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SR QC REVIEWER (2 OF 2)
  Posted 4 days ago    Oxford Global Resources    Seattle, WA

Summary:Perform tactical work and review a variety of documents, protocols, and reports.Project Details:Exhibit varying levels of experience and a solid progression of work and/or trainingDocument, review and batch disposition of API and drug product used in Phase 1-3 clinical studiesReview and approve manufacturing records, change controls, investigations and analytical dataReview and approve test methods and method validationsReview manufacturing validation protocol and reportsJob Experience:Experience in small molecule manufacturing and contract manufacturingBachelor's degree in Engineering, Chemistry, Biology, or other related disciplineA minimum of 5+ years' work experience in the Quality organization of a Medical Device and/or Pharmaceutical companyKnowledge and experience in CAPA; Root Cause Investigation; Validation (Process, Test Method, Software, and Design); Environmental Monitoring, Manufacturing operat

Source: Talroo

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