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Catalent

Global contract drug formulation, manufacturing, packaging

Commercial Manufacturing Quality Assurance Specialist

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

About the Job

Requirements

  • A Master's degree in a scientific discipline with no experience; or a Bachelor's degree in a scientific discipline with at least 1 year of experience in Quality Assurance, Quality Control, or Regulatory Compliance in a Good Manufacturing Practice environment; or an Associate's degree with at least 3 years of experience in an FDA-regulated field and at least 1 year in Quality Assurance, Quality Control, or Regulatory Compliance; or a high school diploma with at least 5 years of experience in an FDA-regulated field and at least 1 year in Quality Assurance, Quality Control, or Regulatory Compliance.
  • Six Sigma or American Society for Quality certification is preferred.

Responsibilities

  • Perform batch record review, product release, and disposition.
  • Draft, review, and approve technical documents such as procedures or master batch records.
  • Ensure products are manufactured, tested, and released according to applicable FDA guidelines, regulations, Good x Practices, and internal standard operating procedures.
  • Participate in developing and maintaining quality assurance programs, procedures, and controls to ensure products meet established standards and agency guidelines.
  • Train, coach, and mentor others on technical, personal development, or business issues.
  • Assist with data compilation for annual product review.
  • Provide quality assurance advisement for project outcomes and customer interactions.
  • Participate in developing and implementing process-related improvements.
  • Assist with manufacturing floor activities, including equipment and room approval and facility compliance.
  • Perform other duties as assigned.

Desired Qualifications

  • Six Sigma or American Society for Quality certification.

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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