Quality Engineer
Stockton, CA - USA
Job Summary
Location:Stockton CA
Employment Type:Full-Time / Exempt
About Us:Vander-Bend is a U.S.-based manufacturer dedicated to building the precision infrastructure that powers tomorrows 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 Vantedges 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 / Skills:
Education & Experience
- Bachelors 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).
Technical Knowledge
- 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).
Skills & Competencies
- 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
Benefits:
- Medical Dental Vision Life Insurance
- Vacation and Sick Pay
- 401k