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Quality Engineer
Quality EngineerVantedge Medical • Stockton, CA, US
Quality Engineer

Quality Engineer

Vantedge Medical • Stockton, CA, US
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  • [job_card.full_time]
  • [job_card.permanent]
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Job Description

Job 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.
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