Manufacturing Engineer II - Shockwave

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

Manufacturing Engineer II at Johnson & Johnson, focusing on supporting production, designing/developing/testing/implementing processes, tooling, and fixtures for commercial products in the medical device sector. Responsibilities include sustaining production lines, resolving issues, identifying improvement projects, performing testing, participating in new product introductions, maintaining documentation (FMEAs, MPIs, DMRs, BOMs, LHRs), supporting quality events, creating label files, and executing process validation protocols. Requires a Bachelor's degree in engineering, 3-5 years of experience in a medical device environment, and knowledge of quality system requirements.

What you'd actually do

  1. Actively collaborate with Production to provide sustaining support in resolving product/process/equipment problems.
  2. Actively identify and participate in process/product, tooling, equipment, fixtures and cost reduction improvement projects.
  3. Coordinate and/or perform functional and destructive testing to support Engineering Reports.
  4. Participate as an extended team member for new product introduction, including scaling up, stabilizing and transfer to alternate sites.
  5. Participate in development and maintenance of process FMEAs, Manufacturing Process Instructions (MPIs), and Device Master Record (DMR) documents.

Skills

Required

  • Bachelor's degree in engineering
  • 3-5 years of experience in a medical device environment
  • Knowledge of and compliance with applicable Quality System requirements such as QSRs, FDA, ISO, MDD, MDR and other applicable regulations
  • Understanding of Lean and Six Sigma concepts
  • Experience with Validation of Medical Devices (IQ-OQ-PQ)

Nice to have

  • Basic understanding of Statistics (Cpk, Hypothesis Testing, DOE’s, Gage R&R)
  • Able to create and maintain Drawings in SolidWorks
  • Experience with MES and ERP (Oracle)

What the JD emphasized

  • medical device environment
  • Validation of Medical Devices (IQ-OQ-PQ)
  • Quality System requirements