R&d Assembler II - Shockwave Medical

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

This role is for an R&D Assembler II at Johnson & Johnson's Shockwave Medical division, focusing on the assembly, testing, and inspection of in-development, non-commercial medical devices. The assembler will follow R&D engineer directions, record data on Lot History Records, and comply with quality, safety, and environmental policies. Responsibilities include building prototypes, performing in-process inspections, preparing packaging, documenting scrap, and adhering to controlled environment room procedures and Lean Manufacturing principles.

What you'd actually do

  1. Builds prototypes, subassemblies, and/or final assemblies per MPIs or engineering documentation.
  2. Performs in‑process inspections of components/materials, subassemblies, and final assemblies to ensure that specifications are met for data collection and analysis.
  3. Uses documented guidelines provided by engineers and provides feedback for improved manufacturing methods to assist in the product development process.
  4. Monitors equipment parameters and results of in‑process inspection(s); as necessary, adjusts according to documented procedures to ensure product meets appropriate quality specifications.
  5. Records details of work and completes required portions of LHR to ensure traceability of each finished product lot.

Skills

Required

  • High school diploma or equivalent experience.
  • Ability to read and communicate in English.
  • Ability to use various hand tools to assemble small parts.
  • 1-3 years of experience in a manufacturing environment with small parts.
  • Ability to work in and abide by Controlled Environment Room (CER) procedures.
  • Ability to assemble, and test medical devices, including soldering, gluing, and assembly under the microscope while following Manufacturing Process Instructions (MPI), Standard Operating Procedures (SOP), Work Instructions (WI), etc.
  • Capable of filling out detailed LHRs while following Good Documentation Practices (GDP).
  • Ability to work in a fast-paced environment while adhering to SWMI safety standards.

Nice to have

  • Medical device manufacturing experience is preferred.