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Senior Quality Engineer
Senior Quality EngineerDandy • Arlington, TX, US
Senior Quality Engineer

Senior Quality Engineer

Dandy • Arlington, TX, US
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About The Role

Dandy is transforming the massive and antiquated dental industry—an industry worth over $200B. Backed by some of the world's leading venture capital firms, we're on an ambitious mission to simplify and modernize every function of the dental practice through technology. As we expand our reach globally, Dandy is building the operating system for dental offices around the world—empowering clinicians and their teams with technology, innovation, and world-class support to achieve more for their practices, their people, and their patients.

About The Role

Dandy is seeking a skilled and proactive Quality Engineer to join our fast-growing, venture-backed team. The ideal candidate for this role is someone with strong technical depth in quality control excited to redefine industry best practices and find solutions to challenging new problems to help enable Dandy's goals. The ideal candidate will have a strong continuous improvement background, insatiable curiosity and a desire to learn and grow.

Responsibilities

  • Establish, refine, and document quality control standards, inspection methods, and testing protocols.
  • Monitor the production process to ensure adherence to quality standards at every stage.
  • Lead CAPA initiatives with external partners to determine root cause and ensure necessary actions to correct are implemented.
  • Work with onsite Quality Manager to train and mentor production staff on quality practices and compliance requirements.
  • Investigate and resolve production issues by analyzing root causes and implementing corrective actions.
  • Collect, analyze, and summarize quality data to generate actionable insights and detailed reports.
  • Act as a liaison for customer feedback, adapting processes to meet quality expectations and regulatory standards.
  • Innovate on existing quality processes and work with software and automation engineering teams to build tooling that supports product quality.
  • Support the ISO certification process and prepare the organization for ISO recertification audits.

What We're Looking For

  • Proven experience in a quality engineering or leadership role within a manufacturing environment.
  • Hands-on experience managing ISO 13485 or ISO 9001 quality management systems, including documentation, internal audits, and compliance activities.
  • Demonstrated ability to lead teams through ISO certification and external audit processes, including gap assessments and CAPA closure.
  • Experience in quality validation of new equipment and processes, including creation of validation protocols (IQ / OQ / PQ), risk assessments, and ensuring compliance with regulatory requirements.
  • Strong problem-solving skills with a data-driven approach to root cause analysis, nonconformance management, and preventive action planning.
  • Proficiency in statistical methods, process capability analysis, and using tools such as Minitab, Excel, or JMP.
  • Familiarity with quality elements of design and manufacturing transfer, particularly in dental prosthetics or other Class I / II medical devices.
  • Ability to interpret and apply regulatory and standard requirements (e.g., 21 CFR Part 820, ISO 13485 : 2016, MDSAP).
  • Excellent communication, collaboration, and training skills with a track record of guiding cross-functional teams.
  • High attention to detail and the ability to operate effectively under fast-paced, deadline-driven conditions.
  • Ability to independently manage quality projects and deliver compliant results with minimal supervision.
  • Bonus Points For

  • Experience working in a fast-paced startup environment, wearing multiple hats across quality, operations, and compliance.
  • Direct involvement in New Product Introduction (NPI) or product launches, including design transfer, process validation, and first-article quality reviews.
  • Building or scaling quality systems from the ground up, especially in early-stage or rapidly growing organizations.
  • Demonstrated ability to thrive in ambiguity and implement structured quality processes in evolving environments.
  • For full-time positions, Dandy offers a wide range of best-in-class, comprehensive, and inclusive benefits tailored to each country where we operate. Our local benefits packages typically include healthcare, dental, mental health support, parental planning resources, retirement savings options, and generous paid time off—ensuring our team members are supported no matter where they live and work.

    Dandy is proud to be an equal-opportunity employer. We are committed to building a diverse and inclusive culture that celebrates authenticity to win as one. We do not discriminate on the basis of race, religion, color, national origin, gender, gender identity, sexual orientation, age, marital status, disability, protected veteran status, citizenship or immigration status, or any other legally protected characteristics.

    Dandy also fully complies with the Americans with Disabilities Act (ADA). We are dedicated to embracing challenges and creating an accessible, inclusive workplace for all individuals. If you require any accommodations for your interview or have any questions beforehand, we will do everything we can to meet your needs.

    Seniority level

  • Mid-Senior level
  • Employment type

  • Full-time
  • Job function

  • Quality Assurance
  • Industries

  • Medical Equipment Manufacturing
  • J-18808-Ljbffr

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