Employer: Stryker Corporation
Job Title: Staff Engineer, Systems Engineering
Job Requisition: 1006.23.2
Job Location: Fully remote from anywhere in U.S.
Job Type: Full Time
Duties: Research, design, develop, modify, and verify medical device systems. Translate user needs to system requirements. Modify existing system architectures or test designs. Create new system architectures or test designs for simple products or features. Allocate and decompose requirements on a multidisciplinary (electrical, mechanical, software) project using modeling, simulation, budgeting, or mathematical techniques. Lead Concept Phase activities for a feature. Analyze and correct complex product design issues using independent judgment. Lead analytical studies, including trade studies, sensitivity studies, optimization studies, performance assessments, and design assessments. Lead system integration testing and verification activities. Contribute to Product Risk Management activities. Advance solutions by applying in-depth knowledge of customer needs, market, and competitive offerings. Apply detailed knowledge of clinical procedures to author design inputs. Support Voice of Customer sessions internally and with clinicians. Be proficient with and mentor others in usage of industry standards, including design requirements and test strategies per applicable regulations. Lead creation and refinement of engineering documentation, such as the Design History file. Follow and mentor others on R&D procedures like design controls and risk management, per the Quality Management System. Work cooperatively with all stakeholders to ensure project success. Identify and support the creation of or improvements to procedures, policies, processes, systems, and technology. Support and execute segments of complex multifunctional teams to advance projects through the design /development/launch process. Deliver high quality results with passion, energy, and drive to meet business priorities. Collaborate with cross-functional teams to build partnership to achieve business objectives. Telecommute benefit: Fully remote.
Requirements: Bachelor’s degree in Computer Science, Software Engineering, Systems Engineering, Biomedical Engineering or related field (willing to accept foreign educational equivalent) and four (4) years of experience in an engineer-related role or project management role, within a regulated medical device industry driving projects to completion. Demonstrated Expertise (quantitative experience requirements not applicable to this section): develop and optimize system requirements, design and verification documentation; requirements management and systems modeling tool/software, including Jama; change management software; and, quality control systems and change management for FDA-regulated systems.
Contact: [email protected]. Must reference job 1006.23.2
