We're partnering with a leading pharmaceutical company to appoint a Project Manager to lead end-to-end project execution. From imminent deal signature through to successful product registration and launch.

This critical role owns timeline, risk, governance, and communication across multiple functions including Regulatory Affairs, Quality, Branding and Communications, and Executive leadership.

Key responsibilities:

• Lead cross-functional workflows from deal signature to product registration.
• Manage project timelines, risk, governance, and stakeholder communications.
• Ensure documentation (NPRF, final artwork) meets FDA, EMA, GCC, and local regulatory standards.
• Oversee introduction of new product lines and process enhancements.
• Build and manage integrated project plans, RAID reviews, and governance forums.

Requirements:

• 6–10 years’ experience in project management, business operations, or integration within pharmaceuticals, biotech, or healthcare.
• Experience leading at least two full product registrations or line extensions.
• Strong understanding of regional regulatory frameworks.
• Advanced skills in MS Project, Excel, and Power BI.
• Excellent coordination and influencing skills across cross-functional teams.

If you’re an experienced Project Manager with a strong regulatory and commercial understanding of pharmaceutical operations, we’d love to hear from you.