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Resilience

Biologics and sterile injectables CDMO

Manufacturing Technician 2 - Inspection, Nights

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

About the Job

Requirements

  • Experience in a pharmaceutical or cGMP-regulated environment is required.
  • The candidate must be able to understand, read, write, communicate, and follow instructions in English.
  • The candidate must maintain attention to detail, keep accurate records, and perform mathematical calculations.
  • The candidate must acquire and maintain all certifications and qualifications required for the assigned work area.
  • Some overtime may be required with minimal advance notice to support business needs.

Responsibilities

  • Operate assigned machinery, including servicing automated inspection equipment, monitoring equipment status, reintroducing materials, manually palletizing inspected materials, and assuring a smooth flow of product.
  • Perform manual visual, cosmetic, and physical inspection of material, promptly escalating concerns to the Lead and Manager/Supervisor as needed; obtain and maintain visual inspection qualification.
  • Start up equipment, make minor machinery adjustments, remove jams, perform minor troubleshooting, and carry out minor assembly or disassembly for cleaning.
  • Use material handling equipment such as motorized and manual pallet jacks and non-motorized lifts.
  • Perform cleaning, housekeeping, and line-clearance activities for assigned areas as required to maintain a cGMP environment.
  • Complete batch-record and GMP documentation entries, maintain records and logs required for job responsibilities, and perform mathematical computations when needed.
  • Maintain knowledge of product security controls and material handling equipment.
  • Be responsible for the outgoing quality level.
  • Follow job-related safety procedures and understand hazards, including personal protective equipment, ergonomics, lockout/tagout, human safety, material handling, waste handling, chemical handling, and spill controls; report discrepancies to the process facilitator.
  • Perform work 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.
  • Learn to print standard operating procedures and forms through ECMS.
  • Support lean activities and process improvement, including performing 5S in the work area, participating in problem-solving, and manually tracking overall equipment effectiveness and process performance data.
  • Review operational standard operating procedures, forms, and batch records for accuracy; identify and suggest process improvements while maintaining quality and cGMP compliance.
  • Support other work areas as needed and perform other assigned duties with minimal supervision under the direction of the process facilitator or designee.
  • When trained and given access, transfer materials in and out of cold rooms.
  • If trained and certified as a trainer, train and evaluate other team members on assigned equipment and process tasks.
  • Develop novice-to-intermediate knowledge of SAP inventory movements and inventory management, including moving items between storage locations and goods-issuing items to process orders.

Desired Qualifications

  • Prior production experience.
  • Experience working in a lean manufacturing environment.
  • Knowledge of current Good Manufacturing Practices and Food and Drug Administration policies and procedures.
  • Prior inspection experience in a pharmaceutical manufacturing environment.

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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