Responsibilities
• Lead multiple concurrent QC laboratory digitization and master data projects across global manufacturing sites.
• Drive day-to-day project execution, ensuring milestones, deliverables, and timelines are met.
• Track and report project metrics, KPIs, risks, dependencies, and action items.
• Coordinate cross-functional teams including QC, Digital, Validation, IT, and site stakeholders.
• Support LabWare to Veeva LIMS deployment initiatives and Business-as-Usual (BAU) activities.
• Escalate risks and proactively resolve project roadblocks.
• Challenge site teams, ask the right technical questions, and ensure project assumptions and timelines are validated.
• Drive accountability across project teams to ensure successful execution.
Required Qualifications
• 8+ years of project management experience supporting pharmaceutical QC or laboratory informatics projects.
• Strong QC laboratory background with an understanding of laboratory workflows and regulated environments.
• Experience managing LIMS, Empower, laboratory digitization, or master data initiatives.
• Experience tracking project metrics, KPIs, budgets, risks, and project performance.
• Ability to work closely with global site teams and challenge requirements where appropriate.
• Experience working within GxP/CSV regulated environments.
Qualifications
• Experience with Veeva LIMS and/or LabWare LIMS.
• Familiarity with laboratory master data and QC applications.
• PMP or equivalent project management certification.
• Experience supporting global deployments across multiple manufacturing sites.