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Resilience

Biologics and sterile injectables CDMO

Process Engineer 3 - Inspection

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeWest Chester Township, OH, USAIn-person

About the Job

Requirements

  • Significant experience supporting automated inspection or vision systems in a GMP-regulated manufacturing environment.
  • Experience with equipment validation (IQ/OQ/PQ) and lifecycle management.
  • Experience leading technical investigations, root cause analysis, and change control processes.
  • Strong understanding of equipment reliability principles (MTBF, MTTR, FMEA, risk management).

Responsibilities

  • Own the reliability strategy for automated inspection systems, ensuring sustained performance against established KPIs, including OEE, false rejects, defect rates, MTBF, MTTR, and downtime.
  • Develop and maintain preventive and predictive maintenance strategies for inspection equipment, including vision systems, cameras, sensors, and reject mechanisms.
  • Analyze performance, reject-rate data, and trends to identify failure modes; implement corrective and preventive actions and vision recipe improvements.
  • Lead complex troubleshooting efforts for mechanical, electrical, controls, and vision-related issues.
  • Serve as the technical subject matter expert for automated inspection systems.
  • Provide mentorship and technical guidance to engineering, maintenance, and operations teams.
  • Provide on-call technical support as required.
  • Ensure automated inspection systems remain validated and inspection-ready in accordance with FDA and global regulatory expectations.
  • Author and/or approve URS, FAT/SAT protocols, commissioning documentation, and IQ/OQ/PQ protocols and reports related to inspection equipment.
  • Support validation lifecycle activities, including revalidation following changes or performance drift.
  • Lead technical investigations for inspection-related deviations, non-conformances, and customer complaints.
  • Support change control activities, including appropriate risk assessments and validation impact evaluations.
  • Serve as the inspection equipment subject matter expert during regulatory inspections and internal audits.
  • Lead long-term reliability and performance improvement initiatives focused on false-reject reduction, detection capability optimization, equipment downtime reduction, OEE improvement, obsolescence management, and inspection process improvements (such as SOR/EOR).
  • Implement data-driven monitoring strategies and statistical analysis to ensure sustained inspection effectiveness.
  • Support new equipment installations, upgrades, and lifecycle planning.
  • Drive continuous improvement initiatives using Lean and Six Sigma methodologies.

Desired Qualifications

  • Experience with automated vision systems, camera-based inspection platforms, and PLC/controls troubleshooting.
  • Experience supporting regulatory inspections.
  • Experience with CMMS systems and reliability analytics.
  • Project management experience in capital or long-term reliability initiatives.
  • Lean Manufacturing or Six Sigma certification.

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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