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San Diego, California, United States · On-site
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San Diego, California, United States · On-site
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San Diego, California, United States · On-site
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San Diego, California, United States · On-site
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Lead quality oversight for manufacturing operations, contract manufacturers, and suppliers to ensure compliance with regulatory requirements. Establish robust manufacturing processes, lead process validations (IQ/OQ/PQ), and drive continuous improvement through statistical tools and CAPAs.
Requires a Bachelor's degree in Engineering or a related field and at least 7 years of quality engineering experience in an FDA-regulated medical device environment. Preferred candidates have ISO 13485 Lead Auditor certification and experience with Class III implantable devices.
About Synchron
Synchron’s vision is to build non-surgical brain–computer interfaces at global scale that protect the fundamental human rights of freedom of expression and autonomy. Our first mission is to develop motor decoders that restore the ability of 15 million people with paralysis to interact with the digital world. Our second mission is to develop whole-brain cognitive decoders that enable hundreds of millions of people with cognitive decline to preserve and expand their agency as cognition changes over time. In pursuing these goals, we aim not only to help humans flourish, but also to drive fundamental discoveries in human intelligence. Our team operates at the intersection of healthcare and technology, translating breakthrough research into real-world, safety-critical systems.
Senior Quality Engineer (Operations)
Quality
Location: San Diego, CA (On-site)
Employment Type: Full-Time
About the Role
As Senior Quality Engineer (Operations), you will serve as the Quality lead supporting Synchron’s manufacturing operations, contract manufacturers, and supplier network to ensure products are manufactured safely, consistently, and in compliance with applicable regulatory requirements. You will partner closely with Manufacturing Engineering, Supply Chain, Operations, and R&D to establish robust manufacturing processes, support design transfer activities, and drive continuous improvement across production operations.
You will also assist in the development and implementation of Synchron’s QMS. This is a hands-on role requiring regular engagement on the manufacturing floor, with suppliers, and across cross-functional teams.
Key Responsibilities
Required Qualifications
Preferred Qualifications
Compensation
The base salary range for this role is $130,000 – $150,000 depending on experience, skills, and qualifications.
In addition to base salary, this role may be eligible for discretionary bonuses and/or equity grants, subject to board approval and company policy.
Visa Sponsorship
We are unable to offer visa sponsorship for this position at this time.
Benefits (for W-2, full-time, exempt employees in the US only) ***Intern positions not eligible
Equal Employment Opportunity (EEO)
Synchron is an equal opportunity employer. We are committed to creating an inclusive environment for all employees and applicants and provide equal employment opportunities without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, veteran status, or any other characteristic protected by applicable law.
If you need a reasonable accommodation during the application or interview process, please let us know.
Join Us
At Synchron, you will be part of a transformative mission, and you will work alongside driven people who believe in the power of collaboration and innovation to make a lasting impact. If you are excited to stretch your skills and contribute to something meaningful, apply now and build the future with us.
Brain Computer Interface
Synchron is developing implantable neurotechnology to unlock the brain and solve unmet medical needs at scale
Offices: Brooklyn, Brooklyn, New York 11205, US
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