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Quality Engineer

Job in Stockton, San Joaquin County, California, 95219, USA
Listing for: Vantedge Medical
Full Time position
Listed on 2026-07-02
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 87000 - 115000 USD Yearly USD 87000.00 115000.00 YEAR
Job Description & How to Apply Below

Quality Engineer

Full-time | Permanent

Salaried | $87K - $115k

We are not currently working with third party agencies on this role.

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's Vander-Bend Sheet Metal Manufacturing business in Stockton, CA. Areas of assignment may include product/process improvement efforts, equipment validations, supplier quality performance and quality systems support.

Responsibilities:

  • Analyze quality data (CAPA, complaints, yield trends) to identify systemic issues and lead cross-functional improvement initiatives to enhance product and process performance.
  • Partner with Supply Chain and suppliers to drive supplier quality improvements, including corrective actions and performance monitoring.
  • Develop, track, and report key process performance metrics (KPIs) to ensure manufacturing processes meet quality and yield targets.
  • Lead or support APQP/PPAP activities, including pFMEA, Control Plans, process capability studies, and GR&R.
  • Manage nonconforming materials (NCMR), customer complaints, and returns, ensuring timely root cause analysis and effective corrective/preventive actions.
  • Support and maintain compliance with ISO 9001 and ISO 13485 Quality Management Systems (QMS), including audit readiness and documentation control.
  • Author, review, and update standard operating procedures (SOPs), work instructions, and quality documentation.
  • Develop and execute equipment validation protocols (IQ/OQ/PQ) and generate validation reports.
  • Collaborate cross-functionally with Manufacturing, Engineering, and Quality teams to resolve quality issues and implement sustainable solutions.
  • Perform additional duties as assigned to support departmental and organizational objectives.

Requirements:

  • Bachelor's degree in Quality, Mechanical, Industrial Engineering, or related field.
  • Minimum 2+ years of quality engineering experience in a manufacturing environment (sheet metal or similar preferred).
  • Strong knowledge of quality systems and standards, including ISO 9001 and/or ISO 13485.
  • Experience with core quality tools and methodologies:
    • Root cause analysis (5 Whys, Fishbone)
    • FMEA (Design/Process)
    • Statistical Process Control (SPC)
    • Process capability (Cp/Cpk)
    • Familiarity with APQP/PPAP processes and documentation requirements.
    • Experience with measurement system analysis (MSA/GR&R).
    • Knowledge of statistical analysis software (Minitab, JMP, or equivalent).
    • Strong analytical and problem-solving skills with a data-driven approach.
    • Ability to interpret technical drawings, specifications, and manufacturing processes.
    • Effective communication and collaboration skills across cross-functional teams.
    • Strong documentation and technical writing abilities (procedures, reports, validations).
    • Ability to manage multiple priorities in a fast-paced manufacturing environment.
    • 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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