--- title: 'Quality Technician at Neptune Medical' canonical: 'https://feeny.ai/job/quality-technician-neptune-medical-burlingame-california-j0n2sxnq30gv' type: 'job' last_seen: '2026-09-14' --- # Quality Technician at Neptune Medical - **Company:** Neptune Medical - **Location:** Burlingame California, United States - **Posted:** 2026-05-21 - **Last confirmed live:** 2026-09-14 - **Apply:** https://job-boards.greenhouse.io/neptunemedical/jobs/4698546005 ## Job description Neptune Medical, is an innovative, venture capital funded medical device startup headquartered in Burlingame, CA. We have already commercialized novel medical devices using our technology. Now the team at Neptune is building something truly unique: a fully flexible medical robot that enables doctors to reach deep into human anatomy. Triton Robotic Endoscopy will disrupt flexible endoscopy and set a new standard in outcomes for decades to come. TITLE:  Quality Technician POSITION SUMMARY: The Quality Technician will support manufacturing operations by ensuring in-process and finished medical devices meet established quality requirements, specifications, and regulatory standards. This role is responsible for identifying and documenting quality issues on the production floor, supporting investigations and root cause analysis, managing nonconforming materials, and collecting process and product data to drive continuous improvement. The technician works closely with Manufacturing, Quality Engineering, and cross-functional teams to ensure rapid response to quality concerns and compliance with applicable quality system regulations (e.g., FDA 21 CFR Part 820, ISO 13485). ## ROLES AND RESPONSIBILITIES Manufacturing Quality & Inspection - Perform incoming, in-process, and final inspections of components, subassemblies, and medical devices in accordance with approved procedures, drawings, and sampling plans - Ensure product compliance with specifications, GMP, and regulatory requirements - Accurately document inspection and test results in device history records (DHRs) and other quality records - Maintain traceability of materials and finished goods throughout production Nonconformance & Investigation Support - Identify, document, and segregate nonconforming materials - Support containment activities, including line clearance, product holds, and sorting/rework activities - Assist in root cause investigations and corrective and preventive actions (CAPA) - Collaborate with Quality Engineers to analyze trends and recurring issues Data Collection & Continuous Improvement - Collect and analyze in-process quality data to support process monitoring and improvement initiatives - Provide input on quality metrics, yield trends, and defect data - Partner with Manufacturing and Engineering teams to implement process improvements and error-proofing solutions Equipment & Testing - Operate, maintain, and calibrate inspection and test equipment (e.g., calipers, microscopes, gauges) - Support equipment calibration and environmental monitoring programs as needed - Perform basic product or material testing in accordance with validated methods Documentation & Quality Systems Support - Review Device History Records (DHRs) and other quality documentation for completeness and accuracy - Maintain quality records in compliance with document control procedures and regulatory requirements - Support audits (internal/external) by providing documentation and participating in audit activities - Ensure adherence to Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) Cross-Functional Collaboration - Work closely with Production, Manufacturing Engineering, and Quality Engineering to ensure timely resolution of quality issues - Communicate quality concerns clearly and escalate issues as appropriate - Support training of production personnel on quality requirements and procedures ## REQUIRED QUALIFICATIONS: - High school diploma or equivalent required; Associate degree or technical certification preferred - 3–5+ years of experience in Quality Assurance/Quality Control in a manufacturing environment (medical device industry strongly preferred) - Working knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or ISO 13485 - Experience with inspection methods, sampling plans, and interpreting engineering drawings and specifications - Proficiency in Microsoft Office and electronic quality management systems ## PREFERRED QUALIFICATIONS: - Experience in a regulated medical device or life sciences environment - Familiarity with nonconformance systems, CAPA, and root cause analysis tools (e.g., 5 Whys, Fishbone) - Hands-on experience with dimensional and visual inspection equipment - Understanding of validation activities (IQ/OQ/PQ) - Experience supporting audits and regulatory inspections Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART Station. Our job titles may span more than one career level. The starting hourly rate for this role is between $35-$40/hour depending on experience. The actual base pay is dependent upon many factors, such as: education, training, transferable skills, work experience, business needs, and location. The base pay range is subject to change and may be modified in the future. This role may also be eligible for equity, benefits and 401(K) with matching. Neptune Medical provides equal employment opportunities to all applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. ## About Neptune Medical ## Company Overview - **One-liner**: Neptune Medical is a venture-backed medical device company creating the future of endoscopy with its proprietary Dynamic Rigidization™ technology, enabling unprecedented control and precision in gastrointestinal procedures. - **Entity Type**: Private (Series D, venture-backed) - **Headquarters**: Burlingame, California, United States - **Founded**: 2016 - **Founders**: Alex Tilson (Founder & CEO) ## Core Business - **Primary industry**: Medical devices – gastrointestinal endoscopy - **Target customers**: Hospitals, academic medical centers, and gastroenterologists (B2B) - **Mission or purpose**: “To go where no one has gone, and do what no one has done” – advancing minimally invasive care through innovation ## Products & Services - **Pathfinder®**: FDA-cleared dynamic rigidizing overtube that enhances endoscope stability and control during upper and lower GI procedures; used in over 15,000 patients at leading U.S. hospitals. - **Triton™ Robotic Endoscopy System**: A fully flexible robotic system designed for easy navigation, precision, and control throughout the entire colon. Currently in clinical trials (first-in-human study completed with 100% cecal intubation rate and no adverse events). Not yet for sale in the U.S. or international markets. - **Dynamic Rigidization™ Technology**: Proprietary platform that allows an endoscope to transition between flexible and rigid states on demand, enabling challenging therapeutic and diagnostic procedures. ## Market Standing - **Valuation**: Not publicly disclosed - **Key Metric**: Total funding – $97M (Series D, August 2024) - **Notable Investors/Partners**: Sonder Capital (lead), Olympus Corporation of the Americas, Korea Omega Investment, Shangbay Capital, Scientific Health Development. Board includes Fred Moll (co-founder of Intuitive Surgical) and Mir Imran (InCube Ventures). - **Growth Signals**: - 128 employees as of mid-2026 (+26.3% year-over-year) - 12 active job postings (+20% year-over-year) - Positive first-in-human study results for Triton (May 2026) – 100% cecal intubation, 67.5% polyp detection rate - Spun out Jupiter Endovascular subsidiary in 2024 to sharpen focus on GI robotics ## Competitive Advantages - **Proprietary Dynamic Rigidization™ technology** – a unique, patented platform that no competitor has replicated. - **First-mover with FDA-cleared Pathfinder** – already adopted in 15,000+ procedures, building clinical evidence and physician trust. - **Strategic investor backing** – Olympus (global endoscopy leader) and Sonder Capital provide deep industry expertise and capital. - **Strong patent portfolio** – 54 patents covering endoscopy, medical equipment, and digestive system procedures. - **Triton robotic system** – aims to combine the benefits of flexible endoscopy with robotic precision, addressing colonoscopy demand and physician fatigue. ## Strategic Focus - **Primary priority**: Commercializing the Triton robotic endoscopy system, including regulatory submissions (FDA/CE Mark) and expanding clinical data. - **Continued Pathfinder adoption** – scaling sales to more hospitals and academic centers. - **Talent acquisition** – actively hiring across engineering (mechanical, electrical, software, systems), quality, clinical affairs, and manufacturing to support product development and scale-up. ## Why Work Here - **Culture**: Described as “collaborative, innovative, ambitious” – a nimble start-up environment where employees contribute directly to groundbreaking medical technology. - **Work model**: Likely on-site at the Burlingame lab/office (state-of-the-art clean room and bench facilities). Location is adjacent to SFO airport, BART, and Caltrain for easy commuting. - **Benefits**: Medical, dental, and vision insurance; matching 401(k); daily lunch, drinks, and snacks; stock option grants. - **Engineering culture**: Strong focus on robotics, hardware, and software – teams work on everything from Linux software platforms to NPI process development. Many hires come from Intuitive, Boston Scientific, Johnson & Johnson MedTech, and Auris Health. - **Growth opportunity**: Joining at a pivotal stage (post-Series D, pre-commercial launch of Triton) offers significant career growth and equity upside. ## Sources 1. [neptunemedical.com](https://neptunemedical.com/) 2. [linkedin.com](https://www.linkedin.com/company/neptunemedical) 3. [cbinsights.com](https://www.cbinsights.com/company/neptune-medical) 4. [greenhouse.io](http://job-boards.greenhouse.io/neptunemedical) ## Other roles at Neptune Medical - [Materials Specialist](https://feeny.ai/job/materials-specialist-neptune-medical-burlingame-california-9bd6z1g7yby5) — Burlingame California, United States - [Senior Mechanical Engineer, Hardware](https://feeny.ai/job/senior-mechanical-engineer-hardware-neptune-medical-burlingame-california-7qcma9j4vjm1) — Burlingame California, United States - [Manufacturing Engineering Technician (I/II/III), NPI](https://feeny.ai/job/manufacturing-engineering-technician-i-ii-iii-npi-neptune-medical-burlingame-6w5wkf017yvq) — Burlingame California, United States - [Senior NPI Process Development Engineer](https://feeny.ai/job/senior-npi-process-development-engineer-neptune-medical-burlingame-california-h04paemwf3ka) — Burlingame California, United States - [Product Development Engineer II](https://feeny.ai/job/product-development-engineer-ii-neptune-medical-burlingame-california-5b2pe2m27k4n) — Burlingame California, United States - [R&D Manager, Mechanical Design](https://feeny.ai/job/r-d-manager-mechanical-design-neptune-medical-burlingame-california-j3j0rsddjx8m) — Burlingame California, United States - [Senior Manager of Clinical Affairs](https://feeny.ai/job/senior-manager-of-clinical-affairs-neptune-medical-burlingame-california-04h01rj4td9r) — Burlingame California, United States - [Senior/Staff Electrical Engineer](https://feeny.ai/job/senior-staff-electrical-engineer-neptune-medical-burlingame-california-0pyqen6g52fx) — Burlingame California, United States - [Senior/Staff Linux Software Engineer – Robotics Platform](https://feeny.ai/job/senior-staff-linux-software-engineer-robotics-platform-neptune-medical-5vskkc0b1cd3) — Burlingame California, United States - [Senior/Staff Systems Engineer](https://feeny.ai/job/senior-staff-systems-engineer-neptune-medical-burlingame-california-m6s9z426grag) — Burlingame California, United States