Are you passionate about ensuring the highest standards in pharmaceutical manufacturing? Viatris, a global leader in generic and branded generic drugs, including antiretrovirals (ARVs) for HIV/AIDS treatment, is hosting a walk-in recruitment drive for Quality Control (QC) and Quality Assurance (QA) positions at their Oral Solid Dosage (OSD) Manufacturing Facility in Nashik. This is your chance to join a company dedicated to improving global health through innovative pharmaceuticals. The recruitment event is scheduled for Sunday, September 14, 2025, at Fern Kesarval Hotel & Spa, Goa, from 10:00 AM to 3:00 PM. Explore exciting career opportunities in quality control and assurance with Viatris, a subsidiary of Mylan Laboratories Limited, now part of a globally renowned pharmaceutical powerhouse.
Job Responsibilities
As a QC/QA professional at Viatris’s Nashik facility, you will play a critical role in maintaining the quality and compliance of pharmaceutical products. Key responsibilities include:
- Quality Control (QC):
- Perform testing and analysis using advanced instruments like HPLC, GC, UV, IR, Dissolution, and Malvern Particle Sizer to ensure product quality.
- Conduct Microbiology analysis, including MLT testing and EM testing, for product safety.
- Maintain laboratory equipment calibration and ensure compliance with cGMP and GLP standards.
- Participate in OOS/OOT investigations, deviation reporting, and CAPA implementation using tools like Trackwise.
- Retain and review analytical records, logbooks, SOPs, and raw data sheets.
- Quality Assurance (QA):
- Oversee IPQA, QMS, documentation, and AQA processes to ensure regulatory compliance.
- Review and close OOS/OOT cases and monitor CAPA implementation.
- Support regulatory audits (e.g., FDA, MHRA) and ensure compliance with corrective actions.
- Maintain documentation as per GMP requirements and support quality management systems.
Qualifications
To excel in these roles, candidates should meet the following criteria:
- Education: M.Sc. (Chemistry), B.Pharm, or M.Pharm (Pharmaceutical Analysis).
- Experience: 1–4 years in Quality Control or Quality Assurance within a pharmaceutical manufacturing environment.
- Skills:
- Hands-on experience with HPLC, GC, UV, IR, Dissolution, LIMS, and other analytical instruments for QC roles.
- Proficiency in Microbiology analysis (MLT, EM testing) or CSV experience for QC roles.
- Expertise in IPQA, QMS, documentation, and AQA for QA roles.
- Candidates with experience in FDA or MHRA audits are preferred.
- Strong understanding of cGMP, GLP, and regulatory compliance.
Benefits of Joining Viatris
Working at Viatris offers more than just a job—it’s an opportunity to make a global impact. Benefits include:
- Career Growth: Access to learning and development programs to advance your pharmaceutical career.
- Global Exposure: Work with a leading pharmaceutical company known for its ARV innovations.
- Competitive Salary: Estimated salary range of INR 3,00,000–6,00,000 per annum, based on experience and qualifications.
- Supportive Environment: Collaborate with a team dedicated to quality and innovation in healthcare.
How to Apply
Join Viatris at their walk-in recruitment drive:
- Date: Sunday, September 14, 2025
- Time: 10:00 AM to 3:00 PM
- Venue: Fern Kesarval Hotel & Spa, Verna, Edapally–Panvel Hwy, Cortalim, Goa
- Requirements: Bring an updated resume, educational certificates, experience letters, and a valid ID. Be prepared for on-the-spot interviews and technical assessments.
- Note: Candidates with relevant qualifications and experience in QC/QA are encouraged to attend. For inquiries, visit Pharmabharat.com or contact Viatris directly.
FAQs
1. What types of roles are available at the Viatris Nashik recruitment drive?
The recruitment drive offers positions in Quality Control (Lab, Microbiology, CSV) and Quality Assurance (IPQA, Documentation, QMS, AQA) at the Nashik OSD facility.
2. Who can attend the walk-in interviews?
Candidates with 1–4 years of experience in QC/QA, holding an M.Sc. (Chemistry), B.Pharm, or M.Pharm (Pharmaceutical Analysis), and relevant skills in HPLC, GC, or regulatory audits are eligible.
