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Tier-1 brand, metro location, generalist PM title, and broad stakeholder requirements increase applicant competition.
Role requires specialized QC laboratory, GMP and regulatory experience, limiting cross-industry transferability.
Requires domain-specific QC, GMP, regulatory and technology-transfer expertise making filters stringent.
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Own and coordinate QC Laboratory technology and analytical method transfers with local CMOs within APAC strategic localisation programmes.
Provide technical, quality, and project leadership to ensure compliance with Novo Nordisk Quality standards, EU GMP, FDA, and local regulatory requirements.
Manage milestones, risks, and interfaces while supporting laboratory design, setup, qualification, validation, and ramp-up to stable routine operation.
Advanced degree in Chemistry, Pharmacy, Engineering, or a similar discipline.
Strong experience in QC Laboratories including analytical methods, validation, and GMP compliance.
Proven project management experience in complex, multi-stakeholder environments involving technology transfer and lab readiness.
Work Experience Required: Not explicitly mentioned in the JD.
Experienced in handling technology transfer and analytical method transfer within QC Laboratories in regulated environments.
Comfortable operating in complex cross-functional settings with multiple stakeholders including local CMOs and regulatory entities.
Capable of managing projects end-to-end with focus on compliance and laboratory operational readiness across the APAC region.