Manufacturing Technician II

6010-Biosense Webster Inc. Legal Entity

Milpitas (CA)

On-site

USD 70,000 - 95,000

Full time

3 days ago

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Job summary

Johnson & Johnson is hiring a Manufacturing Technician II for the OTTAVA Surgical Robotic Platform in Milpitas, CA. You will perform electro‑mechanical assembly of robotic modules and support production with a focus on quality and regulatory compliance.

The role requires hands‑on experience in automated assembly, GDP, GMP, and the ability to work on a structured production line with occasional overtime. This position offers growth opportunities within a leading medical device portfolio.

Qualifications

2+ years of manufacturing or assembly experience in medical devices or related regulated environments.
Hands-on GDP and regulated environments experience.
Proficiency with common assembly tools listed in the requirements.

Responsibilities

Assemble electro‑mechanical robotic modules per engineering docs with minimal supervision.
Maintain ISO 13485, FDA QSR, GDP compliance on the production line.
Perform functional, electrical, and mechanical tests with calibrated tools.
Identify basic issues and escalate complex problems to engineering.
Document production activities and test results in MES/ERP systems.

Skills

Administrative Support

Agile Manufacturing

Assembly Operations

Communication

Execution Focus

Good Manufacturing Practices

Innovation

Learning Agility

Manufacturing Processes

MSAT

Mechanical Equipment

Plant Operations

Process Oriented

Prototyping

Repair Management

Structural Fabrication

Technologically Savvy

Tools

Torque wrenches

Screwdrivers

Calipers

Multimeters

Presses

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 & Information

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

About Medtech Surgery Fueled by innovation at the intersection of biology and technology, we’re developing 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 team that’s reimagining 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 world’s most prevalent conditions such as obesity, cardiovascular disease and cancer. Patients are waiting. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

We are searching for the best talent for Manufacturing Technician II, in support of the OTTAVA Surgical Robotic Platform.

The Manufacturing Technician II 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 technician capable of working independently and supporting both manufacturing and engineering activities. This position offers hands‑on experience with innovative technology and opportunities for long‑term career development.

Key Responsibilities

Perform intermediate level electro‑mechanical assembly of robotic system modules including joints, control modules, and cable harnesses using engineering documentation and established work instructions with minimal supervision.
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 across multiple product modules.
Conduct functional, electrical, and mechanical tests using calibrated tools, test fixtures, torque equipment, and multimeters.
Identify, and troubleshoot basic electrical and mechanical issues (e.g., miswiring, misalignment, sensor faults) and elevate complex or systemic issues to engineering.
Perform minor mechanical and electrical repairs to support production continuity, escalating complex issues to engineering.
Maintain compliance with ESD controls, clean manufacturing protocols, and contamination‑control standards appropriate for medical device manufacturing.
Accurately document production activities, test outcomes, and inspection data in MES, ERP/SAP, and electronic DHR systems following GDP.
Perform in‑process inspections and contribute to quality verifications to ensure adherence to workmanship and regulatory standards.
Assist in process updates by providing feedback on assembly sequences, documentation accuracy, and fixture/tool improvements.
Support manufacturing engineering on the line setup, fixture validation, new product introduction (NPI) builds, and continuous improvement initiatives.
Support training, knowledge‑sharing, and guidance for new or entry‑level technicians.
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 three designated modules while meeting all safety, quality, and training requirements.

Qualifications

2+ years of experience in manufacturing or assembly within medical devices, electromechanical systems, capital equipment calibration and validation knowledge or related regulated industries.
Hands‑on experience with Good Documentation Practices (GDP) and regulated 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.

Preferred

Ability to work with Kanban operations, MES, and software‑based test procedures.
Experience with Learning Management Systems (ComplianceWire), MES, SAP, or similar systems.
Exposure to robotics or surgical device assembly and troubleshooting.
Experience with calibration and validation activities for electromechanical or robotic systems.
Ability to interpret technical documentation, assembly instructions, and engineering documentation.
Basic electrical troubleshooting skills: use of multimeter, grounding, and isolation for problem‑solving.

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.

Equal Opportunity Employment

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, internal employees contact AskGS to be directed to your accommodation resource.

Required Skills