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Resilience

Biologics and sterile injectables CDMO

Maintenance Technician 3

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

About the Job

Requirements

  • Experience in a regulated production environment, specifically responsible for equipment maintenance and performance.
  • Experience with some of the following automation systems: programmable logic controllers, human-machine interfaces, supervisory control and data acquisition, Rockwell Inductive (Ignition), Aveva (Wonderware), Siemens, Emerson (GE), or B&R.
  • 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.
  • Proficiency with computerized maintenance management systems such as Maximo or SAP.

Responsibilities

  • Complete emergency repair, rebuilding, changeover, and inspection work on process-related equipment. Install, inspect, test, adjust, repair, and perform line turnarounds, changeovers, and preventative maintenance according to established procedures in a timely and efficient manner.
  • Troubleshoot automation systems, including programmable logic controllers, human-machine interfaces, and supervisory control and data acquisition systems.
  • Interpret diagrams, drawings, programmable logic controller code, and other schematics.
  • Complete documentation and required functions in the work order system to close out activities in compliance with current Good Manufacturing Practices.
  • Monitor data within the assigned operating area to maintain equipment and system performance.
  • Use testing tools and measuring equipment to maintain and troubleshoot electronic, environmental monitoring, pneumatic, hydraulic, and mechanical line equipment.
  • Train operators in equipment setup and minor adjustments or repairs.
  • Install new equipment and oversee equipment upgrades according to site standard operating procedures.
  • Perform 5S activities and maintain the organization of operating areas.
  • Perform work responsibly in accordance with standard operating procedures, current Good Manufacturing Practices, established safety procedures, and Occupational Safety and Health Administration requirements and guidelines.
  • Be familiar with Material Safety Data Sheets for area chemicals.
  • Complete batch record and Good Manufacturing Practice documentation entries; maintain records and logs as required, including mathematical computations where needed.
  • Work with minimal supervision under the direction of the Maintenance Facilitator, Process Facilitator, Engineer, or other activity leads.
  • Perform Technician and Mechanical Technician roles 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 procedures and inventory control.
  • Serve as a project resource to PET to support 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 current Good Manufacturing Practice environment.
  • Perform other similar and related responsibilities as assigned by area management.
  • Work overtime with prior notice to support business needs; emergency overtime may be required with little notice to ensure manufacturing equipment operation.

Desired Qualifications

  • High school graduate, vocational school graduate, or equivalent.
  • Associate degree in Engineering or a related discipline, or graduation from an equivalent mechanical trade school.
  • 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 materials requirements planning systems.
  • Experience with overall equipment effectiveness, total productive maintenance, 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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