Manufacturing Tech II

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

The Manufacturing Technician II is responsible for performing electro-mechanical assembly of robotic modules and components for the OTTAVA Surgical Robotic Platform, supporting production schedules, and maintaining compliance with medical device regulations. This role involves interpreting assembly procedures, conducting tests, troubleshooting basic issues, and documenting production activities within a regulated environment.

What you'd actually do

  1. 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.
  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 across multiple product modules.
  4. Conduct functional, electrical, and mechanical tests using calibrated tools, test fixtures, torque equipment, and multimeters.
  5. Identify, and troubleshoot basic electrical and mechanical issues (e.g., miswiring, misalignment, sensor faults) and escalate complex or systemic issues to engineering.

Skills

Required

  • High School diploma equivalent with 1-2 years’ experience or 3-4 years of experience in manufacturing or assembly within medical devices, electromechanical systems, or related regulated industries.
  • Hands-on experience with Good Documentation Practices (GDP) and regulated environments.
  • Basic electrical troubleshooting skills: use of multimeter, grounding, and isolation for problem-solving.
  • 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.
  • Capability to work both independently and collaboratively, demonstrating adaptability to evolving operational requirements.

What the JD emphasized

  • medical device regulations
  • Good Documentation Practices (GDP)
  • regulated environments