Sr Engineer Quality Engineering
Job in
Milpitas, Santa Clara County, California, 95035, USA
Listed on 2026-06-05
Listing for:
Johnson & Johnson
Full Time
position Listed on 2026-06-05
Job specializations:
-
Engineering
Quality Engineering, Biomedical Engineer, Process Engineer
Job Description & How to Apply Below
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:
Irvine, California, United States of America, Milpitas, California, United States of America
Job Description:
Johnson & Johnson Vision, a member of the Johnson & Johnson family of companies, is recruiting for a Sr Engineer Quality Engineering, located in Milpitas, CA or Irvine, CA.
About Med Tech
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at
The Sr Engineer Quality Engineering provides quality and technical leadership to ensure new and existing medical devices meet their intended use.
Key Responsibilities:
* Quality leadership on product project teams and ensures the Critical to Quality (CTQs) attributes cascading requirements (for user needs to product, process, raw materials and test methods) are established, implemented and met.
* Ensures effective risk management or product harms and hazards and improves capability of processes.
* Leads development team in design control strategy and implementation
* Collaborates with functional business partners to proactively address quality issues during new product development, design changes and product verification/validation.
* Leads activities associated with risk management and human factors. This includes working with engineers and product development to identify areas of high risk within their processes; establishing, monitoring and implementing risk mitigation plans; and ensuring management awareness of risks, gaining support for mitigation efforts and tracking progress.
* Quality Management Systems support including Design Control, Risk Management, Change Control, Non-Conformance and
* Corrective Actions and Audits.
Qualifications
Education:
* Bachelors or equivalent university degree in Engineering or other related technical field is required.
Experience and Skills:
Required:
* 4 years working experience in Design/Process Engineering/Science/Statistics in a regulated industry.
* Strong communication, interpersonal and organizational skills.
* Practical understanding of QSR/ISO medical device regulations especially design controls, and risk management.
* Ability to function in a team environment and deliver on team objectives.
* Strong attention to detail.
* Strong written and verbal communication skills.
* Developed presentation skills.
Preferred:
* Experience in Medical Device industry.
* Candidates should be familiar with general quality management system concepts, including good documentation practice
* (GDP), corrective and preventive action (CAPA), and document change control practices
* Human Factors Engineering experience.
Other:
* Up to 10% domestic travel is required.
* Relocation assistance will not be provided
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…
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