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Specialist Technical Writing

West Greenwich, RI
Top 3 Must Have Skill Sets:    
  • Previous technical writing experience
  • Previous experience In investigation process (RCA)
  • Drug Substance Experience
Day to Day Responsibilities:
  • Perform investigation, project manager the owning deviations, CAPA generations, lead functional team, communicate with management when situation is holding the progress of the deviations
Summary
  • Ideal- Must have previous Amgen experience. Must have previous technical writing experience, experience In investigation process (RCA) and Drug Substance Experience.
  • 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 (develops, writes, edits), perform investigation, project manager the owning deviations, CAPA generations, lead functional team, communicate with management when situation is holding the progress of the deviations. 

Skills: ; 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; May require communication through a variety of media (e.g., CD, intranet, on-line training, etc.); Skills: ; MS Office expertise ; previous technical writing experience ; regulated environment experience ; document version control experience ; excellent communication/writing skills

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

 
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