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