Sr. Project Manager, Medical Device

Our global medical device client is seeking an experienced Senior Project Manager in the Medical Device space to support critical system separation initiatives. This role will lead the planning, execution, and transition of regulated systems being stood up, cloned, or remediated for the newly formed organization. The ideal candidate brings hands‑on experience working within a medical device environment, understands regulated systems and processes, and can confidently manage complex, cross‑functional projects through separation timelines.

• Global Make/Deliver Labeling
• Electronic Instructions for Use (eIFU)
• Global UDI

• Manage system separation projects through agreed‑upon timelines, ensuring delivery aligns with regulatory, quality, and business requirements.
• Lead day‑to‑day project execution across multiple work streams, maintaining clear plans, milestones, risks, and dependencies.
• Drive coordination across Quality, Regulatory, Operations, IT, and business stakeholders.
• Oversee system cloning, data cleansing, configuration, and validation activities for New Co readiness.
• Partner closely with IT to support system design, environment setup, testing, and cutover planning aligned to the new organizational model.
• Ensure system testing (including UAT) is planned, executed, and documented appropriately for a regulated environment.
• Support procedure development, updates, and alignment required for system separation and New Co operations.
• Ensure documentation meets medical device quality and compliance expectations.
• Develop and execute transition plans to support a smooth handoff of systems, processes, and knowledge to the New Co organization.
• Facilitate structured knowledge transfer sessions and documentation to ensure long‑term sustainability post‑separation.
• Act as a key liaison between business teams and IT, ensuring alignment between system capabilities and operational needs.
• Provide clear status updates, issue escalation, and decision support to program and executive stakeholders.

• Experience managing system‑focused projects within a medical device or highly regulated environment.
• Strong understanding of regulated systems, validation, and compliance expectations (e.g., labeling, UDI, eIFU).
• Proven ability to lead complex initiatives through separation, carve‑out, or transformation timelines.
• Experience partnering closely with IT teams on system implementation, cloning, testing, and deployment.
• Strong project management skills with the ability to operate independently and drive outcomes.

• Direct experience with labeling systems, eIFU platforms, or UDI programs in a global medical device context.
• Experience supporting New Co stand‑up, separation, or divestiture initiatives.
• Familiarity with global Make/Deliver or supply chain‑related systems in regulated environments.
• Local to the Raynham, MA area, or able to be onsite in Raynham during the workweek as project needs require.
• Comfortable working in a fast‑moving, ambiguous environment typical of separation initiatives.