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Quality Assurance Manager

L6

ambioGrovetown, GAtoday
Job Description
Primary Responsibilities:
  • Maintains and creates appropriate validation/Qualification- SOPs, files and
  • Coordinates all quality activities with outside laboratories and partners including AmbioPharm.
  • Ensure decisions made meet external and internal Quality compliance expectations for API and finished
  • Communicate and coordinate with other departments and/or key stake-holders as required to resolve issues and concerns detected during review, assure issues are appropriately documented, investigated, corrections and preventative actions implemented, effectiveness evaluated, and trended for periodic
  • Ensure quality systems are compliant and efficient at all contract manufacturers
  • Actively participate in all the FDA related PAI preparation onsite and at the CMOs/CDMOs as required.
  • Implement and maintain Corrective and Preventative Action (CAPA)
  • To assist with the evaluation of planned changes (change control) to validated processes, equipment, procedures and organize re-qualification/re-validation studies where
  • To assist with the review of validation protocols and reports for processes, equipment and computerized systems
  • Ensure the implementation of effective corrective and preventative actions arising from QA monitoring/ inspection
  • To maintain tracking for deviations, corrective and preventative actions, service complaints and change controls
  • To assist with the investigation of result and complaints and ensure that effective immediate follow up actions are
  • To perform internal audits against defined quality performance measures and ensure that effective immediate follow up actions are
  • Manage or assist in external inspections and verify the completion of corrective action as required by the reports of the inspectors
  • To assist with the management of quality documentation and the review and approval of all quality documents, e.g. SOPsTo interact with personnel from other sections on any issues that may arise
  • To respect information obtained in the course of duties performed, and refrain from disclosing such information without the consent of the employee/patient, or person entitled to act on their behalf, except where disclosure is required by law or by the order of a Court, or is necessary in the public
Qualifications:
  • Fundamental knowledge of drug product compliance principles 5+ years experience in the pharmaceutical industry, in a QA role
  • A good understanding of auditing principles
  • Proficient in the use of Microsoft (Access, Excel, Word)
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Level

LeadL6

Location

Grovetown, GA

Occupation

Quality Control Systems Managers

Industry

Pharmaceutical Preparation Manufacturing

Posted

today

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