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Resilience

Biologics and sterile injectables CDMO

Facilities Engineer 3 - HVAC Utilities

Building Services EngineeringConfirmed live in the last 24 hours
Full-timeWest Chester Township, OH, USAIn-person

About the Job

Requirements

  • Experience supporting facilities systems in a Good Manufacturing Practice environment.
  • Prior experience in maintenance or technical documentation.
  • Strong interpersonal skills and self-motivation.
  • Strong organizational skills.
  • Strong written and verbal communication skills.
  • Preferred: Bachelor's degree in engineering.
  • Preferred: 5–7 years of engineering experience in a Good Manufacturing Practice environment.

Responsibilities

  • Provide engineering oversight and technical support for site heating, ventilation, and air conditioning systems, including chilled water, hot water, air handling units, exhaust systems, and cleanroom environments.
  • Support temperature-controlled chambers, including cold rooms, controlled warehouse space, and standalone reach-in units.
  • Apply cleanroom HVAC design requirements and understand the HEPA filter certification process.
  • Develop and execute preventive and predictive maintenance programs to ensure system reliability and uptime.
  • Provide Facilities support on capital projects and follow site specifications for all projects.
  • Participate in new equipment design specification and collaborate with cross-functional teams, contractors, and vendors to deliver engineering solutions.
  • Use good engineering and documentation practices during job activities.
  • Troubleshoot Facilities utilities and systems, identify temporary and permanent fixes, and support system issues or improvements.
  • Maintain technical documentation, standard operating procedures, system drawings, and certification records; apply knowledge of piping and instrumentation diagrams.
  • Lead and coordinate investigations and studies.
  • Use a computerized maintenance management system to manage logistics.
  • Initiate appropriate actions when process deviations occur.
  • Own change controls, corrective actions, impact assessments, change-control action items, deviations, and periodic reviews.
  • Monitor records for regulatory compliance and monitor equipment and systems for performance and problem indicators.
  • Coordinate with representatives from other departments and attend team meetings to discuss progress, initiatives, and other matters.
  • Perform data entry and answer compliance and Facilities questions from others.
  • Read, understand, and comply with cGMP and standard operating procedures, including general safety and lockout procedures.
  • Communicate policies and procedures to employees.
  • Establish visual tracking and other tools to enhance audit readiness and trend analysis.
  • Lead process-improvement activities and teams to meet strategic goals.

About the Company

Resilience

Biologics and sterile injectables CDMO

Resilience is a North American CDMO focused on biologics and sterile drug products. It provides end-to-end services from development through commercial production, including biologics development and drug substance manufacturing, aseptic fill/finish, device assembly, packaging, logistics, regulatory support, and tech transfer, all coordinated via a stage-gate process and a digital quality management system. It differentiates itself with North American-based, integrated biologics and sterile capabilities, a focus on sterile injectables and device assembly, and recent expansion into injectable pen devices for diabetes and obesity medicines. Its goal is to broaden access to complex medicines while protecting North American biopharma supply chains with dependable capacity and strong regulatory support from clinical development to commercial scale.

Company size
1,001-5,000
Company stage
Growth Equity (Venture Capital)
Total funding
$3.2B
Headquarters
Blue Ash, OH
Founded
2020

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