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Resilience

Biologics and sterile injectables CDMO

Manufacturing Technician 2 - Process Execution Team

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

About the Job

Requirements

  • Must be able to understand, read, write, communicate, and follow instructions in English.
  • Must have good attention to detail and be capable of keeping accurate records and performing mathematical calculations.

Responsibilities

  • Operate equipment and perform in-process monitoring, line clearances, OEE data collection, cosmetic inspection, cleaning, and batch record entries in accordance with current good manufacturing practices.
  • Operate assigned machinery, service filling machines with materials, remove finished materials from machine tables, and assure smooth product flow.
  • Assemble, disassemble, operate, and sanitize various filling equipment.
  • Execute filter integrity testing as needed per standard operating procedures.
  • Perform cleaning and housekeeping activities for assigned areas to maintain a current good manufacturing practice environment.
  • Start up machinery and make minor adjustments.
  • Enter data into computer systems, including supervisory control and data acquisition and human-machine interface systems, as required.
  • Perform visual and physical checks of in-process and finished materials as requested.
  • Work with printing devices, including printing mats.
  • Complete batch record and good manufacturing practice documentation entries, and maintain records and logs required for job responsibilities, including mathematical computations where needed.
  • Use knowledge of product security controls and material handling equipment; be responsible for outgoing quality levels.
  • Understand aseptic behaviors and media fills, including line interventions, and maintain basic knowledge of viable and non-viable monitoring equipment.
  • Perform inventory control and reconciliation activities, including limited use of SAP as needed.
  • Perform work in accordance with standard operating procedures, current good manufacturing practices, and established safety procedures and Occupational Safety and Health Administration requirements and guidelines.
  • Be familiar with material safety data sheets for area chemicals and job-related safety procedures and 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.
  • Assist mechanical staff with preventive maintenance procedures as required.
  • Support lean activities and process improvement, including 5S, Single Minute Exchange of Die, problem-solving, and manual tracking of OEE performance data for process improvement analysis.
  • Assist with executing validation and engineering protocols for processes and equipment.
  • Identify and suggest process improvements while maintaining quality and current good manufacturing practice compliance.
  • Train and support other filling functions as needed.
  • Perform other assigned duties with minimal supervision under the direction of the process facilitator or designee.
  • Acquire and maintain required certifications and qualifications for the assigned work area.
  • Learn new skills and develop capabilities on an ongoing basis to contribute to the Process Execution Team.
  • Work some overtime with minimal advance notice as required by business needs.

Desired Qualifications

  • Prior production experience.
  • Experience working in a pharmaceutical or current good manufacturing practice-regulated environment.
  • Experience working in a lean manufacturing environment.
  • Knowledge of current good manufacturing practices and Food and Drug Administration policies and procedures.
  • High school graduate, vocational school graduate, or equivalent.

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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