Life Sciences Project Leader for GMP Facility Upgrades

Hargrove Life Sciences, LLC; Philadelphia (Philadelphia County); On-site; USD 90,000 - 140,000; Full time

Benefits offered by this job

401(k)

Health insurance

Paid holidays

PTO

Job summary

Hargrove Life Sciences, LLC is seeking a Project Manager to lead multidisciplinary engineering and design projects for clients across biotechnology, pharmaceutical, and specialty chemical industries. You will manage planning, budgeting, scheduling, and client communications to ensure successful delivery from front-end planning through startup.

The role requires 8+ years of relevant experience in GMP-regulated environments, with an engineering background and PMP preferred.

Qualifications

• 8+ years of engineering, design, or project execution experience in life sciences or manufacturing environments.
• Experience managing projects through full lifecycle in GMP-regulated facilities.
• Familiarity with FDA-regulated environments and life sciences standards.

Responsibilities

• Lead multidisciplinary engineering and design projects for biotechnology, pharmaceutical, and specialty chemical clients.
• Manage project planning, budgeting, scheduling, and resource coordination.
• Serve as primary client contact and build strong relationships to meet project objectives.
• Coordinate process, mechanical, piping, electrical, instrumentation, controls, structural, and architectural teams.
• Ensure deliverables meet technical, quality, regulatory, and client requirements.

Skills

Project management

Cross-functional leadership

Communication skills

Client relationship management

Budgeting

Regulatory compliance

Team coordination

Microsoft Office

Education

Bachelor or Master of Science in Mechanical, Electrical, Chemical or Civil Engineering

Tools

Microsoft Office

Job description

Hargrove Life Sciences, LLC is seeking a Project Manager to lead multidisciplinary engineering and design projects for clients across biotechnology, pharmaceutical, and specialty chemical industries. You will manage planning, budgeting, scheduling, and client communications to ensure successful delivery from front-end planning through startup.

The role requires 8+ years of relevant experience in GMP-regulated environments, with an engineering background and PMP preferred.