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Specialist Quality Assurance

West Greenwich, RI
Top 3 Must Have Skill Sets:
  • 2-3 years of Technical Writing         
  • 1+ years Project management knowledge

Day to Day Responsibilities:
  • Call meetings, lead functional team, technical write deviations, work cross functionally with multiple Amgen teams (PD, Mfg, QA, QC, SC, Warehouse).    

Job Details:
  • Responsible for supporting the deviation of major event related large molecule Bulk Drug Substances (BDS) manufactured at Amgen Rhode Island (ARI).
  • Primary responsibilities of this position include support the investigation process, perform investigation, project manager the owning deviations, CAPA generations, lead functional team, communicate with management when situation is holding the progress of the deviations.
  • knowledge of process and faculty equipment, and the ability to interpret and apply Good Manufacturing Practices (GMP); quality assurance or manufacturing experience in the pharmaceutical industry; written and spoken fluency required in specific language needed

 "This posting is for Contingent Worker, not an FTE"
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