Process Engineer II - Downstream - Site Based, Redmond, WA

Role: Process Engineer II specializing in downstream bioprocessing at a cGMP manufacturing site utilizing continuous processing platforms. Objectives include supporting all downstream operations, process understanding, and continuous improvement initiatives. Responsibilities: develop and review technical documentation, authoring SOPs and change controls, leading investigations, monitoring process performance, and providing 24/7 on-call support. Collaborates with global MSAT, Operations, and Quality teams, acting as technical SME, and applying Operational Excellence principles. Qualifications: Bachelor's or Master's in Engineering with 2+ (up to 5+) years in biotech/pharma, with hands-on experience in downstream purification, disposable manufacturing technologies, and GMP environments. Proven leadership, stakeholder influence, and risk management skills are essential. High-value specifics: biologics, biopharmaceuticals, cell/gene therapy, supporting clinical-scale cGMP manufacturing, with a focus on process development, change management, and continuous process improvement. Work setup: not explicitly stated, but involves 24/7 operations and on-call support.