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American Regent

Produces sterile injectable medications for healthcare

Materials Quality Supervisor

Validation, Compliance & Quality SystemsPosted on Nov 11
Full-timeNew Albany, OH, USANo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree or equivalent work experience.
  • At least five years of industry experience.
  • Experience in quality inspection, auditing, and testing.
  • Experience writing investigations and implementing corrective action programs.
  • Product- or industry-specific experience.
  • Knowledge of relevant regulatory requirements.
  • Proficiency in Microsoft Word, Excel, and Outlook.
  • Strong oral and written communication skills.
  • Strong time-management and organizational skills, with the ability to delegate tasks.
  • 20/20 vision, corrected if necessary.
  • Ability to pass the D15 color blindness screening.

Responsibilities

  • Ensure that raw materials, primary containers, and packaging components used in product manufacturing meet established quality standards.
  • Supervise and coordinate workers engaged in sampling, inspecting, and testing raw materials and primary packaging, applying quality assurance standards and procedures.
  • Supervise and coordinate workers engaged in supplier notification activities.
  • Direct workers in quality assurance inspection and testing to ensure compliance with standard operating procedures and regulatory standards.
  • Assign training of new workers to qualified workers.
  • Review and approve reports; confer with quality assurance, production, management, and engineering personnel to resolve work-related problems.
  • Draft and revise quality assurance policies and procedures.
  • Interpret and implement quality assurance standards.
  • Evaluate the adequacy of quality assurance standards.
  • Devise sampling procedures and directions for recording and reporting quality data.
  • Review implementation and efficiency of quality and inspection systems.
  • Collect and compile statistical quality data.
  • Initiate events; perform root cause analysis, impact assessments, corrective and preventive actions, and effectiveness checks related to incoming materials; assist other departments with investigations as required.
  • Manage the destruction approval process for material, including assigning approval numbers and determining disposition of material to be disposed of.
  • Facilitate and evaluate audit findings and implement appropriate corrective actions.
  • Drive quality culture and Core Competency Model initiatives to support enhanced organizational performance.
  • Perform other tasks and duties as assigned by management.

About the Company

American Regent

Produces sterile injectable medications for healthcare

American Regent is a pharmaceutical company that develops, manufactures, and supplies sterile injectable medicines for U.S. and Canadian healthcare providers, including brands and generic injectables. Its products are produced in sterile form and used by hospitals, clinics, and other providers to treat patients. The company operates manufacturing sites in New York, Ohio, and Pennsylvania and ships across the United States and Canada, aiming to ensure a steady, broad portfolio of injectable therapies for patients. It differentiates itself through its commitment to reliable supply and through ongoing investments to modernize and expand its U.S. manufacturing capabilities, supporting sustainable growth and the well-being of its employees and customers. Its goal is to maintain a steady supply of high-quality injectable medicines by expanding capacity and improving efficiency to serve the healthcare marketplace.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
New York, NY
Founded
Not listed

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