Mylan Laboratories (Viatris) Recruitment Drive for Quality Control at Nashik Facility – Indore Interview

Join Viatris, a global healthcare leader formed in 2020 through the merger of Mylan Laboratories Limited and Pfizer’s Upjohn unit. With a presence in 165+ countries, Viatris operates a USFDA, WHO-GMP, and ISO 9001:2015-certified Oral Solid Dosage (OSD) manufacturing facility in Nashik, Maharashtra, producing tablets and capsules for markets like the US, EU, and Emerging Markets.

We’re hosting a recruitment drive in Indore for Quality Control (QC) professionals to support our Nashik facility, focusing on analytical excellence in pharmaceutical manufacturing.

Event Details: Recruitment Drive

This recruitment drive targets QC professionals with 2-6 years of experience for our Nashik OSD facility. The walk-in interview will be held in Indore, with candidates expected to work at Nashik post-selection.

Date and Time

• Date: Sunday, May 18, 2025
• Time: 10:00 AM – 3:00 PM IST

Venue

The Red Maple Hill Hotel
Jhoomer Ghat, Rasalpura Rau, Indore, Madhya Pradesh – 453331

Job Location

• Mylan Laboratories Limited (A Viatris Company), Plot No. H-1, MIDC, Malegaon, Sinnar, Nashik, Maharashtra – 422113

Job Opportunity: Quality Control (QC)

We’re hiring QC Officers and Executives to ensure product quality at our Nashik facility, a Zero Liquid Discharge (ZLD) site compliant with cGMP standards.

Position

• Officer / Executive – Quality Control

Department

• Quality Control (OSD Manufacturing)

Qualification

• M.Sc. (Chemistry)
• B.Pharm
• M.Pharm (Pharmaceutical Analysis preferred)

Experience

• 2-6 years in Quality Control within USFDA/MHRA-regulated OSD facilities

Number of Openings

• Multiple (likely 4-6 based on typical QC hiring drives)

Key Responsibilities

• Analytical Testing:
  • Analyze raw materials, in-process samples, finished products, and stability samples using HPLC, GC, UV, IR, and Dissolution testers
  • Perform method validation and transfer per ICH Q2(R1)
• Compliance:
  • Ensure adherence to cGMP, GLP, and USFDA/MHRA standards
  • Maintain accurate documentation in LIMS and quality reports
• Investigations:
  • Conduct OOS/OOT investigations and implement CAPA
  • Support laboratory deviation analysis and root cause identification
• Audit Support:
  • Prepare for and participate in regulatory audits (USFDA, MHRA)
  • Address audit findings related to analytical processes
• Instrument Handling:
  • Operate and maintain analytical instruments (HPLC, GC, UV, IR, Dissolution)
  • Calibrate equipment and ensure operational efficiency

Key Skills

• Hands-on expertise in HPLC, GC, UV, IR, Dissolution, and LIMS
• Knowledge of cGMP, GLP, and ICH Q2(R1) guidelines
• Experience with method validation, method transfer, and stability studies
• Familiarity with QMS (OOS, OOT, CAPA, deviations)
• Strong documentation and regulatory audit exposure
• Analytical problem-solving and attention to detail

Salary

• ₹3.5–7.0 Lakhs/year (estimated based on Glassdoor and AmbitionBox for Nashik QC roles)

Why Join Viatris?

Viatris, with 38,000+ employees globally, is rated 4.1/5 on AmbitionBox for salary (4.3/5 at Nashik) and job security (4.2/5). Our Nashik facility, one of four OSD sites in India, supports global markets with antiretrovirals, antidiabetics, and more.

Employees praise cGMP practices and benefits but note work culture challenges (3.9/5) due to middle management. Recent FDA scrutiny at our Indore site highlights ongoing data integrity remediation, underscoring our commitment to quality.

Key Benefits

• Work in a USFDA-approved, ZLD OSD facility
• Support global markets with high-quality generics
• Gain expertise in advanced analytical tools like HPLC and LIMS
• Join a Nashik-based team with a 4.1/5 employee rating
• Contribute to Viatris’ mission of healthier lives

How to Apply

Attend the walk-in interview on May 18, 2025, from 10:00 AM to 3:00 PM at The Red Maple Hill Hotel, Indore, or email your CV to Abhinay.kharde@viatris.com with subject “QC Officer/Executive – Nashik”. Bring:

• Updated resume (original and photocopy)
• Educational certificates (M.Sc., B.Pharm, M.Pharm)
• Experience letters and last 3 months’ payslips
• Aadhar and PAN cards
• CTC and notice period details
• Preparation:
  • Review HPLC, GC, and ICH Q2(R1) guidelines
  • Be ready to discuss OOS investigations and USFDA/MHRA audits
  • Expect technical questions on analytical method validation
• Note: Viatris does not charge recruitment fees; verify communications via @viatris.com emails. Candidates unable to attend can email their CV by May 15, 2025, for consideration.

About Viatris

Viatris, formed by merging Mylan and Upjohn, operates 50+ manufacturing sites globally, including four OSD facilities in India (Nashik, Indore, Aurangabad, Jadcherla). Our Nashik plant, certified for ISO 14001 and ISO 45001, supports 100+ markets with generics and branded generics. With a Hyderabad R&D center for OSDs, we drive innovation in pharmaceutical manufacturing.

Our Mission

• Empower healthier lives through quality medicines
• Uphold cGMP and global regulatory standards
• Foster innovation and sustainability

Attend the recruitment drive on May 18, 2025, in Indore or email Abhinay.kharde@viatris.com to join Viatris’ Nashik QC team. Advance your career with a global pharma leader!