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American Regent

Produces sterile injectable medications for healthcare

Quality Assurance Manager

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBrea, CA, USA$117.9k - $124k /yr

About the Job

Requirements

  • A bachelor's degree in Engineering or a science discipline or related field is required.
  • A minimum of 8 years of experience in Pharmaceutical Quality Assurance is preferred, with preference for External Quality Management and sterile injectables.
  • Strong working knowledge of current Good Manufacturing Practices, FDA requirements, and ICH Q8/9/10/12 guidelines.
  • Direct experience participating in and supporting regulatory inspections and submissions is preferred.
  • Ability to work independently without supervision and as part of a team.
  • Ability to effectively plan and organize work activities and prioritize task completion to meet schedules and deadlines.
  • Strong problem-solving and analytical skills, attention to detail, and ability to manage multiple projects simultaneously.
  • Ability to travel domestically or internationally 5–10% is preferred.
  • Experience with Microsoft Office.
  • Excellent organizational and interpersonal skills and strong oral and written communication skills.
  • Demonstrated experience with the use or governance of electronic Quality Systems is preferred.

Responsibilities

  • Provide day-to-day quality input and oversight for lifecycle development and commercialization of pharmaceuticals at external manufacturing partners globally, ensuring operations comply with current Good Manufacturing Practices, Quality Agreements, regulatory standards, and the company's Quality Management System.
  • Establish Quality KPI scorecards to monitor third-party finished-product contract manufacturers’ compliance and performance.
  • Drive timely decisions and facilitate active communication and information flow between contract manufacturers and internal functional teams.
  • Ensure quality and compliance matters meet appropriate Good Manufacturing Practices and regulatory requirements so products are safe, pure, and effective.
  • Support supply chain operations for commercial product distribution and timely new-product launches.
  • Serve as the Quality lead for technical transfer activities at external manufacturing partners.
  • Support manufacturing activities related to regulatory filings, including on-site presence for engineering, validation, and registration-batch manufacturing, and timely review and approval of documents.
  • Facilitate approval or release of commercial products based on conformance to specifications, current Good Manufacturing Practices requirements, and contractual agreements.
  • Verify that corrective actions intended to prevent recurrence are completed promptly and are consistent with the stated corrective action.
  • Investigate and determine the need for field alerts or recalls and withdrawals of company products manufactured by third-party contract manufacturers, and manage those actions as needed.
  • Review and approve third-party quality records and documentation, including product and process change controls, master batch records, active pharmaceutical ingredient and raw-material records, product specifications, analytical methods, stability and validation protocols and reports, quality incidents and investigation reports, quality agreements, and technical-transfer documentation.
  • Perform on-site visits during manufacturing and packaging of company products and create a quality business review process.
  • Initiate and attend periodic meetings with contract manufacturers as the company Quality Assurance representative.
  • Make quality decisions on contract manufacturer and supplier-related tasks and events.
  • Provide status updates on contract-manufacturer-related tasks and action items to multiple internal departments.
  • Monitor and track the relationship between company batches and contract manufacturer batches.
  • Provide information and documentation needed for shipping products between the company and contract manufacturers.
  • Monitor, track, and trend contract manufacturer batch dispositions; create and update tracking documents for contract-manufacturer-related tasks and share them with multiple departments.
  • Review and approve contract manufacturer and supplier executed batch records and batch-disposition documents.
  • Create and provide documents requested by contract manufacturers.
  • Notify contract manufacturers of internal events requiring third-party notifications and follow up on third-party review status as applicable.
  • Review and approve company batch-disposition documents and create Certificates of Conformance.
  • Support regulatory agency inspections.
  • Establish working relationships with all internal functional areas.
  • Participate in regulatory and company inspections of external manufacturing partners to support successful inspection outcomes and maintain inspection readiness at those sites.
  • Perform quality risk assessments and drive risk-reduction improvement plans and remediation where necessary.
  • Develop and revise company policies and procedures for managing third-party contract manufacturers and external service providers.
  • Develop and foster positive relationships with contract manufacturers while holding them accountable.
  • Perform work requiring independent decision-making and the exercise of independent judgment and discretion.
  • 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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