Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy.
Post : Manager QA
Job Description
Quality Management at Novo Nordisk is a critical department which ensuring the implementation and compliance of Novo Nordisk’s Quality Management System (QMS) in the affiliate.
As a Manager QA your roles & responsibilities are as follows :
• Maintain the affiliate's QMS, continually evaluating and monitoring its suitability and adequacy for the commercial business. Act as a backup Quality Responsible Person (QRP).
• Facilitate and manage corporate quality audits and regulatory audits and drive the Supplier Qualification Program, including the identification, evaluation through audits, monitoring, maintenance, and re-qualification of vendors.
• Handle Commercial and Distribution Quality Management by reviewing and approving Changes, Deviations, Investigations, Market Complaints, mock recall/ actual recall and CAPA within the Veeva Quality system.
• Handle temperature excursions by conducting proper review and evaluation to ensure product compliance. Manage the release of imported and repacked products through thorough review and evaluation.
• Support QA operations, KPIs, and deliverables, ensuring all Quality KPIs are met on target.Coordinate with entity management to facilitate Quality Management Review (QMR) activities.
• Manage monthly & quarterly quality objective reporting, escalate issues with QMS impact, and ensure the closure of open actions from previous QMR meetings.
• Ensure compliance with all major quality system activities, including document control, record control, training, CAPA, change control, deviation, risk management, quality agreements and internal audit.
Candidate Profile
• Master’s degree in Pharmacy or a Science-related discipline.
• 10-14 years of experience in Commercial Quality/ Distribution quality/ Corporate Quality Assurance.
• Minimum 5 years of exp. in drafting CAPAs, evaluating Deviations and managing Change Control and drafting quality agreements.
• Hands-on experience with electronic QMS platforms, specifically Veeva Quality Suite, is highly preferred.
• Hands-on Experience in hosting and managing regulatory inspections (e.g., CDSCO) and corporate audits.
• Experience in Cold Chain qualification would be an added advantage.
• Strong understanding of risk management principles.
• Proven ability to lead, influence, and work effectively in a cross-functional team environment.
Additional Information
Experience : 10-14 years
Qualification : Master’s degree in Pharmacy
Location : Bangalore, Karnataka
Industry Type : Pharma/ Healthcare/ Clinical research
Department : Legal Compliance and Quality
End Date : 12th December 2025
QA Manager : Apply here
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