Facilities Engineer

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

Facility Engineer
Location: Englewood, CO, 80112
Industry: Pharmaceutical Manufacturing
Work Environment: GMP-Regulated Manufacturing Facility Position Summary

A leading pharmaceutical manufacturing organization is conducting a search for a Facility Engineering Manager to support facility engineering operations, capital projects, utilities, equipment, and infrastructure within a highly regulated manufacturing environment.

Key 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.
• Conduct and/or coordinate performance inspections of HVAC, plumbing, electrical, boilers, mechanical systems, and other facility utilities.
• Manage site activities necessary for successful execution of facility and capital projects.
• Coordinate with internal teams and external vendors to ensure projects are executed safely, efficiently, and according to established requirements.
• Ensure facility operations comply with applicable OSHA, cGMP, FDA, and other regulatory requirements.
• Collaborate with Maintenance teams to develop and implement effective preventive maintenance programs.
• Ensure Engineering, Project, and Maintenance documentation remains accurate and up to date.
• Partner with Production and Quality teams to ensure facility readiness for manufacturing operations.
• Support the identification and resolution of facility technical issues throughout the equipment and facility lifecycle.
• Ensure equipment and facility systems are properly handed over to end users following repairs, preventive maintenance, modifications, and projects.
• Apply facilities engineering expertise to improve operating procedures, design specifications, technical documentation, and departmental processes.
• Support vendor management and third-party contractors involved in facility projects and modifications.
• Ensure all facility-related work is performed safely and in accordance with applicable industry standards.
• Support continuous improvement initiatives across Facilities and Engineering operations.
• Perform other duties as assigned by senior Facilities and Engineering leadership.

Required Qualifications

• Minimum 5 years of experience managing facilities or facility engineering within 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.
• Experience managing capital projects and facility remodels involving GMP-regulated spaces.
• Strong understanding of facility systems, including HVAC, electrical, plumbing, mechanical systems, boilers, and utilities.
• Strong written and verbal communication skills, including presentation capabilities.
• Strong organizational skills and ability to manage multiple priorities.
• Results-oriented approach with strong problem-solving and decision-making abilities.
• Proficiency with Microsoft Project, Outlook, Excel, and Word.