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Catalent

Global contract drug formulation, manufacturing, packaging

Associate Biomanufacturing - Upstream

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeMadison, WI, USANo salary listed

About the Job

Requirements

  • A high school diploma or equivalent plus at least four years of relevant experience, or a Bachelor's or Associate degree in a scientific, engineering, or biomanufacturing discipline with at least one year of experience, or a Master's in Science, Technology, Engineering, or Mathematics without formal experience.
  • Ability to use Microsoft Word, Excel, and other Office systems.
  • Ability to perform the stated physical tasks, including frequent lifting or moving of up to 10 pounds and occasional lifting or moving of up to 50 pounds, and comply with Environmental Health and Safety responsibilities.
  • Ability to work in a controlled cleanroom environment as needed.

Responsibilities

  • Perform basic troubleshooting and upstream cell culture activities, including aseptic manipulation in a Grade A environment, large-scale culture in single-use bioreactors, clarification of bulk harvest product, and cell bank vialing.
  • Follow manufacturing Batch Production Records and Standard Operating Procedures in accordance with current Good Manufacturing Practices, focusing on right-first-time execution.
  • Document activities in compliance with Good Documentation Practices in Batch Production Records, forms, and other quality documentation.
  • Recognize deviations from intended procedures and raise awareness through the Rapid Response process; identify safety, quality, and efficiency improvements.
  • Participate in the Catalent Way continuous improvement culture, lead “Just Do It” activities, and engage in continuous improvement projects.
  • Coach junior team members on basic execution activities and act as an onboarding buddy for new hires.
  • May become a Certified Trainer and take responsibility for final sign-off of training completion for basic execution activities.
  • Interact with clients during Person In Plant or virtual observations to provide updates on batch schedule and status.
  • Participate in daily shift huddles and lead shift exchange activities.
  • Perform general cleanroom housekeeping, including room and equipment cleaning, waste disposal, and maintenance of 5S standards.
  • Perform other duties as assigned.

Desired Qualifications

  • Experience in Good Manufacturing Practice manufacturing is preferred.
  • Preferred experience with TrackWise, ComplianceWire, JD Edwards, DeltaV, and chromatography software such as Unicorn.

About the Company

Catalent

Global contract drug formulation, manufacturing, packaging

Catalent provides end-to-end contract development and manufacturing services for pharmaceutical, biotechnology, and consumer health products. Its offerings cover drug formulation, large-scale manufacturing, clinical supply, and packaging under long-term partnerships, coordinating through a connected supply chain to move products from development to market. It differentiates itself with a broad, integrated service platform and long-standing customer relationships that help clients accelerate development and ensure reliable supply. The company aims to help clients bring products to market efficiently while balancing quality, cost, and sustainability across the product lifecycle.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Franklin Township, NJ
Founded
1996

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