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:
Calyxo is seeking a Staff Systems Engineer to architect, validate, and own the system-level behavior of a complex medical device ecosystem throughout the entire product development lifecycle.
You will define and own the end-to-end system architecture, translate user and business needs into robust system and subsystem requirements, validate architectural decisions through prototyping and bench testing, and proactively de‑risk critical technical challenges. This role carries direct accountability for system-level requirements ownership and verification.
The ideal candidate combines hands-on medical device experience, strong systems thinking, and the technical leadership expected of a staff-level engineer operating across hardware, software, disposables, and clinical use environments.
In This Role, You Will:
System Architecture:
- Architect systems with a strong focus on technical and patient risk mitigation.
- Establish and control system interfaces, including fluidic, mechanical, electrical, and software-control boundaries.
- Drive architectural trade studies using bench testing, prototyping, and simulation to validate design decisions.
- Ensure architectural robustness across intended use, misuse, fault conditions, and edge cases.
Requirements Ownership & Decomposition:
- Own creation, maintenance, and verification of system-level requirements, with particular emphasis on performance, safety, and reliability.
- Decompose user, clinical, and business needs into clear, testable system and subsystem requirements.
- Ensure complete traceability from user needs through requirements, risks, mitigation, and verification.
- Write requirements that are technically precise, non-prescriptive, and verification-ready.
Risk Reduction & Technical Validation:
- Lead identification and mitigation of system-level risks.
- Own or significantly contribute to system-level dFMEAs, ensuring strong linkage between requirements, risk controls, and verification activities.
- Define and support system-level verification strategies, ensuring requirements are objectively testable and clinically relevant.
- Actively de-risk novel or critical aspects of the system through early experimentation and focused learning cycles.
Cross-Functional Technical Leadership:
- Serve as the systems subject-matter expert across mechanical, electrical, firmware, software, clinical, quality, and product teams.
- Lead architecture reviews, requirements reviews, and system-level design discussions.
- Work closely with other technical leads (mechanical, electrical, and SW) to ensure a fully functional system.
- Provide clear technical direction and interface control to external development partners, ensuring alignment with Calyxo’s system architecture and verification strategy.
- Mentor engineers on systems thinking, requirement quality, and architectural rigor.
Who You Will Report To:
- Sr. Manager, Systems and Test Engineering
Requirements:
Education & Experience:
- Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or related field; Master’s or PhD strongly preferred.
- 12+ years of experience in medical device development, with significant ownership of system architecture.
- Strong hands-on experience with both:
- Single-use disposable systems.
- Capital equipment incorporating pumps, sensors, and closed-loop control.
Technical Expertise:
- Experience architecting systems that integrate hardware, disposables, and software.
- Proven ownership of system-level requirements and verification.
- Proficiency with Jama (or equivalent), dFMEAs, fault-tree analysis, and requirements traceability.
- Strong working knowledge of relevant medical device standards (e.g., ISO 14971, IEC 62304, IEC 60601 family).
- Track record of writing high-quality, testable requirements that scale across complex systems.
Leadership & Communication:
- Staff-level technical judgment and decision-making capability.
- Ability to lead through influence and technical authority rather than direct reporting lines.
- Clear, concise technical communicator across disciplines and experience levels.
- Comfortable operating in ambiguity, making informed trade-offs, and driving alignment.
Work Conditions:
- Location: Pleasanton, CA (on-site presence expected 4–5 days per week).
- Travel: Minimal (<10%).
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 range of $195,000 - $205,000 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 [email protected]. If you receive a request for information from any other domain, please contact us directly at [email protected] 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.
Skills Required
- Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related field
- Master's degree or PhD
- 12+ years of experience in medical device development
- Significant ownership of system architecture
- Hands-on experience with single-use disposable systems
- Hands-on experience with capital equipment incorporating pumps, sensors, and closed-loop control
- Experience architecting systems integrating hardware, disposables, and software
- Ownership of system-level requirements and verification
- Proficiency with Jama or equivalent requirements-management software
- Experience with dFMEAs, fault-tree analysis, and requirements traceability
- Working knowledge of ISO 14971, IEC 62304, and IEC 60601 family standards
- Track record of writing high-quality, testable requirements for complex systems
- Staff-level technical judgment and decision-making capability
- Ability to lead through influence and technical authority
- Clear, concise cross-disciplinary technical communication
- Ability to operate in ambiguity, make trade-offs, and drive alignment
What We Do
Calyxo, Inc. is an innovation-driven medical device company focused on improving care for patients with kidney stones, a common and painful condition that consumes vast amounts of healthcare resources today. Founded in 2016, Calyxo is led by executives and investors with a strong track record of commercializing paradigm-shifting solutions in the field of urology. Our team features some of the most talented, high-achieving and brightest minds in the medical device industry who are compelled by a desire to make a difference in kidney stone care. We are proud of our collaborative, diverse, fun and dynamic culture. We drive our actions based on our core values which we call ‘F.I.T to WIN.’ Find Joy: We celebrate wins and enjoy the journey! Integrity: We are truthful, honorable, and reliable. Transparency: We share what’s going on in our business. We are open, honest and have a clear communication across our organization. Win as a Team: We are earnest collaborators. We hold ourselves and each other accountable.
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