Manufacturing Manager - Nights, Site Based, Redmond, WA

Role: Manufacturing Operations Manager specializing in purification for biotherapeutics, overseeing 24/7 shift operations with significant on-the-floor presence. Responsibilities: supervise staff, ensure cGMP compliance, generate and maintain technical documentation, troubleshoot and lead investigations, execute plant start-up, commissioning, validation, and support technology/process transfer. Contribute to regulatory inspections and budget inputs. Qualifications: Master’s degree with 3+ years or Bachelor’s with 5+ years in manufacturing/operations; strong knowledge of cGMP and purification processes including chromatography, viral inactivation, filtration, UF/DF; proven leadership skills, effective communication, technical troubleshooting, and project management. Preferred: experience managing staff, participation in audits, advanced knowledge of purification equipment and disposable manufacturing tech, process automation (DeltaV), and technology transfers for clinical or commercial manufacturing. High-value: biotherapeutic purification, cGMP compliance, process transfer, validation, troubleshooting, staff leadership, validation activities, and cross-functional collaboration. Work setup details not specified; the role involves significant on-site operational management.