Pharmaceutical - Senior Project Manager / PMO (No C2C or H1)

Kankakee, IL, US • Posted 3 days ago • Updated 3 days ago
Full Time
On-site
$150,000 - $160,000/yr
Fitment

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Job Details

Skills

  • Project management exp
  • Exp. in pharmaceutical or biotech or life sciences environments
  • Exp. delivering capital projects
  • validation
  • manufacturing or compliance initiatives
  • Exp. with Good Manufacturing Practices (GMP) and/or FDA
  • Exp. working within or alongside a formal PMO
  • Exp. with engineering design
  • or process scale-up

Summary

Pharmaceutical - Senior Project Manager / PMO
Duration: Full Time Direct Hire
Location: Kankakee, IL (Onsite)

Position Description :

Summary:


We are seeking an experienced Senior Project Manager / PMO leader with a strong background in engineering or scientific disciplines and proven delivery experience within the pharmaceutical or biotech industry. This role is responsible for leading complex, cross-functional CAPEX projects (manufacturing, laboratories, utilities, engineering, construction) utilizing the best PMO standards, governance, and execution discipline.

or US Permanent Resident.

This is a hands-on leadership role-not purely administrative-requiring ownership of project outcomes, stakeholder alignment, and technical understanding of regulated environments.

Responsibilities

Project Leadership & Delivery

  • Lead end-to-end execution of capital projects, within pharmaceutical manufacturing and laboratories, from inception / business case development, through to project execution and closure.
  • Manage many projects simultaneously (typically three to four), typically ranging between $1-10M, but the actual values may fluctuate (sometimes there are larger projects).
  • Manage scope, schedule, cost, and quality across multiple concurrent projects, provide regular status updates & reporting on projects
  • Drive project planning (charters, schedules, resource plans) and ensure realistic execution strategies
  • Identify risks early and proactively manage mitigation plans in regulated environments. Escalate & resolve issues proactively.
  • Document, manage and monitor action items, issues, decisions, risks.

PMO Governance & Standards

  • Utilize world class PMO best practices, tools, and reporting structures for executing capital projects
  • Work with project controls specialists on schedule tracking, cost forecasting, change management.
  • Lead stage-gate processes aligned with GMP and validation requirements
  • Provide portfolio-level visibility to leadership (KPIs, dashboards, resource loading)

Cross-Functional Coordination

  • Requires interfacing / managing many stakeholders including engineering, construction, manufacturing, EHS, IT, QA, QC, Regulatory, maintenance, calibration, in a high paced manufacturing environment.
  • Act as the central point of coordination between internal stakeholders and external vendors/contractors
  • Manage third-party engineering firms, system integrators, and construction partners

Regulatory & Compliance

  • Ensure projects align with U.S. Food and Drug Administration expectations and GMP requirements
  • Oversee validation lifecycle activities (IQ/OQ/PQ), commissioning, and documentation readiness
  • Maintain audit-ready project documentation

Stakeholder Management

  • Communicate effectively with senior leadership and site-level teams
  • Translate technical issues into business impacts and actionable decisions
  • Drive accountability across teams without direct authority

Qualifications

Education

  • Bachelor s degree in Engineering, Life Sciences, Scientific or related field
  • Advanced degree (MBA, MS) is a plus

Certifications (Preferred, but not required)

  • PMP (Project Management Professional) Project Management Institute

Experience

  • 8 15+ years of project management experience
  • 5+ years within pharmaceutical, biotech, or life sciences environments
  • Demonstrated experience delivering capital projects, validation, manufacturing or compliance initiatives
  • Experience working within or alongside a formal PMO

Technical & Industry Knowledge

  • Strong understanding of GMP, validation, and regulated project environments
  • Familiarity with systems such as MES, LIMS, ERP (e.g., SAP), or automation platforms is highly desirable, but not required.
  • Experience with engineering design, construction, or process scale-up is highly desirable, but not required.

Core Competencies

  • Strong execution mindset (not just reporting)
  • Ability to manage ambiguity and drive decisions
  • High accountability and ownership of outcomes
  • Commercial awareness (cost, ROI, timelines)
  • Ability to challenge stakeholders constructively
  • Multi-tasking, escalating, reporting, tracking, documentation
  • Working in a fast paced environment in a large organization
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 10527923
  • Position Id: 8954968
  • Posted 3 days ago
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