Quality Assurance

Roles & Responsibilities
• Review and approve manufacturing and packing batch records
• Manage change control, deviation handling, and risk assessments
• Perform in-process checks and line clearance activities
• Support validation, qualification, and internal/external audit activities
• Ensure GMP compliance, finished product integrity, and documentation accuracy
• Maintain quality systems in accordance with regulatory and vaccine industry standards

Qualifications
• B.Pharm / M.Pharm /B.sc /M.Sc (Life Sciences or related discipline)

Experience
• 3–16 years of experience in sterile manufacturing, vaccine, or injectable operations
• Prior exposure to GMP-compliant environments is mandatory

Skills
• Strong knowledge of quality systems and GMP documentation
• Experience in audits, validation, qualification, and risk management
• Ability to handle batch record review and compliance activities
• Good understanding of sterile and vaccine manufacturing processes
• Strong attention to detail and regulatory mindset

Walk-In Interview Details
Date: 14 February 2026
Time: 10:00 AM – 2:00 PM
Venue: Chiron Behring Vaccines Pvt. Ltd., Plot No. 3502, G.I.D.C. Estate, P.B. No. 136, Ankleshwar, Dist. Bharuch, Gujarat – 393002, India

Documents Required
• Updated resume
• Passport-size photograph
• Aadhaar card & PAN card
• Educational certificates
• Experience letters (if applicable)

About the Organization
Chiron Behring Vaccines Pvt. Ltd., part of the Bharat Biotech network, is a key contributor to India’s vaccine manufacturing ecosystem, operating advanced GMP-compliant facilities focused on producing high-quality, life-saving vaccines for global health needs.