The Quality Engineer II will support Manufacturing Engineering and Production by ensuring compliance with quality systems and regulations. Responsibilities include design assurance, risk management, quality function implementation, and collaboration with various teams to improve manufacturing processes, conduct audits, and maintain supplier conformances.

The Senior Systems Manager will lead medical device system development, supervise technical teams, manage design verification and validation, and ensure compliance with industry standards and regulations. Responsibilities include overseeing device development, documentation, project management, and collaborating with internal and external resources.