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Catalent

Global contract drug formulation, manufacturing, packaging

Associate Quality Assurance

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeKansas City, MO, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in a scientific discipline or at least one year of Manufacturing or Quality Assurance experience in a Good Manufacturing Practice environment.
  • Ability to follow instructions, guidance, and direction from others.
  • Ability to use existing procedures to solve routine problems.
  • Ability to apply all elements of the quality system to identify, classify, and control the status of finished products.
  • Ability to follow written, oral, diagram, or schedule instructions.
  • Strong mathematical and scientific reasoning skills.
  • Ability to identify abnormal data and potential quality or compliance concerns and escalate them to management.
  • Written and verbal communication skills with internal and external stakeholders.
  • Ability to recognize unmet needs within the department and business.
  • Ability to collaborate effectively with peers and demonstrate leadership capabilities in a matrix environment.
  • Time management and efficiency skills; organization and multitasking abilities; ability to work effectively under pressure to meet deadlines.
  • Proficiency with computer technology, including hardware and software for common tasks such as Word, Excel, Outlook, and PowerPoint basics.

Responsibilities

  • Oversee Quality support functions associated with manufacturing products.
  • Review batch records, cleaning records, and logbooks.
  • Ensure products are manufactured according to applicable current Good Manufacturing Practices, FDA guidelines, MHRA guidelines, regulations, and internal Standard Operating Procedures.
  • Identify deviations during manufacturing and provide direction on appropriate corrective actions.
  • Review and approve batch documentation for adherence to Standard Operating Procedures and current Good Manufacturing Practices.
  • Participate in Quality Assurance programs, procedures, and controls to ensure products meet established standards and agency guidelines.
  • Complete monthly and daily facility audits.
  • Assist with manufacturing floor activities, including equipment and room approval and facility compliance.
  • 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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