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0026V6130 Pharma Project Manager Consultant

Two River Consulting Partners
Posted 6 days ago, valid for 15 days
Location

West Chester, OH 45071, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • The Project Manager Consultant position focuses on leading capital projects in a pharmaceutical manufacturing environment, including planning, budgeting, and execution.
  • Candidates must have a Bachelor’s degree in Engineering and a minimum of 7-10 years of experience in pharmaceutical manufacturing, particularly in CQV Engineering projects and GMP processes.
  • The role requires strong technical expertise in managing multi-disciplinary projects, vendor management, and adherence to compliance standards.
  • Proficiency in Microsoft Project for scheduling and budgeting is essential, along with excellent leadership and communication skills to influence cross-functional teams.
  • This position is based 100% onsite in West Chester, OH, with a competitive C2C salary offered.
0026V6130 Project Manager Consultant
Please contact Amanda Mazza, amanda@tworivercp.com

Project Manager Key Responsibilities:

  • Capital Project Management:
    Lead and manage full lifecycle of capital projects, including: planning, budgeting, execution, and closeout, ensuring alignment with site and corporate goals
  • Technical Leadership:
    Lead and oversee multi-disciplinary pharmaceutical manufacturing engineering projects, including equipment upgrades, site-wide system modernizations, utility and infrastructure improvements, and facility security enhancements, ensuring compliance with GMP requirements, validated system expectations, and operational reliability standards
  • Budget & Financial Oversight:
    Develop and maintain accurate project budgets and forecasts; monitor project spend, track variances, and ensure financial accountability for capital expenditures
  • Documentation & Phase Deliverables:
    Ensure adherence to established project documentation, phase gates, and change management processes for technical and operational projects
  • Cross-Functional Collaboration:
    Partner with Manufacturing, Quality, Validation, and other cross-functional stakeholders to deliver integrated project outcomes and support site readiness for commercial and clinical operations
  • Vendor & Contractor Management:
    Manage external engineering firms, equipment vendors, and contractors to ensure adherence to project scope, quality, safety, and schedule requirements

Qualifications & Requirements

  • Education:
    Bachelor’s degree in Engineering (Mechanical, Chemical, Industrial, or related discipline). Advanced degree preferred
  • Experience:
    • Minimum 7–10 years of experience in pharmaceutical manufacturing with a focus on CQV Engineering projects/upgrades, GMP processes, equipment qualification
    • Proven track record in capital project management, managing multiple projects at once
    • Construction experience
  • Technical Expertise:
    • Strong understanding of multi-disciplinary pharmaceutical manufacturing engineering projects, including equipment upgrades, site-wide system modernizations, utility and infrastructure improvements, and facility security enhancements, ensuring compliance with GMP requirements, validated system expectations, and operational reliability standards
    • Knowledge of pharmaceutical packaging, modern controls and safety devices, and equipment validation
    • Familiarity with process utilities and equipment qualification protocols (IQ/OQ/PQ)
  • Project & Financial Skills:
    • Highly skilled utilizing Microsoft Project for schedule/project plan development
    • Skilled in budgeting, forecasting, and cost control within complex, regulated environments
  • Soft Skills:
    • 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
LOCATION
100% onsite in West Chester, OH

EMPLOYMENT
Competitive C2C
 



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