Mylan Laboratories Limited, a Viatris Company, has announced a Walk-In Recruitment Drive for experienced Quality Control (QC) and Quality Assurance (QA) professionals at its OSD Manufacturing Facility in Jadcherla, Telangana. Candidates holding M.Sc (Chemistry), B.Pharm, or M.Pharm qualifications with 3–8 years of pharmaceutical experience are invited to attend the recruitment drive on 9 August 2026.
This is an excellent opportunity for pharma professionals seeking QC Jobs in Telangana, QA Officer Jobs, Mylan Laboratories Careers, and Viatris Pharma Jobs 2026 in one of India’s leading pharmaceutical manufacturing facilities.
Mylan Laboratories Recruitment 2026 – Overview
| Particular | Details |
|---|---|
| Company | Mylan Laboratories Limited (A Viatris Company) |
| Facility | OSD Manufacturing Facility |
| Department | Quality Control (QC), Quality Assurance (QA) |
| Position | Officer / Executive |
| Qualification | M.Sc (Chemistry), B.Pharm, M.Pharm |
| Experience | 3–8 Years |
| Job Location | Jadcherla, Mahabubnagar, Telangana |
| Interview Type | Walk-In Interview |
| Walk-In Date | 9 August 2026 |
| Timing | 9:30 AM – 5:00 PM |
Available Positions
Quality Control (QC)
Openings are available in:
- Raw Material (RM)
- Packaging Material (PM)
- Stability
- Validation
- Finished Product (FP)
- Analytical Method Transfer
Quality Assurance (QA)
Openings in:
- IPQA (In-Process Quality Assurance)
Educational Qualification
Candidates should possess any of the following qualifications:
- M.Sc (Chemistry)
- B.Pharm
- M.Pharm
Experience Required
- Minimum: 3 Years
- Maximum: 8 Years
- Experience in pharmaceutical manufacturing and quality systems is preferred.
Key Responsibilities
Quality Control
- Perform analytical testing of raw materials, finished products, and stability samples.
- Conduct validation and analytical method transfer activities.
- Ensure compliance with GMP, GLP, and regulatory requirements.
- Prepare laboratory documentation and analytical reports.
- Handle laboratory instruments and troubleshoot analytical issues.
Quality Assurance
- Perform IPQA activities during manufacturing operations.
- Review batch manufacturing and packaging records.
- Monitor GMP compliance across manufacturing areas.
- Participate in deviation investigations, CAPA, and change control.
- Support regulatory and internal audits.
Preferred Skills
- Good Manufacturing Practices (GMP)
- GLP Documentation
- Analytical Method Validation
- Pharmaceutical Quality Systems
- Stability Testing
- Documentation Compliance
- Investigation & CAPA
- Strong communication skills
- Teamwork and problem-solving abilities
Walk-In Interview Details
Date: 9 August 2026
Time: 9:30 AM – 5:00 PM
Venue:
Mylan Laboratories Limited (A Viatris Company)
S-16 & 17/A, SEZ, Green Industrial Park, Polepally (V),
Jadcherla (M), Mahabubnagar District, Telangana
