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The Process Engineer III will support downstream tech transfer and manufacturing processes, focusing on late-stage and commercial biologics, documentation creation, and regulatory compliance.

The Senior Automation Engineer will oversee the AVEVA PI system deployment, integration with process control systems, and ensure data governance in a global manufacturing environment.

The Process Engineer II will design and develop new equipment, evaluate technologies, assist with project integration, and support regulatory submissions in a biopharmaceutical environment.

Serve as strategic HR partner advising senior leaders on HR strategy, policies, org design, performance management, employee relations, talent acquisition, and HR programs. Lead annual HR cycles, analyze HR metrics to drive improvements, coach managers, and support organizational change from design through implementation.

The Automation CSV Engineer supports validation, compliance, and testing for GMP automation systems, ensuring they remain compliant and operational. Responsibilities include documentation, testing, collaboration across teams, and maintaining regulatory standards.

The Principal Process Engineer leads technology transfer and validation for clinical and commercial biologics manufacturing, ensuring compliance and process optimization.

Lead global MSAT technology transfer and process validation for late-stage and commercial biologics. Drive site-to-site transfers, develop global templates/protocols (PPQ, PQ, batch records), perform gap/risk analyses and mitigation, analyze process data and annual reviews, support regulatory CMC documentation and inspections, and mentor junior engineers.