Work Flexibility: Onsite What You Will Do Support the ongoing manufacturing of medical devices by designing, documenting, and improving manufacturing processes and operations that ensure product safety, quality, and performance. Lead process qualification, verification, and validation activities to support manufacturing operations and regulatory compliance. Analyze, troubleshoot, and resolve manufacturing issues impacting product quality, safety, delivery, or cost. Design, develop, and implement manufacturing equipment, tooling, and fixtures to support production requirements. Design and coordinate engineering tests and experiments; analyze data, draw conclusions, and communicate recommendations. Support product development and sustaining engineering activities through technology development, specification creation, process studies, material testing, and technical reporting. Participate in risk management and design control activities, including FMEA and design reviews. Partner with operators, technicians, production supervisors, quality engineers, and cross-functional teams to address production floor challenges and improve manufacturing performance. Manage engineering project activities including planning, documentation, scheduling, progress tracking, and implementation. Evaluate and implement process or product alternatives to optimize manufacturing performance. Provide technical guidance and training to operators and technicians. Collaborate with suppliers and external partners to support equipment, process, and product initiatives. Champion patient safety, product quality, and compliance with Stryker's Quality Management System and applicable regulatory requirements. What You Need Required

Qualifications

Bachelor's degree in Engineering. 2+ years of relevant experience supporting manufacturing processes and operations in a production environment.

Experience

conducting process, equipment, or product qualification, verification, and validation activities.

Experience

troubleshooting manufacturing, process, or quality-related issues and implementing effective solutions.

Experience

designing, developing, or supporting manufacturing equipment, tooling, and fixtures. Ability to create, read, and interpret engineering drawings using standard engineering software. Strong analytical and problem-solving skills, including statistical, geometric, and mathematical analysis. Ability to manage technical responsibilities with limited supervision.

Preferred Qualifications

Experience

within the medical device industry or another regulated manufacturing environment. Proficiency with Minitab or similar statistical software.

Experience

participating in design control activities, including risk analysis and FMEA.

Experience

selecting suppliers and assessing supplier capabilities and performance.

Experience

supporting materials testing, process studies, and manufacturing investigations. $89,400 - $148,900 USD Annual Travel Percentage: 10% 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.