We are looking for great teammates with a passion for working in a laboratory and thriving 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 will work in a manufacturing laboratory environment that adheres to Good Laboratory Practice (GLP) and current Good Manufacturing Practice (cGMP). Responsibilities include collection, labeling, analysis, and results recording for raw materials, intermediate products, finished goods, packaging materials, and other samples. You will also perform tracking, trend analysis, and other Quality Control (QC) related responsibilities as directed by laboratory systems. Additionally, there are roles for a QC Analyst that involve writing control documents like Standard Operating Procedures (SOPs), delivering training, performing system health assessments, on-floor coaching, product disposition, and facilitating or participating in quality system failure investigations, while maintaining cGMP principles and Good Documentation practices.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree