Medley Pharmaceuticals Ltd is conducting a Walk-in Interview Drive for experienced professionals in Quality Control (QC) roles at its Daman manufacturing facility. Being a USFDA, UK-MHRA, and WHO-GMP approved organization, Medley offers excellent career growth opportunities for candidates with strong expertise in stability studies and analytical testing.
Job Details
| Category | Details |
|---|---|
| Company Name | Medley Pharmaceuticals Ltd |
| Job Roles | Asst. Manager / Executive – QC Stability QC Officer – RM, FP & Stability |
| Department | Quality Control (QC) |
| Industry Type | Pharmaceuticals |
| Experience Required | 2 – 14 Years (Role-specific) |
| Salary Package | Not Disclosed |
| Job Location | Daman (U.T.) |
| Employment Type | Full-Time |
| Walk-in Date | 12th April 2026 (Sunday) |
| Interview Timings | 9:00 AM – 2:00 PM |
| Venue | Medley Pharmaceuticals Ltd, Survey No. 378/7, 379/2&3, Kachigam, Daman – 396210 |
| Contact Email | keval@medleylab.com |
| Contact Numbers | 0260-715400 / 0260-715408 |
Open Positions Breakdown
1. Asst. Manager / Executive – QC Stability Section
- Experience: 7 – 14 Years
- Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
Responsibilities:
- Preparation of stability protocols and reports
- Knowledge of ICH stability guidelines
- Stability data review and summary report preparation
- Monitoring of stability chambers
- Coordination with QC team for sample analysis
2. QC Officer – RM, FP & Stability Section
- Experience: 2 – 5 Years
- Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
Responsibilities:
- Analysis of raw materials, finished products, and stability samples
- Hands-on experience with HPLC (Chromeleon), GC
- Conduct QC testing and ensure compliance
Skills Required
- Strong knowledge of QC and stability studies
- Experience with HPLC, GC, and analytical instruments
- Understanding of ICH guidelines and GMP compliance
- Attention to detail and documentation skills
Key Highlights
- Work in a USFDA, UK-MHRA, WHO-GMP approved facility
- Opportunity for career growth in a reputed pharma company
- Exposure to global regulatory standards
Important Instructions
- Carry updated resume and required documents
- Candidates unable to attend can email their CV
- Ensure relevant QC/stability experience before applying
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