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 in Riyadh to lead technology transfer and analytical method transfers for a localization program with local partner SaudiBIO.
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 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
- Fluency in English, written and spoken
Full Job Posting
Position Overview
- Senior Project Manager – QC Laboratory
- Category: Project Management & Agile
- Location: Riyadh, Saudi Arabia
- GCM DP RoW Projects
The position
- Act as Work Package Owner (WPO) for the QC Laboratory aseptic manufacturing scope, supporting local partner SaudiBIO in technology transfer, laboratory readiness, analytical method transfer and ramp up of operations.
- Ensure full alignment with Novo Nordisk Quality standards and regulatory requirements.
- Report to the Program Head and be part of the program localization management team.
Your new role
- Acting as Senior Project Manager and QC Laboratory Work Package Owner gives you the opportunity to work on a large and strategic localization program with high visibility.
- Drive and coordinate Novo Nordisk's QC Laboratory support activities across the program.
- Day to day tasks include: Acting as Work Package Owner for the QC Laboratory, coordinating technology transfer and analytical method transfer, supporting QC Laboratory design and validation, providing guidance and training, safeguarding compliance, managing milestones and risks, and supporting ramp
Your new department
- In Global Manufacturing & Supply, we cover the full value chain from drug and device development to marketed Novo Nordisk products.
- You will join GCM DP RoW, part of Novo Nordisk's Global Manufacturing Services (GMS) organization, supporting establishment of sustainable manufacturing capabilities in markets where local presence is required.
- The KSA localization program is a multi phase initiative developing local pharmaceutical manufacturing capabilities in Saudi Arabia in collaboration with SaudiBIO.
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.
- Fluency in English, written and spoken.
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