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Resilience

Biologics and sterile injectables CDMO

CSV Engineer 3

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeWest Chester Township, OH, USA

About the Job

Requirements

  • Demonstrated experience in validation or process engineering.
  • Demonstrated ability to independently lead validation studies and projects from planning through execution with minimal supervision.
  • Hands-on experience with automation and computer system validation (CSV).
  • Working knowledge of GxP regulations and validation standards for computerized systems, including 21 CFR Part 11, GAMP 5, and data integrity (ALCOA+) principles.
  • Ability to expertly read and interpret engineering drawings, P&IDs, and system diagrams.
  • Strong analytical skills with keen attention to detail.
  • Strong written and verbal communication skills, including technical report writing.
  • Strong problem-solving abilities and sound independent judgment.
  • Ability to prioritize and manage own time and workload across concurrent projects.
  • Ability to coach peers and provide technical guidance to less-experienced team members.
  • Work may require gowning and adherence to cleanroom, personal protective equipment, and safety requirements.
  • Occasional lifting of up to 25 lbs and the ability to stand, walk, and access equipment on the manufacturing floor for extended periods.
  • May require work outside standard business hours to support production schedules, shutdowns, or time-sensitive validation activities.

Responsibilities

  • Independently plan, author, and execute validation deliverables — validation plans, protocols (IQ/OQ/PQ), and summary reports — for automation and computerized systems in accordance with GAMP 5 and applicable cGMP requirements.
  • Lead the qualification and lifecycle management of automated equipment and GxP computer systems (e.g., PLC, SCADA, DCS), including 21 CFR Part 11 and data integrity (ALCOA+) compliance.
  • Serve as a technical advisor on validation strategy and risk-based approach across the facility, utility, process, and cleaning validation portfolio.
  • Lead and coordinate validation studies and investigations with minimal supervision, applying independent technical judgment to resolve complex issues.
  • Communicate project priorities, risks, and progress to the process team on a continuing basis.
  • Identify and drive continuous-improvement opportunities in validation methodology, automation, and documentation practices.
  • Prepare and review validation documentation, ensuring activities, actions, and results are accurate, complete, and audit-ready.
  • Answer compliance and process questions from cross-functional partners and serve as a subject-matter resource during regulatory and internal audits.
  • Initiate and document appropriate corrective action when process deviations or system non-conformances occur, escalating issues beyond established procedures as needed.
  • Maintain validated state through change control, periodic review, and requalification activities.
  • Provide technical coaching and guidance to less-experienced engineers and technicians on validation methodology and automation best practices.
  • Build alignment across engineering, quality, and operations on validation requirements and acceptance criteria.
  • May oversee and direct the validation activities of others within assigned projects.
  • Perform work in a combination of office, laboratory, and cGMP manufacturing environments.
  • Work 8 hours Monday through Friday, with some flexibility; the employer may modify schedules based on business needs.

Desired Qualifications

  • Bachelor’s degree in Engineering, Computer Science, or a related discipline.
  • 5+ years of experience in validation or process engineering, including hands-on automation and computer system validation.
  • Experience in a regulated or cGMP manufacturing environment.
  • Familiarity with structured software development lifecycle (SDLC), configuration management, and scripting for automated and computerized systems.
  • Hands-on experience with industrial automation platforms (e.g., Rockwell/Allen-Bradley, Siemens, or Emerson DeltaV PLC/SCADA/DCS) and data historians.
  • Familiarity with automated testing tools and validation lifecycle management (VLM) software.

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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