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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Get Access To All JobsWorking Location: Brazil, Sao Paolo; Massachusetts, Westborough
Workplace Flexibility: Hybrid
For more than 100 years, Olympus has focused on making people’s lives healthier, safer and more fulfilling. Every day, we live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care so people everywhere can fulfill their desires, dreams, and lives. Our five Core Values empower us to achieve Our Purpose: Patient Focus, Integrity, Innovation, Impact and Empathy.
Job Description
This role is responsible for supplier management activities including but not limited to Supplier Qualifications, Audits, Quality Assurance Agreement negotiations, and Supplier Risk Improvement. This role is within supplier quality function with focus on the Latin American region.
Job Duties
- Determines appropriate supplier level (risk category) based on Supplier usage by Olympus.
- Qualifies new and remediates qualifications of existing suppliers.
- Develops documented risk improvement strategy for suppliers not meeting the minimum requirements.
- Carries out supplier audits, supplier surveys, and Quality Assurance Agreement notifications.
- Identifies gaps in suppliers' capabilities / technical project risks.
- Makes decisions on acceptance or rejection of supplier input.
- Leads improvement projects at the supplier.
- Acts as primary interface to supplier regarding systemic quality matters.
- Supports facility audits by outside agencies (i.e., FDA, ISO/ MDSAP / ISP / ANVISA / COFEPRIS).
- Serves as first escalation path for supplier quality engineering part-level concerns.
Job Requirements
Required:
- BA/BS degree or equivalent in a Life Science, Engineering, or Physical Science with an advanced technical degree required.
- Minimum of 5 years in a related field.
- FDA & Medical Device experience.
- Must be fluent in English and either Portuguese and/or Spanish.
- Very good knowledge of Quality tools and methods.
- Comfortable with Microsoft Office (Word, Excel, Outlook, and PowerPoint) and operating a variety of websites.
- Expert level knowledge of ISO 9001 & ISO 13485.
- Basic project management skills.
- Ability to travel up to 40% of time domestically and internationally.
Why join Olympus?
We offer a holistic employee experience supporting personal and professional well-being through meaningful work, equitable offerings, and a connected culture.
Equitable Offerings you can count on:
- Competitive salaries, annual bonus and 401(k)* with company match
- Comprehensive medical, dental, vision coverage effective on start date
- 24/7 Employee Assistance Program
- Free live and on-demand Wellbeing Programs
- Generous Paid Vacation and Sick Time
- Paid Parental Leave and Adoption Assistance*
- 12 Paid Holidays
- On-Site Child Daycare, Café, Fitness Center**
Connected Culture you can embrace:
- Work-life integrated culture that supports an employee centric mindset
- Offers onsite, hybrid and field work environments
- Paid volunteering and charitable donation/match programs
- Employee Resource Groups
- Dedicated Training Resources and Learning & Development Programs
-
Paid Educational Assistance
-
US Only
Center Valley, PA and Westborough, MA
Are you ready to be a part of our team?
The anticipated base pay range for this full-time position in this location is $100,263.00 - $135,355.00 / year, plus potential for annual bonus (subject to plan eligibility and other requirements).
Olympus considers a variety of factors when determining actual compensation for this position, including level of experience, working location, and relevant education and certifications.
At Olympus, we are committed to Our Purpose of making people’s lives healthier, safer and more fulfilling. As a global medical technology company, we partner with healthcare professionals to provide best-in-class solutions and services for early detection, diagnosis and minimally invasive treatment, aiming to improve patient outcomes by elevating the standard of care in targeted disease states.
For more than 100 years, Olympus has pursued a goal of contributing to society by producing products designed with the purpose of delivering optimal outcomes for its customers around the world.
Headquartered in Tokyo, Japan, Olympus employs more than 31,000 employees worldwide in nearly 40 countries and regions. Olympus Corporation of the Americas, a wholly owned subsidiary of Olympus Corporation, is headquartered in Center Valley, Pennsylvania, USA, and employs more than 5,200 employees throughout locations in North and South America.
You Belong at Olympus
We are deeply committed to fostering a respectful, fair, and welcoming workplace for all individuals, perspectives, and lifestyles. We believe in fostering a non-discriminatory, inclusive work environment where everyone feels a sense of belonging, in full compliance with legal standards. Empathy and unity are core to our company culture, empowering employees to contribute fully and flourish. We warmly encourage all who wish to bring their talents to Olympus to apply.
Applicants Requesting Accommodations: Olympus is committed to the full inclusion of all qualified individuals. As part of this commitment, Olympus will ensure that persons with disabilities are provided reasonable accommodations for the hiring process. If reasonable accommodation is needed, please contact OCAAccommodations@olympus.com. If your disability impairs your ability to email, you may call our HR Compliance Manager at 1-888-Olympus (1-888-659-6787).
Let’s realize your potential, together.
It is the policy of Olympus to extend equal employment and advancement opportunity to all applicants and employees without regard to race, color, national origin (including language use restrictions), citizenship status, religious creed (including dress and grooming practices), age, sex (including pregnancy, childbirth, breastfeeding, medical conditions related to pregnancy, childbirth and/or breastfeeding), gender, gender identity and expression, sexual orientation, marital status, disability (physical or mental) and/or a medical condition, genetic information, ancestry, veteran status or service in the uniformed services, and any other characteristic protected by applicable federal, state or local law.
Posting Notes: || United States (US) || Massachusetts (US-MA) || Westborough || Quality & Regulatory Affairs (QA/RA)
Nearest Major Market: Worcester
Job Segment: QA, Quality Assurance, Senior Quality Engineer, Quality Engineer, Medical Device Engineer, Quality, Technology, Engineering
Working Location: Brazil, Sao Paolo; Massachusetts, Westborough
Workplace Flexibility: Hybrid
For more than 100 years, Olympus has focused on making people’s lives healthier, safer and more fulfilling. Every day, we live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care so people everywhere can fulfill their desires, dreams, and lives. Our five Core Values empower us to achieve Our Purpose: Patient Focus, Integrity, Innovation, Impact and Empathy.
Job Description
This role is responsible for supplier management activities including but not limited to Supplier Qualifications, Audits, Quality Assurance Agreement negotiations, and Supplier Risk Improvement. This role is within supplier quality function with focus on the Latin American region.
Job Duties
- Determines appropriate supplier level (risk category) based on Supplier usage by Olympus.
- Qualifies new and remediates qualifications of existing suppliers.
- Develops documented risk improvement strategy for suppliers not meeting the minimum requirements.
- Carries out supplier audits, supplier surveys, and Quality Assurance Agreement notifications.
- Identifies gaps in suppliers' capabilities / technical project risks.
- Makes decisions on acceptance or rejection of supplier input.
- Leads improvement projects at the supplier.
- Acts as primary interface to supplier regarding systemic quality matters.
- Supports facility audits by outside agencies (i.e., FDA, ISO/ MDSAP / ISP / ANVISA / COFEPRIS).
- Serves as first escalation path for supplier quality engineering part-level concerns.
Job Requirements
Required:
- BA/BS degree or equivalent in a Life Science, Engineering, or Physical Science with an advanced technical degree required.
- Minimum of 5 years in a related field.
- FDA & Medical Device experience.
- Must be fluent in English and either Portuguese and/or Spanish.
- Very good knowledge of Quality tools and methods.
- Comfortable with Microsoft Office (Word, Excel, Outlook, and PowerPoint) and operating a variety of websites.
- Expert level knowledge of ISO 9001 & ISO 13485.
- Basic project management skills.
- Ability to travel up to 40% of time domestically and internationally.
Why join Olympus?
We offer a holistic employee experience supporting personal and professional well-being through meaningful work, equitable offerings, and a connected culture.
Equitable Offerings you can count on:
- Competitive salaries, annual bonus and 401(k)* with company match
- Comprehensive medical, dental, vision coverage effective on start date
- 24/7 Employee Assistance Program
- Free live and on-demand Wellbeing Programs
- Generous Paid Vacation and Sick Time
- Paid Parental Leave and Adoption Assistance*
- 12 Paid Holidays
- On-Site Child Daycare, Café, Fitness Center**
Connected Culture you can embrace:
- Work-life integrated culture that supports an employee centric mindset
- Offers onsite, hybrid and field work environments
- Paid volunteering and charitable donation/match programs
- Employee Resource Groups
- Dedicated Training Resources and Learning & Development Programs
-
Paid Educational Assistance
-
US Only
Center Valley, PA and Westborough, MA
Are you ready to be a part of our team?
The anticipated base pay range for this full-time position in this location is $100,263.00 - $135,355.00 / year, plus potential for annual bonus (subject to plan eligibility and other requirements).
Olympus considers a variety of factors when determining actual compensation for this position, including level of experience, working location, and relevant education and certifications.
At Olympus, we are committed to Our Purpose of making people’s lives healthier, safer and more fulfilling. As a global medical technology company, we partner with healthcare professionals to provide best-in-class solutions and services for early detection, diagnosis and minimally invasive treatment, aiming to improve patient outcomes by elevating the standard of care in targeted disease states.
For more than 100 years, Olympus has pursued a goal of contributing to society by producing products designed with the purpose of delivering optimal outcomes for its customers around the world.
Headquartered in Tokyo, Japan, Olympus employs more than 31,000 employees worldwide in nearly 40 countries and regions. Olympus Corporation of the Americas, a wholly owned subsidiary of Olympus Corporation, is headquartered in Center Valley, Pennsylvania, USA, and employs more than 5,200 employees throughout locations in North and South America.
You Belong at Olympus
We are deeply committed to fostering a respectful, fair, and welcoming workplace for all individuals, perspectives, and lifestyles. We believe in fostering a non-discriminatory, inclusive work environment where everyone feels a sense of belonging, in full compliance with legal standards. Empathy and unity are core to our company culture, empowering employees to contribute fully and flourish. We warmly encourage all who wish to bring their talents to Olympus to apply.
Applicants Requesting Accommodations: Olympus is committed to the full inclusion of all qualified individuals. As part of this commitment, Olympus will ensure that persons with disabilities are provided reasonable accommodations for the hiring process. If reasonable accommodation is needed, please contact OCAAccommodations@olympus.com. If your disability impairs your ability to email, you may call our HR Compliance Manager at 1-888-Olympus (1-888-659-6787).
Let’s realize your potential, together.
It is the policy of Olympus to extend equal employment and advancement opportunity to all applicants and employees without regard to race, color, national origin (including language use restrictions), citizenship status, religious creed (including dress and grooming practices), age, sex (including pregnancy, childbirth, breastfeeding, medical conditions related to pregnancy, childbirth and/or breastfeeding), gender, gender identity and expression, sexual orientation, marital status, disability (physical or mental) and/or a medical condition, genetic information, ancestry, veteran status or service in the uniformed services, and any other characteristic protected by applicable federal, state or local law.
Posting Notes: || United States (US) || Massachusetts (US-MA) || Westborough || Quality & Regulatory Affairs (QA/RA)
Nearest Major Market: Worcester
Job Segment: QA, Quality Assurance, Senior Quality Engineer, Quality Engineer, Medical Device Engineer, Quality, Technology, Engineering
See all 250+ H-1B Visa Supplier Quality Engineer Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new H-1B Visa Supplier Quality Engineer Jobs.
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.