Project Executive (Life Sciences)
Role Overview
Serve as an owner's representative on complex life science, pharmaceutical, and biotechnology construction projects.
Lead strategic planning, stakeholder alignment, project planning, budgeting, negotiation, and delivery of critical initiatives.
This is a full-time, permanent position.
Key Skills for This Role
Full Job Posting
Role Overview
Serve as an owner's representative on complex life science, pharmaceutical, and biotechnology construction projects.
Lead strategic planning, stakeholder alignment, project planning, budgeting, negotiation, and delivery of critical initiatives.
This is a full-time, permanent position.
Workplace and Travel
- Work may alternate between the Durham, North Carolina headquarters office and client locations.
- The role includes office and site-based work, site travel, and construction-site inspections in varied weather conditions.
- A valid driver's license is required.
Responsibilities
- Direct construction projects from conception through completion.
- Develop execution strategies, logistics plans, safety plans, budgets, schedules, and work plans.
- Review contracts, construction documents, and project processes.
- Track project costs, budget, schedule, quality, risks, and overall performance.
- Conduct site walkthroughs and provide feedback to contractors and subcontractors.
- Manage quality control, document control, communications, and contractor and consultant contracts.
- Prepare project reports and implement improvements to efficiency, quality, and safety.
- Build collaborative relationships with clients, owners, users, design teams, contractors, and local authorities.
Required Qualifications
- Requires 15–20 years managing complex life science capital projects.
- Requires a related technical bachelor's degree or equivalent experience.
- Requires experience managing life science projects over $20M, including construction, renovation, and infrastructure upgrades.
- Requires cGMP facility design, build, qualification, and maintenance expertise.
- Requires experience with pharmaceutical, biotechnology, or life sciences facility design, construction, commissioning, and operation.
- Requires regulated-environment knowledge including FDA regulations, GEP, cGMP, GDP, and applicable CFR requirements.
- Requires strong budgeting, scoping, estimating, stakeholder management, and cross-functional leadership skills.
Relevant Technologies
- Relevant experience may include manufacturing and utilities systems, clean and aseptic rooms, CIP, SIP, autoclaves, VHP sterilization, and sterile-fill facilities.
- Relevant platforms may include controlled environments, pharmaceutical manufacturing processes, GMP warehousing, and automated storage and retrieval systems.
Physical Requirements
- Must use required on-site safety gear, including hard hat, glasses, and safety harness.
- Must be able to traverse construction sites, perform inspections, and may lift up to 30 pounds.
Benefits
- Benefits include 401(k) with employer contribution, cell phone allowance, employer-paid life and long-term disability insurance, medical, dental, vision, paid time off, and holidays.
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