QA Specialist - Lot Disposition, Site Based, Redmond, WA

Role: QA Specialist responsible for executing day-to-day quality assurance activities in GMP biologics manufacturing, ensuring compliance with cGMPs and internal procedures. Objectives include batch release documentation, review of deviations and change controls, and facilitating lot disposition meetings. Responsibilities: compile lot release data, ensure documentation completeness, partner with Manufacturing, QC, and QA teams, and escalate significant quality risks. Requirements: Bachelor's in biological or engineering sciences, minimum 3 years in biopharma/pharmaceutical cGMP environments, strong attention to detail, and effective cross-functional communication skills. Preferred: experience working with biologics in a GMP setting, knowledge of lot disposition processes. High-Value: biologics manufacturing, GMP, cGMP compliance, GMP QA, batch release, deviation review, cross-functional collaboration. WorkSetup: on-site in Seattle, WA; role is site-based.