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Tier-1 employer and metro locations increase density, but niche QC lab and regulatory specialization reduce applicant breadth.
High pharma QC, GMP, and analytical method transfer specialization limits cross-industry transferability.
Requires advanced degree, specific QC/method transfer and GMP experience, plus proven project leadership.
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Own and coordinate QC Laboratory technology and analytical method transfers for Novo Nordisk's localisation programmes in APAC, primarily India.
Lead QC Laboratory design, setup, qualification, validation readiness, and ramp-up to stable operations with local CMO partners.
Ensure compliance with EU GMP, FDA, Novo Nordisk quality standards and local regulatory requirements, managing risks and cross-work package interfaces.
Advanced degree in Chemistry, Pharmacy, Engineering, or similar discipline.
Strong experience with QC Laboratories including analytical methods, validation, GMP compliance, and technology transfer.
Proven project management experience in complex, multi-stakeholder environments.
Based in India (Bangalore or Hyderabad) with ability to travel 5-10 days/month to local partners and possibly across APAC.
Experienced senior professional skilled in managing end-to-end QC laboratory technology and method transfers for pharmaceutical manufacturing.
Able to lead cross-functional, multi-stakeholder teams including local and external partners with strong stakeholder management skills.
Comfortable operating in complex, regulated environments ensuring global and local compliance during laboratory localisation and scale-up.