{"schemaVersion":"jobsearcher.job.v1","id":"04d566e8ded5f7cc785cccd6","url":"https://jobsearcher.com/jobs/04d566e8ded5f7cc785cccd6","canonicalUrl":"https://jobsearcher.com/jobs/04d566e8ded5f7cc785cccd6","title":"Process Engineer","description":"Process Engineer\n\nJob type: Full Time · Department: Process Engineering · Work type: On-Site · USD 70,000-85,000 / year\n\nAddison, Texas, United States\n\nABOUT PRECISION NEUROSCIENCE\nPrecision Neuroscience is building a next-generation brain–computer interface (BCI) to heal and empower millions of people living with neurological conditions.\n\nPrecision Neuroscience's first product, Layer 7, is designed to help people with severe paralysis operate digital devices using only their thoughts—opening up new possibilities for daily life.\n\nOur team brings together experts in neurosurgery, AI and machine learning, microfabrication, electrical engineering, clinical science, and more. We combine deep technical rigor with a people-first mindset to turn breakthrough research into real-world medical solutions.\n\nAs a Precision employee, you’ll join one of the fastest-moving and best-capitalized companies in the emerging field of brain–computer interfaces. Since our founding in 2021, we have raised more than $180 million, advanced our technology through validation, and initiated human trials with leading hospitals across the country.\n\nOur Values:\n\nWe build for human impact , measuring progress by the lives our work can change.\n\nWe do no harm , holding ourselves to the highest standards of safety, integrity, and responsibility.\n\nWe innovate with urgency because the stakes are high and our users can’t wait.\n\nWe bring sharp minds, open ears , pairing expertise with curiosity, humility, and respect.\n\nAnd we lead the way , taking ownership of our work and helping to shape the future of our field.\n\nWe are seeking a Process Engineer to support device assembly and clinical builds for our next-generation neural implants in our Addison, Texas facility.\n\nThis is a hands‑on role building, assembling, and testing medical devices that are used in the clinic. Working under the direction of senior engineers, you will author and maintain process documentation (SOPs and work instructions) and contribute to yield enhancement and quality control efforts. It is an ideal role for someone who is detail‑oriented, enjoys building and troubleshooting hardware, and is excited to grow into a process engineering career in a regulated medical‑device environment.\n\nThis position will be based in our Addison, TX office. We are unable to consider remote workers or individuals who are not currently based in the US and legally authorized to work in the US.\n\nSkills & Qualification\n\nBuild and assemble microfabricated devices into finished headstage assemblies, including PCB and cable integration.\n\nPerform basic electrical testing (continuity, impedance, functional checks) to verify device integrity.\n\nAuthor and revise Standard Operating Procedures (SOPs) and Work Instructions (WI) for assembly and production processes; keep documentation accurate and current under change control.\n\nSupport production lot dispositions — gather and organize build and inspection data, help prepare records, and assist engineers in lot review and release activities.\n\nSupport excursion and nonconformance handling — help document deviations, participate in investigations, and assist with corrective and preventive actions.\n\nSupport yield enhancement and quality control efforts — collect and analyze process and yield data, apply basic statistical process control (SPC), and help identify and implement improvement opportunities.\n\nAssist with process characterization, metrology, inspection, and in‑process quality checks during builds.\n\nMaintain accurate records and follow good documentation practices under the Quality Management System (QMS) for Class III medical implant manufacturing.\n\nSkills, Knowledge and Expertise\nRequired:\n\nEducation + experience:\nBS in Engineering or a related technical field + 0–2 years relevant experience (internships, co‑ops, research, and academic project work count)\n\nMS in Engineering + 0–1 years relevant experience\n\nHands‑on aptitude — comfortable working with tools, equipment, instrumentation, or in a lab, cleanroom, or production environment.\n\nFoundational understanding of engineering fundamentals and basic data analysis and statistics.\n\nStrong written and verbal communication with strong attention to detail (important for authoring SOPs and work instructions and for maintaining records).\n\nAbility to follow detailed procedures precisely and to work collaboratively in a fast‑paced, team‑oriented environment.\n\nEagerness to learn, take direction, and grow technically.\n\nGood communication skills and comfort flagging issues early\n\nPreferred:\n\nInternship, co‑op, or academic experience in a cleanroom, microfabrication, MEMS, medical device, or other regulated manufacturing environment.\n\nExposure to quality systems (ISO13485, FDAQSR /21CFRPart820 /QMSR) or good documentation practices (GDP).\n\nExperience with assembly of small or precision components, microscopy, or visual/dimensional inspection.\n\nExposure to SPC, DOE, or data‑analysis tools (e.g., JMP, Minitab, Python, or Excel).\n\nDiverse workforces create the best culture, company, and products. We at Precision are committed to an inclusive culture that celebrates the uniqueness and contributions of everyone.\n\nAs an equal opportunity employer, Precision does not discriminate on the basis of sex, race, religion, national origin, disability status, protected veteran status, or any other characteristic protected by law.\n\nThe actual base salary offered is determined by a number of variables, including, as appropriate, the applicant's qualifications for the position, years of relevant experience, distinctive skills, level of education attained, certifications or other professional licenses held, and the location of residence and/or place of employment.\n\nWe prioritize candidate security. Please be aware that job offers will only come from emails ending with precisionneuro.io\n\nFor roles based in Massachusetts it is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.\n\n#J-18808-Ljbffr","company":"Neara","rawCompany":"neara","city":"Addison","state":"TX","isRemote":false,"isActive":false,"createdAt":"2026-09-02T04:01:03.029Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2031.00","title":"Bioengineers and Biomedical Engineers","slug":"bioengineers-and-biomedical-engineers"}],"industries":[{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer","description":"Process Engineer\n\nJob type: Full Time · Department: Process Engineering · Work type: On-Site · USD 70,000-85,000 / year\n\nAddison, Texas, United States\n\nABOUT PRECISION NEUROSCIENCE\nPrecision Neuroscience is building a next-generation brain–computer interface (BCI) to heal and empower millions of people living with neurological conditions.\n\nPrecision Neuroscience's first product, Layer 7, is designed to help people with severe paralysis operate digital devices using only their thoughts—opening up new possibilities for daily life.\n\nOur team brings together experts in neurosurgery, AI and machine learning, microfabrication, electrical engineering, clinical science, and more. We combine deep technical rigor with a people-first mindset to turn breakthrough research into real-world medical solutions.\n\nAs a Precision employee, you’ll join one of the fastest-moving and best-capitalized companies in the emerging field of brain–computer interfaces. Since our founding in 2021, we have raised more than $180 million, advanced our technology through validation, and initiated human trials with leading hospitals across the country.\n\nOur Values:\n\nWe build for human impact , measuring progress by the lives our work can change.\n\nWe do no harm , holding ourselves to the highest standards of safety, integrity, and responsibility.\n\nWe innovate with urgency because the stakes are high and our users can’t wait.\n\nWe bring sharp minds, open ears , pairing expertise with curiosity, humility, and respect.\n\nAnd we lead the way , taking ownership of our work and helping to shape the future of our field.\n\nWe are seeking a Process Engineer to support device assembly and clinical builds for our next-generation neural implants in our Addison, Texas facility.\n\nThis is a hands‑on role building, assembling, and testing medical devices that are used in the clinic. Working under the direction of senior engineers, you will author and maintain process documentation (SOPs and work instructions) and contribute to yield enhancement and quality control efforts. It is an ideal role for someone who is detail‑oriented, enjoys building and troubleshooting hardware, and is excited to grow into a process engineering career in a regulated medical‑device environment.\n\nThis position will be based in our Addison, TX office. We are unable to consider remote workers or individuals who are not currently based in the US and legally authorized to work in the US.\n\nSkills & Qualification\n\nBuild and assemble microfabricated devices into finished headstage assemblies, including PCB and cable integration.\n\nPerform basic electrical testing (continuity, impedance, functional checks) to verify device integrity.\n\nAuthor and revise Standard Operating Procedures (SOPs) and Work Instructions (WI) for assembly and production processes; keep documentation accurate and current under change control.\n\nSupport production lot dispositions — gather and organize build and inspection data, help prepare records, and assist engineers in lot review and release activities.\n\nSupport excursion and nonconformance handling — help document deviations, participate in investigations, and assist with corrective and preventive actions.\n\nSupport yield enhancement and quality control efforts — collect and analyze process and yield data, apply basic statistical process control (SPC), and help identify and implement improvement opportunities.\n\nAssist with process characterization, metrology, inspection, and in‑process quality checks during builds.\n\nMaintain accurate records and follow good documentation practices under the Quality Management System (QMS) for Class III medical implant manufacturing.\n\nSkills, Knowledge and Expertise\nRequired:\n\nEducation + experience:\nBS in Engineering or a related technical field + 0–2 years relevant experience (internships, co‑ops, research, and academic project work count)\n\nMS in Engineering + 0–1 years relevant experience\n\nHands‑on aptitude — comfortable working with tools, equipment, instrumentation, or in a lab, cleanroom, or production environment.\n\nFoundational understanding of engineering fundamentals and basic data analysis and statistics.\n\nStrong written and verbal communication with strong attention to detail (important for authoring SOPs and work instructions and for maintaining records).\n\nAbility to follow detailed procedures precisely and to work collaboratively in a fast‑paced, team‑oriented environment.\n\nEagerness to learn, take direction, and grow technically.\n\nGood communication skills and comfort flagging issues early\n\nPreferred:\n\nInternship, co‑op, or academic experience in a cleanroom, microfabrication, MEMS, medical device, or other regulated manufacturing environment.\n\nExposure to quality systems (ISO13485, FDAQSR /21CFRPart820 /QMSR) or good documentation practices (GDP).\n\nExperience with assembly of small or precision components, microscopy, or visual/dimensional inspection.\n\nExposure to SPC, DOE, or data‑analysis tools (e.g., JMP, Minitab, Python, or Excel).\n\nDiverse workforces create the best culture, company, and products. We at Precision are committed to an inclusive culture that celebrates the uniqueness and contributions of everyone.\n\nAs an equal opportunity employer, Precision does not discriminate on the basis of sex, race, religion, national origin, disability status, protected veteran status, or any other characteristic protected by law.\n\nThe actual base salary offered is determined by a number of variables, including, as appropriate, the applicant's qualifications for the position, years of relevant experience, distinctive skills, level of education attained, certifications or other professional licenses held, and the location of residence and/or place of employment.\n\nWe prioritize candidate security. Please be aware that job offers will only come from emails ending with precisionneuro.io\n\nFor roles based in Massachusetts it is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.\n\n#J-18808-Ljbffr","datePosted":"2026-09-02T04:01:03.029Z","dateModified":"2026-09-02T04:01:03.029Z","hiringOrganization":{"@type":"Organization","name":"Neara","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Addison","addressRegion":"TX","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"04d566e8ded5f7cc785cccd6"},"url":"https://jobsearcher.com/jobs/04d566e8ded5f7cc785cccd6"}}