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Resilience

Biologics and sterile injectables CDMO

Automation Engineer 1

Controls & Automation EngineeringPosted on Nov 12
Full-timeWest Chester Township, OH, USAIn-person

About the Job

Requirements

  • Experience with some of the following automation systems: programmable logic controllers, human-machine interfaces, or supervisory control and data acquisition systems, including Rockwell, Inductive (Ignition), Aveva (Wonderware), Siemens, Emerson (GE), or B&R.
  • Ability to work independently with attention to detail and a desire to learn about manufacturing technologies.

Responsibilities

  • Participate in and support the design, optimization, commissioning, or validation of newly procured or existing equipment as the automation subject matter expert.
  • Interface with equipment and systems including programmable logic controllers, supervisory control and data acquisition systems, human-machine interfaces, servers, and other automation equipment.
  • Consult cross-functionally and assist system owners in process development as the automation subject matter expert.
  • Review and approve requirements, specifications, drawings, coding procedures, and guidelines.
  • Provide technical guidance and train others on systems, software, equipment, machines, procedures, or processes.
  • Use technical expertise and a troubleshooting approach to identify temporary and permanent fixes to address issues.
  • Review and approve documentation needed for equipment and process qualification.
  • Author, review, and revise standard operating procedures and specifications to maintain equipment, systems, or facilities, and comply with all standard operating procedures.
  • Ensure proper documentation practices during maintenance processes.
  • Recommend and initiate activities to ensure areas and equipment are maintained in a state of compliance.
  • Assess and implement improvements in productivity, waste generation, quality, and cost.
  • Lead and coordinate investigations and studies with little supervision.
  • Interact with regulatory agency personnel during audits and inspections.
  • Perform quality audits to ensure devices are in proper working condition.
  • Provide 24/7 support to others as part of a rotating on-call support system.

Desired Qualifications

  • Bachelor’s degree in Engineering, Computer Science, or a related discipline.
  • Experience with data historian and visualization systems such as Aveva PI (OSI PI).
  • Knowledge of change control, deviation, corrective and preventive action, validation, and qualification principles.

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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