Pharmaceutical Project Manager
Core
Day-to-day project lead for validated environment and laboratory construction projects (e.g., cleanrooms, biosafety cabinets, containment suites) across a campus, ensuring compliance with regulatory expectations and operational excellence.
Role type
Senior IC project manager (validated environments)
Builds
Validated laboratory and cleanroom facilities for biopharma, medical devices, and healthcare sectors
Domain
Construction + Life Sciences/Pharmaceuticals
Required skills
Project management, validated environment delivery (GMP/GLP/ISO 17025), contract administration, budgeting, risk management, stakeholder coordination, regulatory compliance, data integrity, change order management
Preferred skills
Master's degree, PMP certification, CQV/CSV experience, FDA 21 CFR Part 11/EU Annex 11 knowledge, datacenter-adjacent facility experience, continuous improvement in validation processes
Technologies
Primavera P6, MS Project, MS Office, Solution Navigator
Responsibilities
Plan and execute validated environment projects; coordinate Owners, Architects, Engineers, and Contractors; manage project scope, schedule, and budget; develop validation strategies and documentation; mitigate project risks; report performance to leadership; manage vendor/subcontractor performance; prepare for regulatory inspections; foster safe and compliant project environments
Seniority
Senior, hands-on IC with potential supervision of junior team members