At Stryker Robotics, manufacturing engineering plays a critical role in delivering reliable, high-quality robotic systems that support healthcare providers around the world. In this role, you will partner across engineering, quality, operations, and supply chain teams to improve manufacturing performance, support new product introductions, and drive operational excellence on the production floor.
This position provides hands-on manufacturing engineering support for the assembly of complex electromechanical systems while leveraging data, process improvements, and problem-solving methodologies to enhance quality, efficiency, throughput, and cost performance.
What You Will Do
- Provide direct manufacturing engineering support to production operations by troubleshooting process issues, leading root cause investigations, and driving timely resolution of manufacturing challenges.
- Execute manufacturing process validation and equipment qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), in compliance with quality and regulatory requirements.
- Analyze manufacturing data using statistical tools to improve process capability, support measurement system analysis, and identify opportunities to improve quality, throughput, ergonomics, and cost.
- Collaborate with Quality, Research & Development, Advanced Operations, and Supply Chain teams to support design for manufacturability, new product introductions, production readiness activities, and continuous improvement initiatives.
- Develop and maintain manufacturing documentation, including work instructions, standard operating procedures, process failure mode and effects analyses, control plans, and visual aids in accordance with quality management system requirements.
What You Will Need
Required:
- Bachelor’s degree in Mechanical Engineering, Industrial Engineering, Biomedical Engineering, Electrical Engineering, Manufacturing Engineering, Robotics Engineering, or a related engineering discipline.
- Minimum 2 years of manufacturing engineering experience.
- Experience supporting complex mechanical and/or electromechanical assemblies.
- Experience working within a regulated manufacturing environment.
Preferred:
- Experience in medical device, robotics, high-tech assembly, or other regulated manufacturing industries.
- Experience supporting nonconformance investigations, corrective and preventive actions, process validation, and continuous improvement initiatives.
- Knowledge of FDA Quality System Regulations, ISO 13485, ISO 14971, and risk-based validation methodologies.
- Proficiency with engineering and statistical analysis tools such as SolidWorks, Minitab, and Geometric Dimensioning & Tolerancing (GD&T).
United States of America Pay Ranges:
$77,700 - $129,500 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.
Skills Required
- Bachelor's degree in Mechanical, Industrial, Biomedical, Electrical, Manufacturing, Robotics Engineering, or a related engineering discipline
- At least 2 years of manufacturing engineering experience
- Experience supporting complex mechanical and/or electromechanical assemblies
- Experience working within a regulated manufacturing environment
- Experience in medical device, robotics, high-tech assembly, or another regulated manufacturing industry
- Experience with nonconformance investigations, corrective and preventive actions, process validation, and continuous improvement
- Knowledge of FDA Quality System Regulations, ISO 13485, ISO 14971, and risk-based validation methodologies
- Proficiency with SolidWorks, Minitab, and Geometric Dimensioning & Tolerancing
Inari Medical Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Inari Medical and has not been reviewed or approved by Inari Medical.
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Fair & Transparent Compensation — Pay is considered competitive for many roles, with employees described as 'extremely happy' with total compensation including pay, stock, equity, and benefits. Feedback suggests above‑average salary levels across departments contribute to strong pay sentiment.
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Healthcare Strength — Benefits include comprehensive medical, dental, and vision coverage, with 100% employer‑paid premiums for employees cited in multiple descriptions. Additional options like critical illness, accident, hospital indemnity, and wellness programs reinforce the healthcare offering.
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Leave & Time Off Breadth — Time off is characterized by unlimited PTO, cited as a top benefit by employees. Paid holidays and flexible hours are also referenced, expanding the range of time‑off options.
Inari Medical Insights
What We Do
Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.









