Senior Manager

Responsibilities

• Manage QC testing of raw materials, in-process samples, and finished products
• Ensure compliance with GMP, GLP, ISO standards, and regulatory guidelines
• Review and approve QC test results and batch release documentation
• Maintain and improve laboratory systems, SOPs, and testing procedures
• Review and approve change control, deviation reports, and investigation reports
• Monitor calibration, validation, testing, and inspection activities
• Support CAPA (Corrective and Preventive Action) implementation
• Investigate OOS (Out of Specification) and OOT (Out of Trend) results
• Lead and supervise QC analysts and officers, providing necessary training

Requirements

• B.Sc / M.Sc / B.Pharm / M.Pharm or a related science field
• 8–15 years of QC experience in the pharmaceutical or medical device industry
• Strong knowledge of GMP, GLP, and ISO 13485 standards
• Experience with regulatory compliance (CDSCO, FDA, or CE)
• Proficiency with analytical instruments and laboratory systems

About the Company

Founded in 2006, Meril is a global medical device company dedicated to the innovation, design, and development of state-of-the-art healthcare solutions. We manufacture a diverse range of products, including vascular intervention devices, orthopaedic supplements, in-vitro diagnostics, and endo-surgery products. Headquartered in India with a global presence in over 100 countries, Meril is committed to improving the quality of human life through advanced medical technology and research.