Vacancy caducado!
Job Description
Job Details: Responsible for supporting the deviation of major event related large molecule Bulk Drug Substances (BDS) manufactured at client 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
Additional Information
2-3 years of Technical WritingProject management knowledge1+ years
Call meetings, lead functional team, technical write deviations, work cross functionally with multiple client teams (PD, Mfg, QA, QC, SC, Warehouse).
Vacancy caducado!