Manufacturing Technician I (Entry-Level Medical Devices)

Key Responsibilities: Perform electro-mechanical assembly of robotic system modules including joints, control modules, and cable harnesses by following detailed work instructions and engineering within a structured production line environment to meet daily build targets while maintaining compliance with ISO 13485, FDA QSR, and Good Documentation Practices (GDP).Interpret and apply defined assembly procedures to correctly build, verify, and validate mechanical and electromechanical components. Conduct basic functional, electrical, and mechanical tests using calibrated tools, test fixtures, torque equipment, and multimeters. Identify and escalate assembly, component, or test issues to senior technicians or engineering in a timely manner. Follow clean manufacturing, ESD protection, and contamination control requirements for regulated medical device assembly. Accurately record build steps, inspection results, and test outcomes in MES, ERP/SAP, and electronic DHR systems. Participate in in-process inspections and quality verifications to ensure work aligns with workmanship and quality standards. Maintain clean and organized work areas in accordance with safety, quality, and 6S standards. Support manufacturing engineering during line setup, process clarifications, or simple troubleshooting tasks as assigned. Prepare production lines by performing line clearance, verifying equipment maintenance and calibration status, and ensuring material readiness—which includes accurate material transactions, cycle counts of raw materials, sub-assemblies, and WIP, as well as proactively identifying and reporting shortages or discrepancies to prevent build interruptions and support efficient production scheduling. Maintain certification and demonstrate proficiency on at least one designated module while meeting all safety, quality, and training requirements.

Work Schedule: Primary work location: Milpitas, CA.Regular work schedule: Monday-Friday, 2:00 PM - 10:30 PM.Initial training will be conducted at the Santa Clara site on the regular shift schedule of 6:00 AM - 2:30 PM.Occasional weekend work may be required. Overtime may be required based on production demand. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.