QA Engineer Jobs in USA with Visa Sponsorship
QA engineers have a strong path to H-1B visa sponsorship since the role requires a technical degree and is firmly in the specialty occupation category. Tech companies of all sizes, from startups to enterprise software firms, sponsor for QA roles. The distinction between manual QA and automation-focused QA matters for sponsorship, with automation engineers being in higher demand and commanding stronger petitions. TN visa and E-3 visas are also options for eligible nationalities. For detailed occupation requirements, see the O*NET profile.
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Get Access To All JobsWork Schedule
First Shift (Days)
Environmental Conditions
Office
Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Location/Division Specific Information:
The Drug Product Division - North America (DPD-NA) is one of the five divisions that make up the Pharma Services Group. We are made up of approximately 4400 colleagues across six sites who specialize in taking sterile injectable and oral solid dose drug products from development to commercialization.
How You Will Make an Impact
Join Thermo Fisher Scientific as a Lead QA Technician and contribute to ensuring product quality and regulatory compliance. As a member of our Quality team, you'll help enable our mission of making the world healthier, cleaner and safer through quality oversight of pharmaceutical manufacturing operations. Your expertise will help maintain high standards of quality while supporting production of life-changing medicines. Shift is Monday-Friday, 8hr days.
A Day in the Life
- Provide independent quality oversight of GMP manufacturing operations, including aseptic processing
- Perform and lead batch record review to ensure accuracy and compliance with regulatory and internal requirements
- Lead and support deviation investigations, root cause analysis, and CAPA development and effectiveness checks
- Utilize electronic quality systems such as TrackWise and Documentum to manage documentation and workflows
- Partner with Manufacturing, Validation, Engineering, and Regulatory teams to support compliant operations
- Support and participate in regulatory inspections, internal audits, and customer audits
- Apply knowledge of aseptic manufacturing controls, cleanroom operations, and gowning practices
- Mentor and provide technical guidance to QA Technicians and peers
- Identify opportunities for continuous improvement and quality system enhancements
- Ensure compliance with site procedures, safety requirements, and data integrity standards
Education:
- High School Diploma or equivalent required.
- Preferred Fields of Study: Chemistry, Pharmacy, Biology, Biotechnology or related scientific field
Experience
- Minimum of three (3) years of experience in pharmaceutical quality assurance or related GMP environment, four (4) years preferred.
- Equivalent combinations of education, training, and relevant work experience may be considered
Knowledge, Skills, and Abilities
- Expertise in batch record review, deviation investigations and CAPA management
- Strong understanding of aseptic manufacturing processes and controls
- Professional communication skills both written and spoken
- Ability to manage multiple priorities in a dynamic environment
- Strong attention to detail and analytical problem-solving skills
- Effective interpersonal and communication abilities
- Project management and organizational capabilities
- Experience supporting regulatory inspections and customer audits
- Demonstrated ability to work effectively with cross-functional teams
- Proficiency with Microsoft Office applications
- Ability to work various shifts as required
- Demonstrated ability to guide and develop team members
- Ability to understand and interpret technical procedures and specifications
Work Schedule
First Shift (Days)
Environmental Conditions
Office
Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Location/Division Specific Information:
The Drug Product Division - North America (DPD-NA) is one of the five divisions that make up the Pharma Services Group. We are made up of approximately 4400 colleagues across six sites who specialize in taking sterile injectable and oral solid dose drug products from development to commercialization.
How You Will Make an Impact
Join Thermo Fisher Scientific as a Lead QA Technician and contribute to ensuring product quality and regulatory compliance. As a member of our Quality team, you'll help enable our mission of making the world healthier, cleaner and safer through quality oversight of pharmaceutical manufacturing operations. Your expertise will help maintain high standards of quality while supporting production of life-changing medicines. Shift is Monday-Friday, 8hr days.
A Day in the Life
- Provide independent quality oversight of GMP manufacturing operations, including aseptic processing
- Perform and lead batch record review to ensure accuracy and compliance with regulatory and internal requirements
- Lead and support deviation investigations, root cause analysis, and CAPA development and effectiveness checks
- Utilize electronic quality systems such as TrackWise and Documentum to manage documentation and workflows
- Partner with Manufacturing, Validation, Engineering, and Regulatory teams to support compliant operations
- Support and participate in regulatory inspections, internal audits, and customer audits
- Apply knowledge of aseptic manufacturing controls, cleanroom operations, and gowning practices
- Mentor and provide technical guidance to QA Technicians and peers
- Identify opportunities for continuous improvement and quality system enhancements
- Ensure compliance with site procedures, safety requirements, and data integrity standards
Education:
- High School Diploma or equivalent required.
- Preferred Fields of Study: Chemistry, Pharmacy, Biology, Biotechnology or related scientific field
Experience
- Minimum of three (3) years of experience in pharmaceutical quality assurance or related GMP environment, four (4) years preferred.
- Equivalent combinations of education, training, and relevant work experience may be considered
Knowledge, Skills, and Abilities
- Expertise in batch record review, deviation investigations and CAPA management
- Strong understanding of aseptic manufacturing processes and controls
- Professional communication skills both written and spoken
- Ability to manage multiple priorities in a dynamic environment
- Strong attention to detail and analytical problem-solving skills
- Effective interpersonal and communication abilities
- Project management and organizational capabilities
- Experience supporting regulatory inspections and customer audits
- Demonstrated ability to work effectively with cross-functional teams
- Proficiency with Microsoft Office applications
- Ability to work various shifts as required
- Demonstrated ability to guide and develop team members
- Ability to understand and interpret technical procedures and specifications
See all 2,054+ QA Engineer Jobs
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Get Access To All JobsTips for Finding Visa Sponsorship as a QA Engineer
Build expertise in both manual and automated testing
QA engineers who can perform exploratory manual testing and write automated test scripts are more versatile than those who only do one. Demonstrating proficiency in test design methodology (boundary value analysis, equivalence partitioning) alongside automation frameworks shows the specialized training that supports an H-1B petition.
Learn in-demand test automation tools
Selenium WebDriver, Cypress, Playwright, and Appium for mobile testing are the most requested QA automation tools. Pairing these with API testing tools like Postman or REST Assured and CI/CD integration (Jenkins, GitHub Actions) makes your profile immediately valuable to employers.
Target tech companies with large QA organizations
Microsoft, Salesforce, Oracle, and enterprise SaaS companies maintain dedicated QA teams and regularly sponsor H-1B visas. These companies value QA engineers who can work within agile teams and contribute to test strategy, not just execute test cases.
Use STEM OPT to demonstrate end-to-end quality ownership
Computer science degrees qualify for the 24-month STEM OPT extension. During the 36-month OPT window, aim to own the quality strategy for at least one product feature or release cycle. This level of ownership makes you harder to replace and strengthens the sponsorship argument.
Frequently Asked Questions
Do companies sponsor H-1B visas for QA engineers?
Yes. QA engineer roles are classified as specialty occupations under software-related SOC codes, and many tech companies actively sponsor QA engineers. Large employers like Microsoft, Amazon, and enterprise software companies have consistent demand for QA professionals. Roles that involve test automation, test architecture, or quality strategy tend to receive sponsorship more readily than pure manual testing positions.
How to find QA Engineer jobs with visa sponsorship?
Start by using Migrate Mate, a specialized platform for visa sponsorship opportunities that connects QA Engineers with employers offering H-1B visa, L-1 visa, and other work visas. Focus your search on tech companies, software development firms, and financial services organizations that frequently sponsor international talent. These industries actively seek QA Engineers and have established visa sponsorship programs to attract skilled testing professionals.
Is QA engineering considered less prestigious than software development for visa purposes?
No. From a visa perspective, QA engineering roles are classified the same way as other software engineering roles and carry the same specialty occupation standing. The prevailing wage is determined by the specific SOC code and geographic location. Many companies use titles like Software Development Engineer in Test (SDET) or Quality Engineer, which are treated equivalently in H-1B filings.
What degree do I need for a QA engineer H-1B petition?
A bachelor's degree in computer science, software engineering, information technology, or a related technical field is typically required. Some employers accept degrees in mathematics or engineering with demonstrated programming experience. The degree must relate directly to the QA engineering job duties described in the petition.
Can QA engineers transition to software development roles on the same visa?
If both roles fall under the same or similar SOC code and the new role's requirements are substantially similar, an amendment may not be required. However, a significant change in job duties, location, or SOC code would require the employer to file an H-1B amendment. Consult your employer's immigration attorney before making any role changes to ensure compliance.
What is the prevailing wage requirement for sponsored QA Engineer jobs?
When a U.S. employer sponsors a foreign worker for a work visa, they are legally required to pay at least the "prevailing wage" — the average wage paid to workers in the same occupation, in the same geographic area, with similar experience. This is set by the Department of Labor to prevent employers from hiring foreign workers at below-market rates. The prevailing wage varies significantly by role, location, and experience level — for example, a qa engineer in California will have a different prevailing wage than the same role in a smaller state. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search.