Senior Project Manager - QC Laboratory
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Key skills for this role
About the Role
Novo Nordisk seeks a Senior Project Manager for QC Laboratory to lead technology transfer and analytical method transfer for a localization program in Riyadh. The role involves coordinating QC lab readiness, ensuring GMP compliance, and managing milestones.
Key Skills for This Role
Responsibilities
- Act as Work Package Owner for the QC Laboratory, representing Novo Nordisk towards SaudiBIO
- Coordinate QC Laboratory technology transfer and analytical method transfer activities
- Support QC Laboratory design, setup, qualification and validation readiness
- Provide guidance, training and mentoring to the local partner in line with Novo Nordisk standards
- Safeguard compliance with EU GMP, Novo Nordisk Quality requirements and local regulatory expectations
- Manage milestones, risks and interfaces with other work packages
- Support the QC Laboratory ramp up until stable routine operation is achieved
Requirements
- Advanced degree in Chemistry, Pharmacy, Engineering or similar discipline
- Strong experience within QC Laboratories, including analytical methods, validation and GMP compliance
- Proven experience with technology transfer and QC Laboratory readiness
- Solid project management experience in complex, multi stakeholder environments
- Strong stakeholder management and communication skills
- Fluency in English, written and spoken
Full Job Posting
Position Overview
- Senior Project Manager – QC Laboratory within GCM DP RoW Projects, Riyadh, Saudi Arabia.
- Act as Work Package Owner for QC Laboratory aseptic manufacturing scope, supporting local partner SaudiBIO in technology transfer, laboratory readiness, analytical method transfer and ramp up of operations.
Your New Role
- Acting as Work Package Owner for the QC Laboratory, representing Novo Nordisk towards SaudiBIO.
- Coordinating QC Laboratory technology transfer and analytical method transfer activities.
- Supporting QC Laboratory design, setup, qualification and validation readiness.
- Providing guidance, training and mentoring to the local partner in line with Novo Nordisk standards.
- Safeguarding compliance with EU GMP, Novo Nordisk Quality requirements and local regulatory expectations.
- Managing milestones, risks and interfaces with other work packages.
- Supporting the QC Laboratory ramp up until stable routine operation is achieved.
Your New Department
- Global Manufacturing & Supply covers full value chain from drug and device development to marketed products.
- Join GCM DP RoW, part of Novo Nordisk's Global Manufacturing Services organization, supporting establishment of sustainable manufacturing capabilities.
Your Skills & Qualifications
- An advanced degree in Chemistry, Pharmacy, Engineering or a similar discipline.
- Strong experience within QC Laboratories, including analytical methods, validation and GMP compliance.
- Proven experience with technology transfer and QC Laboratory readiness.
- Solid project management experience in complex, multi stakeholder environments.
- Strong stakeholder management and communication skills, with ability to influence and build trust.
- Fluency in English, written and spoken.
What We Offer
- Opportunities to learn and develop, benefits designed with your career and life stage in mind.
Deadline
- 7 July 2026. Applications reviewed on an ongoing basis.
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