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The Process Controls Engineer designs and integrates clean environment subsystems within regulated devices, ensuring environmental performance, contamination control, and compliance throughout the device development lifecycle.

The Senior Test Engineer will develop test plans, assess device performance, contribute to regulatory submissions, and mentor junior staff.

As a Junior Control Systems Engineer, you'll design and develop control systems for medical devices and automation solutions, collaborating with engineers to integrate hardware and optimize performance.

The Junior Salesforce Administrator will manage Salesforce operations, support workflows, maintain data integrity, and assist cross-functional teams with Salesforce solutions.

The QA Admin manages document control processes, supports QA functions, oversees training documentation, and ensures compliance in a medical device R&D environment.

As a Quality Engineer, you'll lead failure investigations, analyze data, support corrective actions, ensure compliance, and drive product improvements in a regulatory environment.

The PCB Layout Designer will translate electrical schematics into optimized PCB layouts, collaborating with engineers, ensuring design integrity, and managing the workflow for manufacturing.

As a Senior Software Quality Engineer, you will support the development of medical devices by leading test strategy, requirements capture, and configuration of software tools, ensuring compliance with regulatory standards.

The Quality Engineer will provide quality guidance, lead risk management, conduct investigations, ensure compliance with standards, and participate in audits.

As a Product Development Automation Engineer at DEKA, you will specify, design, validate, and support automated manufacturing equipment while ensuring effective communication with engineering, operations, and quality departments.