About Company:
Mylan Laboratories Limited, now a subsidiary of Viatris, is a global pharmaceutical company with a strong focus on developing and manufacturing generic and branded generic drugs, including antiretrovirals (ARVs) for HIV/AIDS treatment. It was previously known as Matrix Laboratories before being acquired by Mylan NV in 2007. Mylan, and now Viatris, is a significant player in the global pharmaceutical market, particularly in the area of ARVs, where it is a leading manufacturer.
Mylan Laboratories Limited, now part of Viatris, is holding a recruitment drive for Quality Control (QC) / Quality Assurance (QA) positions at their OSD Manufacturing Facility in Nashik on Sunday, 14th September, 2025, from 10:00 AM to 15:00 PM.
Viatris is more than just a place to work. It’s a place where you can learn, grow and make an impact in the world. Mylan Laboratories Limited (A Viatris Company) is hiring for it’s OSD Manufacturing Facility at Nashik.
Recruitment Drive for Quality Control / Quality Assurance for Nashik Locations @ GOA.
Job Details:
- Department: QC / QA
- Experience: 1 to 4 years in QC / QA. QC (Competent to handle instruments like HPLC/GC/UV/Dissolution/IR)) QA (IPQA/QMS/Documentation / AQA)
- Qualification: M.Sc. (Chemistry) / B. Pharm / M. Pharm (Pharmaceutical Analysis)
Job Skills:
- Hands on experience in HPLC, GC, UV, IR, Dissolution, LIMS and other instrument analysis required for QC / Competent to perform Microbiology analysis like MLT testing and EM testing / CSV experience.
- IPQA, QMS, Documentation and AQA experience required for QA
- Candidate who have faced regulatory Audits like FDA & MHRA Audit will be preferred.
Walk-In Interview Details:
- Date: 14th Sep’ 2025
- Time: 10:00 Hrs. to 15:00 Hrs.
- Venue Location: Fern Kesarval Hotel & Spa, Verna, Edapally – Panvel Hwy, Cortalim, Goa.
We have Openings in Both QC (Lab / Microbiology / CSV) and QA(IPQA / Documentation / QMS / AQA) .
Seeking for candidates (Male/Female) with sound qualification background to ensure the testing of drug product in Quality control lab and to ensure every product is of the highest quality. They shall be concerned with sampling, specifications, testing, documentation, release procedures which ensure that the necessary and relevant tests are carried out under the norms of cGMP.
Role & responsibilities
- Candidate must have relevant experience in Quality control OSD and QMS and able to operate & maintain laboratory equipment/instruments (HPLC, GC, Malvern Particle sizer, dissolution apparatus etc.) as per procedure.
- To maintain documents as per GLP requirements.
- To ensure the calibration status of laboratory equipment & instruments.
- To report and involve in incidence/Deviation/OOS/OOT investigations.
- Candidate must have sound exposure in the Quality Control Laboratory to supervise and maintain documents and retention of records as per GMP requirements.
- To ensure the review of QC documents like analytical reports SOPS, Qualification, Logbooks, Raw data sheet, analytical records, calibration and ensuring compliance to observations with proper root cause and justifications.
- Candidates participate in initiation, review, and closure of OOS/OOT and monitor the CAPA with implementation in Track wise.
- To ensure the compliance of the Corrective and Preventive Actions (CAPA) necessitated through various activities such as Regulatory Audits, Market Complaints, and Product Recall & Annual Product Review in the QC if applicable.
- To support Quality Assurance / Compliance /Regulatory Systems, Processes and ensure Monitoring, Execution, Initiation of the Quality Management Systems in Quality Control laboratory.
