Quality Assurance Project Manager

Quality & Regulatory Affairs Project Specialist

About the Role

Key Responsibilities

• Coordinate Quality & Regulatory project activities across sites and functions.
• Maintain project plans, action trackers, risks, milestones, and status reports.
• Coordinate meetings, actions, deliverables, and stakeholder communication.
• Support QMS activities , quality documentation, CAPAs, deviations, change controls, and transition activities.
• Support Regulatory Affairs activities and maintain regulatory trackers.
• Create and maintain dashboards and project reporting, ideally using Power BI .
• Identify risks, delays, dependencies, and escalate where required.
• Support operational readiness and transition/cutover activities.

Your Profile

• Experience in Project Management / PMO / Project Coordination .
• Solid experience in Quality / Quality Assurance / QMS within a regulated environment.
• Experience in pharma, biotech, medical devices, diagnostics, IVD, or similar life sciences industries .
• Hands-on experience with Power BI, dashboards, or data visualization .
• Strong organizational and stakeholder management skills.
• Experience coordinating cross-functional and/or international projects.
• Regulatory Affairs experience is a strong advantage.
• Experience with divestiture, separation, transition, merger, or transformation projects is a plus.

Start: ASAP

Duration: 10 months

Location: Remote

Workload: 100%