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Catalent

Global contract drug formulation, manufacturing, packaging

Associate 1 - Quality Assurance, On the Floor

Validation, Compliance & Quality SystemsUpdated on Nov 13
Full-timeMadison, WI, USA

About the Job

Requirements

  • A Bachelor's degree in a STEM field and 0 or more years of experience, or an Associate's degree in a STEM field and at least 1 year of experience, or a high school diploma and at least 4 years of experience.

Responsibilities

  • Execute the Quality Assurance on the Floor program.
  • Conduct manufacturing walkthroughs.
  • Provide quality support to operations.
  • Issue controlled production documents, such as batch records and labels.
  • Review batch records, test data, and logs.
  • Release solutions and materials.
  • Inspect final product containers.
  • Escalate quality and regulatory issues.
  • Maintain controlled records.
  • Perform other duties as assigned.

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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