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Director of QA

Philadelphia Metro Area, PA

Posted: 01/23/2019 Job Type: Scientific Job Number: JN -012019-23471
  • BS/MS in Scientific Field with 10+ years of Pharmaceutical Industry Compliance experience and leadership
  • Drug development, NDA and Regulatory Experience is required
  • Responsible for system wide quality, system implementation and process improvement
  • Oversight of pharmaceutical quality assurance including component, intermediate, bulk and finished product release, equipment cleaning verification, qualifying equipment , document management, internal and external audits, regulatory relations, complaint handling, NDA submissions, cGMP training of employees, and other duties as assigned.
  • Review, approval, and release of raw materials
  • Support manufacturing and analytical services along with the QA team
  • Document control through management, issuance, authoring, and approval of documents (SOPs, Monographs, Investigations)
  • Responsible for the training of all employees with regards to quality and cGMP
  • Lead supplier, client and FDA audits
  • Root Cause, CAPA, Manufacturing Investigations
  • Interface with FDA when audits are conducted
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