Facilities Engineer

Actalent; Louisville (CO); On-site; USD 44,964 - 55,572; Full time

Benefits offered by this job

Medical, dental & vision

401(k)

Life Insurance

Disability

HSA

Time Off

Job summary

Actalent is seeking a Facilities Engineering Technician for a hands-on, on-site role at a state-of-the-art lentiviral vector manufacturing facility in Louisville, CO. You will perform corrective and preventative maintenance on building systems and lab equipment, ensuring cGMP and FDA compliance through accurate documentation in CMMS.

The role requires 5+ years in facilities maintenance, an Associate's degree, and hands-on experience with HVAC, electrical, plumbing, and life-safety systems, plus

Qualifications

• 5+ years in facilities maintenance or facilities engineering in regulated environments
• Associate’s degree in a technical field or closely related discipline
• Hands-on experience with equipment in manufacturing/lab settings
• Ability to troubleshoot mechanical systems (motors, pumps, boilers)
• Ability to troubleshoot electrical systems and power distribution
• Familiarity with GMP/FDA regulations and cGMP documentation
• Experience documenting maintenance in CMMS
• Physical ability to stand, bend, kneel, lift up to 30 lb

Responsibilities

• Perform corrective and preventative maintenance on building systems and lab equipment to ensure safe, reliable operations
• Inspect and repair HVAC, plumbing, electrical, and life-safety systems daily
• Troubleshoot mechanical, electrical, plumbing, pneumatic and hydraulic issues
• Work hands-on with motors, pumps, chillers, boilers, autoclaves and cryogenic units
• Maintain GMP documentation of maintenance activities in CMMS (Blue Mountain preferred)
• Operate and monitor building automation systems (BMS, EMS, PLCs)
• Collaborate with cross-functional teams to support production and facility improvements
• Follow cGMP and FDA requirements for maintenance activities

Skills

Facilities maintenance

Electrical systems

Mechanical systems

CMMS documentation

Blue Mountain CMMS

Cross-functional teamwork

On-site work

Safety compliance

Education

Associate's degree in a technical field

Tools

CMMS software

Blue Mountain CMMS

Job description

Job Title: Facilities Engineering Technician

The Facilities Engineering Technician plays a key role in maintaining a state-of-the-art lentiviral vector manufacturing facility by performing corrective and preventative maintenance on building systems and laboratory equipment. This position ensures the reliable operation of mechanical, electrical, plumbing, and life-safety systems while maintaining strict cGMP and FDA compliance through accurate documentation in a CMMS. The technician troubleshoots complex facility issues, supports off-hours emergency repairs, and oversees external vendors to ensure high-quality work and adherence to safety and regulatory standards. This is a hands-on, on-site role within a high-tech, mission-driven biotechnology environment.

Responsibilities

• Perform corrective and preventative maintenance on building systems and laboratory equipment to ensure safe and reliable facility operations.
• Inspect, maintain, and repair HVAC, plumbing, electrical, and life-safety systems daily to minimize downtime and support uninterrupted operations.
• Troubleshoot mechanical, electrical, plumbing, pneumatic, and hydraulic issues across the facility and implement effective solutions.
• Work hands-on with motors, pumps, chillers, boilers, and laboratory equipment such as autoclaves and cryogenic units to keep equipment in optimal condition.
• Maintain accurate and timely GMP documentation of all maintenance activities using CMMS software, preferably Blue Mountain, in alignment with FDA and cGMP standards.
• Operate, monitor, and adjust building automation systems, including BMS, EMS, and PLCs, to maintain proper environmental and process conditions.
• Collaborate with cross-functional teams in a manufacturing and laboratory environment to support production needs and facility improvements.
• Follow cGMP and FDA regulatory requirements for all maintenance activities to support a compliant, audit-ready facility.

Essential Skills

• At least 5 years of experience in facilities maintenance or facilities engineering roles, preferably within regulated or manufacturing environments.
• Associate’s degree in a relevant technical field or closely related discipline.
• Strong hands-on experience with chemical manufacturing equipment in an industrial or laboratory setting.
• Proven ability to troubleshoot and repair mechanical systems, including motors, pumps, chillers, and boilers.
• Proven ability to troubleshoot and repair electrical systems, including facility power distribution and equipment-level components.
• Familiarity with GMP environments and FDA regulations, including working under cGMP guidelines.
• Experience maintaining cGMP-compliant documentation of maintenance activities using CMMS software.
• Physical ability to perform job duties, including standing, bending, kneeling, and lifting up to 30 pounds.

Additional Skills & Qualifications

• Experience working in biopharma, biotechnology, or cell-and-gene therapy facilities.
• Experience in facilities that operate under strict cGMP guidelines and FDA oversight.
• Hands-on experience with building automation systems beyond basic operation, including configuration or optimization.
• Strong organizational skills and attention to detail for maintaining accurate records and documentation.
• Interest in contributing to mission-driven work supporting advanced therapeutic manufacturing.

Work Environment

The Facilities Engineering Technician works on-site in a state-of-the-art lentiviral vector manufacturing facility located in Louisville, Colorado. This is a fully on-site, hands-on role that requires daily presence in a high-tech, cGMP-compliant environment. The facility operates under strict cGMP and FDA guidelines, with high standards for safety, quality, and documentation. The culture emphasizes cross-departmental collaboration, values diverse perspectives, and promotes a joyful, accountable, and solution-oriented approach to work. The technician supports both routine and dynamic operations, including participation in on-call rotations and response to emergency maintenance needs. Personal protective equipment such as gloves, protective clothing, and safety glasses is regularly required, and the role involves physical activity including standing, bending, kneeling, and lifting up to 30 pounds. The facility features advanced building automation systems and modern manufacturing and laboratory equipment, offering a technologically sophisticated work setting within a vibrant regional biotech community.

Job Type & Location

This is a Contract position based out of Louisville, CO.

Pay and Benefits

The pay range for this position is $32.64 – $40.34/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan — Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Louisville,CO.

Application Deadline

This position is anticipated to close on Jul 29, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.