R

Resilience

Biologics and sterile injectables CDMO

Manufacturing Technician 2

Machine & Process OperationConfirmed live in the last 24 hours
Full-timeWest Chester Township, OH, USAIn-person

About the Job

Requirements

  • Prior experience in a regulated manufacturing environment.
  • Working knowledge of product security controls and material handling equipment.
  • Demonstrated documentation and data entry skills, including accurate completion of batch records and logbooks.
  • Basic mathematical skills, including the ability to perform routine calculations such as weights, measures, and conversions.
  • Ability to effectively read, write, speak, and understand English to interpret standard operating procedures, batch records, and work instructions.
  • Ability to follow written procedures and work instructions with minimal supervision, escalating issues as needed.
  • Basic problem-solving skills and the ability to identify deviations or inconsistencies in processes or documentation.
  • Ability to work effectively as part of a team in a fast-paced production environment.
  • Ability to pass an eye exam during onboarding.
  • Ability to perform a primarily non-sedentary role, including climbing, kneeling, repetitive motion, working in changing temperatures, and exerting up to 100 pounds of force to move objects.
  • Visual acuity for working with data and figures, viewing a computer terminal, extensive reading, operating machinery or motor vehicles, and observing facilities.
  • Participation in an occupational health program, which may include medical assessment, surveillance, vaccination, and testing.
  • Ability to use personal protective equipment, which may include respirators, personal air-purifying respirators, gowns, gloves, face protection, and other barrier equipment.
  • Adherence to the established Quality Management System, Quality Policy, Standard Operating Procedures, current Good Manufacturing Practices, and other regulations and standards applicable to the role.

Responsibilities

  • Operate assigned machinery by servicing machines with materials, monitoring equipment status, reintroducing materials, manually palletizing finished materials, and ensuring smooth product flow.
  • Start up machinery, including equipment setup, recipe selection, data entry on SCADA and HMI, making minor adjustments, and performing critical sensor challenges.
  • Perform manual packaging tasks, including hand packaging and rework of in-process and finished material.
  • Operate light material-handling equipment, including motorized and manual pallet jacks and non-motorized lifts, to safely move, store, or deliver material.
  • Perform visual quality inspection and sampling of in-process materials, and promptly escalate concerns to the Lead and Management as needed.
  • Perform minor troubleshooting, including clearing minor jams and identifying equipment defects, and escalate issues to the Lead and Management as needed.
  • Perform inventory control and reconciliation activities using SAP and WES.
  • Perform cleaning, housekeeping, and line-clearance activities for assigned areas to maintain a current Good Manufacturing Practices environment.
  • Perform batch record and Good Manufacturing Practices documentation entries, and perform mathematical computations as required.
  • Follow job-related safety procedures, including personal protective equipment, lockout/tagout, ergonomics, material, chemical, and waste handling, spill controls, and human safety.
  • Support lean activities and process-improvement work, including 5S, problem-solving, and manual data collection.
  • Execute protocols as required for equipment qualification and process validation work.
  • Provide flexible support to other areas of the Manufacturing Team as needed.
  • Acquire and maintain all required certifications and qualifications for the assigned work area.
  • Attend and actively participate in daily Tier 0 meetings.

Desired Qualifications

  • High school graduate, vocational school graduate, or equivalent.
  • At least one year of experience in a pharmaceutical, biotechnology, or current Good Manufacturing Practices-regulated manufacturing environment.
  • Experience working in a lean manufacturing environment.
  • Working knowledge of current Good Manufacturing Practices principles, including documentation practices, safety procedures, and compliance expectations.
  • 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

Recently Posted Jobs

Explore more opportunities at Resilience

See more jobs