Stryker Group
Staff Engineer- Product Engineering R&D Systems
Stryker Group, Irvine, California, United States, 92713
At Stryker’s Inari Medical, we are transforming the lives of patients suffering from venous and other vascular diseases through purpose-driven innovation. As a fast-growing medical device company, we develop breakthrough technologies that treat life-threatening conditions with speed, safety, and precision. Join us in shaping the future of vascular health.
We are currently seeking a Staff R&D Engineer to join our team of passionate innovators and engineers.
The Staff R&D Engineer supports and leads project teams in the development of medical device products - this includes writing or verifying specifications, developing testing and product processes, and designing fixtures to ensure the concepts and/or prototypes meet requirements.
The Staff R&D Engineer actively participates in cross-functional product strategy development and in broader initiatives within the R&D organization.
Know more about the Division Here:
Inari Medical You will need to live within commuting distance to our 6001 Oak Canyon STE 100, Irvine, CA office. You will need to be in the office 5 days a week. What you will do
Independently research, design, develop, modify, and verify mechanical components for medical devices. Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success. Analyze and correct complex product design issues using independent judgment. Advance solutions by applying in-depth knowledge of customer needs, market and competitive offerings. Conduct or design advanced prototyping and testing. Apply detailed knowledge of clinical procedures to author design inputs. Support Voice of Customer sessions internally and with clinicians. Be proficient with and mentor others in usage of industry standards, including design requirements and test strategies per applicable regulations. Lead creation and refinement of engineering documentation, such as the Design History file. Follow and mentor others on R&D procedures like design controls and risk management, per the Quality Management System. Identify and support the creation of or improvements to procedures, policies, processes, systems, and technology. Support and execute segments of complex multifunctional teams to advance projects through the design /development/launch process.
What you need
Required Qualifications:
Bachelor’s Degree in Mechanical Engineering, Biomedical Engineering or related discipline 4+ years of work experience in R&D Demonstrated mechanical engineering problem-solving skills Experience with 3D CAD modeling (Solidworks Preferred) Preferred Qualifications:
Experience in creating engineering drawings, models, applying GD&T, and CAE tools to optimize the design Adept at applying knowledge of materials and manufacturing processes to product design Pre-Clinical and/or Clinical experience. 510(k) and/or PMA experience. $87,600 - $186,700 salary plus bonus eligible + benefits. Actual minimum and maximum may vary based on location.Individual pay is based on skills, experience, and other relevant factors.
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Inari Medical You will need to live within commuting distance to our 6001 Oak Canyon STE 100, Irvine, CA office. You will need to be in the office 5 days a week. What you will do
Independently research, design, develop, modify, and verify mechanical components for medical devices. Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success. Analyze and correct complex product design issues using independent judgment. Advance solutions by applying in-depth knowledge of customer needs, market and competitive offerings. Conduct or design advanced prototyping and testing. Apply detailed knowledge of clinical procedures to author design inputs. Support Voice of Customer sessions internally and with clinicians. Be proficient with and mentor others in usage of industry standards, including design requirements and test strategies per applicable regulations. Lead creation and refinement of engineering documentation, such as the Design History file. Follow and mentor others on R&D procedures like design controls and risk management, per the Quality Management System. Identify and support the creation of or improvements to procedures, policies, processes, systems, and technology. Support and execute segments of complex multifunctional teams to advance projects through the design /development/launch process.
What you need
Required Qualifications:
Bachelor’s Degree in Mechanical Engineering, Biomedical Engineering or related discipline 4+ years of work experience in R&D Demonstrated mechanical engineering problem-solving skills Experience with 3D CAD modeling (Solidworks Preferred) Preferred Qualifications:
Experience in creating engineering drawings, models, applying GD&T, and CAE tools to optimize the design Adept at applying knowledge of materials and manufacturing processes to product design Pre-Clinical and/or Clinical experience. 510(k) and/or PMA experience. $87,600 - $186,700 salary plus bonus eligible + benefits. Actual minimum and maximum may vary based on location.Individual pay is based on skills, experience, and other relevant factors.
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