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Senior Quality Engineer

Job in Irvine, Orange County, California, 92604, USA
Listing for: J&J Family of Companies
Full Time, Part Time position
Listed on 2026-07-17
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer
Salary/Wage Range or Industry Benchmark: 140774 - 149220 USD Yearly USD 140774.00 149220.00 YEAR
Job Description & How to Apply Below
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:*
* Quality

** Job Sub*
* ** Function:*
* Quality Assurance

** Job Category:*
* Professional

** All Job Posting Locations:*
* Irvine, California, United States of America

*
* Job Description:

*
* *
* Employer:

** Biosense Webster, Inc.

*
* Job Title:

** Senior Quality Engineer

** Job Code:
** A011.5775

*
* Job Location:

** Irvine, CA

** Job Type:
** Full-Time

** Rate of Pay:**      $140,774 - $149,220

*
* Job Duties:

** Lead Quality Engineering for the New Product Development Core team developing new technologies for the treatment of various cardiac arrhythmias. Responsible for design verification and validation activities for device in development. Support the development of design solutions. Perform complex tests and analyses to ensure that products are aligned with established specifications. Perform statistical analysis of data generated, including but not limited to: process capability, Cpk, Ppk, Gauge R&R, ANOVA, Sample Size determination, and variable/attribute data analysis against predetermined acceptance criteria.

Compile data and prepare reports on findings, to identify trends and propose corrective action as needed. Recommend and implement revisions, corrections, and changes to applicable test equipment, procedures, and methods. Troubleshoot defective products during the development and testing phases. Perform risk management activities to prevent unforeseen failure modes and improve the capacity of the processes, including FMEAs (Design, Application, Process).

Utilize output, confidence, and reliability to determine appropriate sample size for product verification testing. Perform, review, and approve component qualifications, drawings, and work instructions. Create, revise and approve Engineering Change Orders (ECOs) and Change Notices (CNs) on cPDM/Windchill for device/component/sub-assembly specifications, and for work/process instructions in pre-production and at production level.

Requires up to 20% travel (domestic & international). May telecommute 2 days per week.

** Requirements:
** Employer will accept a Master's degree in Biomedical Engineering or related field and 4 years of experience in the job offered or in a Senior Quality Engineer-related occupation.

This job posting is anticipated to close on  
** 7/21/2026** .

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 candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please contact us via  or contact AskGS to be directed to your accommodation resource.

Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).

This position is eligible to participate in the Company's long-term incentive program.

Subject to the terms of their respective policies and…
Position Requirements
10+ Years work experience
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