley Pharmaceuticals Ltd., one of India’s leading pharmaceutical companies, has announced a walk-in interview for experienced professionals at its manufacturing facility in Daman. The company operates a USFDA, UK-MHRA, and WHO-GMP approved manufacturing site and is looking for skilled candidates in Quality Control and Packing departments.

This is an excellent opportunity for B.Pharm, M.Pharm, B.Sc, and M.Sc graduates seeking career growth in the pharmaceutical manufacturing industry.

Company Overview

Company Name: Medley Pharmaceuticals Ltd.
Industry: Pharmaceutical Manufacturing
Location: Daman, India
Regulatory Approvals: USFDA, UK-MHRA, WHO-GMP

Medley Pharmaceuticals is recognized among the top pharmaceutical companies in India and is known for maintaining high-quality manufacturing standards and regulatory compliance.

Available Positions

1. QC Officer (RM, PM, FP & Stability Section)

Experience Required: 2–6 Years

Qualification:

• B.Sc
• M.Sc
• B.Pharm
• M.Pharm

Job Responsibilities

• Raw Material (RM), Packing Material (PM), Finished Product (FP), and Stability Analysis
• HPLC (Chromeleon Software) operation and analysis
• Gas Chromatography (GC) analysis
• Analytical method execution and documentation
• GMP compliance and laboratory practices
• Data Integrity implementation
• Regulatory documentation and reporting

Required Skills

• Hands-on experience in HPLC and GC
• Knowledge of GMP guidelines
• Documentation and laboratory compliance
• Stability studies and analytical testing
• Data integrity and quality systems

2. Packing Officer / Supervisor (Tablet & Liquid)

Experience Required: 1–4 Years

Qualification:

• B.Pharm
• M.Sc
• B.Sc

Job Responsibilities

• Tablet and Liquid Packing Operations
• Primary and Secondary Packaging Activities
• Track & Trace System Management
• Serialization Process Handling
• Liquid Oral Formulation Packing
• Production and packing documentation

Required Skills

• Experience in pharmaceutical packaging operations
• Knowledge of serialization systems
• Understanding of packaging compliance
• Good documentation practices
• Team handling and operational coordination

Walk-In Interview Details

Interview Date: 11th October 2026

Interview Time: 09:00 AM to 02:00 PM

Interview Venue

Medley Pharmaceuticals Ltd.
Survey No. 378/7, 379/2 & 3,
Zari Causeway Road, Kachigam,
Daman (U.T.) – 396210

Application Process

Candidates unable to attend the walk-in interview may send their updated CV via email.

Email ID: keval@medleylab.com

Contact Number: 0260-7151400

Why Join Medley Pharmaceuticals?

• USFDA Approved Manufacturing Facility
• UK-MHRA & WHO-GMP Compliant Plant
• Career Growth Opportunities
• Learning & Development Programs
• Professional Working Environment
• Exposure to Global Regulatory Standards

Technical FAQs

1. What is the role of HPLC in pharmaceutical quality control?

HPLC (High Performance Liquid Chromatography) is used to identify, quantify, and verify the purity of pharmaceutical products, raw materials, and stability samples.

2. What is Stability Testing in pharmaceuticals?

Stability testing evaluates how a drug product maintains its quality, safety, and efficacy under different environmental conditions over time.

3. What is GMP compliance?

Good Manufacturing Practices (GMP) are quality guidelines ensuring pharmaceutical products are consistently produced and controlled according to regulatory standards.

4. What is Serialization in pharmaceutical packaging?

Serialization is the process of assigning a unique identification code to each product pack for traceability, anti-counterfeiting, and regulatory compliance.

5. What is Data Integrity in pharmaceutical manufacturing?

Data Integrity ensures that all records and electronic data are complete, accurate, consistent, and reliable throughout the product lifecycle.