CQV Project Manager/Program Manager Consultant jobs in United States
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Ecocareers · 1 month ago

CQV Project Manager/Program Manager Consultant

Confidential company is seeking a CQV Project Manager/Program Manager Consultant. The role involves leading and managing the full lifecycle of capital projects in pharmaceutical manufacturing, ensuring alignment with corporate goals and overseeing engineering activities.

Staffing & Recruiting

Responsibilities

Lead and manage full lifecycle of capital projects, including planning, budgeting, execution, and closeout, ensuring alignment with site and corporate goals
Oversee engineering activities for projects including but not limited to: Facilities/Utilities supporting Oral Solid Dosage Manufacturing and Packaging, GMP processes, Automation upgrades, and QC Lab equipment
Develop and maintain accurate project budgets and forecasts; monitor project spends, track variances, and ensure financial accountability for capital expenditures
Ensure adherence to established project documentation, phase gates, and change management processes for technical and operational projects
Partner with Manufacturing, Quality, Validation, and other cross-functional stakeholders to deliver integrated project outcomes and support site readiness for commercial and clinical operations
Manage external engineering firms, equipment vendors, and contractors to ensure adherence to project scope, quality, safety, and schedule requirements

Qualification

Pharmaceutical ManufacturingGMP ProcessesProject ManagementFacilities/UtilitiesMicrosoft ProjectBudgetingForecastingLeadershipCommunicationDetail-oriented

Required

Bachelor's degree in engineering (Mechanical, Chemical, Industrial, or related discipline)
Minimum 7–10 years of experience in pharmaceutical manufacturing with a focus on Oral Solid Dosage Manufacturing and Packaging, GMP processes, Automation upgrades, and QC Lab equipment
Proven track record in capital project management, managing multiple projects at once
Strong understanding of Facilities/Utilities supporting Oral Solid Dosage Manufacturing and Packaging, GMP processes, Automation upgrades, and QC Lab equipment
Knowledge of pharmaceutical packaging, modern controls and safety devices, tablet inspection systems, SCADA/Client-X integrations, and equipment validation
Familiarity with process utilities and equipment qualification protocols (IQ/OQ/PQ)
Highly skilled utilizing Microsoft Project for schedule/project plan development
Skilled in budgeting, forecasting, and cost control within complex, regulated environments
Strong leadership and communication skills, with the ability to influence cross-functional teams
Highly organized, detail-oriented, and capable of managing multiple priorities in a dynamic environment
Willingness to work onsite at a GMP manufacturing facility

Preferred

Advanced degree preferred

Company

Ecocareers

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Funding

Current Stage
Early Stage
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