Pharmaceutical Project Manager
Core
Day-to-day project lead for validated environment and laboratory construction projects (cleanrooms, biosafety cabinets, containment suites) ensuring operational excellence and regulatory compliance.
Role type
Senior IC project manager (validated environments)
Builds
Validated laboratory and cleanroom facilities for biopharma, medical devices, and healthcare sectors
Domain
Life sciences construction and facility validation
Required skills
Project management, validated environment delivery, regulatory compliance (GMP/GLP/ISO), cross-functional coordination, risk mitigation, contract administration, budget management, stakeholder communication, project scheduling, vendor management
Preferred skills
Master's degree, PMP certification, CQV/CSV experience, FDA 21 CFR Part 11 knowledge, datacenter-adjacent facility experience, continuous improvement program contribution
Technologies
Primavera P6, MS Project, MS Office
Responsibilities
Plan and execute multi-site validated projects; coordinate Owners, Architects, Engineers, and Contractors; develop validation strategies and documentation; manage project scope, schedule, and budget; mitigate project risks; report performance to executive leadership; manage change orders and procurement; prepare teams for regulatory inspections; foster safe and compliant project environments
Seniority
Senior, hands-on IC with potential supervision of junior team members
