Quality Engineer I, Product and Process Quality Resume Hector Turner Quality Engineer I, Product and Process Quality (608) 555-1842 hector.turner@example.com linkedin.com/example/hectorturner Madison, WI 53703 STRENGTHS Evidence Based Investigation Built root cause evidence for nonconformances and CAPA cases. Teams gained clearer decisions when facts felt scattered. Quiet Process Improvement Used Lean reviews and process data to reduce variation. Small changes made daily production work smoother. Supplier Quality Partnership Reviewed capability data and corrective actions with suppliers. Practical questions often opened better conversations. Validation Discipline Connected IQ, OQ, PQ, and V&V records with acceptance evidence. Reviewers could follow each decision. Cross Functional Communication Translated statistical findings for engineering, manufacturing, and quality partners. Clear evidence helped groups move forward. SKILLS Quality engineering Validation CAPA SCARs FMEA DOE Lean Six Sigma Supplier quality Quality audits IQ/OQ/PQ V&V ISO 9001 ISO 13485 Minitab LANGUAGES English Native 40 Spanish Intermediate 20 MY CAREER 2.9 Years Quality Engineer I, Regulated Manufacturing at Alder Medical Components (1.9 Years) Quality Engineering Research Assistant, Applied Quality Lab at University Applied Quality Lab (1 Years) SUMMARY Quality Engineer with two years supporting regulated products and manufacturing operations across validation, nonconformance investigation, supplier controls, audits, and continuous improvement . Bachelor’s trained mechanical engineer with practical application of ISO 9001, ISO 13485, FDA requirements, 21 CFR Part 820 , IQ/OQ/PQ , V&V, CAPA, SCARs, FMEA, DOE, Lean, and Six Sigma. Uses Excel, Minitab, and JMP to turn production and validation data into clear quality decisions. Experience includes molded diagnostic device components, injection molding process controls, supplier qualification, technical compliance documentation , and audit preparation. Works closely with R&D, Manufacturing, Quality, Engineering, and supplier teams while managing parallel priorities independently. Brings a calm, evidence based approach to corrective action, risk reduction, and repeatable product performance across regulated manufacturing environments. EXPERIENCE Quality Engineer I, Regulated Manufacturing Alder Medical Components October 2024 - Present Madison, WI Support lifecycle quality for molded diagnostic device components from design transfer through routine production. Own validation records, deviation investigations, supplier quality activities, risk documentation, audit evidence, and focused improvement work. Partner with Manufacturing, R&D, Quality, Engineering, and external suppliers to protect compliant and repeatable product performance. Supported molded diagnostic component transfer through production using lifecycle quality controls and manufacturing data. Executed IQ/OQ/PQ protocols in Minitab, documenting acceptance evidence for validated production processes. Investigated nonconformances with root cause analysis , CAPA records, and SCARs, then verified corrective actions. Updated FMEAs after tooling changes, linking failure risks with controls, sampling, inspection, and verification. Qualified suppliers through capability data, change records, incoming trends, and corrective action reviews. Prepared ISO 13485 and 21 CFR Part 820 audit evidence for regulated manufacturing reviews. Coordinated Lean improvement work that reduced process variation and supported repeatable product performance. Quality Engineering Research Assistant, Applied Quality Lab University Applied Quality Lab September 2023 - September 2024 Milwaukee, WI Supported supervised quality engineering studies involving polymer processing, measurement systems, prototype assembly, and supplier quality cases. Applied statistical analysis , DOE, FMEA, verification methods, and corrective action planning while presenting findings that supported process standardization and waste reduction. Analyzed manufacturing datasets in Excel and JMP, separating common cause variation from actionable signals. Built DOE matrices for polymer processing trials and summarized factor effects for follow up experiments. Created FMEA records for prototype assembly, connecting failure modes with practical process controls. Drafted verification protocols and test reports for fixture and measurement system studies. Prepared root cause evidence and corrective action plans for simulated CAPA and supplier quality cases. Presented statistical findings that supported process standardization and waste reduction decisions. PROJECTS Polymer Processing DOE Study 2024 Built a structured DOE study for polymer processing trials, helping reviewers see factor effects, follow up needs, and practical paths toward more stable manufacturing performance. Diagnostic Component Validation Framework 2025 Organized validation evidence across IQ, OQ, PQ, and V&V activities, giving cross functional reviewers a clearer path from process requirements through documented acceptance. LEADERSHIP & AWARDS Earned ASQ Certified Quality Improvement Associate recognition in 2025. Completed Lean Six Sigma Green Belt certification in 2025. Presented applied statistical findings that supported process standardization and waste reduction. EDUCATION Bachelor's Degree in Mechanical Engineering University of Wisconsin-Milwaukee GPA: 4.0 2024 Milwaukee, WI Coursework: Quality engineering, statistical methods, manufacturing processes, design of experiments CERTIFICATIONS ASQ Certified Quality Improvement Associate 2025 Lean Six Sigma Green Belt 2025 TECHNICAL SKILLS Quality Systems: ISO 9001, ISO 13485, 21 CFR Part 820 Validation Methods: IQ, OQ, PQ Verification Practices: V&V, validation protocols, validation reports Corrective Action: CAPA, SCARs, root cause analysis Risk Management: FMEA, process controls, risk review Statistical Analysis: Minitab, JMP, Excel Process Improvement: Lean, Six Sigma, waste reduction Manufacturing Processes: Injection molding, process standardization, production controls Supplier Quality: Supplier qualification, capability data, corrective action reviews Regulatory Documentation: Design History Files, product certifications, audit evidence SKILLS Quality engineering Validation CAPA SCARs FMEA DOE Lean Six Sigma Supplier quality Quality audits IQ/OQ/PQ V&V ISO 9001 ISO 13485 Minitab PROFESSIONAL AFFILIATIONS ASQ community participant with interest in quality systems and continuous improvement. University applied quality lab contributor focused on manufacturing data and validation methods. LANGUAGES English (Native) Spanish (Intermediate) ADDITIONAL INFORMATION Work Status : Authorized to work in United States. No sponsorship required. ADDITIONAL INFORMATION Work Status : Authorized to work in United States. No sponsorship required. REFERENCES AVAILABLE ON REQUEST
  • File
  • Preview
  • Show Styles
  • PDF Download
  • US English
File
Styles Download Buy Log In
Bootstrap
> JP 1 1
PDF Footer and Margins Setup
The margins are applied to the document, and the footer shows up in the preview and the PDF

Footer Font Settings

Are you applying for a specific job
so we can tailor your resume to it? Are you applying for a specific job
so we can tailor your cover letter to it?
Type your details as text to generate a personalized resume Type your details as text to generate a personalized cover letter
Website link found! Ready to create resume from:
Skip this Step
Drag the into the box to verify you're human.
Drop here

My Resumes

Displaying {number_of_files} files (out of {total_of_all_files} total)
Name File Type Last Modified: Description:

Rename File

Filename already exists!

Delete Files

Warning: This action is irreversible. Once you click submit, the files will be permanently deleted.

Heading text
Upload From Computer Upload
Select From Existing
LinkedIn
Drag & Drop files anywhere in this tab, or

Uploaded Files

Delete Name Last Updated Use This File
Select this to use the file for generating your resume and cover letter. Only one source—uploaded file, selected file, or LinkedIn text—can be used.

My Files

Resumes or cover letters you create will appear here. No files available yet.
Delete Name Last Updated Use This File
Select this to use the file for generating your resume and cover letter. Only one source—uploaded file, selected file, or LinkedIn text—can be used.

Add LinkedIn Profile PDF

You can download your LinkedIn profile as a PDF by opening linkedin.com in a web browser, clicking your profile photo, selecting the “More” or “Resources” button, and choosing “Save to PDF.” You can then attach the PDF using the Upload From Computer tab.

Paste Your LinkedIn Profile Text

If you have copied the LinkedIn profile text, paste it below. See how to copy your profile from LinkedIn

   
Select this to use the LinkedIn profile text for generating your resume and cover letter. Only one source—uploaded file, selected file, or LinkedIn text—can be used.
-->
Select this to use the LinkedIn profile text for generating your resume and cover letter. Only one source—uploaded file, selected file, or LinkedIn text—can be used.

Try these controls

<
>