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Quality Assurance Specialist

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; written and spoken fluency required in specific language needed 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.

ACTIVE

Manager is open to Post Grad candidates that has technical writing experience from school.<br/><br/>Job Details: Responsible for supporting the deviation of major event related large molecule Bulk Drug Substances (BDS) manufactured at *** 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. 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; written and spoken fluency required in specific language needed

Specialist Quality Assurance

OQSIE

West Greenwich, RI

About the Company

OQSIE