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As a Senior Product Quality Engineer, you will manage product field investigations, perform root cause analysis, and drive continuous improvement in product quality and processes in the medical device industry.

The manager will develop regulatory strategies for medical devices, manage a regulatory team, lead FDA submissions, and ensure compliance with global regulations.

The Technical Project Manager will lead lifecycle projects for medical devices, ensuring compliance, project planning, execution, and collaboration across teams while improving product quality.

The role involves testing embedded systems software and desktop applications, defining testing strategies, developing protocols, and ensuring quality adherence in regulated environments.

The Sr. Quality Engineer provides quality engineering support, leads investigations for nonconformances, drives CAPA initiatives, and ensures compliance with FDA and ISO standards.

The Quality Control Manager leads inspection and compliance activities in manufacturing, ensuring product quality and regulatory adherence. They oversee QC teams, drive continuous improvement initiatives, and manage nonconformance processes to enhance operational efficiency.

The Manufacturing Manager leads manufacturing operations, ensuring production goals are met in quality, safety, delivery, and cost while driving continuous improvement and collaborating cross-functionally.

The Senior Automation Engineer will lead the development and validation of automation equipment and processes, driving continuous improvement and collaboration across teams to enhance manufacturing efficiency and compliance.

The Senior Manager leads engineering teams for high-volume medical device manufacturing, focusing on team development, PCBA testing, compliance, and continuous improvement.