H-1B Visa Supplier Quality Engineer Jobs
Supplier Quality Engineer roles sit firmly within H-1B visa specialty occupation territory, requiring at minimum a bachelor's degree in engineering or a related field. Employers across automotive, aerospace, and manufacturing regularly sponsor H-1B petitions for SQE candidates, and the role's reliance on technical standards like PPAP, APQP, and IATF 16949 strengthens the specialty occupation case at filing.
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Argon Medical Devices is a global manufacturer of specialty medical products, headquartered in Plano, Texas. Argon offers a broad line of medical devices for Interventional Radiology, Vascular Surgery, Interventional Cardiology and Oncology. Argon’s brand is recognized for best-in-class products that improve patient outcomes via percutaneous, image-guided procedures. Our values describe what we believe in and how we operate. These values are our moral compass which guide our decisions and define the deeply held beliefs and principles of our organizational culture. Argon Medical is a family of individuals united by a mission and culture which continue to grow stronger every day.
ARGON MEDICAL DEVICES IS NOT LEVERAGING SEARCH FIRMS
Position Overview:
We are looking for a motivated Supplier Quality Engineer to join our quality team. In this role, you will be managing our supplier relationships, performance, and assist with investigations until resolved. You will work to improve the site’s incoming inspection capabilities including inspection methods, sampling plans, and approved supplier/materials list. You’ll work closely with subject matter experts within the quality, manufacturing, engineering and procurement departments to improve product quality and schedule adherence.
What you will do:
The supplier quality engineer will be responsible for managing the supplier relationships and overseeing the site's incoming inspection processes. The key responsibilities are outlined below:
Supplier Management:
- Issue/resolve nonconforming products through the SCAR/NCR process with suppliers.
- Provide supplier scorecards based on performance categories.
- Work with suppliers on their changes through the supplier notification process (SNC) and be the representative for the Wheeling location.
- Onboarding new suppliers and/or materials with cross functional collaboration.
Incoming Inspection:
- Improve incoming inspection process by refining process flow, utilizing existing equipment, and/or purchasing new equipment.
- Manage Dock-To-Stock (DTS) program based on supplier performance.
- Manage incoming AQL switching rules program.
Skills for Success:
- BS Degree in Engineering required.
- 3+ years of experience as a Quality Engineer required.
- Previous experience in FDA/ISO regulated industry required. SO 13485 Medical Device industry preferred.
- CQE and CQA preferred.
- Ability to interpret engineering drawings, GD&T, and technical specifications required.
- Hands-on experience with audits, inspections, and statistical analysis required.
Company Overview:
Argon Medical Devices is a global manufacturer of specialty medical products, headquartered in Plano, Texas. Argon offers a broad line of medical devices for Interventional Radiology, Vascular Surgery, Interventional Cardiology and Oncology. Argon’s brand is recognized for best-in-class products that improve patient outcomes via percutaneous, image-guided procedures. Our values describe what we believe in and how we operate. These values are our moral compass which guide our decisions and define the deeply held beliefs and principles of our organizational culture. Argon Medical is a family of individuals united by a mission and culture which continue to grow stronger every day.
ARGON MEDICAL DEVICES IS NOT LEVERAGING SEARCH FIRMS
Position Overview:
We are looking for a motivated Supplier Quality Engineer to join our quality team. In this role, you will be managing our supplier relationships, performance, and assist with investigations until resolved. You will work to improve the site’s incoming inspection capabilities including inspection methods, sampling plans, and approved supplier/materials list. You’ll work closely with subject matter experts within the quality, manufacturing, engineering and procurement departments to improve product quality and schedule adherence.
What you will do:
The supplier quality engineer will be responsible for managing the supplier relationships and overseeing the site's incoming inspection processes. The key responsibilities are outlined below:
Supplier Management:
- Issue/resolve nonconforming products through the SCAR/NCR process with suppliers.
- Provide supplier scorecards based on performance categories.
- Work with suppliers on their changes through the supplier notification process (SNC) and be the representative for the Wheeling location.
- Onboarding new suppliers and/or materials with cross functional collaboration.
Incoming Inspection:
- Improve incoming inspection process by refining process flow, utilizing existing equipment, and/or purchasing new equipment.
- Manage Dock-To-Stock (DTS) program based on supplier performance.
- Manage incoming AQL switching rules program.
Skills for Success:
- BS Degree in Engineering required.
- 3+ years of experience as a Quality Engineer required.
- Previous experience in FDA/ISO regulated industry required. SO 13485 Medical Device industry preferred.
- CQE and CQA preferred.
- Ability to interpret engineering drawings, GD&T, and technical specifications required.
- Hands-on experience with audits, inspections, and statistical analysis required.
See all 366+ H-1B Visa Supplier Quality Engineer Jobs
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Get Access To All JobsTips for Finding H-1B Visa Sponsorship as a Supplier Quality Engineer
Align your degree to SQE job requirements
USCIS evaluates whether your specific degree directly relates to the role. A degree in mechanical, industrial, or manufacturing engineering maps cleanly. Materials science or quality management degrees work too, but prepare a brief equivalency statement linking your coursework to supplier quality functions.
Target manufacturers enrolled in E-Verify
STEM-adjacent manufacturing employers enrolled in E-Verify are already set up for compliant hiring. Cross-reference DOL LCA disclosure data by SOC code 17-2112 to identify which manufacturers have filed for quality engineering roles specifically, not just engineering broadly.
Search verified H-1B sponsors on Migrate Mate
Filter by SOC code or job title on Migrate Mate to find employers with documented LCA filing history for Supplier Quality Engineer roles. This surfaces companies that have already navigated the specialty occupation argument for this position, reducing your vetting work significantly.
Request the prevailing wage tier before offer stage
Ask your recruiter which DOL wage level the employer intends to file at before accepting an offer. SQE roles span Levels I through III depending on supplier complexity and autonomy. A Level I designation on a senior-scope role creates compliance risk and can weaken your petition.
Document your PPAP and audit experience precisely
USCIS officers scrutinize whether SQE duties genuinely require a specialized degree. Your resume and support letter should name specific quality systems you've worked within, such as IATF 16949, AS9100, or AIAG standards, connecting each directly to engineering judgment rather than inspection or clerical work.
Verify the prevailing wage using OFLC Wage Search
Before your employer files the LCA, confirm the posted wage matches or exceeds the DOL prevailing wage for your metro area and experience level. Use OFLC Wage Search with SOC code 17-2112 and your actual worksite zip code, not the employer's headquarters if they differ.
H-1B Visa Supplier Quality Engineer: Frequently Asked Questions
Does a Supplier Quality Engineer role qualify as an H-1B specialty occupation?
Yes. USCIS treats Supplier Quality Engineer as a specialty occupation because the role typically requires at minimum a bachelor's degree in mechanical, industrial, or manufacturing engineering. The position involves applying engineering theory to supplier qualification, root cause analysis, and quality system audits, which supports the specialty occupation argument. Your employer's job description should tie each duty to specific degree-level knowledge to strengthen the petition.
Which industries sponsor H-1B visas most often for Supplier Quality Engineers?
Automotive, aerospace, medical device, and electronics manufacturing are the highest-volume industries for SQE H-1B sponsorship. These sectors operate under strict regulatory and certification frameworks like IATF 16949, AS9100, and ISO 13485, which require degree-level engineering expertise. You can browse employers with verified LCA filing history for this role on Migrate Mate, filtered by industry or location.
What SOC code applies to Supplier Quality Engineer for H-1B filing purposes?
Most SQE roles are filed under SOC code 17-2112, Industrial Engineers, or 17-2141, Mechanical Engineers, depending on the employer's framing of the role. The SOC code determines which prevailing wage tier applies, so confirm the code your employer intends to use before the LCA is submitted. You can check the O*NET profile for each code to verify the duties align with your actual job responsibilities.
Can a Supplier Quality Engineer on H-1B work across multiple supplier sites?
Yes, but worksite compliance requires attention. If your role involves regular work at supplier facilities in different metro areas, your employer may need to file amended LCAs or additional H-1B petitions for each worksite. Short-term placements under 30 days in a 12-month period have different posting requirements under DOL rules. Clarify the worksite structure with your employer before filing to avoid compliance issues.
How does changing employers affect an H-1B Supplier Quality Engineer?
You can change employers under H-1B portability rules once USCIS has approved your first H-1B and you've maintained lawful status. Your new employer must file an H-1B transfer petition before your start date. Because SQE roles vary in scope across industries, the new employer's job description should independently satisfy the specialty occupation requirement, not simply reference your previous approval.