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American Regent

Produces sterile injectable medications for healthcare

QA Batch Record Review 2

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeNew Albany, OH, USANo salary listed

About the Job

Requirements

  • A high school diploma or GED equivalent is required.
  • A minimum of two years of equivalent experience with current Good Manufacturing Practice batch-record documentation is required.
  • Quality Assurance, compliance, and auditing experience in a current Good Manufacturing Practice manufacturing environment is required.
  • Strong attention to detail and adherence to Standard Operating Procedures are required.
  • Intermediate skills in Microsoft Word and Excel are required.
  • Organizational, interpersonal, and written and oral communication skills are required.
  • Analytical thinking and problem-solving skills are required.
  • Ability to manage multiple activities simultaneously and produce results is required.
  • Ability to take feedback constructively and work in a team-oriented environment is required.
  • Ability to work overtime as needed is required.
  • Ability to occasionally lift and/or move up to 25 pounds is required.

Responsibilities

  • Perform critical review of executed batch-record documentation.
  • Enter data into applicable spreadsheets and databases.
  • Update metric reports for trending.
  • Work with personnel to ensure errors and corrections are resolved according to Standard Operating Procedure requirements.
  • Identify quality-process improvements to increase quality and efficiency in systems, operations, and personnel.
  • Ensure all work is performed and documented in accordance with company policies and procedures, the Code of Federal Regulations, mutually recognized agreements with international regulatory bodies, and health and safety requirements.
  • Submit error-free batch records for product release.
  • Submit Change Requests as needed.
  • Support investigations and Corrective Actions/Preventative Actions, including report writing.
  • Apply basic knowledge of current Good Manufacturing Practices and supporting regulatory documents.
  • Mentor and provide guidance to less-senior Quality Assurance Batch Record Review Associates.
  • Provide guidance to plant personnel on batch-record corrections.
  • Perform other tasks and duties as assigned by management.
  • Travel between American Regent facilities.

Desired Qualifications

  • An associate or bachelor's degree is preferred.
  • Ability to meet and maintain clean gowning requirements is preferred.

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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