Project Manager
Listed on 2026-10-13
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Business
Workstream Facilitation: Plan and lead high-value cross-functional workshops, alignment sessions, and recurring Tier 2 workstream execution huddles.
Schedule Management: Build, maintain, and baseline workstream-level integrated schedules on , ensuring logic ties and milestone alignment with the Master Integrated Schedule (IS).
Workstream Cost Control: Track financial performance for assigned work streams, monitoring PO drawdowns, invoice approvals, vendor spend, and cost variance reporting.
Resource Loading Support: Assist Workstream Leads in resource loading and capacity planning to prevent operational bottlenecks during ramp-up phases.
RAID Log & Action Management:Maintain and actively drive resolution for assigned workstream RAID logs (Risks, Assumptions, Issues, Dependencies) and Action Item registers.
Governance Reporting: Support Workstream Leads in drafting standard 3-page status reports, 4-pillar health checks, exception reports, and executive summaries for Tier 2 and Tier 3 governance forums.
Qualifications & Experience RequirementsEducation: B.S. in Engineering, Life Sciences, Business, or related technical field. PMP certification preferred.
Industry
Experience:
Minimum 5–7 years of project management experience within cGMP Bio Pharma / Pharmaceutical Site Start-Up, commissioning, or tech transfer operations.
Platform Expertise: Advanced proficiency in , MS Project, Excel, and Google Workspace (Docs, Sheets, Slides, Drive).
Key
Competencies:
Strong workshop facilitation, stakeholder management, cross-functional risk mitigation, and fluency in pharma manufacturing terminologies.
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