Senior Mechanical Design Engineer(Hybrid) at Stryker - Poland

Portage, Michigan, United States -

Full Time

Start Date

Immediate

Expiry Date

26 Mar, 26

Salary

0.0

Posted On

26 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Mechanical Engineering, Medical Device Design, CAD Modeling, Problem Solving, Cross-Functional Collaboration, Quality Management, Risk Management, Engineering Specifications, Prototyping, Customer Insight, Clinical Procedures, Design Controls, Manufacturing Processes, Statistical Methods, GD&T, FEA

Industry

Medical Equipment Manufacturing

Description

Work Flexibility: Hybrid or Onsite At Stryker, we share a bold mission: Together with our customers, we are driven to make healthcare better. Every day, we push boundaries to improve lives through groundbreaking medical technologies. Our Interventional Spine team leads the way in creating minimally invasive solutions that restore mobility, relieve pain, and transform patient outcomes. We’re looking for a Senior Design Mechanical Engineer to join our dynamic team of innovators at our Portage, Michigan headquarters. This hybrid role requires at least three days onsite, offering the perfect blend of collaboration and flexibility. As a Senior Design Engineer, you’ll partner across disciplines—Quality, Manufacturing, Regulatory, Clinical Sciences, Marketing, and Project Management—to drive success. Under minimal supervision, you’ll have the chance to work on cutting-edge systems and play a pivotal role in designing and delivering next-generation spine devices that truly make a difference. Learn more about our business here: Stryker IVS What you will do Design & Development: Research, design, develop, and verify medical device components and sub-systems with minimal supervision. Specifications & Solutions: Translate design inputs into engineering specifications; develop and prototype solutions to validate concepts. Problem Solving: Apply fundamental and advanced engineering principles to analyze and resolve complex issues. Customer & Clinical Insight: Demonstrate a strong understanding of customer needs, product use, and clinical procedures. Compliance & Documentation: Adhere to industry standards and regulatory requirements; create and refine engineering documentation, including Design History Files. Quality & Risk Management: Follow design controls and risk management processes per the Quality Management System. Cross-Functional Collaboration: Work closely with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management to ensure project success. Ownership & Leadership: Prioritize work independently, contribute to complex projects, and build strong team relationships. What you need Required Qualifications: Bachelor of Science in Engineering, Mechanical Engineering, BioMedical, or related discipline. 2+ years of relevant work experience. Working knowledge and understanding of mechanical engineering practices and design principles. Preferred Qualifications: Experience working in the medical device industry. Knowledge of design and concept generation CAD or CAE modeling tools (Creo preferred) Knowledge of analysis tools (i.e., DFMECA, Fault Tree Analysis, FEA, Stack-ups, etc.) and statistical methods (i.e., leveraging Minitab for ANOVA, normality testing, confidence calculations, etc.). 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. Travel Percentage: 20% Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability. Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. Stryker 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.

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Responsibilities

The Senior Mechanical Design Engineer will research, design, develop, and verify medical device components and sub-systems with minimal supervision. They will collaborate across various disciplines to ensure project success and adhere to industry standards and regulatory requirements.