Senior Manufacturing Technician (Advanced Manufacturing & Troubleshooting)

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at .

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Supply Chain Manufacturing

Job Sub Function:

Manufacturing Assembly

Job Category:

Business Enablement/Support

All Job Posting Locations:

Milpitas California United States of America Santa Clara California United States of America

Job Description:

AboutMedtechSurgery

Fueled by innovation at the intersection of biology and technologyweredeveloping the next generation of smarter less invasive more personalized treatments.

Are you passionate about improving and expanding the possibilities of surgery Ready to join a teamthatsreimagining how we heal Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the worlds most prevalent conditions such as obesity cardiovasculardiseaseand cancer. Patients are waiting.

Your unique talents will help patients on their journey to wellness. Learn more at are searching for the best talent for Manufacturing Technician III for 2nd shift in support of the OTTAVA Surgical Robotic Platform.

Manufacturing Technician III is responsible for performing electro-mechanical assembly of robotic modules and components supporting production schedules and maintaining compliance with medical device regulations. This role reports into the Surgical Robotics (OTTAVA) Manufacturing organization.

We are seeking a detail-oriented and experienced individual who thrives in a fast-paced environment and is comfortable working independently while supporting manufacturing and engineering needs. This position offers hands-on experience with innovative technology and opportunities for long-term career development.

Key Responsibilities

• Perform advanced electromechanical assembly and systemlevel integration of robotic system modules including joints control modules sensors and cable harnesses using detailed work instructions and engineering documentation.
• Lead complex assembly and testing activities across multiple robotic modules with minimal supervision.
• Operate within a structured production environment to meet build throughput and schedule commitments while maintaining compliance with ISO 13485 FDA QSR GDP and GMP requirements
• Interpret and apply assembly procedures MPIs TPIs and engineering documents to correctly build verify and validate mechanical and electromechanical components across multiple product modules.
• Conduct functional basic electrical mechanical and diagnostic testing using calibrated equipment torque tools multimeters and approved software-based test procedures.
• Troubleshoot diagnose and rework complex electrical and mechanical issues including alignment sensor faults and calibration mismatches and escalate systemic issues to engineering.
• Maintain compliance with ESD controls clean manufacturing practices hazardous waste handling and safety standards; promptly address safety concerns and support riskmitigation activities.
• Accurately document production activities inspection results rework actions and test outcomes in MES ERP/SAP and electronic DHR systems following GDP and GMP standards.
• Perform inprocess inspections and contribute to quality verifications to ensure adherence to workmanship and regulatory standards.
• Actively participate in quality improvement initiatives by identifying issues supporting engineering in investigations corrective and preventive action implementation.
• Collaborate closely with Manufacturing leadership NPI engineering Quality and Operations teams to resolve manufacturing challenges and support successful pilot builds and product introductions as well as identifying improvement opportunities.
• Support validation and calibration activities for assemblies fixtures and test systems as defined by engineering and quality requirements.
• Provide clear actionable feedback to Engineering to improve MWIs/MPIs/TPIs and manufacturability.
• Support training knowledge-sharing and onthejob guidance for Manufacturing Technician I and II team members including assistance with complex assemblies and/or troubleshooting tasks.
• Maintain certification and demonstrate multimodule proficiency across at least five major robotic system modules while upholding all safety quality and compliance requirements.
• 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.
• Contributes to process efficiency efforts by identifying workflow bottlenecks recommending improvements and supporting implementation of incremental process enhancements.

Qualifications

Required

• 4 years of experience in medical device or electromechanical capital equipment manufacturing with demonstrated use of Good Documentation Practices (GDP) in a regulated environment.
• Strong troubleshooting capability with familiarity in 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 consistently meeting workmanship safety and productivity expectations.
• Knowledge of ESD principles and hands-on application of ESD controls in production environments.
• Proficiency with precision assembly tools such as torque wrenches screwdrivers hand drivers calipers multimeters presses etc.
• Familiarity with ISO 13485 FDA QSR requirements and clean manufacturing practices for medical device production.
• Effective communication and collaboration skills with the ability to work 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.
• Demonstrated initiative with a commitment to continuous improvement and adherence to GDP/GMP expectations.

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

• Experience with robotics motion-control systems or surgical device assembly involving advanced troubleshooting.
• Working knowledge of process validation activities and fixture validation.
• Exposure to continuous improvement methodologies and the ability to identify opportunities for workflow or process optimization.
• Ability to interpret complex electromechanical schematics and system-level documentation.
• Strong mechanical aptitude with ability to troubleshoot and support rootcause investigation of complex assembly-level issues.

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 and 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 please email the Employee Health Support Center() or contact AskGS to be directed to your accommodation resource

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Required Skills:

Preferred Skills:

Accountability Agile Manufacturing Assembly Operations Data Savvy Execution Focus Good Manufacturing Practices (GMP) Manufacturing Processes Manufacturing Science and Technology (MSAT) Mechanical Equipments Organizing Plant Operations Predictive Analytics Predictive Maintenance Process Oriented Repair Management Technologically Savvy