Design Engineer

Sitka Inc.; Phoenix (AZ); Hybrid; USD 140,000 - 190,000; Full time

Benefits offered by this job

Stock Ownership Plan

Comprehensive benefits package

Job summary

Gore is seeking an experienced Design Engineer for our Phoenix, AZ facility. You will join a cross-functional team to design, develop, and commercialize medical devices, applying DFMA and industry standards.

Hybrid work arrangement in the United States is available. The role requires extensive SolidWorks modeling, mold flow analysis, and GD&T expertise, with opportunities to document designs for IP protection and collaborate across disciplines.

Qualifications

• Bachelor's degree in Engineering or Science with 15+ years of engineering/R&D experience.
• SolidWorks modeling and Simulation experience with CSWP certification.
• Proficiency with mold flow analysis software (MoldFlow, Moldex3D).

Responsibilities

• Design, develop, and commercialize innovative medical devices with DFMA.
• Contribute to cross-functional core teams and drive risk reduction.
• Document designs using standards: ISO 10993, 21 CFR 820, ASME Y14.5.
• File invention disclosures with IP/legal teams.
• Maintain CAD, GD&T, tolerance analyses, and FEA expertise.
• Deliver design packages with specs, CAD models, material sets, and data.
• Interface with suppliers to communicate design needs.
• Support product lines through tech transfers and CAPAs.
• Apply structured problem-solving to root-cause design issues.
• Understand Gore device portfolio and manufacturing methods.

Skills

Cross-functional collaboration

Analytical thinking

Technical communication

Travel flexibility

Education

Bachelor's degree in Engineering or Science

Tools

SolidWorks

MoldFlow

Moldex3D

GD&T

FEA

Job description

Category: Engineering, Scientists & Technicians

Experience Level: Experienced

Work Arrangement: Hybrid

Posting Start Date: 10/7/26

Posting End Date: 10/21/26

About the Role

We are looking for an experienced Design Engineer to join our team. In this role, you will design new medical products or support existing products with a diverse, cross-functional team of Gore associates and external partners. As an integral contributor to the success of Gore's product portfolio, this position will involve interactions with a variety of disciplines across Gore Medical.

Diversity is a core value at Gore. We are passionate about building and sustaining an inclusive and equitable work environment for all Associates. We believe every member of our team enriches our work environment by exposing us to a broad range of perspectives to understand and engage with our customers, suppliers, and each other.

This position will be located at our facility in Phoenix, Arizona , with the possibility of a hybrid work arrangement.

Responsibilities

• Design, develop, and commercialize innovative medical devices and accessories, leveraging new and existing technologies, while incorporating Design for Manufacture and Assembly principles (DFMA). Drive and participate in structured design reviews and act as a formal technical reviewer within the Quality System where appropriate.
• Work as a new product development core team member to generate design concepts and develop them into detailed product designs that meet Design Input Requirements and stakeholder needs, scoping design work in collaboration with cross-functional partners and driving risk reduction efforts to deliver on project priorities and timelines.
• Drive and document design development efforts using good engineering practices (e.g. research, design and execution of experiments, tolerance analysis, etc.) within a quality system, including incorporating existing industry and regulatory standards (e.g. ISO 10993, 21 CFR Part 820, ASME Y14.5) into design requirements, contributing to the standardization of best practices, templates, and design engineering tools within the function.
• Document designs and concepts for patent or trade secret protection, collaborating with legal/IP functions to submit invention disclosures when appropriate.
• Maintain and grow expertise in core design skills (e.g., CAD, GD&T, tolerance analysis, FEA), pursue relevant certifications (e.g., CSWP, ASME GDTP, CAM-F) and develop an understanding of medical device core material sets and manufacturing methods (e.g., forming, additive, and subtractive manufacturing)
• Deliver design packages which include specifications, tolerance analyses, CAD models, material sets, summaries of the performance, and analyses, data, and rationales supporting the design choices.
• Represent the technical needs of the device design and inspection requirements to suppliers.
• Support commercial product lines through technology transfers, design changes, specification updates and improvements, and input on CAPAs, NCRs, or other areas where the design may be impacted.
• Apply structured problem-solving techniques to determine root cause for non-conforming products and design issues (e.g., raw materials, components, assemblies, and systems).
• Develop and maintain a fundamental understanding of the portfolio of Gore device designs, capabilities, materials, and manufacturing methods to incorporate best practices and support standardization.

Required Qualifications

• Bachelor’s degree in Engineering or Science, with a minimum of fifteen years of experience in engineering, R&D, or related fields, or an equivalent combination of education and professional experience
• Significant SolidWorks modeling and Simulation analysis experience, demonstrated with a Solidworks Professional Certification (CSWP)
• Proficiency with mold flow analysis software (e.g., MoldFlow, Moldex3D)
• Experience with R&D development cycles and participating in technical design reviews, either providing technical input or incorporating feedback on design outputs
• Excellent verbal and written communication skills with both technical and non-technical audiences
• Demonstrated ability to apply engineering evaluation methods, such as tolerance analyses, material assessments, and performance testing, that inform design direction
• Demonstrated experience developing and documenting product specifications in compliance with ASME standards and applicable quality system requirements, including the application of geometric dimensioning and tolerancing (GD&T)
• Demonstrated ability to complete projects per quality system requirements that balance customer service, fitness for use, manufacturability, and time to market
• Experience with data-driven decision making and structured problem-solving techniques to determine root cause and identify countermeasures
• Demonstrated ability to foster an inclusive environment that engages and empowers fellow Associates
• Ability to travel up to 10%

Desired Qualifications

• Software skills (e.g. ABAQUS, Python, Rhino, Grasshopper, Simpleware, JMP statistical analysis, NX, CREO)
• Experience with nitinol stent design, catheter design, injection molded component design, prototyping, manufacturing, and/or testing
• Ability and willingness to learn new technical skills and apply them to product development activities with significant technical uncertainties and tight timelines

This position offers a hybrid work arrangement in the country from which the Associate is employed. Eligibility is dependent on the responsibilities of the role and business needs, and the Associate must agree to comply with Gore’s work arrangement policies.

What We Offer

Our success is based on the capability and creativity of our Associates, and we are proud to offer a comprehensive and competitive total rewards program that supports your everyday and helps you build your tomorrow.
We provide benefits that offer choice and flexibility and promote overall well-being. And in keeping with our belief that every Associate should share in the collective success of the enterprise; we provide a distinctive Associate Stock Ownership Plan in each country as well as potential opportunities for profit-sharing. Learn more at gore.com/careers/benefits
Gore is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, national origin, ancestry, age, status as a qualified individual with a disability, genetic information, pregnancy status, medical condition, marital status, sexual orientation, status as a protected veteran, gender identity and expression, and any other characteristic protected by applicable laws and regulations.
Gore is committed to a drug-free workplace. All employment is contingent upon successful completion of drug and background screening. Gore will consider qualified applicants with criminal histories, e.g., arrest and conviction records, in a manner consistent with the requirements of applicable laws.
Gore requires all applicants to be eligible to work within the United States. Gore generally will not sponsor visas unless otherwise noted on the position description.

For over 65 years, Gore has improved lives through discovery, product innovation and rewarding careers for Associates. We push the boundaries of what's possible - not just through our products and technologies but also through individual growth and development.

We believe in the strength of a diverse and inclusive workplace. With diverse perspectives, ideas and experiences, we uncover new possibilities and make a greater impact in the world. Our Associates build on a rich history of innovation, upholding Gore's values and supporting an inclusive work environment where we treat each other and our external partners with fairness, dignity and respect.

Copyright 2025 W. L. Gore & Associates, Inc.