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Vantedge Medical
Posted 1mo ago

Quality Engineer

Vantedge Medical
Stockton, California, United States
$87k-$115k/yrOnsiteFull Time
Responsibilities
  • analyzing data
  • leading improvements
  • validating equipment
Requirements
  • Bachelor's in engineering
  • 2+ years quality engineering in manufacturing
  • Knowledge of ISO 9001/13485
  • APQP/PPAP, FMEA, SPC
  • MSA/GR&R
  • Statistical software (Minitab/JMP)
  • Root-cause analysis
  • Validation, and technical documentation
Technical tools mentioned
ISO 9001ISO 13485APQPPPAPFMEApFMEAStatistical Process Control (SPC)Cp/CpkMSAGR&RIQ/OQ/PQMinitabJMPDoE

Job description

Job Type
Full-time
Description

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.

About Vantedge Medical

Manufacturer of precision metal components for medical device OEMs.

Year founded
1979
Employees
1200
Organization type
Private
Latest investment
Raised $90.00M Private Equity (2023) — led by Aterian Investment Partners
Headquarters
US

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