Manufacturing Technician III

Johnson & Johnson

. Perform advanced electro-mechanical assembly and system-level integration of robotic system modules and components .

Posted 9/17/2026full-timeMilpitas • California • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in advanced electro-mechanical assembly, system-level integration, and troubleshooting of robotic systems while adhering to ISO 13485 and FDA QSR standards. Proficient in using precision assembly tools and conducting thorough testing and quality verification in a regulated manufacturing environment.

Highest-signal resume keywords

Electro-Mechanical AssemblyTroubleshooting CapabilityISO 13485 ComplianceGood Documentation PracticesPrecision Assembly Tools

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Electro-Mechanical AssemblyTroubleshootingValidation ActivitiesElectrical TestingMechanical TestingQuality VerificationProcess ImprovementRoot-Cause InvestigationSchematic InterpretationRobotics Assembly

Soft Skills

Effective CommunicationCollaborationInitiativeFlexibilityIndependence

Tools & Technologies

MultimetersTorque WrenchesCalipersHand DriversPressesMES SystemsERP/SAP Systems

Industry Keywords

ISO 13485FDA QSRGood Documentation PracticesGMPClean Manufacturing PracticesMedical Device ManufacturingElectromechanical Capital Equipment

Tech Stack

Tools & technologies

AssemblyERP

About the role

Key responsibilities & impact

Perform advanced electro-mechanical assembly and system-level integration of robotic system modules and components
Lead complex assembly and testing activities across multiple robotic modules
Meet production throughput and schedule commitments while complying with ISO 13485, FDA QSR, GDP, and GMP requirements
Interpret assembly procedures, MPIs, TPIs, and engineering documents
Conduct functional, electrical, mechanical, and diagnostic testing using calibrated equipment, torque tools, multimeters, and approved software
Troubleshoot, diagnose, and rework complex electrical and mechanical issues; escalate systemic issues to engineering
Maintain ESD controls, clean manufacturing practices, hazardous waste handling, and safety standards
Document production activities, inspections, rework, and test outcomes in MES, ERP/SAP, and electronic DHR systems
Perform in-process inspections and support quality verifications
Participate in quality improvement initiatives, investigations, and corrective and preventive actions
Collaborate with Manufacturing, NPI Engineering, Quality, and Operations teams on manufacturing challenges, pilot builds, and product introductions
Support validation and calibration activities for assemblies, fixtures, and test systems
Provide feedback to Engineering on work instructions and manufacturability
Support training and on-the-job guidance for Manufacturing Technician I and II team members
Maintain certification and multi-module proficiency across at least five major robotic system modules
Prepare production lines through line clearance, equipment verification, material readiness, transactions, cycle counts, and shortage reporting
Identify workflow bottlenecks and support incremental process improvements

Requirements

What you’ll need

4+ years of experience in medical device or electromechanical capital equipment manufacturing
Demonstrated use of Good Documentation Practices (GDP) in a regulated environment
Strong troubleshooting capability and familiarity with validation-related activities
Solid electrical troubleshooting capability, including proficiency with multimeters, grounding/isolation techniques, and diagnostic evaluation of module failures
Ability to execute multiple assembly and testing tasks while meeting workmanship, safety, and productivity expectations
Knowledge and hands-on application of ESD controls in production environments
Proficiency with precision assembly tools such as torque wrenches, screwdrivers, hand drivers, calipers, multimeters, and presses
Familiarity with ISO 13485, FDA QSR requirements, and clean manufacturing practices for medical device production
Effective communication and collaboration across manufacturing, engineering, quality, and operations teams
Ability to work independently in a fast-paced environment while managing priorities and supporting production continuity
Flexibility to work overtime, early shifts, and weekends based on business needs
Initiative and commitment to continuous improvement and GDP/GMP expectations
Preferred: experience with robotics, motion-control systems, or surgical device assembly involving advanced troubleshooting
Preferred: working knowledge of process and fixture validation
Preferred: exposure to continuous improvement methodologies
Preferred: ability to interpret complex electromechanical schematics and system-level documentation
Preferred: strong mechanical aptitude and root-cause investigation experience

Benefits

Comp & perks

Inclusive work environment
Long-term career development opportunities
Overtime opportunities based on production demand