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Catalent

Global contract drug formulation, manufacturing, packaging

Technician - Biomanufacturing, Downstream/Mrna

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 two years of relevant experience is required, or an associate's or bachelor's degree in a scientific, engineering, or biomanufacturing discipline without formal experience.
  • Ability to use Microsoft Word, Excel, and other Office systems.
  • Ability to 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 to perform the listed movement and computer-screen tasks.
  • Must comply with environmental, health, and safety responsibilities for the position.
  • Ability to operate in a cleanroom environment as needed.

Responsibilities

  • Perform basic downstream purification and mRNA production activities, including in-vitro transcription reactions, chromatography, tangential flow filtration, viral filtration, 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.
  • Identify safety, quality, and efficiency improvements, and participate in the Catalent Way continuous-improvement culture.
  • May lead Just Do It continuous-improvement activities and participate in implementing continuous-improvement projects.
  • May coach more junior team members on basic execution activities and serve as an onboarding buddy to help new team members learn the culture and basic workplace expectations.
  • Perform general cleanroom housekeeping, including room and equipment cleaning, waste disposal, and maintenance of 5S standards.
  • Perform other duties as assigned.

Desired Qualifications

  • GMP manufacturing experience is preferred.
  • Experience with TrackWise, ComplianceWire, JD Edwards, DeltaV, or chromatography software is preferred.

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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