R

Resilience

Biologics and sterile injectables CDMO

Manufacturing Technician 2 - Formulation

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

About the Job

Requirements

  • Prior experience in a regulated manufacturing environment.
  • Working knowledge of automated and semi-automated equipment, such as pumps and mixers, and light material handling equipment.
  • Ability to read, write, speak, and understand English to follow detailed instructions and communicate with team members.
  • Ability to accurately complete batch records, logbooks, and other controlled documentation.
  • Basic problem-solving and mathematical skills, including routine calculations such as weights, measures, and conversions.
  • Ability to follow standard operating procedures, written procedures, and work instructions with minimal supervision, and escalate issues as needed.
  • 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 climb, kneel, perform repetitive motions, tolerate temperature changes, and exert 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 general facility observation.
  • Participation in an occupational health program, which may include medical assessment, surveillance, vaccination, and testing.
  • Ability to use required personal protective equipment, including respirators, powered air-purifying respirators, gowns, gloves, face protection, and other barrier equipment.
  • Ability to pass an eye exam during onboarding.

Responsibilities

  • Perform start-up, equipment operation, batch execution, material handling, cleaning, housekeeping, and line clearance activities to maintain a current Good Manufacturing Practice environment.
  • Work collaboratively with mechanic technicians and lead technicians to resolve production-related issues involving batch setup and execution, documentation, equipment operations, standard operating procedures, and safety and quality inspection procedures.
  • Monitor process execution, materials, and supply levels to support successful production-floor operations; coordinate production tasks such as batch execution.
  • Perform clean-in-place and steam-in-place procedures on process lines according to standard operating procedures.
  • Set up and create single-use connections, including single-use bags.
  • Perform filter integrity testing as needed according to standard operating procedures.
  • Perform parts washing and dispensing operations as necessary.
  • Assemble, disassemble, and sanitize equipment.
  • Operate automated and semi-automated equipment, including pumps and mixers.
  • Assist technical staff with preventive maintenance procedures as required.
  • Support lean activities, including 5S, problem-solving, process-improvement analysis, and manual tracking of performance data for overall equipment effectiveness.
  • Perform inventory control using SAP.
  • Complete batch record and Good Manufacturing Practice documentation entries, including mathematical computations.
  • Follow job-related safety procedures for personal protective equipment, lockout/tagout, ergonomics, material handling, chemical, waste and spill controls, and human safety.
  • Perform work in accordance with standard operating procedures, current Good Manufacturing Practices, established safety procedures, and Occupational Safety and Health Administration requirements and guidelines; report discrepancies to process facilitators.
  • Acquire and maintain required certifications and qualifications for the assigned work area.
  • Cross-train and support other work areas as needed.
  • Attend and actively participate in daily tier meetings.
  • Adhere to the Quality Management System, including the Quality Manual, Quality Policy, standard operating procedures, current Good Manufacturing Practices, and other regulations and standards applicable to the role.

Desired Qualifications

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

Recently Posted Jobs

Explore more opportunities at Resilience

See more jobs