How would you describe what you did at
amgen?
Managed analytical sample submission and compilation of test results for clinical trials, manufacturing, research, toxicology, and pharmacokinetics.
* Reviewed pre-clinical/clinical batch records in collaboration with analysts to correct documentation errors, reducing time to lot release.
* Refined a clinical trial, toxicology, and PK study sample management process, catching labeling errors and improving chain-of-custody tracking/documentation.
* Trained manufacturing/quality new hires on LIMS, sample management and analytical equipment and client consultation
* Redesigned QC sample distribution center, creating one centralized hub serving research through manufacturing. Reduced costly delays and misplaced samples by 30%.
* Successfully prepared labs and performed training audits for FDA inspections.
Posted @ 12:50AM, July 03, 2007
by Matt Holland | Permalink
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