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Senior Project Manager

Job in Madison, Dane County, Wisconsin, 53774, USA
Listing for: TAI
Full Time position
Listed on 2026-08-22
Job specializations:
  • Engineering
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 150000 - 215000 USD Yearly USD 150000.00 215000.00 YEAR
Job Description & How to Apply Below

About The Role

The Senior Project Manager will play a central role in driving major capital expansion projects for a growing pharmaceutical manufacturing campus. Acting as the client’s Owner’s Representative, this leader oversees projects from initial concept through engineering, construction, commissioning, and final handover. The position is deeply embedded in the evolution of a complex, cGMP-regulated environment, guiding cross-functional teams, external partners, and large-scale facility initiatives to successful, compliant, and efficient delivery.

This is a high-impact role for someone who thrives in steering multifaceted technical programs and shaping the future capabilities of a cutting-edge biologics manufacturing operation.

About

The Role

The Senior Project Manager will play a central role in driving major capital expansion projects for a growing pharmaceutical manufacturing campus. Acting as the client’s Owner’s Representative, this leader oversees projects from initial concept through engineering, construction, commissioning, and final handover. The position is deeply embedded in the evolution of a complex, cGMP-regulated environment, guiding cross-functional teams, external partners, and large-scale facility initiatives to successful, compliant, and efficient delivery.

This is a high-impact role for someone who thrives in steering multifaceted technical programs and shaping the future capabilities of a cutting-edge biologics manufacturing operation.

About TAI

TAI brings together engineering, construction, systems integration, on-site services, and technical services - combining proven execution with trusted expertise to support clients across the entire project lifecycle. Team members at TAI are capable, well-rounded, flexible, and optimistic. We have found that the best employees are the ones who recognize the importance of what they do and the ones who let that guide them in the actions they take.

More than any skill, we seek people who make decisions that support the common good. We work for our clients, and we work for one another.

Here's a Glimpse Into Your Day To Day
  • Lead the full lifecycle (cradle-to-grave) execution of capital projects from conceptual planning through engineering, construction, commissioning, qualification, and closeout.
  • Manage project scope, schedules, budgets, and resources for large-scale facility and manufacturing initiatives.
  • Coordinate cross-functional teams including Engineering, Facilities, Manufacturing, Quality, Validation, Procurement, and external engineering and construction partners.
  • Oversee contractor selection, design reviews, procurement activities, construction execution, and project controls.
  • Identify and mitigate project risks while managing scope changes and budget performance.
  • Ensure compliance with cGMP, FDA, OSHA, and company engineering standards throughout project execution.
  • Provide regular project updates to leadership and key stakeholders while driving projects to successful completion.
  • Support continuous improvement initiatives that enhance facility performance, manufacturing capacity, and operational efficiency.
You’ll Be a Perfect Fit If You Have
  • Bachelor's degree in Engineering, Construction Management, or a related technical discipline.
  • 10-15 years of experience managing capital projects with full lifecycle (cradle-to-grave) responsibility.
  • 5+ years of experience managing capital projects within pharmaceutical, biotechnology, or other cGMP manufacturing environments.
  • Demonstrated success delivering capital projects valued at $100 million or greater.
  • Strong knowledge of pharmaceutical facility design (biologics manufacturing), manufacturing infrastructure, construction management, and project controls.
  • Experience managing multidisciplinary teams, EPC firms, contractors, and equipment vendors.
  • Working knowledge of cGMP regulations, commissioning, qualification, and validation practices.
  • Experience supporting biologics manufacturing, cleanroom environments, and single-use bioprocess systems.
  • Familiarity with commissioning, qualification, and validation (CQV) processes.
  • Excellent leadership, communication, and organizational skills.
Compensation And…
Position Requirements
10+ Years work experience
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