We’re looking for great teammates who have a passion for working in a laboratory and thrive in a dynamic environment. This role cultivates good manufacturing practices (GMPs) and company quality principles to deliver product performance and quality. As a QC Laboratory Analyst, you could work in an analytical or microbiological laboratory environment that stays in sync with Good Laboratory Practice (GLP) and current Good Manufacturing Practice (cGMP). The work will require collection, labeling, analysis, and results recording related to raw materials, intermediate products, finished goods, packaging materials and other samples. Tracking, trend analysis, and other Quality Control (QC) related responsibilities will be performed as directed by laboratory systems. In addition to laboratory testing, QC Analysts may be required to write control documents like Standard Operating Procedures (SOPs), deliver training, perform system health assessments, carry out “on the floor” coaching, and facilitate or participate in quality system failure investigations. Maintain cGMP principles and Good Documentation practices.
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Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree