Manufacturing Technician I

6267-Auris Health Inc. Legal Entity; Santa Clara (CA); On-site; USD 40,000 - 65,000; Full time

Job summary

Johnson & Johnson MedTech in Santa Clara, CA seeks a Manufacturing Technician I to join the Ottava production team. You will perform electro‑mechanical assembly of robotic modules, support schedules, and maintain compliance with medical device regulations in a fast-paced environment.

You will work under ISO 13485 and GDP standards, documenting build steps and tests while collaborating with engineering and quality teams to ensure line efficiency and product quality.

Qualifications

• GDP knowledge and familiarity with FDA/ISO environments.
• Experience in regulated manufacturing or assembly is a plus.
• Strong attention to detail and written/verbal communication.

Responsibilities

• Perform electro-mechanical assembly of robotic modules per work instructions.
• Maintain ISO 13485, FDA QSR, and GDP compliance in daily tasks.
• Interpret procedures to build, verify, and test components.
• Conduct basic functional, electrical, and mechanical tests with calibrated tools.
• Identify and escalate issues to senior staff promptly.
• Adhere to cleanroom/ESD and contamination control requirements.
• Accurately record build steps and test results in MES/ERP/DHR systems.
• Participate in in-process inspections and quality verifications.
• Support manufacturing engineering during line setup and troubleshooting.
• Prepare production lines with material readiness and cycle counts.

Skills

Administrative Support

Agile Manufacturing

Assembly Operations

Detail-Oriented

Execution Focus

Factory Acceptance Test

Good Manufacturing Practices

Innovation

Learning Agility

Manufacturing Processes

MSAT

Mechanical Equipments

Plant Operations

Process Oriented

Prototyping

Repair Management

Structural Fabrication

Technologically Savvy

Tools

MES

SAP

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through 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 humanity.Learn more at jnj.com

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: Santa Clara, California, United States of America

Job Description: About MedTech Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal. Through 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 humanity.Learn more at https://www.jnj.com/.

An internal pre-identified candidate for consideration has been identified. However, all applications will be considered. We are searching for the best talent for Manufacturing Technician I Job Description:

Johnson & Johnson MedTech, a member of Johnson & Johnson's Family of Companies, is currently recruiting for a Manufacturing Technician I to join the dynamic Ottava production team. The Manufacturing Technician I 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 individual who thrives in a fast-paced environment and is eager to learn and grow. This position offers hands‑on experience with innovative technology and opportunities for long-term career development.

Key Responsibilities

• Perform electro‑mechanical 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 elevate 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.
• 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—including 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.

Qualifications

• High School diploma equivalent or 0–2 years of experience in manufacturing or assembly within medical devices, electromechanical systems, or related regulated industries.
• Knowledge of Good Documentation Practices (GDP) and familiarity with FDA‑regulated or ISO‑certified 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.
• Strong written and verbal communication skills, with the ability to interact effectively across all levels of the organization.
• Ability to perform in a fast‑paced, dynamic environment while managing multiple priorities and maintaining accuracy.
• Strong attention to detail with a willingness to learn, receive feedback, and develop technical skills over time.
• Capability to work both independently and collaboratively, demonstrating adaptability to evolving operational requirements.

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 individual’s 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 Monday–Friday, 6:00 AM–2:30 PM (onsite). Occasional evening or 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.

Required Skills

• Administrative Support
• Agile Manufacturing
• Assembly Operations
• Detail-Oriented
• Execution Focus
• Factory Acceptance Test (FAT)
• Good Manufacturing Practices (GMP)
• Innovation
• Learning Agility
• Manufacturing Processes
• Manufacturing Science and Technology (MSAT)
• Mechanical Equipments
• Plant Operations
• Process Oriented
• Prototyping
• Repair Management
• Structural Fabrication
• Technologically Savvy

Preferred Skills

• Administrative Support
• Agile Manufacturing
• Assembly Operations
• Detail-Oriented
• Execution Focus
• Factory Acceptance Test (FAT)
• Good Manufacturing Practices (GMP)
• Innovation
• Learning Agility
• Manufacturing Processes
• Manufacturing Science and Technology (MSAT)
• Mechanical Equipments
• Plant Operations
• Process Oriented
• Prototyping
• Repair Management
• Structural Fabrication
• Technologically Savvy

The anticipated base pay range for this position is : $40,250.00 - $64,802.50

Additional Description for Pay Transparency: Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Company’s long-term incentive program. Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits: Vacation –120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year Holiday pay, including Floating Holidays –13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year Caregiver Leave – 80 hours in a 52-week rolling period10 days Volunteer Leave – 32 hours per calendar year Military Spouse Time-Off – 80 hours per calendar year or additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through 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 humanity.Learn more at https://www.jnj.com/. Do Not Sell or Share My Personal Information Limit the Use of My Personal Information