{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/neptunemedical/jobs/4672750005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4424542005,"location":{"name":"Burlingame, California, United States"},"metadata":null,"id":4672750005,"updated_at":"2026-03-12T16:36:54-04:00","requisition_id":"285","title":"Manufacturing Engineering Technician (I/II/III), NPI","company_name":"Neptune Medical","first_published":"2026-03-12T16:36:54-04:00","language":"en","application_deadline":null,"content":"\u0026lt;p\u0026gt;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\u0026amp;nbsp;decades to come.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;TITLE:\u0026lt;/strong\u0026gt; \u0026lt;strong\u0026gt;Manufacturing Engineering Technician (I/II/III), NPI\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As an NPI Engineering Technician you will be responsible for supporting NPI Manufacturing Engineering in developing our Endoscopes from concept to product commercialization. They will support manufacturing prototypes, process development, equipment maintenance, and executing test protocols.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate would act with passion and intensity in a medical device start-up that is fast paced and collaborative and display the ability to perform to the requirements outlined below. For the right person, this position will be a tremendously exciting and career-defining opportunity, making core contributions to a genuinely new type of medical robotic platform.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;ROLES AND RESPONSIBILITIES:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with R\u0026amp;amp;D and NPI engineers to evaluate and assemble new designs and manufacturing methods with the ability to work with little to no written instructions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manufacture medical devices for prototype, process development, design verification, and commercialization phases.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists engineering with defining manufacturing process instructions, and identifies critical equipment, fixtures, and tooling to aid in implementation of new designs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and investigate process, quality, and workmanship issues and assist engineering in documenting and implementing process improvements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support engineers in executing test protocols to collect data to characterize manufacturing processes, Equipment Installation Qualifications (IQ), and Operational Qualifications (OQ), and Process Qualifications (PQ).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable supporting manufacturing of multiple sub-assembly builds with the use of hand tools and equipment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Keep work area, equipment and materials clean, organized and properly identified.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct cross training with technicians and production assemblers and provide technical support as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience with manufacturing processes such as coil winding, braiding, lamination, die bonding, hot box, adhesive dispensing, UV curing, and cutting techniques.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working directly with engineering during development and design transfer to refine process, equipment/tooling development, and inspection.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills – ability to communicate in English orally and via writing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Positive demeanor with a strong work ethic and desire to be a big part of a growing organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 5 years working in a medical device manufacturing industry preferably in catheter manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High school diploma or GED\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART Station.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our job titles may span more than one career level. The starting hourly rate for this role is between $35 to $50 pr 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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026lt;/p\u0026gt;","departments":[{"id":4130564005,"name":"Mechanical Engineering","child_ids":[],"parent_id":null}],"offices":[{"id":4001265005,"name":"Triton Headquarters","location":"Burlingame, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/neptunemedical/jobs/4676821005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4426537005,"location":{"name":"Burlingame, California, United States"},"metadata":null,"id":4676821005,"updated_at":"2026-03-24T12:50:15-04:00","requisition_id":"291","title":"Materials Specialist","company_name":"Neptune Medical","first_published":"2026-03-24T12:50:15-04:00","language":"en","application_deadline":null,"content":"\u0026lt;p\u0026gt;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\u0026amp;nbsp;decades to come.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;TITLE: Materials Specialist\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Materials Specialist will focus on supporting the manufacturing team’s commercial preparation. This role will engage in cross-functional collaboration to manage materials in-house to ensure smooth rollout of manufacturing activities. The successful candidate will possess a passion for medical device operations/supply chain with a record of successful management of multiple products.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate will act with passion and intensity in a medical device start-up that is fast paced and collaborative and will display the ability to perform to the requirements outlined below. For the right person, this position will be a tremendously exciting and career-defining opportunity, making core contributions to a genuinely new type of medical robotic platform.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;ROLES AND RESPONSIBILITIES:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Performs daily routine tasks: receives, stores, labeling, kitting, picks, packs, ships and/or distribute materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain MIN MAX and ROP for production material and manage to ensure no production part shortages.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepares domestic and International for shipment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;May assist with work orders, as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;May assist with purchase orders, as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Verifies goods received against documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performs an initial quality check on incoming items.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare materials for production \u0026amp;amp; R\u0026amp;amp;D, including picking and staging components according to work orders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage BOM and inventory, performing regular cycle counts to ensure accurate part counts and inventory reconciliation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with production teams to fulfill material transfer requests and support manufacturing schedules.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist R\u0026amp;amp;D with Material Transfer Requests\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;When needed, assist in the packaging and shipment of finished goods, as necessary.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage incoming and outgoing material shipments for offsite storage.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Main point of contact to monitor/track shipments, obtain missing shipment documentation or corrections, and resolve accounts payable issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support company goals and objectives, policies and procedures that comply with FDA Quality System Regulations (QSR), ISO 13485, and any other applicable domestic.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain a clean and organized work environment, adhering to Good Manufacturing Practices (GMP) and safety guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other responsibilities to support Manufacturing Operations as required.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;REQUIRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;High school diploma required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2 years’ work experience in a regulated industry (e.g., medical device, pharma industry, aerospace).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to lift fifty-five (20) pounds.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Impeccable organizational skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience collaborating with cross functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding time management and multi-tasking skills - able to appropriately prioritize tasks and work efficiently under pressure.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Capable of reading and understanding part prints\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A driven outlook and with a strong desire to succeed as an individual Material Specialist Operations Coordinator, as a team, and as a company\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;PREFERRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience with Propel Quality system.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with NetSuite system.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting medical devices and capital equipment BOMs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in a start-up environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience creating, setting up, and/or managing inventory systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with packaging and shipping of products\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART Station.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026lt;/p\u0026gt;","departments":[{"id":4130565005,"name":"Manufacturing","child_ids":[],"parent_id":null}],"offices":[{"id":4001265005,"name":"Triton Headquarters","location":"Burlingame, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/neptunemedical/jobs/4671559005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4424008005,"location":{"name":"Burlingame, California, United States"},"metadata":null,"id":4671559005,"updated_at":"2026-03-10T13:03:17-04:00","requisition_id":"283","title":"Product Development Engineer II","company_name":"Neptune Medical","first_published":"2026-03-10T13:03:17-04:00","language":"en","application_deadline":null,"content":"\u0026lt;p\u0026gt;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\u0026amp;nbsp;decades to come.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;TITLE: Product Development Engineer II\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Product Development Engineer II will focus on testing the performance of our product and using test results to drive product improvement. A successful candidate will possess a passion for medical device engineering and a record of developing test methods for hardware devices in engineering R\u0026amp;amp;D environments. This role will engage in cross-functional collaboration to define requirements and test acceptance criteria, perform risk management, and design experiments to reliably measure the performance of our product.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate will act with passion and intensity in a medical device start-up that is fast paced and collaborative and will display the ability to perform to the requirements outlined below. For the right person, this position will be a tremendously exciting and career-defining opportunity, making core contributions to a genuinely new type of medical robotic platform.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;ROLES AND RESPONSIBILITIES:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute test methods for a complex, robotically driven medical device.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design, prototype and build custom electromechanical fixturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop software scripts to control robotic platforms and tools to perform data post-processing and analysis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Apply principles of systems engineering, design controls and risk management to the development of a medical device.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and maintain design requirements based on stakeholder needs and product safety.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Use statistical analysis techniques to support data-driven decision making and define acceptance criteria for design verification testing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and root cause product issues or defects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implement test process improvements to drive better accuracy, repeatability, and reproducibility of results.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author, release and maintain robust documentation in a product lifecycle management (PLM) system.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and present technical read-outs to cross-functional audiences including engineers, quality and regulatory personnel, and leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Emphasize product quality, patient safety, data integrity and other principles of GxP.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support company goals and objectives, policies and procedures that comply with FDA Quality System Regulations (QSR), ISO 13485, and any other applicable domestic regulations including Cal FDB, OSHA and Cal-OSHA.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;REQUIRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;B.S. or M.S. in Mechanical, Biomedical or related field of Engineering.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3+ years of work experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience working with cross functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with test engineering and/or design verification.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of design controls and risk management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A driven outlook and with a strong desire to succeed as an engineer, as a team, and as a company.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;PREFERRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience working in the medical device industry and/or other regulated environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with disposables/consumables.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with electromechanical and/or robotic systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in a start-up environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with PLM/ALM tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience using statistical techniques to analyze quantitative data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with rapid prototyping.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with test method validation, fixture qualification and/or non-product software validation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient with Minitab.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient with Solidworks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient with Linux-based operating systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient with Python.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART Station\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our job titles may span more than one career level. The starting base salary for this role is between $100,000 and $130,000 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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026lt;/p\u0026gt;","departments":[{"id":4141967005,"name":"Engineering Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4001265005,"name":"Triton Headquarters","location":"Burlingame, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/neptunemedical/jobs/4698546005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4437197005,"location":{"name":"Burlingame, California, United States"},"metadata":null,"id":4698546005,"updated_at":"2026-05-21T14:54:53-04:00","requisition_id":"300","title":"Quality Technician","company_name":"Neptune Medical","first_published":"2026-05-21T14:54:53-04:00","language":"en","application_deadline":null,"content":"\u0026lt;p\u0026gt;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\u0026amp;nbsp;decades to come.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;TITLE:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;strong\u0026gt;Quality Technician\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY:\u0026lt;/strong\u0026gt; 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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;ROLES AND RESPONSIBILITIES\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Manufacturing Quality \u0026amp;amp; Inspection\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform incoming, in-process, and final inspections of components, subassemblies, and medical devices in accordance with approved procedures, drawings, and sampling plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure product compliance with specifications, GMP, and regulatory requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accurately document inspection and test results in device history records (DHRs) and other quality records\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain traceability of materials and finished goods throughout production\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Nonconformance \u0026amp;amp; Investigation Support\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Identify, document, and segregate nonconforming materials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support containment activities, including line clearance, product holds, and sorting/rework activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in root cause investigations and corrective and preventive actions (CAPA)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Quality Engineers to analyze trends and recurring issues\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Data Collection \u0026amp;amp; Continuous Improvement\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collect and analyze in-process quality data to support process monitoring and improvement initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide input on quality metrics, yield trends, and defect data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Manufacturing and Engineering teams to implement process improvements and error-proofing solutions\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Equipment \u0026amp;amp; Testing\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Operate, maintain, and calibrate inspection and test equipment (e.g., calipers, microscopes, gauges)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support equipment calibration and environmental monitoring programs as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform basic product or material testing in accordance with validated methods\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Documentation \u0026amp;amp; Quality Systems Support\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Review Device History Records (DHRs) and other quality documentation for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain quality records in compliance with document control procedures and regulatory requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support audits (internal/external) by providing documentation and participating in audit activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure adherence to Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Cross-Functional Collaboration\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Work closely with Production, Manufacturing Engineering, and Quality Engineering to ensure timely resolution of quality issues\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate quality concerns clearly and escalate issues as appropriate\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support training of production personnel on quality requirements and procedures\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;REQUIRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;High school diploma or equivalent required; Associate degree or technical certification preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3–5+ years of experience in Quality Assurance/Quality Control in a manufacturing environment (medical device industry strongly preferred)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or ISO 13485\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with inspection methods, sampling plans, and interpreting engineering drawings and specifications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in Microsoft Office and electronic quality management systems\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;PREFERRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience in a regulated medical device or life sciences environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with nonconformance systems, CAPA, and root cause analysis tools (e.g., 5 Whys, Fishbone)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with dimensional and visual inspection equipment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of validation activities (IQ/OQ/PQ)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting audits and regulatory inspections\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART Station.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026lt;/p\u0026gt;","departments":[{"id":4130566005,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4001265005,"name":"Triton Headquarters","location":"Burlingame, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/neptunemedical/jobs/4668039005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4422528005,"location":{"name":"Burlingame, California, United States"},"metadata":null,"id":4668039005,"updated_at":"2026-05-28T11:57:43-04:00","requisition_id":"282","title":"R\u0026D Manager, Mechanical Design","company_name":"Neptune Medical","first_published":"2026-03-02T17:22:58-05:00","language":"en","application_deadline":null,"content":"\u0026lt;p\u0026gt;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\u0026amp;nbsp;decades to come.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;TITLE: R\u0026amp;amp;D Manager, Mechanical Design\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Product Development Manager, Mechanical Design will manage a group of engineers developing the drive mechanism and interface to robotic capital equipment for a novel robotic endoscopy system.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate will act with passion and intensity in a medical device start-up that is fast paced and collaborative and will display the ability to perform to the requirements outlined below. For the right person, this position will be a tremendously exciting and career-defining opportunity, making core contributions to a genuinely new type of medical robotic platform.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;ROLES AND RESPONSIBILITIES:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage 5-7 direct reports, including career development and performance reviews\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Plan team staffing and recruitment to ensure project success\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive performance and technical requirement development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead risk management activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide project management for device handles development, including defining milestones, cross-functional interdependencies, risks, and opportunities to expedite launch timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent team in updates to senior management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with NPI to develop processes and device assembly procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead vendor selection activities for tooling, component, and subassembly sourcing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Upgrade our manufacturing processes to ensure proper DFM and maximum scalability of our medical devices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Initiate and implement programs to continuously improve quality, cost and cycle time\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Emphasize quality and utilize a risk-driven approach to ensure compliance to risk management policies and practices and ensure GMP.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support company goals and objectives, policies and procedures that comply with FDA Quality System Regulations (QSR), ISO 13485, and any other applicable domestic regulations including Cal FDB, OSHA and Cal-OSHA.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;REQUIRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;B.S. or M.S. in Mechanical or Related Engineering\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8+ years of work experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2+ years in technical leadership or management role\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience working with cross functional teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience developing and launching high volume medical devices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Capable with CAD modeling, engineering drawing generation, DFM, tolerance analysis and tooling design\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience creating and managing schedules, budgets, and plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of design controls and risk management\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;PREFERRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience managing engineers, technicians, or interns as direct reports\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with disposables/consumables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with design and sourcing high volume injection molded components\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developed products from invention to market release\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in a start-up environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient with SolidWorks.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART Station\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our job titles may span more than one career level. The starting base salary for this role is between $180,000 and $231,000 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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026lt;/p\u0026gt;","departments":[{"id":4130564005,"name":"Mechanical Engineering","child_ids":[],"parent_id":null}],"offices":[{"id":4001265005,"name":"Triton Headquarters","location":"Burlingame, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/neptunemedical/jobs/4658668005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4418260005,"location":{"name":"Burlingame, California, United States"},"metadata":null,"id":4658668005,"updated_at":"2026-02-06T12:47:28-05:00","requisition_id":"279","title":"Senior Manager of Clinical Affairs","company_name":"Neptune Medical","first_published":"2026-02-06T12:47:28-05:00","language":"en","application_deadline":null,"content":"\u0026lt;p\u0026gt;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\u0026amp;nbsp;decades to come.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;TITLE: Senior Manager of Clinical Affairs\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY:\u0026lt;/strong\u0026gt; The Clinical Affairs Senior Manager/Associate Director will be responsible for the design, execution and monitoring of clinical studies and will provide scientific expertise throughout the development and implementation of the studies. This role is accountable for the end-to-end clinical strategy, design, execution, oversight, and reporting of clinical studies supporting product development, regulatory submissions, and commercialization. S/he will work closely with R\u0026amp;amp;D, Regulatory Affairs, Quality and external stakeholders to ensure high-quality, compliant, and efficient clinical programs and interact with regulatory agencies as needed to support regulatory submissions and audits.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate would act with passion and intensity in a medical device start-up that is fast paced and collaborative and display the ability to perform to the requirements outlined below. For the right person, this position will be a tremendously exciting and career-defining opportunity, offering the opportunity to shape clinical strategy for a novel medical robotic platform and to contribute meaningfully to the company’s long-term success.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;ROLES AND RESPONSIBILITIES:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Clinical Strategy and Leadership\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the development and execution of the overall clinical strategy aligned with company and regulatory objectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide expert input into clinical development plans, trial design, and evidence-generation strategies across the product lifecycle.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advise senior leadership on clinical risks, opportunities, and trade-offs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Study Design, Execution, and Oversight\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversee the design, initiation, execution, monitoring, and closeout of clinical studies, ensuring adherence to timelines, budgets, and quality standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic oversight of CROs, vendors, investigators, and internal teams to ensure effective study conduct.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and monitor study performance metrics; proactively identify risks and lead cross-functional mitigation strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in the development of clinical strategy and trial design.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Scientific and Regulatory Contributions\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the development and review of key clinical documents, including protocols, amendments, investigator brochures, informed consent forms, case report forms, and clinical study reports.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interpret and synthesize clinical, scientific, and risk data to support regulatory submissions, scientific publications, and labeling claims.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitate regulatory submissions and communications. Interacts with regulatory agencies as needed and use scientific and medical knowledge to write strategic responses to questions from regulatory bodies about submissions.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Data Review, Safety, and Quality\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide oversight of clinical data review, including safety and adverse event evaluation, throughout study conduct and reporting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure clinical activities are conducted in compliance with GCP, FDA, ISO, and applicable international regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Quality to develop and implement SOPs, support audits, complaint review, and implementation of corrective and preventive actions.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Operational and Financial Management\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic oversight of clinical trial budgets, timelines, and resource planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead or oversee contract negotiations with investigators, institutions, CROs, and other vendors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive continuous improvement of clinical processes, systems, and best practices.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;REQUIRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;B.S. in Biomedical Engineering, Life Sciences or similar\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;7-10+ years of progressive experience in clinical research within the medical device industry, including leadership of complex clinical studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience developing and executing clinical strategies that support regulatory submissions and product approvals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong working knowledge of Good Clinical Practice (GCP), FDA and international regulations, ISO standards and clinical research best practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to lead cross-functional teams and influence without direct authority.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication, skills including experience presenting to senior leadership and regulatory agencies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High attention to detail and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Fluent in medical terminology and sound knowledge of anatomy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical, problem-solving, and decision-making skills with high professional judgment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to thrive in a fast-paced, evolving startup environment with a hands-on, ownership-oriented mindset\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Takes initiative and acts quickly to drive to solutions with a driven outlook and with a strong desire to succeed as a team player, and as a key part of a company\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel up 20% domestically and internationally\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;PREFERRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience in medical robotics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Master’s degree or higher in Biomedical Engineering, Life Sciences, or a related discipline\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience or knowledge of the GI/endoscopy space\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART Station\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our job titles may span more than one career level. The starting base salary for this role is between $182,500 and $229,000 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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4130567005,"name":"Clinical","child_ids":[],"parent_id":null}],"offices":[{"id":4001265005,"name":"Triton Headquarters","location":"Burlingame, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/neptunemedical/jobs/4674286005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4425331005,"location":{"name":"Burlingame, California, United States"},"metadata":null,"id":4674286005,"updated_at":"2026-03-18T10:32:41-04:00","requisition_id":"288","title":"Senior Mechanical Engineer, Hardware","company_name":"Neptune Medical","first_published":"2026-03-17T16:17:07-04:00","language":"en","application_deadline":null,"content":"\u0026lt;p\u0026gt;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\u0026amp;nbsp;decades to come.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;TITLE:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;strong\u0026gt;Senior Mechanical Engineer, Hardware\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;In this role you will be tasked with designing and building complex robotic test systems inclusive of subsystem bench test development and large system end-of-line test systems for endoscope and capital products. In this role you will own the architecture and mechanical design, assembly, and test of the systems. You will be responsible for requirements, design outputs, prototypes, functional test, cross-functional design reviews, and final system assembly and delivery.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate will act with passion and intensity in a medical device start-up that is fast paced and collaborative and will display the ability to perform to the requirements outlined below. For the right person, this position will be a tremendously exciting and career-defining opportunity, making core contributions to a genuinely new type of medical robotic platform.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;ROLES AND RESPONSIBILITIES:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Design structural and electromechanical aspects of complex robotic test systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and select motors, gear boxes, drivetrains and sensors to meet performance targets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design structural and interface elements as defined by cross functional needs and requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Rapidly iterate test systems through 3D printed concepts to machined parts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engage in cross functional collaboration with Endoscopy, Systems and Manufacturing teams to generate elegant test capabilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create and maintain Solidworks CAD models, interconnect diagrams, specifications and detailed drawings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create manufacturing methods and fixtures, including assembly fixtures and in-line/end-of-line test fixtures, to ensure final capital and endoscopy products meet specifications and safety.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and participate in technical design reviews.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with colleagues to brainstorm, collaborate, and share knowledge, demonstrating a team forward mentality with honest work ethic.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively within the confines of a regulated, quality-system driven, FDA-monitored medical device environment. \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;REQUIRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;B.S. in Mechanical Engineering with 5+ years experience. Related degrees are acceptable, but you should be able to convince us that you are very competent in mechanical design.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience designing and building mechanical mechanisms, interfaces, and structures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to document designs and assemblies in a manner that is reproducible and follows good documentation practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience testing, iterating, and documenting prototype solutions to undefined problems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of various types of motors, encoders, sensors, power transmission, and drive-train-related components.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in electromechanical design.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience using various rapid prototyping techniques and basic machinery such as 3D printing machines and basic machinery (mill/lathe).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience designing novel solutions to unsolved problems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An inventive aptitude balanced with discipline and detail-orientation.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;PREFERRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience with test bench and complex test system design.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience in mechanical analysis including modeling tolerance stacks, static and dynamic analysis, FEA and thermal analysis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience designing for manufacturability and understanding common manufacturing processes such as machining, sheet metal, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with risk analysis and risk mitigation to develop robust systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to generate original ideas by history of patents and IP.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience creating and managing schedules, budgets, and plans.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART Station.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our job titles may span more than one career level. The starting base salary for this role is between $150,000 and $180,000 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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026lt;/p\u0026gt;","departments":[{"id":4136569005,"name":"Hardware","child_ids":[],"parent_id":null}],"offices":[{"id":4001265005,"name":"Triton Headquarters","location":"Burlingame, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/neptunemedical/jobs/4672321005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4424356005,"location":{"name":"Burlingame, California, United States"},"metadata":null,"id":4672321005,"updated_at":"2026-04-22T18:24:13-04:00","requisition_id":"284","title":"Senior NPI Process Development Engineer","company_name":"Neptune Medical","first_published":"2026-03-11T18:35:29-04:00","language":"en","application_deadline":null,"content":"\u0026lt;p\u0026gt;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\u0026amp;nbsp;decades to come.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;TITLE:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;strong\u0026gt;Senior NPI Process Development Engineer\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior NPI Process Development Engineer will focus on further developing our product and then transferring it into a manufacturing setting. The successful candidate will possess a passion for medical device engineering and a record of successful process, tooling and equipment design.\u0026amp;nbsp; This role will engage in cross-functional collaboration to accelerate the product development process, reduce cost of goods, and enable more complex designs through manufacturing improvements.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate will act with passion and intensity in a medical device start-up that is fast paced and collaborative and will display the ability to perform to the requirements outlined below. For the right person, this position will be a tremendously exciting and career-defining opportunity, making core contributions to a genuinely new type of medical robotic platform.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;ROLES AND RESPONSIBILITIES:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Work with product development to design and prototype novel manufacturing processes and equipment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop new processes to manufacture our products to meet device performance and cost targets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and prototype novel manufacturing equipment and fixturing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create and maintain necessary Manufacturing Process Instructions (MPI’s), test methods, product drawings, and component specifications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Upgrade our manufacturing processes to ensure proper DFM and maximum scalability of our medical devices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Initiate and implement programs to continuously improve quality, cost and cycle time\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prototype fixtures using 3-D printers, lathe, drill press, band saw, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides technical support and performing failure analysis for non-conforming components, assemblies, and process defects\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build the assembly line for our clinical launches\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Specify, support and maintain the proper CER space to manufacture our medical devices under defined environmental quality controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the flow of WIP through Lean practices including Kanban and 5S.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain relationships with key vendors and suppliers and support supplier validations and supplier management best practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Emphasize quality and utilize a risk-driven approach to ensure compliance to risk management policies and practices and ensure GMP.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support company goals and objectives, policies and procedures that comply with FDA Quality System Regulations (QSR), ISO 13485, and any other applicable domestic regulations including Cal FDB, OSHA and Cal-OSHA.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;REQUIRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;B.S. or M.S. in Mechanical or Related Engineering\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;4+ years of work experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience working with cross functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of generating and managing manufacturing documentation from concept to commercialization for medical device product (MPIs, LHRs, BOM, flowcharts, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Capable with CAD modeling, engineering drawing generation, DFM, tolerance analysis and tooling design\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possess knowledge of process validation, GMP, and state-of-the-art manufacturing processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A driven outlook and with a strong desire to succeed as an engineer, as a team, and as a company.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of design controls\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success developing catheter manufacturing processes including braiding, coil winding, extruding, lamination, adhesive joining, die bonding, and laser welding.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;PREFERRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience with catheter or similar manufacturing (lamination, bonding, dip coating, ultrasonic welding, etc)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with disposables/consumables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing lab technicians and assemblers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developed products from invention to market release.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in a start-up environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient with SolidWorks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience creating and managing schedules, budgets, and plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with packaging and shipping validations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART station.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our job titles may span more than one career level. The starting base salary for this role is between $140,000 and $175,000 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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026lt;/p\u0026gt;","departments":[{"id":4130564005,"name":"Mechanical Engineering","child_ids":[],"parent_id":null}],"offices":[{"id":4001265005,"name":"Triton Headquarters","location":"Burlingame, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/neptunemedical/jobs/4702968005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4439245005,"location":{"name":"Burlingame, California, United States"},"metadata":null,"id":4702968005,"updated_at":"2026-06-11T12:40:10-04:00","requisition_id":"301","title":"Senior Quality System Specialist (Temporary)","company_name":"Neptune Medical","first_published":"2026-06-04T11:22:07-04:00","language":"en","application_deadline":null,"content":"\u0026lt;p\u0026gt;Neptune Medical is a venture backed medical device company based in Silicon Valley. We design, manufacture, and commercialize medical devices based on our proprietary Dynamic Rigidization™ technology. Pathfinder® is our first FDA-cleared commercial device incorporating this novel technology. This advanced endoscopy device is being used at a growing list of leading U.S. hospitals and academic medical centers. 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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;TITLE: Senior Quality System Specialist (Temporary)\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Quality System Specialist ensures the integrity and compliance of the Quality Management System (QMS) for medical devices, with a focus on document control, calibration, equipment control, audits, and training. This role supports regulatory compliance (FDA, ISO 13485, EU MDR), drives continuous improvement, and collaborates with cross-functional teams to maintain high-quality standards throughout the product lifecycle. This position plays a critical role in managing and overseeing the document control processes and systems, ensuring that all documents are properly controlled, maintained, and accessible to authorized personnel.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate will act with passion and intensity in a medical device start-up that is fast paced and collaborative and display the ability to perform to the requirements outlined below. For the right person, this position will be a tremendously exciting and career-defining opportunity, making core contributions to a genuinely new type of medical robotic platform.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;ROLES AND RESPONSIBILITIES:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversee and maintain document control systems, ensuring all quality and regulatory documents (SOPs, Device/Batch Records, MDFs, Design \u0026amp;amp; Development Files, change orders) are current, accurate, and compliant with industry standards (FDA QMSR, ISO 13485, EU MDR).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support and improve quality system processes, including CAPA management, data integrity, and continuous improvement initiatives (e.g. QMSR Gap Assessment).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee and improve document control procedures, including revision/version control, document tracking, and secure archiving.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee Complaints Handling system. Lead monthly complaint meeting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the Neptune Medical Approved Supplier List, including annual review.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide Management Review input. Own approval of Management Review output.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in Process Nonconformance (PNRs) and Material Nonconformance (MRRs) review, as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own CAPAs, as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage post market surveillance activities in the applicable jurisdictions (USA \u0026amp;amp; EU). Author applicable reports.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Incorporate new and updated external documents (e.g., regulations, standards, guidance) into the Neptune Medical QMS. Perform an annual audit of the External Documents List.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate and maintain calibration programs for inspection, measurement, and test equipment, ensuring timely calibration and proper documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee equipment control, including preventive maintenance schedules, equipment ID assignment, and equipment history file maintenance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, deliver, and track quality system training for staff to ensure understanding and adherence to QMS requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure training plans are established for Neptune Medical employees.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Update/assign training plans in eQMS.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Train new hires on eQMS software and training program.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Plan, conduct, and support internal and external audits; coordinate audit responses and corrective actions to ensure ongoing compliance with regulatory standards (FDA QMSR, ISO 13485, EU MDR)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact with regulatory bodies and auditors during inspections, providing documentation and ensuring readiness for audits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent areas of responsibility in the front room of both internal and external quality audits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact with regulatory bodies and auditors during inspections, providing documentation and ensuring readiness for audits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent areas of responsibility in internal and external quality audits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform analysis for Quality metrics, Management Review, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work in accordance with quality system procedures.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;REQUIRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Science, Engineering, or a related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 7 years of experience in quality assurance or quality systems within the medical device industry, with hands-on experience in document control, equipment management, and audits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience using an electronic quality management system, e.g., Arena, EtQ. Experience using Propel is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of 21 CFR 820 and ISO 13485 quality system requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work well under pressure and to meet multiple and occasional competing deadlines while maintaining a cooperative working relationship with other people.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work in a highly detailed environment where mental focus and accuracy of work output is essential.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong proficiency using MS Office Suite (e.g., Word, Excel, PowerPoint) and PDF software.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Be results-oriented with appropriate urgency.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Good organizational, oral and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to work in a startup environment and adapt to changing needs and priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Eagerness to learn new things.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART Station\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our job titles may span more than one career level. The starting base pay for this role is between $57.50 and $72.00 per 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 will initially be a temporary role, with the possibility of being made permanent at the end of the year.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026lt;/p\u0026gt;","departments":[{"id":4130566005,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4001265005,"name":"Triton Headquarters","location":"Burlingame, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/neptunemedical/jobs/4646254005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4412434005,"location":{"name":"Burlingame, California, United States"},"metadata":null,"id":4646254005,"updated_at":"2026-01-09T12:01:12-05:00","requisition_id":"272","title":"Senior/Staff Electrical Engineer","company_name":"Neptune Medical","first_published":"2026-01-06T12:38:19-05:00","language":"en","application_deadline":null,"content":"\u0026lt;p\u0026gt;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. Our\u0026amp;nbsp;Triton robot will disrupt flexible endoscopy and set a new standard with Triton Robotic Endoscopy in outcomes for\u0026amp;nbsp;decades to come.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;TITLE: Senior/Staff Electrical Engineer\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Triton Robotics is seeking a highly motivated individual to craft electrical solutions for complex robotic systems that will transform patient care and improve the lives of millions worldwide.\u0026amp;nbsp; As a Senior/Staff Electrical Engineer on the hardware team, you will be responsible for various electrical activities including: PCBA design, cable and system design, and bring-up. Additionally, you will be responsible for ensuring proper integration of robotic peripherals including motion control, sensor interfaces, computing, and power distribution.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You’ll be responsible for ensuring requirements are properly captured, reviewed, and implemented. In addition to design tasks, you will be responsible for creating, documenting, and reviewing all risks in accordance with best design practices and regulatory demands. This is a highly hands-on role that is critical to the success of the product.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate for this role will have 5-10 years of electrical design and bring-up, as well as 4-6 years experience in robotics or medical.\u0026amp;nbsp; You’ll be self-driven and highly motivated to work hands on with a diverse team, be able to take and give constructive feedback, tackle challenges without known solutions, and motivated to drive harder when the solution isn’t obvious.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;WHAT YOU WILL DELIVER:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Execute high-complexity analog and digital PCB designs in Altium, from initial concept through to formal technical reviews and release.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Improve system reliability by diagnosing prototype failures and implementing rapid, well-documented design improvements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bridge the gap between mechanical and electrical disciplines to deliver integrated, high-performance hardware solutions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ownership of all verification activities including board bring up, system integration, testing and documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage external manufacturing partners and lead dFMEA efforts to mitigate risk across the electrical ecosystem.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;WHAT KNOWLEDGE AND SKILLS YOU BRING:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of B.S. in computer science, electrical engineering or similar (M.S. preferred)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;At least 5-10 years of work experience including schematic and layout design of medium to high complexity digital and analog flexible and rigid PCBs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with suppliers to resolve process issues and understand supplier design constraints.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience designing with ESD, EMI, immunity, and thermal considerations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience designing and developing electronic circuits from feasibility through product release.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience and proficiency using Altium Designer and controlled repositories such as GIT and SVN.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to debug and test using high speed oscilloscopes, LCR meters, and other test tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills including presentation of technical content.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;ADDITIONAL SKILLS THAT AN IDEAL CANDIDATE WILL HAVE SOME OF:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience in the medical device field including knowledge of techniques and compliance to standards like 60601-1 and isolation is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with architecture level design in complex systems is welcomed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in motor bring-up and basic programming to facilitate board bring-up and test is desired.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience developing medical devices, including design controls, patient risk analysis, risk mitigation and dFMEA practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;“Nice to have” some experience with firmware.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART station.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our job titles span more than one career level and final offer will be based on experience. The starting base salary for this role is between $160,000 and $220,000 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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026lt;/p\u0026gt;","departments":[{"id":4136569005,"name":"Hardware","child_ids":[],"parent_id":null}],"offices":[{"id":4001265005,"name":"Triton Headquarters","location":"Burlingame, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/neptunemedical/jobs/4626905005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4403266005,"location":{"name":"Burlingame, California, United States"},"metadata":null,"id":4626905005,"updated_at":"2025-11-04T17:18:00-05:00","requisition_id":"257","title":"Senior/Staff Linux Software Engineer – Robotics Platform ","company_name":"Neptune Medical","first_published":"2025-11-04T17:18:00-05:00","language":"en","application_deadline":null,"content":"\u0026lt;p\u0026gt;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\u0026amp;nbsp;decades to come.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;TITLE\u0026lt;/strong\u0026gt;: \u0026amp;nbsp;\u0026lt;strong\u0026gt;Senior/Staff Linux Software Engineer – Robotics Platform \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior/Staff Software Engineer is a key member of the software team who will be responsible for implementing a robust vision compute pipeline on a Linux platform and will actively work with the software and vision teams. As part of the software team responsible for the compute platform for the Triton robot, this candidate will be instrumental in the selection, evaluation and integration of the embedded Linux computers, FPGA bridges and high-speed SerDes links in the novel camera and display system. This member is expected to collaborate on and own parts of the vision software subsystem, helping build a robust and safe software while demonstrating the flexibility and enthusiasm to handle multiple responsibilities in a fast-paced and collaborative start-up environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate will act with passion and intensity in a medical device start-up that is fast paced and collaborative and display the ability to perform to the requirements outlined below. For the right person, this position will be a tremendously exciting and career-defining opportunity, making core contributions to a genuinely new type of medical robotic platform.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;ROLES AND RESPONSIBILITIES:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Design and implement the compute platform for the vision pipeline for the Triton robot.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate and prototype solutions for the control and vision subsystems using different computers and GPUs, optimizing for latency, efficiency and robustness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design, develop, document, verify, and continuously improve software for video pipelines using NVIDIA Jetson embedded systems: control cameras and display low-latency video, record video, composite video streams, and share video and camera metadata.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with deep-learning and computer-vision algorithms engineers to integrate new processing capabilities and AI applications into the product code.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with peer engineers on software design and code reviews.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Document software designs, reviews and processes.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;REQUIRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;B.S. or M.S in CS, ECE, EE or related fields.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5-7 years designing and developing software applications for embedded Linux systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Robust knowledge of C++ and Python.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Linux kernel development and/or NVIDIA’s embedded software stack desired.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability and flexibility to handle multiple responsibilities within the software team based on priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and documentation skills.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART Station.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our job titles may span more than one career level. The starting base salary for this role is between $185,000 and $225,000 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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4130562005,"name":"Software","child_ids":[],"parent_id":null}],"offices":[{"id":4001265005,"name":"Triton Headquarters","location":"Burlingame, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/neptunemedical/jobs/4576398005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4378411005,"location":{"name":"Burlingame, California, United States"},"metadata":null,"id":4576398005,"updated_at":"2025-12-03T13:53:01-05:00","requisition_id":"239","title":"Senior/Staff Systems Engineer","company_name":"Neptune Medical","first_published":"2025-06-13T14:40:58-04:00","language":"en","application_deadline":null,"content":"\u0026lt;p\u0026gt;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\u0026amp;nbsp;decades to come.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;TITLE:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;strong\u0026gt;Senior/Staff Systems Engineer\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;POSITION SUMMARY:\u0026lt;/strong\u0026gt; The Senior/Staff Systems Engineer will take a technical leadership role that is comprised of framing the approach to unstructured design problems of a medical robot, analysis, experimental design, prototyping, and final recommendations to hardware/software teams and senior management. The engineer will also be involved in integrating mechanical, electrical, and software components to bring a surgical robot to life.\u0026amp;nbsp; This individual will be intimately involved across hardware, software, and clinical use of the integrated system.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate would act with passion and intensity in a medical device start-up that is fast paced and collaborative and display the ability to perform to the requirements outlined below. For the right person, this position will be a tremendously exciting and career-defining opportunity, making cre contributions to a genuinely new type of medical robotic platform.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;ROLES AND RESPONSIBILITIES:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead system design discussions to provide design input to hardware and software teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Frame analysis and experimental approaches to drive answers to unstructured design questions without clear solutions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prototype solutions in both software and hardware\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Integrate software and hardware and test the integrated system in clinically relevant conditions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Significantly Contribute to/Lead system risk analysis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Significantly Contribute to/Lead product requirements definition\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical development labs while learning the clinical use case\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;REQUIRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;B.S., M.S. or Ph.D. in Mechanical Engineering, Computer Science, Electrical Engineering, or similar\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;4-12 years of hands-on experience in robotics or other complex electromechanical systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Specific experience and expertise with:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Mechatronics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Robotics fundamentals including kinematics, system dynamics, sensors, and actuators\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Python or Matlab for scripting and data analysis, or other programming language\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communications skills including presentation of technical content\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to work in a startup environment and adapt to changing needs and priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Eagerness to learn new things\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;PREFERRED QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Robot Operating System (ROS)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Embedded and/or real time programming in C, RUST, or C++\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Depth in at least one technical area – mechanical design, C/C++ programming, electrical design, system dynamics and controls etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing projects and leading small technical teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Formal system Verification and Validation (V\u0026amp;amp;V) procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in the regulated medical device environment, including but not limited to document control processes, design control processes, test protocol development, and report writing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with healthcare providers in a hospital environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with using data science techniques to create actionable recommendations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART Station\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our job titles may span more than one career level. The starting base salary for this role is between $170,000 and $220,000 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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4137132005,"name":"Systems","child_ids":[],"parent_id":null}],"offices":[{"id":4001265005,"name":"Triton Headquarters","location":"Burlingame, California, United States","child_ids":[],"parent_id":null}]}],"meta":{"total":12}}