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Resilience

Biologics and sterile injectables CDMO

Supervisor - Multiple Teams

Equipment MaintenanceConfirmed live in the last 24 hours
Full-timeWest Chester Township, OH, USAIn-person

About the Job

Requirements

  • Prior experience in a regulated production environment, specifically responsible for equipment maintenance and performance.
  • Prior people leadership experience, including supervising, mentoring, or developing direct reports.
  • Ability to effectively understand, read, write, communicate, and follow instructions in English.
  • Ability to lift and handle equipment change parts, tooling, and materials associated with equipment maintenance and repair.

Responsibilities

  • Complete emergency repair, rebuilding, changeover, and inspection work on process-related equipment, including installation, inspection, testing, adjustment, repair, line turnarounds, changeovers, and preventative maintenance according to established procedures.
  • Complete documentation and required functions in the work order system to close out activities in compliance with current Good Manufacturing Practices (cGMPs).
  • Monitor data to ensure equipment and system performance within the assigned operating area.
  • Use testing, tools, and measuring equipment to maintain and troubleshoot electronic, environmental monitoring, pneumatic, hydraulic, and mechanical line equipment.
  • Train operators on equipment setup and minor adjustments or repairs.
  • Install new equipment and oversee equipment upgrades according to site standard operating procedures (SOPs).
  • Perform 5S activities and maintain organization of operating areas.
  • Perform work responsibly in accordance with SOPs, cGMPs, and established safety procedures and Occupational Safety and Health Administration (OSHA) requirements and guidelines.
  • Be familiar with Material Safety Data Sheets for chemicals in the area.
  • Perform batch record and Good Manufacturing Practice (GMP) documentation entries; maintain required records and logs, including mathematical computations when needed.
  • Work with minimal supervision under the direction of the Maintenance Manager, Process Managers, Engineer, or other activity leads.
  • Perform Technician and Mechanical Technician duties as required to support daily PET activities.
  • Use appropriate problem-solving and troubleshooting techniques to complete equipment repairs.
  • Follow and maintain compliance with established maintenance, repair, and operations (MRO) procedures and inventory control.
  • Serve as a project resource to PET to assist with timely project follow-up and implementation and validation activities.
  • Maintain aseptic processing and gowning certifications as required for assigned work areas.
  • Perform cleaning and housekeeping activities for assigned areas to maintain a cGMP environment.
  • Perform other similar and related responsibilities as assigned by area management.
  • Work some scheduled overtime and, when necessary, emergency overtime to support business needs and equipment operations within PET.

Desired Qualifications

  • High school graduate, vocational school graduate, or equivalent.
  • Associate degree in engineering or a related discipline, or equivalent mechanical trade school graduate.
  • Previous experience with automated equipment.
  • Training in mechanics, hydraulics, electronics, and testing equipment for electrical and/or mechanical troubleshooting.
  • Knowledge of data and materials maintenance systems such as SAP, KRONOS, or other material requirements planning (MRP) systems.
  • Experience with Overall Equipment Effectiveness (OEE), Total Productive Maintenance (TPM), Lean, or other continuous improvement systems.

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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