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Resilience

Biologics and sterile injectables CDMO

Manufacturing Technician 4 Lead - Inspection

Inspection & TestConfirmed live in the last 24 hours
Full-timeWest Chester Township, OH, USA

About the Job

Requirements

  • Significant experience in a pharmaceutical, biotechnology, or cGMP-regulated manufacturing environment, including demonstrated expertise across all inspection types and equipment and prior experience leading floor execution.
  • Significant experience in a pharmaceutical, biotechnology, or cGMP-regulated manufacturing environment, including knowledge of cGMP requirements, inspection processes, documentation practices, and investigation support.
  • Mastery of visual defect detection and inspection accuracy across all material types handled on the floor.
  • Strong organizational, analytical, and problem-solving skills, with the ability to independently prioritize operations.
  • Ability to effectively read, write, speak, and understand English to communicate technical information cross-functionally.
  • Experience providing on-the-job training or technical guidance to peers while fostering compliance and continuous improvement.
  • Ability to work effectively as part of a team in a fast-paced production environment.
  • Ability to perform non-sedentary work, including climbing, kneeling, repetitive motion, working in temperature changes, and exerting up to 100 pounds of force to move objects.
  • Visual acuity for working with data and figures, viewing computer terminals, extensive reading, operating machinery and motor vehicles, and observing facilities.
  • Participation in an occupational health program, which can include medical assessment, surveillance, vaccination, and testing.
  • Ability to use required personal protective equipment, potentially including respirators, powered air-purifying respirators, gowns, gloves, face protection, and other barrier equipment.
  • Ability to pass an eye exam during onboarding.
  • Ability to adhere to the Quality Management System, Quality Policy, Standard Operating Procedures, current Good Manufacturing Practices, and other applicable regulations and standards relevant to the role.

Responsibilities

  • Lead and monitor inspection process activities to ensure successful production-floor operations.
  • Perform inspection activities as needed to support floor coverage and maintain qualifications.
  • Perform inventory control and reconciliation using SAP and WES.
  • Execute protocols as required for equipment qualification and process validation work.
  • Ensure production-floor work follows requirements in accordance with Standard Operating Procedures and current Good Manufacturing Practices.
  • Support lean activities, including 5S and problem-solving, and serve as a continuous-improvement project resource for the Process Execution Team.
  • Complete advanced batch-record and Good Manufacturing Practice documentation entries on the production floor, including complex or non-routine documentation, and guide team members on documentation accuracy.
  • Access and print current-revision Standard Operating Procedures and forms through ECMS.
  • Follow job-related safety procedures, including personal protective equipment use, lockout/tagout, ergonomics, and chemical handling.
  • Use process documents, including Standard Operating Procedures, forms, and batch records, to guide work in accordance with procedures and current Good Manufacturing Practices.
  • Maintain required certifications and qualifications for the assigned work area.
  • Provide subject-matter guidance to production and mechanical technicians as a technical resource for the team.
  • Act as a certified on-the-job trainer for assigned equipment and process tasks, training and supporting team members.
  • Support team members in maintaining required qualifications and certifications.
  • Collaborate with Process Facilitators and Engineers on inspection-floor initiatives.
  • Apply problem-solving and prioritization skills to make independent decisions and guide team members on daily production activities.
  • Support deviation investigations, corrective and preventive action execution, and Standard Operating Procedure revisions as the inspection-floor subject-matter expert.
  • Attend and actively participate in daily Tier 1 meetings.

Desired Qualifications

  • High school graduate, vocational-school graduate, or equivalent.
  • Four or more years of experience in a pharmaceutical, biotechnology, or cGMP-regulated manufacturing environment.
  • Prior inspection experience.
  • Experience tracking and reporting metrics.
  • Experience contributing to inspection-process improvements, deviation investigations, and qualification programs.
  • Experience working in a lean manufacturing environment.
  • Working knowledge of Microsoft applications, SAP, and/or Veeva Vault.

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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