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Catalent

Global contract drug formulation, manufacturing, packaging

Quality Assurance Supervisor

Validation, Compliance & Quality SystemsUpdated on Nov 13
Full-timePhiladelphia, PA, USANo salary listed

About the Job

Requirements

  • A high school diploma or GED and at least five years of Production Quality Assurance experience are required.
  • A proven track record of monitoring and auditing quality and identifying potential efficiencies in a production environment is required.
  • Experience in a regulated field such as pharmaceutical, food, or automotive is required.
  • Experience working on continuous improvement activities in partnership with other functions, such as Production and Validation, is required.
  • Good computer skills are required.
  • Knowledge of the application of Food and Drug Administration current Good Manufacturing Practices is required.
  • The role requires the ability to be on one's feet and move easily throughout Operations facilities.
  • The role requires the ability to quickly learn and implement Quality Assurance auditing techniques.
  • The role requires the ability to read written documents and use a computer monitor screen frequently.
  • The role requires the ability to sit, stand, and walk regularly and occasionally lift 0–15 pounds.
  • The role requires accessibility to production floor, supply chain, and office staff, and the ability to use required office equipment.

Responsibilities

  • Oversee all Quality Assurance activities related to incoming goods, distribution, destruction, and process auditing.
  • Help ensure the quality and identity of pharmaceutical products during incoming, distribution, and packaging processes.
  • Serve as the Quality partner supporting the Supply Chain and Operations departments.
  • Enforce company policy and regulatory requirements.
  • Serve as the site subject matter expert for Good Manufacturing Practices and Good Distribution Practices.
  • Schedule a daily resource plan to support Supply Chain and Operations activities.
  • Lead investigations into compliance issues involving incoming goods, distribution, returns, destruction, or packaging and production.
  • Develop process excellence and efficiencies before a project begins.
  • Track and report metrics, and identify trends and predictive models.
  • Perform other duties as assigned.

Desired Qualifications

  • A college degree, specifically a Bachelor of Arts or Bachelor of Science, is preferred.
  • At least five years of supervisory experience is preferred.
  • Knowledge of Microsoft Office and an Inventory Management system is a plus.
  • Basic knowledge of Lean Six Sigma methodologies is an advantage.
  • Knowledge of reading engineering drawings and material specifications is a plus.

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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