Quality Engineer at Vantedge Medical

Stockton, California, United States -

Full Time

Start Date

Immediate

Expiry Date

17 Mar, 26

Salary

100000.0

Posted On

17 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Systems, ISO 13485, ISO 9001, Quality Problem Solving, Fishbone Diagrams, 5 Why, FMEA, Process Capability Analysis, Hypothesis Testing, DoE, SPC, Minitab, JMP, Statistical Software

Industry

Medical Equipment Manufacturing

Description

Description Quality Engineer Full-time / Permanent Salaried $87K - $100K About us: Vander-Bend is a U.S.-based manufacturer dedicated to building the precision infrastructure that powers tomorrow’s AI. Our expertise in server racking and power delivery solutions provides the backbone for next-generation data centers, enabling hyperscalers and integrators to innovate and scale globally. With a focus on trusted, domestic manufacturing, we deliver quality, speed, and innovation at scale—redefining AI infrastructure for the future. We are a newly created division of Vantedge Medical, the premier metals-based med-tech solutions partner from concept to full-scale manufacturing. With a steadfast commitment to advancing technology, we take immense pride in the work we do – and have a lot of fun doing it." About the Role: The Quality Engineer will provide support for product/process quality activities within Vantedge Medical. Areas of assignment may include: Product/Process improvement efforts, equipment validations, supplier quality performance and quality systems support. Responsibilities: Generate internal quality reports based on CAPA, complaints and yield. Propose and drive product/process improvement initiatives. Work with suppliers and Vander-Bend’s Supply Chain department to improve overall performance. Maintain metrics to evaluate process performance and work with manufacturing to ensure that expectations are met. Coordinate PPQP activities (pFMEA, CP, Capability reports, GR&R etc.). Assist the Director of Quality in maintaining ISO 13485 QMS. Create/Update work instructions and procedures as needed. Lead and/or create equipment validation protocols and reports. Undertake additional responsibilities or activities as required by Director of Quality. Requirements Requires a 4-year degree in Quality/Mechanical/Industrial engineering or a closely related field. 2+ years of work experience in a related field in a medical device or manufacturing environment. Understand in depth quality systems, ISO 13485 and/or 9001 standards. Ability to create, review, and revise operating procedures, work instructions in English. Specific training and demonstrated success in applying quality problem solving method, such as fishbone diagrams, 5 why, FMEA, process capability analysis, hypothesis testing, DoE, SPC, etc. Minitab, JMP or other statistical software capabilities.

Responsibilities

The Quality Engineer will support product and process quality activities, including generating internal quality reports and proposing improvement initiatives. They will also work with suppliers to enhance overall performance and maintain quality metrics.