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Stryker Corporation R&D Principal Engineer - SW in Portage, Michigan

R&D Principal Engineer - SW for Stryker Corporation to independently balance design tradeoffs while designing a product (3%). Generate and review requirements and design details within a project (5%). Design medical devices in a regulated industry and perform object-oriented design and multi-threaded programming with C/C++ (15%). Lead cooperative efforts with Research and Development (R&D), Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management to ensure project success (2%). Identify and implement breakthrough solutions amongst multiple R&D teams, including demonstrating business and divisional influence (2%). Translate user needs into design inputs and specifications to produce system architectural level layouts and platform designs (3%). Assess and integrate new technologies and capabilities, including prototyping and testing (5%). Contribute, navigate, and influence the intellectual landscape for filings and protection; develop and influence invention disclosures, patents or trade secrets (2%). Partner with customers and key opinion leaders to develop technical strategies and emerging opportunities that meet clinical needs (2%). Strategize and execute customer-facing activities like Voice Of the Customer (VOC) and customer centric design ideas across the business (2%). Act as an independent reviewer and advisor for the creation or refinement of engineering documentation such as the Design History file; act as independent reviewer for design reviews and product development projects (1%). Lead code reviews for subsystems as designer and independent reviewer, applying design principals, coding standards and best practices (2%). Lead and influence the development of standards and regulations, including working closely with functions within and across the business (5%). Lead and support team members to create or improve procedures, policies, processes, systems, and infrastructure (5%). Lead complex product development activities of cross functional teams, including demonstrating best practices in multiple technical areas of expertise (5%). Mentor and grow technical talent within the discipline and function; influences, leads or mentors technical team in design and development of components, sub-systems, and/or systems for medical devices; applies and mentors others on advanced engineering theories, principles, and concepts across various products within the business unit and across business units (5%). Develop, design, including influence and mentor the resolution of complex product design issue (10%). Lead architecture of a complex system and guide design tradeoff decisions (10%). Maintain an in-depth knowledge of the industry and competitive landscape within the business unit (3%). Collaborate on financial and business modeling, including supporting business reviews to validate technical approaches (3%). Act as the divisional expert with extensive experience applying industry standards in device development (5%). Influence the creation and adoption of divisional design control and risk documentation within the quality management system (5%).  Requires: Bachelor's degree in Software Engineering, Computer Science, Electrical Engineering, or Electronics and Communication Engineering (willing to accept foreign education equivalent) plus eight (8) years of experience designing medical devices in a regulated industry and/or performing object-oriented design and multi-threaded programming with C/C++ or, alternatively, a Master's degree in Software Engineering, Computer Science, Electrical Engineering, or Electronics and Communication Engineering (willing to accept foreign education equivalent) and six (6) years of experience designing medical devices in a regulated industry and/or performing object-oriented design and multi-threaded programming with C/C++. Specific skills/other requirements - Must also possess the following (quantitative experience requirements not applicable to this section): Experience

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