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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, or a bachelor's or associate's degree in a scientific, engineering, or biomanufacturing discipline without formal experience.
  • GMP manufacturing experience is preferred.
  • Ability to use Microsoft Word, Excel, and other Office systems.
  • Preferred experience with TrackWise, ComplianceWire, JD Edwards, DeltaV, or chromatography software.
  • Ability to perform the stated physical activities, including frequent lifting or moving up to 10 pounds and occasional lifting or moving up to 50 pounds, and to operate in a cleanroom environment as needed.
  • Must comply with environmental, health, and safety responsibilities for the position.

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 intended procedures 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 act as an onboarding buddy to help new team members learn the culture and basic workplace expectations.
  • Perform general cleanroom housekeeping, including cleaning rooms and equipment, disposing of waste, and maintaining 5S standards.
  • Perform other duties as assigned.

Desired Qualifications

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

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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