Process Engineer

Precision Neuroscience•Addison, TX

4d•Onsite

About The Position

Precision Neuroscience is seeking a Process Engineer to support device assembly and clinical builds for their next-generation neural implants in their Addison, Texas facility. This is a hands-on role focused on building, assembling, and testing medical devices used in clinical settings. The Process Engineer will work under the direction of senior engineers, authoring and maintaining process documentation (SOPs and work instructions), and contributing to yield enhancement and quality control efforts. This role is ideal for a detail-oriented individual who enjoys hardware troubleshooting and is eager to develop a career in process engineering within a regulated medical device environment. The position is based in Addison, TX, and the company is unable to consider remote workers or individuals not currently based in and legally authorized to work in the US.

Requirements

BS in Engineering or a related technical field + 0–2 years relevant experience (internships, co-ops, research, and academic project work count) OR MS in Engineering + 0–1 years relevant experience
Hands-on aptitude — comfortable working with tools, equipment, instrumentation, or in a lab, cleanroom, or production environment.
Foundational understanding of engineering fundamentals and basic data analysis and statistics.
Strong written and verbal communication with strong attention to detail (important for authoring SOPs and work instructions and for maintaining records).
Ability to follow detailed procedures precisely and to work collaboratively in a fast-paced, team-oriented environment.
Eagerness to learn, take direction, and grow technically.
Good communication skills and comfort flagging issues early.

Nice To Haves

Internship, co-op, or academic experience in a cleanroom, microfabrication, MEMS, medical device, or other regulated manufacturing environment.
Exposure to quality systems (ISO 13485, FDA QSR / 21 CFR Part 820 / QMSR) or good documentation practices (GDP).
Experience with assembly of small or precision components, microscopy, or visual/dimensional inspection.
Exposure to SPC, DOE, or data-analysis tools (e.g., JMP, Minitab, Python, or Excel).

Responsibilities

Build and assemble microfabricated devices into finished headstage assemblies, including PCB and cable integration.
Perform basic electrical testing (continuity, impedance, functional checks) to verify device integrity.
Author and revise Standard Operating Procedures (SOPs) and Work Instructions (WI) for assembly and production processes; keep documentation accurate and current under change control.
Support production lot dispositions — gather and organize build and inspection data, help prepare records, and assist engineers in lot review and release activities.
Support excursion and nonconformance handling — help document deviations, participate in investigations, and assist with corrective and preventive actions.
Support 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.
Assist with process characterization, metrology, inspection, and in-process quality checks during builds.
Maintain accurate records and follow good documentation practices under the Quality Management System (QMS) for Class III medical implant manufacturing.