Quality Engineer II
Job in
Santa Clara, Santa Clara County, California, 95053, USA
Listed on 2026-10-24
Listing for:
Biopharma Careers
Full Time
position Listed on 2026-10-24
Job specializations:
-
Engineering
Quality Engineering, Biomedical Engineer, Process Engineer -
Quality Assurance - QA/QC
Quality Engineering
Job Description & How to Apply Below
Quality
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View Full Job & Apply at Johnson & Johnson Johnson & Johnson is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.## About this opportunity
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at .As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
** Job Function:
** Supply Chain Engineering
** Job Sub Function:
** Quality Engineering
** Job Category:
** Scientific/Technology
** All Job Posting Locations:
** Santa Clara, California, United States of America
*
* Job Description:
***
* Employer:
** Shockwave Medical Inc.
*
* Job Title:
** Quality Engineer II
** Job Code:
** A011.10374
*
* Job Location:
** Santa Clara, CA
** Job Type:
** Full-Time
** Rate of Pay:** $105,000 - $115,000 per year
*
* Job Duties:
** Develop, apply, revise and maintain quality standards for processing materials/products into partially or finished products. Design and implement methods and/or procedures for inspecting, testing and evaluating the precision and accuracy of products, components, sub-assemblies and/or production equipment. Support manufacturing and work cross-functionally to resolve technical problems. Participate in decisions on scope of work, risk management, design changes, process improvements, material disposition, and implementation of revised specifications.
Process, investigate, and complete customer complaints. Prepare documentation for inspection/testing procedures, development studies, validation protocols and reports, quality plans, product defect investigations and inspection plans. Assess if components, sub-assemblies, and products meet specification and can initiate, investigate, and resolve non-conformances by working in conjunction with a multidisciplinary team. Participate in developing the risk management documentation including (Hazard assessment, design trace matrix development, DV&V testing, and FMEA).
Practice company safety, quality policies and procedures and participate in internal/external audits.
** Requirements:
** Employer will accept a Bachelor's degree in Bioengineering, Biomedical Engineering or related field and 2 years of experience in the job offered or in a Quality Engineer II-related occupation.
Position requires experience in:
1. Medical device industry;
2. Performing failure/ Product Non-conformance investigations;
3. Production line support including non-conformance investigation and product disposition, supporting process changes and process validation activities including IQ, OQ, and PQ;4. Technical writing skills for investigations, design and process verification and validation protocols and reports;
5. Developing risk management documentation including plans, hazard assessment, design trace matrix development, DV&V testing, and FMEA;
6. Conducting statistical analysis using minitab or equivalent tools for process capability and data normality assessments, analysis of variance, and hypothesis testing, determining appropriate sample sizes, tolerance interval assessments for variable and attribute data, design of experiment (DOE), and variable and attribute sampling plan applications; and
7. ISO, ASTM, and FDA standards for quality within the medical device industry.
This job posting is anticipated to close on
** 10/26/2026.
** Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified…
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