Senior Engineer, R&D

Stryker•Cary, IL

1d•Onsite

About The Position

Work Flexibility: Onsite What You Will Do Technical Responsibilities: Under minimal supervision, research, design, develop, modify, and verify components/modules for medical devices Translate design inputs to engineering specifications and produce sub-system level designs Develop and analyze solutions, prototyping one or more options to provide proof of concept Apply fundamental and some advanced concepts, practices and procedures for problem solving Business Responsibilities: Demonstrate advanced understanding of customer needs and design inputs Demonstrate proficiency with product’s intended use and clinical procedures Learn how the financial models are constructed Med Device Compliance: Follow fundamental industry standards, design requirements and test strategies which apply to regulatory requirements Independently create or refine engineering documentation, such as the Design History file Follow R&D procedure like design controls and risk management, per the Quality Management System General Responsibilities: Under minimal supervision, work with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success Quickly process and assimilate procedures, policies, processes, systems, and technology required Work on complex problems, applying advanced experience and learnings Demonstrate ownership and prioritize work with minimal supervision Works as key member of the team, collaborating with others and solidifying relationships Stryker Corporation is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. We are proud to be named one of the World’s Best Workplaces! For more information, visit: www.stryker.com Work Flexibility Remote – Role allows you to work the majority to 100% of time from an alternate workplace. These roles could have travel expectations, and you must work within the country of the job requisition location. Field-based – You can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary. Almost all sales roles would likely be qualified as field-based. Onsite – Role is 100% located at a Stryker facility. Some ad hoc flexibility may be available depending on role, level, and job requirements. Manufacturing roles and any role that requires physical presence at the office would qualify under this category. Hybrid – You can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager/supervisor.

Requirements

Bachelor of Science in Engineering, Mechanical Engineering, BioMedical or related degree required
2+ years of work experience required

Nice To Haves

Working knowledge and understanding of mechanical engineering practices and design principles
Technical ability to create engineering drawings and models, applying GD&T and CAE tools
Demonstrated ability to apply knowledge of materials and manufacturing processes to product design
Ability to Communicate basic plans and technical information to team members

Responsibilities

Under minimal supervision, research, design, develop, modify, and verify components/modules for medical devices
Translate design inputs to engineering specifications and produce sub-system level designs
Develop and analyze solutions, prototyping one or more options to provide proof of concept
Apply fundamental and some advanced concepts, practices and procedures for problem solving
Demonstrate advanced understanding of customer needs and design inputs
Demonstrate proficiency with product’s intended use and clinical procedures
Learn how the financial models are constructed
Follow fundamental industry standards, design requirements and test strategies which apply to regulatory requirements
Independently create or refine engineering documentation, such as the Design History file
Follow R&D procedure like design controls and risk management, per the Quality Management System
Under minimal supervision, work with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success
Quickly process and assimilate procedures, policies, processes, systems, and technology required
Work on complex problems, applying advanced experience and learnings
Demonstrate ownership and prioritize work with minimal supervision
Works as key member of the team, collaborating with others and solidifying relationships