Manufacturing Tech I - Ottava

Johnson & Johnson Johnson & Johnson · Pharma · Santa Clara, CA +1

This role involves electro-mechanical assembly of robotic modules and components for surgical platforms, supporting production schedules, and ensuring compliance with medical device regulations (ISO 13485, FDA QSR). The technician will interpret procedures, conduct basic tests, identify and escalate issues, and maintain clean manufacturing standards. Responsibilities also include preparing production lines, managing material transactions, and recording build data in MES/ERP systems. Requires a high school diploma or equivalent with 0-2 years of experience in regulated industries, knowledge of GDP, and proficiency with assembly tools.

What you'd actually do

  1. Perform electro‑mechanical assembly of robotic system modules including joints, control modules, and cable harnesses by following detailed work instructions and engineering documentation.
  2. 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).
  3. Interpret and apply defined assembly procedures to correctly build, verify, and validate mechanical and electromechanical components.
  4. Conduct basic functional, electrical, and mechanical tests using calibrated tools, test fixtures, torque equipment, and multimeters.
  5. Identify and escalate assembly, component, or test issues to senior technicians or engineering in a timely manner.

Skills

Required

  • 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.

Nice to have

  • Vocational Certificate or Technical training preferred.
  • Experience with Learning Management Systems (ComplianceWire), MES, SAP, or similar systems
  • Exposure to robotics or surgical device assembly.

What the JD emphasized

  • medical device regulations
  • ISO 13485
  • FDA QSR
  • Good Documentation Practices (GDP)