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A quality control (QC) associate carries out testing and analysis to ensure that biomedical research studies and biomedical products meet specifications and regulatory guidelines. QC associates work in quality control laboratories and in biomanufacturing environments, using complex instrumentation and laboratory equipment to conduct tests and analyses that are used in product quality regulations or scientific research studies. Because the products being developed or manufactured directly impact people’s lives, strict Food and Drug Administration regulations must be followed and documented at every step. In the manufacturing of pharmaceutical products, companies are required to follow SOPs (standard operating procedures) and every step of every process must have a traceable, written record. QC associates are responsible for this documentation. The QC associate performs analytical tests, gathers and assesses data from those tests and writes documentation and reports.

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