Lumicity
Electrical Engineering Manager
Location: Greater Minneapolis–St. Paul Area, MN Annual Salary: $90,000.00-$110,000.00 Responsibilities
May work with R&D leadership to define technical roadmaps aligned with business objectives. Drive continuous improvement in engineering processes and methodologies. Collaborate with Regulatory Affairs, Clinical, Quality and Manufacturing teams etc. throughout product lifecycle. Participate in executive reviews and strategic planning sessions. Maintains substantial knowledge of state-of-the-art principles and theories in their particular area of expertise. Provides critical design and technical problem resolution. Assume technical lead in the design, development, and testing of complex bioelectronic systems comprised of PCB design, stimulation, power management, wireless communication, and sensing technologies, etc. May lead projects or project teams with moderate resource requirements, risk, and/or complexity. Can work independently within functional / divisional policies while maintaining good communication with functional and cross-functional teams. May help with technical recruitment, training, and ongoing support of staff. Provides technical guidance, training and mentorship to less senior staff contributing to their ongoing development within the company. Provides feedback to the development staff on customer specific enhancements as well as new applications for base product in accordance with Quality System requirements. Ensures new products or product enhancements are designed to facilitate transfer to manufacturing in a timely fashion and in accordance with Quality System requirements. Facilitates the process of transferring products from development to manufacturing. Ensures that engineering testing and documentation is in accordance with regulatory requirements for approval of products by the regulatory agencies of the countries into which the products will be marketed. Works with patent attorneys in documenting innovative ideas, reviewing patent application, and supporting Freedom to Operate Analysis. Converts complex information to compelling business context and advice. Presents convincing arguments for complex ideas and projects at cross-functional meetings in a way that persuades others to agree on recommendation and/or approach, when appropriate. Qualifications
Bachelor’s degree in engineering or related discipline or equivalent experience. Master’s degree or higher in engineering is preferred. 10+ years’ experience in medical device design or similar products. Experience working under and knowledge of quality systems designed to meet FDA/EU regulatory requirements. Experience and knowledge of pre-clinical testing of medical products. Ability to travel 20% of the time. Preferred Qualifications
Demonstrates strong proficiency in Electrical Engineering, especially in analog circuit design. Ability to adapt and learn quickly leveraging knowledge towards the contribution of projects. Ability to use Microsoft Office tools for documentation, analyzing data, presenting data or ideas, etc. Ability to use Microsoft Excel and other data analysis tools to manipulate and analyze data sets. Competence in the use of Electronics CAD software (Altium) for schematic capture and PCB layout is preferred. Professional, clear verbal and written communications skills required. Ability to work independently or in a team setting as required. Job Details
Seniority Level: Mid‑Senior level Employment Type: Full‑time Industry: Medical Equipment Manufacturing and Electrical Equipment Manufacturing
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Location: Greater Minneapolis–St. Paul Area, MN Annual Salary: $90,000.00-$110,000.00 Responsibilities
May work with R&D leadership to define technical roadmaps aligned with business objectives. Drive continuous improvement in engineering processes and methodologies. Collaborate with Regulatory Affairs, Clinical, Quality and Manufacturing teams etc. throughout product lifecycle. Participate in executive reviews and strategic planning sessions. Maintains substantial knowledge of state-of-the-art principles and theories in their particular area of expertise. Provides critical design and technical problem resolution. Assume technical lead in the design, development, and testing of complex bioelectronic systems comprised of PCB design, stimulation, power management, wireless communication, and sensing technologies, etc. May lead projects or project teams with moderate resource requirements, risk, and/or complexity. Can work independently within functional / divisional policies while maintaining good communication with functional and cross-functional teams. May help with technical recruitment, training, and ongoing support of staff. Provides technical guidance, training and mentorship to less senior staff contributing to their ongoing development within the company. Provides feedback to the development staff on customer specific enhancements as well as new applications for base product in accordance with Quality System requirements. Ensures new products or product enhancements are designed to facilitate transfer to manufacturing in a timely fashion and in accordance with Quality System requirements. Facilitates the process of transferring products from development to manufacturing. Ensures that engineering testing and documentation is in accordance with regulatory requirements for approval of products by the regulatory agencies of the countries into which the products will be marketed. Works with patent attorneys in documenting innovative ideas, reviewing patent application, and supporting Freedom to Operate Analysis. Converts complex information to compelling business context and advice. Presents convincing arguments for complex ideas and projects at cross-functional meetings in a way that persuades others to agree on recommendation and/or approach, when appropriate. Qualifications
Bachelor’s degree in engineering or related discipline or equivalent experience. Master’s degree or higher in engineering is preferred. 10+ years’ experience in medical device design or similar products. Experience working under and knowledge of quality systems designed to meet FDA/EU regulatory requirements. Experience and knowledge of pre-clinical testing of medical products. Ability to travel 20% of the time. Preferred Qualifications
Demonstrates strong proficiency in Electrical Engineering, especially in analog circuit design. Ability to adapt and learn quickly leveraging knowledge towards the contribution of projects. Ability to use Microsoft Office tools for documentation, analyzing data, presenting data or ideas, etc. Ability to use Microsoft Excel and other data analysis tools to manipulate and analyze data sets. Competence in the use of Electronics CAD software (Altium) for schematic capture and PCB layout is preferred. Professional, clear verbal and written communications skills required. Ability to work independently or in a team setting as required. Job Details
Seniority Level: Mid‑Senior level Employment Type: Full‑time Industry: Medical Equipment Manufacturing and Electrical Equipment Manufacturing
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