Performs activities in support of disposition of product while ensuring compliance with Quality Assurance (QA) policies and procedures, cGMPs, SOPs, and Regeneron Standard Requirement Documents.
As a typical day may include the following: Preparing & reviewing of batch disposition documentation to support QP release of Formulated Drug Substance Reviewing of QC related release data, Documentation review Completing deviation, change control & batch record reports to support disposition Performing status labelling of product as the need arises Representing Quality Assurance in support of deviations...