Description: Performs bioanalytical methods (immunological, in vivo, microbiological, molecular biological, or virological) for various Bio QC Tests on raw materials, in-process, release, or stability samples in compliance with 9CFR, EU, and VICH regulatory guidelines, outlines of production, and special outlines. Responsible for timely communication with supervisors to inform them of testing, compliance, and/or scheduling issues, adhering to company policies, maintaining a safe work environment through site safety KPIs, living out the Lead principles and following appropriate GMP documentation.