Job Description:
Performs functions associated with quality control/quality assurance operations, including working with chemists/microbiologists to conduct simple reviews (reagent review/pH data review, visual data review), complex data review (chromatographic - HPLC/GC, titrator, density meter, FTIR), and perform investigations for OOS/OOT results. Uses electronic programs to evaluate data to assist in assessing and documenting results of quality assurance and control processes. Performs other activities as needed.
Minimum Requirements:
2%2B years working in a GxP laboratory environment.
Proficient in Microsoft Office applications.
Strong written and oral communication skills (English).
Experience working in current Good Manufacturing Practice (cGMP) or other cGxP environments.
Experience performing analytical chemistry data review.
Preferred:
Experience using Laboratory Information Management System (LIMS).
Experience reviewing chromatography data within Empower, LabX, and Omnic software.