Are you an experienced Project Manager (m/f/d) with a proven track record in global regulatory system implementations and governance oversight? Join an exciting international program where you will support the execution of a multi-phase deployment, ensuring critical deliverables, timelines, and go-lives are achieved efficiently. This role provides a unique opportunity to contribute to the governance and planning of a highly visible project in the life sciences sector.

• Lead and support formal validation and consolidated program planning

• Identify the critical path for business go-live and ensure plan baselines are maintained monthly

• Collaborate with Program Management to prepare and close all DG1 tollgate deliverables

• Coordinate cutover management activities (pre-cutover, cutover, post-cutover) in alignment with the PMs

• Support and manage activities related to technical go-lives, identify gaps, and ensure closure of issues

• Monitor and report on critical issues during hypercare, driving resolution through actionable plans

• Provide governance support throughout wave 2, maintaining and updating project baselines and status reports

• Align planning and execution with internal stakeholders across functions and geographies

• 15+ years of experience managing large and complex programs, ideally in the pharmaceutical or life sciences sector

• Extensive experience in Regulatory system implementations and computer system validation (CSV)

• Prior experience working with enterprise environments

• Proven experience as a Cutover Manager in complex implementations

• Advanced user of Smartsheet for planning and progress tracking

• Familiarity with PMO Hub or similar risk management tools

• Strong knowledge of specific IT landscape and legacy platforms (e.g., SubWay, REDI-GO, REDI_RR)

• Experience leading cross-functional and international teams in a matrix organization

• Previous involvement in Veeva Vault implementations; Veeva Vault Platform Certification preferred

• Comfortable working in CET with some overlap to India and US-based teams

• Work remotely from within CET zone

• Contribute to a high-impact program in the life sciences industry

• Collaborate with global cross-functional teams

• Opportunity to lead in a regulated, innovation-driven environment