Facilities Engineering Manager – GMP/Pharma Projects

TalentBridge; Englewood (CO); On-site; USD 90,000 - 125,000; Full time

Job summary

TalentBridge in Englewood, CO seeks a Facility Engineer to oversee facility systems, utilities, equipment, and infrastructure within a GMP-regulated pharmaceutical manufacturing environment. The role supports capital projects and works with Maintenance, Production, and Quality teams to ensure readiness for manufacturing operations.

The ideal candidate has a Bachelor's degree in engineering, 5+ years in facilities within a cGMP/FDA environment, and strong project-management skills to drive

Qualifications

• Minimum 5 years of experience managing facilities or facility engineering in a cGMP/FDA-regulated pharmaceutical manufacturing environment.
• 2+ years of experience in an aseptic processing facility preferred.
• Strong knowledge of cGMP guidelines and pharmaceutical manufacturing standards.
• Bachelor's degree required; technical or engineering degree preferred.
• Demonstrated project management experience.

Responsibilities

• Manage daily Facility Engineering activities, including facility systems, utilities, equipment, and infrastructure.
• Support and manage capital projects, facility modifications, upgrades, expansions, and equipment installations.
• Coordinate with internal teams and external vendors to ensure projects are executed safely, efficiently, and according to established requirements.
• Ensure facility operations comply with OSHA, cGMP, FDA, and other regulatory requirements.
• Collaborate with Maintenance, Production, and Quality teams to ensure facility readiness for manufacturing operations.

Skills

Facility management

Project management

Regulatory compliance

Communication skills

Organization skills

Problem solving

Education

Bachelor's degree in engineering

Tools

Microsoft Project

Outlook

Excel

Word

Job description

TalentBridge in Englewood, CO seeks a Facility Engineer to oversee facility systems, utilities, equipment, and infrastructure within a GMP-regulated pharmaceutical manufacturing environment. The role supports capital projects and works with Maintenance, Production, and Quality teams to ensure readiness for manufacturing operations.

The ideal candidate has a Bachelor's degree in engineering, 5+ years in facilities within a cGMP/FDA environment, and strong project-management skills to drive