Manufacturing Technician II

Johnson & Johnson Innovative Medicine; Milpitas (CA); On-site; USD 55,000 - 75,000; Full time

Job summary

Johnson & Johnson Innovative Medicine is seeking a Manufacturing Technician II to support the OTTAVA Surgical Robotic Platform in Milpitas/Santa Clara, CA. You will perform electro‑mechanical assembly, run tests, and help maintain production schedules in a regulated medical device environment.

Work with engineering and manufacturing teams to troubleshoot issues, document results in GDP‑compliant systems, and contribute to continuous improvement while growing your skills in a cutting‑edge

Qualifications

• 2+ years of experience in manufacturing or assembly within medical devices or regulated environments.
• GDP compliance and working in a regulated environment required.
• Proficiency with common assembly tools and measurement instruments.
• Ability to work flexible schedules including overtime and weekends.

Responsibilities

• Perform intermediate level electro‑mechanical assembly of robotic system modules with minimal supervision.
• Operate in a structured production line to meet daily build targets while maintaining ISO 13485 and GDP compliance.
• Interpret and apply defined assembly procedures to build, verify, and validate components.
• Conduct functional, electrical, and mechanical tests using calibrated tools and equipment.
• Identify and troubleshoot basic issues and escalate complex problems to engineering.
• Maintain ESD controls, clean manufacturing protocols, and GDP documentation.

Skills

Electromechanical assembly

GDP compliance

Quality mindset

Manual dexterity

Tools

Torque wrenches

Multimeters

Calipers

Screwdrivers

Test fixtures

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:

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 technology,we’redeveloping 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 teamthat’sreimagining 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, cardiovasculardiseaseand 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

Required:

• 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.

Additional Information

This job description is intended to outline the general nature and level of work performed. It is