As a PCB Rework Specialist, you will perform electronic assembly and rework tasks in an R&D environment, using specialized tools to repair and inspect PCBs, maintain a clean workspace, and ensure efficient project completion while working with multi-disciplinary teams.

As a Quality Engineer at DEKA, you'll provide Quality guidance for medical device R&D, ensuring compliance with regulations, leading risk management activities, and conducting investigations. Your role includes analyzing data, preparing work plans, and driving system improvements while working cooperatively with design teams and management.

The Senior Software Engineer will develop and evolve DEKA's cloud platform, design scalable infrastructures, and solve technical challenges while ensuring high performance and cybersecurity. The role requires collaboration with cross-functional teams and thorough documentation practices.

As a Senior Software Engineer, you will develop applications for medical devices, tackle technical challenges, ensure applications are secure and scalable, and lead design efforts. You will utilize various technologies including cloud infrastructure, RESTful APIs, and distributed systems.

The Supplier Quality Engineer is responsible for managing supplier quality assurance to ensure products meet specifications. Duties include developing supplier quality initiatives, leading continuous improvement programs, and managing supplier audits and corrective actions. The role requires collaboration with cross-functional teams to monitor supplier performance and drive compliance with DEKA's quality management system.

As a Junior Software Project Manager, you will coordinate software development activities, manage project milestones, prioritize backlogs, and remove roadblocks to ensure timely delivery of high-quality custom solutions while supporting quality and regulatory documentation.

The Senior Systems Engineer will design electro-mechanical systems, manage subsystem integrations, define testing protocols, and conduct hazards analysis. The role involves supporting project management by estimating design efforts and guiding manufacturing processes to meet design goals for a medical device product.

As a Lead Project Quality Engineer, you will provide quality leadership in a medical device R&D team, ensuring compliance with standards and regulations. You will lead investigations, participate in risk management activities, assist in documentation and audits, and drive systematic improvements to foster a quality culture.

The V&V Test Technician at DEKA will join a testing team, perform test procedures, document results, report anomalies, and assist with troubleshooting to ensure that medical products meet FDA standards.

As the Engineering Project Manager at DEKA, you will lead cross-functional teams in developing innovative medical devices, managing project schedules, budgets, and resources while communicating with stakeholders to achieve project goals.

The Senior Test Engineer will write test plans and procedures, assess the performance and reliability of medical devices, create test fixtures, and participate in design failure investigations. This role also involves authoring quality plans and contributing to regulatory submissions while leading an interdisciplinary team.

The Junior Project Manager will assist with daily project activities to overcome technical challenges, manage resources, and drive deliverables in collaboration with the technical team. The role involves defining task priorities and implementing process improvements to ensure product quality aligned with DEKA’s standards.

The Embedded Software Engineer will design, implement, and verify embedded software for a medical device, analyze and update requirements, and solve technical challenges in a dynamic team environment.