Director, Design Quality Assurance

Calyxo, Inc.

Pleasanton, CA 94586

United States

Posted July 1, 2025

{CONTRACTOR,FULL_TIME,INTERN}

Valid until July 31, 2025

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Job Description

Director, Design Quality Assurance - Pleasanton, CA

Join to apply for the Director, Design Quality Assurance - Pleasanton, CA role at Calyxo, Inc.

Director, Design Quality Assurance - Pleasanton, CA

Join to apply for the Director, Design Quality Assurance - Pleasanton, CA role at Calyxo, Inc.

Calyxo, Inc. is a medical device company headquartered in Pleasanton, California, USA. The company was founded in 2016 to address the profound need for improved kidney stone treatment. Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resources each year. Our team is led by executives and investors with a proven track record of commercializing paradigm-shifting devices to meet unmet needs within urology.
Are you ready to change the future of kidney stone treatment? We are seeking high achievers who want to be part of a dynamic team working in a fun, diverse atmosphere.
Summary
The Director, Design Quality Assurance provides strategic representation, planning, management, direction, and guidance to meet quality engineering goals and objectives supporting new product development and sustaining commercial products. This position directs and oversees Quality Engineering staff who contribute to and support new product development and sustaining of commercial products. The role provides leadership in defining and implementing quality engineering policies, principles and processes that facilitate the realization of Calyxo’s product development objectives.
As an integral member of Calyxo’s Quality Leadership Team, this position fosters greater teamwork, alignment, collaboration, accountability, and performance between Quality and R&D.
This position requires experience creating, developing, implementing, managing, overseeing and improving systems and processes, and the ability to drive performance and service at the highest level in a fast-paced, high growth, dynamic medical device environment.
In This Role, You Will

Lead the Design Quality Assurance team and ensure compliance with applicable domestic and international regulatory standards (e.g., FDA, CE marking, etc.).
Oversee Design Quality Assurance and Engineering activities including the development, documentation, implementation and maintenance of quality system requirements and procedures related to design, development, and pre-production manufacturing activities.
Partner with R&D to ensure product development activities and deliverables are compliant with internal procedures, external standards and regulations, and industry best practices.
Provide Quality Engineering leadership, resources, and support to ensure the on-time development and commercialization of quality products.
Oversee and direct Quality staff to ensure ample coverage and support for the R&D team to support new product development (NPD)and sustaining product engineering.
Responsible for overseeing, planning, leading and driving activities such as Risk Management, Biocompatibility, Shelf-Life Studies, Test Method Validation, Reliability Engineering, and Statistical Analysis in support of new product development, product changes, and sustaining product engineering.
Ensure robust design control, software development and risk management practices are followed, driving improvements in test methods, validation, and verification processes.
Champion quality engineering principles and foster a company-wide continuous improvement mindset, promoting shared responsibility for quality.
Responsible for talent management including recruiting, engaging, training, and developing quality staff to ensure the necessary skill sets and competencies to meet business needs.
Establish, foster, and maintain successful cross-functional relations with internal departments/functions such as Operations/Manufacturing, R&D/Engineering, Regulatory and Clinical Affairs.
Interface with all departments to provide leadership on the use of Quality Assurance and Engineering methodologies, tools and regulatory compliance requirements
Serve as Subject Matter Expert for areas of responsibility during internal and external audits
Work in accordance with the quality system procedures related to work activities.
Develop, establish, monitor, and report on functional quality objectives, metrics, and goals.
Manage department expenses in-line with approved department budgets.
Supporting department specific initiatives and projects as assigned.
Contribute to our culture of being collaborative, respectful, transparent, ethical, efficient, high-achieving, and fun!

Who You Will Report To

See Organization Chart

Requirements

Education: Bachelor of Science in Engineering or Life Science discipline.
Minimum 15 years experience in Quality Engineering/Assurance in the medical device industry including 5 years in a managerial role.
Work location: Pleasanton, CA.
Travel: Ability to travel 10 - 15% Domestic and International to suppliers and contract manufacturing sites.
Full-time employment.
Strong knowledge of FDA requirements for design control of medical devices and 21 CFR 820; ISO 13485 and 14971, 62366; IEC 60601-1, IEC 62304 and related regulations.
In depth knowledge of Risk Management, Biocompatibility, and Sterilization.
Strong written, oral, interpersonal skills, analytical skills, problem-solving techniques, and statistical application experience.
Proactive leader who can determine deficiencies, communicate them effectively through the organization, and follow through to resolution.
Excellent level of organizational skills and ability to direct and oversee multiple projects/initiatives at the same time with a high level of attention to detail.
Strategic yet hands-on when needed; high degree of energy and drive; and the ability to continually seek to make improvements to the function, process and people being led.
Excellent leadership and managerial skills with the ability to be flexible, adaptable and to work under pressure.
Experience with FDA Class II sterile devices.
Compliance with relevant county, state, and Federal rules regarding vaccinations.

What We Offer
At Calyxo, you will be part of a knowledgeable, high-achieving, experienced and fun team. You will work in a diverse work environment with experienced, proven leaders and have an opportunity to shape our company culture. You will experience constant learning and dynamic challenges to help you grow and be the best version of yourself.
We Also Offer An Attractive Compensation Package, Which Includes

A competitive base salary of $200,000 - $230,000 and variable incentive plan
Stock options – ownership and a stake in growing a mission-driven company
Employee benefits package that includes 401(k), healthcare insurance and paid vacation

Calyxo is deeply committed to fostering an environment where diversity and inclusion are not only valued but also prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. Diverse viewpoints bring diverse capabilities, which strengthen our focus and fuel our growth.
Calyxo is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics
Legal authorization to work in the United States is required. In compliance with federal law, all persons hired will be required to verify their identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.
Disclaimer
At Calyxo, we prioritize a transparent and structured interview process to ensure the best fit for both our candidates and our team. Please be aware of the following:

Structured Interview Process: Our hiring process includes multiple stages of interviews where you will have the opportunity to communicate directly with Calyxo employees. This ensures that you gain a comprehensive understanding of the role and our company culture.
Verification of Identity: We do not extend job offers without first meeting candidates, either virtually or in person. This step is crucial to maintain the integrity of our hiring process and to ensure mutual alignment.
Beware of Scams: Calyxo will never request sensitive personal information, such as your full name, address, phone number, or identification documents, via email or online forms before an official interview. Calyxo representatives will always contact you using an email format of If you receive a request for information from any other domain, please contact us directly at to verify the legitimacy of the communication.

We appreciate your interest in joining Calyxo and look forward to getting to know you through our official channels.