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Sr. Design Quality Engineer

About The Role

 

The Senior Design Quality Engineer supports product development from concept through commercialization and will serve as the core team member for the cross-functional product development team. The Senior Design Quality Engineer will provide subject matter expertise and guidance to the team on design control and risk management from early development through design transfer, Design for Reliability and Manufacturing, product Development Life Cycle, and Process Validation. In addition, this position will play a working role to ensure that the developed products meet quality standards consistent with Hinge Health's quality processes, while meeting all external design control and regulatory requirements. The role requires solving complex problems with minimal oversight and the ability to articulate complex information to teams, including executive management

 

What You’ll Accomplish

 

  • Design Control and Risk Management Stewardship: Planning and execution of design controls, risk management, and design verification/validation for new products

  • Advocate product design history file and ensure compliance to internal processes and external standards and regulations.

  • Understand user needs and assure they are translated to the design, while ensuring compliance to usability and human factors standards and regulations.

  • Partner with engineering to define design inputs, design outputs, and traceability matrices.

  • Contribute to the strategy and execution of risk-based design verification and validation.

  • Accountable for overall risk management file: participate and support the development of product risk management file, to analyze and assess the product risks associated with user, design, process and supplier.

  • Review and provide feedback on design architectures, selections, requirements, and drawings from early design

  • Collaborate with manufacturing, purchasing, test engineering, and supplier engineering to facilitate transfer of scalable designs into production.

  • Contribute to new product development Technical Reviews and Design Reviews.

  • Support Regulatory Affairs with creating submissions and responding to submission questions.

  • Perform and/or support audits (internal, external, and by regulatory agencies)

  • Coach, mentor, teach, and influence the engineering staff in best quality practices, data analysis, protocol development, and design for quality and reliability methods

Hinge Health Hybrid Model
We believe that remote work and in-person work have their own advantages and disadvantages, and we want to be able to leverage the best of both worlds. Employees in hybrid roles are required to be in the office 3 days per week, for the full 8 hours of a typical business day. The San Francisco office has a dog-friendly workplace program.

Basic Qualifications

  • Bachelor’s degree in electrical, mechanical or system engineering, math, or physics Advanced degree preferred

  • 4+ years of working experience in Quality Engineering or related field and minimum 3 years in medical device design environment

  • 2+ years of working experience in design control and risk management from early design and development through commercialization

  • Experience with electromechanical systems

  • Experience with medical standards compliance including ISO 13485, ISO 14971, IEC 60601, IEC 62304, and 21 CFR 820 with a focus on design controls and risk management

 

Preferred Qualifications

  • Experience with SaMD and SiMD 

  • Able to navigate the quality system with minimal oversight on individual projects

  • Balanced risk decision making to drive product quality, gain consensus, and work through technical challenges

Compensation

This position will have an annual salary, plus equity and benefits. Please note the annual salary range is a guideline, and individual total compensation will vary based on factors such as qualifications, skill level, competencies, and work location. The annual salary range for this position is $120,000 - $180,000.

About Hinge Health

Hinge Health leverages software, including AI, to largely automate care for joint and muscle health, delivering an outstanding member experience, improved member outcomes, and cost reductions for its clients. The company has designed its platform to address a broad spectrum of MSK care—from acute injury, to chronic pain, to post-surgical rehabilitation—and the platform can help to ease members’ pain, improve their function, and reduce their need for surgeries, all while driving health equity by allowing members to engage in their exercise therapy sessions from anywhere. The company is headquartered in San Francisco, California.

What You'll Love About Us

  • Inclusive healthcare and benefits: On top of comprehensive medical, dental, and vision coverage, we offer employees and their family members help with gender-affirming care, tools for family and fertility planning, and travel reimbursements if healthcare isn’t available where you live.

  • Planning for the future: Start saving for the future with our traditional or Roth 401k retirement plan options which include a 2% company match.

  • Modern life stipends: Manage your own learning and development

Diversity and Inclusion

Hinge Health is an equal opportunity employer and prohibits discrimination and harassment of any kind. We make employment decisions without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, age, veteran status, disability status, pregnancy, or any other basis protected by federal, state or local law. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. We provide reasonable accommodations for candidates with disabilities. If you feel you need assistance or an accommodation due to a disability, let us know by reaching out to your recruiter.

By submitting your application you are acknowledging we are using your personal data as outlined in the personnel and candidate privacy policy.


Workday ID

JR805
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Daniel Perez
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Average salary estimate

$150000 / YEARLY (est.)
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$120000K
$180000K

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What You Should Know About Sr. Design Quality Engineer, Hinge Health

Are you a passionate Senior Design Quality Engineer looking to make a real impact in the medical device sector? At Hinge Health, located in sunny San Francisco, California, you’ll be at the forefront of product development from concept to commercialization. This role isn’t just about compliance; it's about being the expert who guides a dynamic cross-functional team through the intricacies of design control and risk management. You'll play a vital role in ensuring our products meet high-quality standards while complying with external regulations. You will solve complex problems with autonomy, ensuring that user needs are translated into fantastic designs while working closely with engineering teams to develop crucial design inputs and outputs. With a focus on risk management, you'll have the responsibility of maintaining the overall risk management file, analyzing potential risks associated with design and manufacturing processes. As a Senior Design Quality Engineer, you’ll also be coaching and mentoring engineering staff on quality practices, making a significant impact on product reliability and safety. You'll enjoy the flexibility of Hinge Health’s hybrid work model, working with us in the office three days a week—plus, our dog-friendly office will make coming to work even more enjoyable. If you're looking for a role where every day brings new challenges and opportunities to innovate, Hinge Health could be the perfect fit for you!

Frequently Asked Questions (FAQs) for Sr. Design Quality Engineer Role at Hinge Health
What are the primary responsibilities of the Senior Design Quality Engineer at Hinge Health?

The Senior Design Quality Engineer at Hinge Health is responsible for overseeing product development, ensuring compliance with design control and risk management standards, and collaborating closely with various teams to facilitate design inputs and outputs. This role requires a deep understanding of product risks and a commitment to maintaining quality throughout the product development lifecycle.

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What qualifications are necessary for the Senior Design Quality Engineer position at Hinge Health?

To qualify for the Senior Design Quality Engineer role at Hinge Health, candidates should possess a bachelor’s degree in engineering, mathematics, or physics, with at least four years of experience in Quality Engineering or a related field. A minimum of three years in a medical device design environment and familiarity with design controls and medical standards like ISO 13485 and IEC 60601 is also essential.

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How does Hinge Health support the professional development of Senior Design Quality Engineers?

At Hinge Health, we believe in continuous learning and development. As a Senior Design Quality Engineer, you'll have access to modern life stipends that help you manage your professional growth, including resources for further training and skill development tailored to your career aspirations.

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What is the work environment like for a Senior Design Quality Engineer at Hinge Health?

The work environment at Hinge Health for the Senior Design Quality Engineer combines a collaborative and inclusive atmosphere with the flexibility of a hybrid work model. As you work in the office three days a week, you'll be supported by a dog-friendly space that enhances productivity and well-being.

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What are the career advancement opportunities for a Senior Design Quality Engineer at Hinge Health?

As a Senior Design Quality Engineer at Hinge Health, there are various pathways for career advancement. You can grow into more senior positions within the quality engineering team or transition into other areas such as product management or regulatory affairs, using your extensive knowledge and experience gained in this role.

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Common Interview Questions for Sr. Design Quality Engineer
Can you describe your experience with design control and risk management?

In response to this question, be prepared to share specific examples of projects where you successfully implemented design controls and managed risks effectively. Highlight any frameworks or methodologies you used and how your approaches contributed to product quality and compliance.

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What steps do you take to ensure compliance with medical standards?

Talk about your familiarity with medical standards such as ISO 13485 and IEC 60601. Discuss your process for staying updated on regulations and how you incorporate compliance checks throughout the design process to ensure all products meet the required standards.

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How would you approach a situation where your team disagrees on a design solution?

Your response should demonstrate your collaborative skills. Explain how you would facilitate open discussions, present data to support your viewpoint, and work toward finding a consensus, ensuring that all team members feel heard and valued.

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What methodologies do you use for effective design verification and validation?

Discuss specific methodologies you have employed, such as V-model or Design Failure Mode and Effects Analysis (DFMEA). Share examples of how these methodologies have helped you in previous projects to validate design decisions and ensure user needs are met.

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Describe how you would mentor a junior engineer in best quality practices.

Showcase your coaching philosophy. Explain how you would provide guidance through hands-on training, regular feedback sessions, and encouraging an open dialogue about quality practices. Mention any tools or resources you would use to enhance their learning experience.

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What challenges have you faced in quality engineering, and how did you overcome them?

Share a specific challenge you've encountered in the field and explain the steps you took to address it. Highlight your problem-solving skills and your ability to adapt to changing environments and requirements.

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How do you prioritize your workload when managing multiple projects?

Talk about your time management skills and any tools you use to keep projects on track. Describe how you assess project urgency and importance and ensure that quality standards are maintained across all initiatives.

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Can you give an example of how you collaborated with cross-functional teams on a recent project?

Provide an example that illustrates your role in a cross-functional team setting, detailing how you communicated effectively, managed expectations, and contributed your expertise to ensure the project’s success.

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What experience do you have with audits related to quality systems?

Discuss your familiarity with internal and external audits, emphasizing your role in preparing for them, participating in audit activities, and addressing any findings. Highlight your understanding of regulatory requirements and how you achieve compliance.

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What tools or software do you consider essential for quality engineering?

List tools that you have found effective in your quality engineering practice, such as statistical analysis software, project management tools, or regulatory compliance platforms. Explain how you use these tools to enhance product quality and streamline processes.

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DATE POSTED
April 24, 2025

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