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Senior Quality Engineer

J&J Family of Companies Milpitas, CA
  • Expired: October 06, 2019. Applications are no longer accepted.

Johnson & Johnson Vision (JJV), a member of Johnson & Johnson's Family of Companies is recruiting for Senior Product Quality Engineer, to be located in Milpitas, CA.

JJV, is a worldwide company with operations in the United States, Japan, Latin America, Asia-Pacific and Europe/Middle East/Africa regions. Research, innovation and new-product development are the focus of our organization. Since we introduced soft disposable contact lenses in 1988, and through the acquisition of Abbott Medical Optics in 2017, no other manufacturer has matched the aggressive expansion of our wide-ranging Surgical Vision (Cataracts and Lasik portfolio) and Vision Care (ACUVUE and Consumer Eye Health solutions) family of products. Our associates around the world are committed to expanding the JJV brand and fortifying our position as the worldwide leader in total eye healthcare solutions.

Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 125 years. We embrace research and science -- bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.

In this role, the Sr. Product Quality Engineer, will be responsible for the development and implementation of customer-based solutions that improves the customer experience and overall product quality. This position will be responsible for design, development and implementation of mechanical and/or electrical enhancements improving on-market products and/or quality release metrics. This position will require cross-functional work with R&D and Program/Product Quality Managers to ensure design intent, manufacture of design related changes and automation groups to ensure design standards have been met.

Additionally, Addresses and corrects product and process complaints. Complete nonconformance and CAPA owner activities such as investigating to root cause, implementing corrective/preventive actions, and monitoring effectiveness. Prepare reports on quality system performance metrics. Analyze all quality system categories to assess compliance to process standards. Ensures comprehensive measurement systems to monitor effectiveness of quality and reliability systems to identify, bracket, correct and prevent defects, & presents reports to management. Provide support for quality system controls and audits, compliance assessment, and for support of steady state manufacturing processes.

Translate customer requirements into product lifecycle improvements aimed at improving the customer experience
Apply strong engineering principles (materials, solid mechanics, DFMEA& reliability) to achieve VOC requirements
Generate and execute protocols/reports with statistical reference
Work with External Manufacturing & Supply Chain to ensure flawless execution
Coordinate the fabrication of prototypes and testing to verify design meets specifications
Design and document test methods
Design and fabricate test fixtures
Contributes technical expertise for systemic Non-Conformances and CAPAs
Adherence to Quality Management Systems and Environmental, Health & Safety
Ability to work within a technical team and as an individual contributor in a fast-paced, changing environment
Ability to communicate effectively horizontally and vertically in a matrix organization
BS in Mechanical, Electrical, Chemical, Biomedical, or Industrial Engineering; Master's Degree in a technical field preferred
Minimum of 4 years' experience product design and/or automation design required
Proficiency in 3D Solid Modeling & tolerancing analysis required
Experience in a Regulated environment required
Experience in Medical Device Industry preferred
Demonstrated technical project leadership capabilities with experience working in a cross-functional team environment is required.
Experience working with Vendors and Suppliers is required.
Knowledge of part manufacturing processes & tooling methodologies are preferred.
This position requires up to 10% travel both domestic and/or international.

BE VITAL in your career; be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.

Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.

Primary Location
United States-California-Milpitas-
AMO Manufacturing USA, LLC (6240)
Job Function
Quality (Eng)
Requisition ID

J&J Family of Companies


Milpitas, CA
95035 USA