Senior Quality Engineer

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

Senior Quality Engineer role at Johnson & Johnson (Shockwave Medical) focused on providing Design Quality Assurance for medical device designs, ensuring compliance with various regulations (ISO 13485, ISO 14971, 21 CFR Part 820, EU MDR, MDSAP). Responsibilities include supporting design reviews, process improvements, risk management, and writing technical documents for regulatory review.

What you'd actually do

  1. Provide Design Quality Assurance to efficiently deliver safe and effective medical device designs for manufacturing.
  2. Provide Quality Assurance support to functions with a focus on process improvements and design control compliance in accordance with ISO 13485, ISO 14971, 21 CFR Part 820, MDD 93/42/EEC, EU MDR, MDSAP and other applicable regulations
  3. Work closely and partner with internal departments to ensure designs are aligned with company policies and procedures.
  4. Participate in design reviews and pre-validation assessments to ensure the safe and environmentally sound initiation of new processes with adequate and appropriate process controls.
  5. Support project teams to ensure that new and existing products are designed and developed in accordance with customer, corporate, and regulatory guidelines, and work closely with Design and Manufacturing Engineering to improve processes where possible.

Skills

Required

  • Master's degree in Mechanical Engineering, Biomedical Engineering or related field
  • 3 years of experience in the job offered or in a Senior Quality Engineer-related occupation

What the JD emphasized

  • ISO 13485
  • ISO 14971
  • 21 CFR Part 820
  • EU MDR
  • MDSAP