Manufacturing Technician I (Entry-Level Medical Devices)

Key Responsibilities

• Perform electromechanical assembly of robotic system modules including joints control modules and cable harnesses by following detailed work instructions and engineering documentation.
• Operate 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 inprocess 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 readinesswhich includes accurate material transactions cycle counts of raw materials subassemblies 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.

Qualifications

Required:

• High School diploma equivalent or 02 years of experience in manufacturing or assembly within medical devices electromechanical systems or related regulated industries or equivalent military experience
• Knowledge of Good Documentation Practices (GDP) or familiarity with FDAregulated or ISOcertified environments.
• Proficiency in assembly tools: torque wrenches screwdrivers calipers multimeters presses etc.
• Ability to work flexible schedules including overtime and weekend shifts in response to business needs.

Additional Information
This job description is intended to outline the general nature and level of work performed. It is not an exhaustive list of all duties responsibilities or qualifications required. Employees may be assigned additional tasks aligned with business needs as per the individuals capabilities.

Preferred:

• Vocational Certificate or Technical training preferred.
• Experience with Learning Management Systems (ComplianceWire) MES SAP or similar systems
• Exposure to robotics or surgical device assembly.

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.