What are the responsibilities and job description for the Owner's Representative Project Manager – GMP Facilities position at ELIQUENT Life Sciences?
We are seeking an experienced Project Manager to lead the delivery of a new GMP-compliant facility, including warehouse, administration, and future manufacturing/QC space. The Project Manager will be responsible for end-to-end execution from design coordination through construction, fit-out, commissioning, and operational readiness.
Key Responsibilities
Project Leadership & Delivery
Act as owner’s representative Project Manager, accountable for full project lifecycle
Lead the project from design coordination through construction, CQV, and operational
readiness
Ensure delivery aligned with scope, schedule, budget, and GMP requirements
Design & Engineering Coordination
Manage and coordinate the engineering partner (A/E firm)
Ensure design meets:
GMP warehouse standards (supporting cell culture manufacturing)
Operational flows (materials, personnel, waste)
Future phase readiness (manufacturing/QC)
Construction & Contractor Management
Oversee general contractor execution of TI scope
Interface with property developer for core & shell coordination
Manage construction integration, interfaces, and change control
GMP & Operational Readiness
Ensure facility design and execution supports:
GMP warehousing (controlled environments, material handling, traceability)
Integration with manufacturing supply chain
Lead transition from construction to operational readiness, including:
Commissioning & qualification coordination (as applicable)
SOP readiness, layout finalization, and turnover
Governance & Reporting
Establish and manage:
Project governance structure
RAID logs, schedule tracking, and budget oversight
Executive reporting and stakeholder communication
Phasing Strategy & Future-Proofing
Ensure Phase 1 delivery does not constrain:
Future manufacturing build-out
QC lab development
Validate infrastructure capacity, layout provisions, and expansion strategy
Education & Qualification Requirements:
10–15 years project management experience in pharmaceutical/biotech facilities
Proven delivery of:
GMP warehouses and/or manufacturing facilities
Tenant improvement projects within developer-delivered buildings
Experience working with:
A/E firms and General Contractors
Multi-party delivery structures (developer tenant contractors)
Technical Competence
Strong understanding of:
GMP requirements (FDA/EU)
Warehouse operations supporting biologics manufacturing
Facility design for material/personnel flows
Familiarity with commissioning and qualification (CQV) and operational startup
Leadership & Delivery Skills
Ability to operate as single point of accountability on the owner side
Strong stakeholder management across:
Internal technical teams
External partners (developer, engineers, contractors)
Experience managing phased projects and future expansion planning
Benefits
What We Offer:
Competitive Compensation: Attractive salary and comprehensive benefits package for full-time and part-time employees, including health, dental, vision, and life insurance, a 401(k) plan with employer match, a generous paid time off policy, and additional perks. Compensation is commensurate with professional experience.
Career Development: Opportunities for professional growth and advancement within a supportive and innovative environment.
Work-Life Balance: Flexible work arrangements and a commitment to maintaining a healthy work-life balance.
Eliquent Life Sciences is proud to be an Equal Opportunity Employer, committed to employee diversity.
Salary : $140 - $160