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Catalent

Global contract drug formulation, manufacturing, packaging

Senior Associate - 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 and at least seven years of relevant experience; alternatively, a bachelor's or associate's degree in a scientific, engineering, or biomanufacturing discipline with at least three years of experience, or a master's degree in STEM with at least one year of experience.
  • Ability to use Microsoft Word, Excel, and other Office systems.
  • Ability to meet the stated physical requirements, including frequent standing, walking, reaching, and lifting or moving up to 10 pounds, and occasional lifting or moving up to 50 pounds.
  • Must comply with environmental, health, and safety responsibilities for the position and be able to work in a controlled cleanroom environment as needed.

Responsibilities

  • Perform advanced troubleshooting and basic 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, focusing 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 procedures and raise awareness through the Rapid Response process; proactively identify safety, quality, and efficiency improvements.
  • Participate in the continuous improvement culture, lead Just Do It continuous improvement activities, and engage in implementing continuous improvement projects.
  • Mentor junior team members on basic execution activities and onboard new team members on workplace culture and basic expectations.
  • May become a Certified Trainer and provide final sign-off for training completion for basic execution activities.
  • Interact with clients during in-person or virtual Person In Plant observations to provide batch schedule and status updates.
  • Participate in daily shift huddles and lead shift exchange activities.
  • Perform cleanroom housekeeping, including room and equipment cleaning, waste disposal, and maintaining 5S standards.
  • Perform other duties as assigned.

Desired Qualifications

  • GMP manufacturing experience is preferred.
  • Experience with TrackWise, ComplianceWire, JD Edwards, DeltaV, and chromatography software such as Unicorn 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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