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Catalent

Global contract drug formulation, manufacturing, packaging

Quality Control Analyst

Inspection & TestPosted on Nov 10
Full-timeWinchester, KY, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in a scientific field is required; an alternative degree in a non-scientific field may be accepted with at least two years of relevant experience in a material testing laboratory.
  • At least two years in a Quality, Laboratory, Clinical, or Chemical manufacturing role is preferred.
  • Ability to assist personnel with lifting liquid containers and other objects weighing more than 50 pounds.
  • Ability to work safely in a dynamic environment with mobile and fixed equipment and changing conditions while completing tasks ranging from simple to complex and multitasking.

Responsibilities

  • Perform reliable, high-quality analytical testing in accordance with USP, NF, EP, JP, FCC, or customer-supplied guidelines. Typical tests may include Dissolution, Titration, Polarimetry, Loss on Drying, Viscosity, Residue on Ignition, Heavy Metal Content, FTIR, HPLC, and GC.
  • Maintain accurate written records of all analyses performed.
  • Interpret analytical results and issues accurately and communicate them effectively.
  • Schedule daily tasks in an organized and efficient manner.
  • Calibrate and maintain laboratory equipment and instrumentation.
  • Operate safely and follow basic laboratory and chemical hygiene practices.
  • Perform peer review of analytical testing and write-ups.
  • Write SOPs as needed.
  • Perform other duties as required in support of Catalent Pharma Solutions.

Desired Qualifications

  • A degree in Chemistry or Biology is preferred.
  • At least two years in a Quality, Laboratory, Clinical, or Chemical manufacturing role 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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