Jobs at Varian

Develops and validates prototype intravascular therapy devices and mechanical components. Responsibilities include requirements definition, SolidWorks design, fabrication planning, testing, flow-model development, quality assurance, technical documentation, FDA-compliant design history files, complaint investigations, and failure analysis. The role also supports microsphere material development, shielded transport containers, vendor-built components, and design verification for regulated medical devices.

As a Quality Assurance Specialist, you will oversee quality processes for sterile injectables, manage audits, ensure compliance, and support training, focusing on continuous improvement in a regulated environment.