Your responsibilities include: Actively contribute to electronics designs from concept to production. Continuously improves process and work methodologies by interfacing with peers/cross-functional groups and analyzing activities to improve workflow and work processes. In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. Provide Technical support, as required, to technology and product development teams. Analyze and assesses technical reports and other information to make recommendations for electronic components and design approaches. Must have good communication and interpersonal skills. Must be a self-starter, manage own time and prioritize tasks based on business priorities. Ability to delegate tasks of larger projects across a development team.
What we’re looking for: Required Qualifications: Bachelor’s degree in electronic, Computer engineering or equivalent 1+ years’ experience in the medical device industry or other similarly regulated field. Experience working with international standards such as IEC 60601 and IEC 61000
Experience Requirements: Strong communication and time management skills for efficient project coordination Expertise in electronic design, including simulation, schematic capture, and PCB layout, with a focus on drive and control electronics for various motors Understanding of Linear and SMPS design principles for robust electronic systems Experience leading DFMEA activities to identify and mitigate design risks Proficient in prototyping and general test equipment setup for effective validation processes. Skilled in PCBA bring-up, troubleshooting, and failure analysis for optimized design performance Experience in designing to address and mitigate EMC issues for regulatory compliance. Strong commitment to meeting product specifications and requirements.
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