R&D Technician-CA

Role details

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.

R&D Technician

Department: Stentrode Kit Team Location: San Diego, CA (On-site)

Employment: Full-Time *Overtime eligible. All overtime hours require prior Manager approval before being worked.

About the Role

We are seeking an R&D Technician to support the hands-on fabrication, assembly, and testing of Synchron’s devices. This individual will work directly alongside engineers to build prototype and pre-production devices, prepare test samples, execute mechanical and functional test procedures, and maintain the lab infrastructure that supports the kit development program.

This is a lab-based, detail-oriented role at the heart of device development. The successful candidate will bring strong manual dexterity, comfort with microscope-based assembly, and a disciplined approach to documentation.

Key Responsibilities

Prototype Fabrication

• Perform hands-on assembly of R&D prototypes
• Assemble procedural accessories and ancillary kit components per documented work instructions
• Support rapid design–build–test iteration cycles by turning around prototype builds on tight timelines

Testing & Sample Preparation

• Prepare test samples, fixtures, and anatomical bench models for device characterization
• Operate lab equipment including force testers (Instron or equivalent), microscopes, laser micrometers, leak detectors, and environmental chambers
• Record, organize, and report test data accurately; flag anomalies or deviations to the engineering team
• Support simulated-use testing and bench model preparation design verification testing

Lab Operations & Equipment

• Maintain clean and organized workspaces in accordance with clean-room, ESD, and contamination control protocols
• Perform routine calibration, preventive maintenance, and upkeep of assembly tools and test instruments
• Manage consumables inventory, raw material stock, and incoming inspection of purchased components
• Operate and maintain specialized equipment such as ovens, laser welders, and polymer processing tools

Documentation & Quality

• Follow and provide feedback on assembly work instructions, test protocols, and standard operating procedures
• Maintain lot traceability, serialization, and device history records (DHR) for all builds
• Participate in non-conformance reporting, CAPA activities, and process improvement efforts as needed
• Support first-article and incoming quality inspections for purchased materials and components

Required Qualifications

• Associate’s degree or technical certificate in biomedical equipment technology, electronics, mechanical technology, or a related field—or equivalent hands-on experience
• 3+ years of experience as a technician in an R&D, manufacturing, or lab environment, ideally in medical devices
• Strong manual dexterity and demonstrated skill with microscope-based assembly of small, delicate components
• Experience with precision manual processes: soldering, adhesive dispensing, wire handling, and mechanical fastening at small scale
• Ability to read and work from engineering drawings, schematics, and written work instructions
• Strong attention to detail and a disciplined approach to documentation and traceability

Preferred Qualifications

• Exposure to mechanical testing equipment (Instron, force gauges, fatigue testers)
• Familiarity with ISO 13485 quality management systems and GDP/GMP practices

Compensation

----------------

The base salary range for this role is $80,000 – $100,000 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.

Benefits (for W-2, full-time, exempt employees in the US only) *Intern positions not eligible

• Subsidized medical and dental insurance coverage for you and your dependent(s)
• Life insurance, short-term disability, long-term disability
• 401k
• Discretionary unlimited PTO
• Flexible Spending Account for you and your dependent(s), with eligible plan elections
• Commuter benefits for NY employees

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 and now and build the future with us.