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Catalent

Global contract drug formulation, manufacturing, packaging

Quality Specialist 1 - Quality Assurance

Validation, Compliance & Quality SystemsConfirmed 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 equivalent knowledge and experience.
  • A high school degree with at least 2 years of Quality Assurance experience in a good manufacturing practice (GMP) manufacturing environment.
  • Pass a 20/30 corrected vision exam with colorblindness testing.
  • Complete a nurse assessment and pulmonary physical.
  • Pass a respirator fit test.
  • Pass a Drug Enforcement Administration background check relating to controlled substance products.
  • Ability to work in refrigerator environments (35°F–46°F / 2°C–8°C) and/or freezer environments (-4°F / -20°C).
  • Ability to work near machinery and packaging equipment.

Responsibilities

  • Participate in continuous improvement initiatives to enhance processes, systems, and procedures related to quality management.
  • Create Certificates of Analysis with supervision and adhere to good manufacturing practice (GMP) standards with guidance while limiting errors.
  • Support clinical trial projects by ensuring compliance with regulatory requirements, good manufacturing practices, and standard operating procedures.
  • Implement and maintain quality assurance processes throughout the product lifecycle.
  • Ensure documentation is accurate, up to date, and properly maintained in accordance with regulatory requirements.

Desired Qualifications

  • Ability to identify aberrant data and potential quality or compliance concerns and escalate them to management.
  • Ability to work effectively under pressure to meet deadlines.

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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