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Catalent

Global contract drug formulation, manufacturing, packaging

Associate – Biomanufacturing - Downstream/Mrna

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeMadison, WI, USA

About the Job

Requirements

  • Have a high school diploma or equivalent and at least four years of relevant experience, or a bachelor's or associate's degree in a scientific, engineering, or biomanufacturing discipline and at least one year of experience, or a master's degree in STEM with no formal experience.
  • Be able to use Microsoft Word, Excel, and other Office systems.
  • Meet the physical requirements, including frequent lifting or moving of up to 10 pounds and occasional lifting or moving of up to 50 pounds, and comply with EHS responsibilities.
  • Be able to work in a controlled, heated, ventilated, and air-conditioned environment and operate in a cleanroom as needed.

Responsibilities

  • Perform basic troubleshooting and downstream purification for mRNA production, including in-vitro transcription reactions, chromatography, tangential flow filtration, viral filtration, bulk drug substance filling, and column packing and qualification.
  • Follow manufacturing Batch Production Records and Standard Operating Procedures in accordance with current Good Manufacturing Practices, with a focus on right-first-time execution.
  • Document activities in accordance with Good Documentation Practices in Batch Production Records, forms, and other quality documentation.
  • Recognize deviations from the intended procedure and raise awareness through the Rapid Response process; proactively identify safety, quality, and efficiency improvements.
  • Participate in the Catalent Way continuous improvement culture, lead Just Do It continuous improvement activities, and engage in implementing continuous-improvement projects.
  • Coach more junior team members on basic execution activities and act as an onboarding buddy to help new team members learn the culture and basic workplace expectations.
  • May become a Certified Trainer and take responsibility for final sign-off of training completion for basic execution activities.
  • Interact with clients during in-person or virtual Person In Plant observations to provide updates on batch schedule and status.
  • Participate in daily shift huddles and lead shift-exchange activities.
  • Perform cleanroom housekeeping, including room and equipment cleaning, waste disposal, and maintenance of 5S standards.
  • Perform other duties as assigned.

Desired Qualifications

  • GMP manufacturing experience.
  • 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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