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Sr. V&V Test Technician needed to execute tests of innovative medical devices using high precision digital balances and various other test equipment. Responsible for independently performing complex tests and collaborating with engineering personnel.

The Senior Systems Engineer will lead the design of electro-mechanical systems, define interfaces between subsystems, develop test strategies, and support program management goals. The role also involves guiding manufacturing processes and contributing to innovative medical device product development.

The Project Quality Engineer will lead quality compliance efforts within a medical device R&D team by managing risk analyses, ensuring adherence to regulatory standards, and facilitating audits. Responsibilities include overseeing investigation processes, approving design changes, and developing quality documentation while promoting quality culture in product development.

The EDA Component Librarian will manage a library of EDA components, ensure adherence to best practices, and maintain data integrity. Responsibilities include creating components in Altium, establishing component workflows, and providing technical support and training to engineers. Strong communication skills and experience in library management are essential.

As a Supplier Quality Specialist at DEKA, you will perform supplier qualifications, maintain the Approved Supplier List, support supplier corrective actions, and facilitate communication between cross-functional teams to drive quality excellence. You'll also monitor supplier performance and assist in the development of management procedures.

This role involves designing electro-mechanical systems, defining interfaces between subsystems, developing test strategies, and conducting hazard analyses. The engineer will also guide project management and manufacturing processes while focusing on cost, size, durability, and serviceability goals.

The V&V Test Manager will lead a team of Test Engineers in developing comprehensive test suites to verify the functionality of medical products, collaborating with Project Managers and System Engineers. Responsibilities include creating test plans, assessing design changes, and contributing to regulatory submissions.