Electrical Engineer for Delivery and Device Research

Lilly is a global health care leader that unites caring with discovery to make life better for people around the world. For more than a century, we have stayed true to a core set of values—excellence, integrity, and respect for people—that guide us in all we do: discovering medicines that meet real needs, improving the understanding and management of disease, and giving back to communities through philanthropy and volunteerism.

We are seeking a highly motivated Electrical Engineer for Lilly’s Delivery and Device Development organization. As an electrical engineer, you will be responsible for conducting electrical engineering activities for drug delivery systems during the development phase. Specifically, this role is responsible for conducting electrical engineering activities in the areas of concept development and prototyping, requirements development, design, risk management, and testing. A strong knowledge of complex electro-mechanical systems as well as experience developing safety critical systems is required for this role.

You must be proficient at developing early phase prototypes as well as developing and designing for finished products. You must possess a history of strong practical engineering knowledge and a proven track record for timely and cost effective project delivery. You will support the development of product development documentation within a regulatory environment for Class I, II and III medical devices. * Broad Electrical Engineering Design responsibilities across analog circuitry, RF antennas, and digital hardware designs that include signal conditioning, amplifiers, microprocessors, and microcontrollers. * Identify unique solutions to complex engineering problems and prove out those solutions through analysis and/or prototype development. * Execute product development activities for safety critical drug delivery devices this may include user needs, use cases, requirements, designs, electrical design, PCB layout, design for manufacturability and testability, risk management and test development. * Performs engineering modeling, simulations, analysis, and measurements. * Candidates should also be able to design, document and fabricate elctro-mechanical prototypes and test fixtures as well as be able to work with vendors for prototype builds for proof of concept as well as verification testing. * Conduct and document development activities for all phases of development in compliance with the Eli Lilly development processes. * Support the development of electrical engineering development procedures that are in compliance with the Eli Lilly development processes and external regulating bodies. * Support the establishment of electrical and software development tools and labs to enable product development activities. * Participation in preparation of time and cost estimates for projects as well as engineering schedules and plans. * Prepares, coordinates, and manages compliance testing for medical devices through nationally recognized testing laboratories. * Generate RFPs for vendors and suppliers and provide engineering guidance and oversight of their activities

**Basic Qualifications** * Bachelors Degree in Engineering (Biomedical, Electrical or Software Engineering preferred) or a Bachelors in a related science field with a MS in engineering. * 8+ years medical device design experience and/or high integrity systems in a regulated environment. * Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position. **Additional Skills/Preferences** * MS, P.E., and/or MBA preferred * Previous medical device / pharmaceutical design / development experience. * Experience with medical device verification of component parts and integrated systems * Strong interpersonal skills and the ability to work productively in an interdisciplinary environment. * Low Frequency RF or RFID experience desired. * Digital Signal Processing experience desired. * Demonstrated record of developing intellectual property * Experience in a start up environment * Experience in contributing to the development of new quality management systems for medical devices and/or connected medical devices * Ability to identify problems and drive issue resolution/improvements * Experience with appropriate regulations (IEC60602, CRF 820.30, ISO13485, ISO 14971, etc) * Effective technical writing skills as well as good verbal communication / presentation skills.