Work Flexibility: Hybrid The Patient Specific Solutions team provides customized devices to those with complex clinical needs, such as oncology, where no other device exists on the market to treat their condition. As a Product Development Engineer, you will transform clinical requirements into patient-specific solutions, partnering with surgeons, operating room staff, clinical teams, and cross-functional stakeholders to deliver designs that support individual patient treatments. You will manage multiple cases, create technical documentation for manufacturing and inspection, and contribute to delivering high-quality solutions within established timelines and regulatory requirements. This role combines engineering design, clinical collaboration, and technical problem-solving in a fast-paced environment where each case presents unique challenges. This is a hybrid role based in Mahwah, NJ, requiring you to be on-site 3 days per week, so candidates must live within a commutable distance. What you will do: Design and develop patient-specific orthopedic implants and associated instruments using clinical imaging data, including X-rays, CT scans, and MRI scans. Create and release technical drawings and 3D CAD models that enable manufacturing and inspection activities. Apply geometric dimensioning and tolerancing (GD&T), finishing specifications, and tolerance stack calculations to support manufacturable designs. Perform engineering calculations and design verification activities to support product design requirements and design validity. Develop surgical planning guides, operating instructions, and supporting documentation for patient-specific devices and instrumentation. Collaborate with surgeons, operating room staff, clinical teams, distributors, and sales representatives to gather design inputs and provide technical support throughout the case lifecycle. Manage multiple patient cases simultaneously while meeting established project timelines and quality requirements. Create and maintain design documentation in accordance with quality system procedures, design controls, risk management processes, and regulatory requirements; attend surgical or clinical cases when required. What You Will Need Required
Qualifications
Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or another Engineering discipline. Minimum 0 years of professional engineering experience.
Preferred Qualifications
Minimum 1 year of experience in product development, mechanical design, medical device engineering, or a related field Completion of an engineering internship, co-op program, or capstone project involving mechanical design, product development, medical devices, manufacturing, or related engineering work.
Experience
using CAD tools such as Creo, 3Matic, Mimics, or similar engineering software. Knowledge of CT segmentation, engineering analysis methods, materials, and manufacturing processes. US20: $83,400 - $133,100 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.