Software Quality Assurance Visa Sponsorship Jobs in North Carolina
North Carolina's software quality assurance job market is anchored by Research Triangle Park, home to major employers like Cisco, Red Hat, and IBM, alongside a growing fintech and healthtech sector in Charlotte. QA engineers with visa sponsorship needs will find consistent demand across Raleigh, Durham, and Charlotte, where tech hiring has expanded steadily in recent years.
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Get Access To All JobsWork Schedule
12 hr shift/days
Environmental Conditions
Able to lift 40 lbs. without assistance, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Title: QA Specialist III – Quality on the Floor (QOTF)
Location: Greenville, NC
Schedule: Day Shift | 6:00 AM – 6:00 PM | 2-2-3 Rotating Schedule
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
Greenville, NC
As part of the Drug Product Division (DPD), our Greenville, North Carolina site is a multi-purpose pharmaceutical development, manufacturing, and packaging campus supporting sterile injectable and oral solid dose drug products from development through commercialization.
This position supports sterile pharmaceutical manufacturing within our Manufacturing Quality Assurance organization. The Quality on the Floor (QOTF) team works directly alongside Manufacturing, Operations, and Quality leadership to maintain regulatory compliance, strengthen aseptic practices, and support continuous improvement.
Unlike traditional desk-based Quality Assurance positions, this role requires a significant manufacturing-floor presence, with approximately 60–75% of the workday spent observing operations, providing guidance, and supporting real-time quality decisions.
How will you make an impact?
As a QA Specialist III – Quality on the Floor (QOTF), you'll play a critical role in maintaining quality and compliance across sterile pharmaceutical manufacturing operations.
This is a highly visible, hands-on position where you'll work directly with manufacturing personnel to observe aseptic practices, assess production activities, identify potential compliance concerns, and provide practical guidance that supports safe and compliant manufacturing.
You'll help maintain a state of inspection readiness by conducting routine manufacturing walkthroughs, evaluating documentation and operational practices, and supporting investigations, deviations, and process improvements.
Success in this role requires more than technical quality knowledge. You'll need strong judgment, problem-solving abilities, and the interpersonal skills to coach employees, influence decisions, and navigate operational challenges while maintaining established quality standards.
This is an excellent opportunity for an experienced Quality professional or manufacturing specialist seeking to transition into a hands-on Quality Assurance role with direct operational impact and opportunities for professional growth.
What will you do?
- Perform routine Quality Assurance oversight of sterile manufacturing, filling, packaging, and inspection activities to ensure compliance with cGMP requirements and site procedures.
- Conduct documented manufacturing-floor walkthroughs, assessing facility conditions, equipment, personnel practices, aseptic technique, and production documentation.
- Observe manufacturing activities and provide real-time coaching, quality guidance, and support to operators and production leadership.
- Identify, document, and escalate potential quality concerns, compliance gaps, and operational risks while supporting appropriate corrective actions.
- Participate in deviation investigations, root cause analysis, RAPID event responses, and change control activities.
- Review and approve manufacturing documentation, batch records, procedures, training materials, and quality records as assigned.
- Collaborate with Manufacturing, Quality, and site leadership to troubleshoot process and equipment issues and identify practical, compliant solutions.
- Support targeted quality oversight initiatives, continuous improvement activities, and ongoing inspection readiness across manufacturing operations.
Education
Bachelor's degree in Engineering, Life Sciences, Microbiology, Technology, or a related technical field is preferred. Equivalent combinations of education, training, and relevant work experience may be considered. Candidates with substantial hands-on manufacturing or quality experience who do not hold a four-year degree are encouraged to apply.
Experience
Minimum of four years of relevant experience in Quality Assurance, Quality Control, manufacturing operations, or a related technical environment. Experience in pharmaceutical manufacturing, sterile operations, aseptic processing, or another regulated industry is strongly preferred. Candidates with transferable quality experience from other regulated manufacturing industries, including automotive or ISO-regulated environments, may also be considered.
Individuals with strong operational knowledge, practical troubleshooting capabilities, and experience supporting quality or compliance activities on the manufacturing floor are particularly encouraged to apply.
Knowledge, Skills and Abilities
- Working knowledge of cGMP, FDA regulatory requirements, and quality systems; familiarity with evolving EU GMP Annex 1 expectations is preferred.
- Understanding of aseptic processing, gowning requirements, and manufacturing-floor quality oversight.
- Strong analytical, troubleshooting, and problem-solving skills with the ability to make sound, risk-based quality decisions.
- Ability to coach employees, communicate concerns constructively, and influence others without direct supervisory authority.
- Strong interpersonal and communication skills with the ability to build productive relationships across Operations and Quality.
- Ability to manage competing priorities, adapt to changing business needs, and respond effectively to urgent quality concerns.
- Experience with deviation investigations, root cause analysis, change control, and technical documentation is preferred.
- Strong attention to detail, organizational skills, and commitment to maintaining regulatory compliance and inspection readiness.
Physical Requirements / Work Environment
This position requires significant time working within sterile pharmaceutical manufacturing areas, including classified cleanrooms and other controlled environments.
Employees must be able to stand and walk for extended periods, periodically bend, stoop, kneel, crouch, and move throughout manufacturing areas. The position may require lifting and moving materials weighing approximately 10–35 pounds.
The role requires appropriate aseptic and non-aseptic gowning, use of designated personal protective equipment, and compliance with established safety and facility procedures.
Candidates must be comfortable working a 12-hour rotating day-shift schedule and maintaining a consistent presence within active manufacturing operations.
BENEFITS
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.
Apply today!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255. Please include your contact information and specific details about your required accommodation to support you during the job application process.
Work Schedule
12 hr shift/days
Environmental Conditions
Able to lift 40 lbs. without assistance, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Title: QA Specialist III – Quality on the Floor (QOTF)
Location: Greenville, NC
Schedule: Day Shift | 6:00 AM – 6:00 PM | 2-2-3 Rotating Schedule
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
Greenville, NC
As part of the Drug Product Division (DPD), our Greenville, North Carolina site is a multi-purpose pharmaceutical development, manufacturing, and packaging campus supporting sterile injectable and oral solid dose drug products from development through commercialization.
This position supports sterile pharmaceutical manufacturing within our Manufacturing Quality Assurance organization. The Quality on the Floor (QOTF) team works directly alongside Manufacturing, Operations, and Quality leadership to maintain regulatory compliance, strengthen aseptic practices, and support continuous improvement.
Unlike traditional desk-based Quality Assurance positions, this role requires a significant manufacturing-floor presence, with approximately 60–75% of the workday spent observing operations, providing guidance, and supporting real-time quality decisions.
How will you make an impact?
As a QA Specialist III – Quality on the Floor (QOTF), you'll play a critical role in maintaining quality and compliance across sterile pharmaceutical manufacturing operations.
This is a highly visible, hands-on position where you'll work directly with manufacturing personnel to observe aseptic practices, assess production activities, identify potential compliance concerns, and provide practical guidance that supports safe and compliant manufacturing.
You'll help maintain a state of inspection readiness by conducting routine manufacturing walkthroughs, evaluating documentation and operational practices, and supporting investigations, deviations, and process improvements.
Success in this role requires more than technical quality knowledge. You'll need strong judgment, problem-solving abilities, and the interpersonal skills to coach employees, influence decisions, and navigate operational challenges while maintaining established quality standards.
This is an excellent opportunity for an experienced Quality professional or manufacturing specialist seeking to transition into a hands-on Quality Assurance role with direct operational impact and opportunities for professional growth.
What will you do?
- Perform routine Quality Assurance oversight of sterile manufacturing, filling, packaging, and inspection activities to ensure compliance with cGMP requirements and site procedures.
- Conduct documented manufacturing-floor walkthroughs, assessing facility conditions, equipment, personnel practices, aseptic technique, and production documentation.
- Observe manufacturing activities and provide real-time coaching, quality guidance, and support to operators and production leadership.
- Identify, document, and escalate potential quality concerns, compliance gaps, and operational risks while supporting appropriate corrective actions.
- Participate in deviation investigations, root cause analysis, RAPID event responses, and change control activities.
- Review and approve manufacturing documentation, batch records, procedures, training materials, and quality records as assigned.
- Collaborate with Manufacturing, Quality, and site leadership to troubleshoot process and equipment issues and identify practical, compliant solutions.
- Support targeted quality oversight initiatives, continuous improvement activities, and ongoing inspection readiness across manufacturing operations.
Education
Bachelor's degree in Engineering, Life Sciences, Microbiology, Technology, or a related technical field is preferred. Equivalent combinations of education, training, and relevant work experience may be considered. Candidates with substantial hands-on manufacturing or quality experience who do not hold a four-year degree are encouraged to apply.
Experience
Minimum of four years of relevant experience in Quality Assurance, Quality Control, manufacturing operations, or a related technical environment. Experience in pharmaceutical manufacturing, sterile operations, aseptic processing, or another regulated industry is strongly preferred. Candidates with transferable quality experience from other regulated manufacturing industries, including automotive or ISO-regulated environments, may also be considered.
Individuals with strong operational knowledge, practical troubleshooting capabilities, and experience supporting quality or compliance activities on the manufacturing floor are particularly encouraged to apply.
Knowledge, Skills and Abilities
- Working knowledge of cGMP, FDA regulatory requirements, and quality systems; familiarity with evolving EU GMP Annex 1 expectations is preferred.
- Understanding of aseptic processing, gowning requirements, and manufacturing-floor quality oversight.
- Strong analytical, troubleshooting, and problem-solving skills with the ability to make sound, risk-based quality decisions.
- Ability to coach employees, communicate concerns constructively, and influence others without direct supervisory authority.
- Strong interpersonal and communication skills with the ability to build productive relationships across Operations and Quality.
- Ability to manage competing priorities, adapt to changing business needs, and respond effectively to urgent quality concerns.
- Experience with deviation investigations, root cause analysis, change control, and technical documentation is preferred.
- Strong attention to detail, organizational skills, and commitment to maintaining regulatory compliance and inspection readiness.
Physical Requirements / Work Environment
This position requires significant time working within sterile pharmaceutical manufacturing areas, including classified cleanrooms and other controlled environments.
Employees must be able to stand and walk for extended periods, periodically bend, stoop, kneel, crouch, and move throughout manufacturing areas. The position may require lifting and moving materials weighing approximately 10–35 pounds.
The role requires appropriate aseptic and non-aseptic gowning, use of designated personal protective equipment, and compliance with established safety and facility procedures.
Candidates must be comfortable working a 12-hour rotating day-shift schedule and maintaining a consistent presence within active manufacturing operations.
BENEFITS
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.
Apply today!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255. Please include your contact information and specific details about your required accommodation to support you during the job application process.
Software Quality Assurance Job Roles in North Carolina
See all 451+ Software Quality Assurance Jobs in North Carolina
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Search Software Quality Assurance Jobs in North CarolinaSoftware Quality Assurance Jobs in North Carolina: Frequently Asked Questions
Which companies sponsor visas for software quality assurance roles in North Carolina?
Companies with a track record of sponsoring visas for QA engineers in North Carolina include Cisco, Red Hat, IBM, and Lenovo, all of which maintain significant operations in Research Triangle Park. Charlotte-based firms in fintech and healthcare technology, such as Bank of America's tech division and Teladoc Health, have also filed H-1B visa petitions for quality assurance positions. Sponsorship activity tends to concentrate at mid-to-large enterprises with established HR infrastructure.
Which visa types are most common for software quality assurance roles in North Carolina?
The H-1B is the most common visa category for software quality assurance engineers in North Carolina, as QA roles typically qualify as specialty occupations requiring at least a bachelor's degree in computer science, information systems, or a related field. Some candidates also enter through OPT or STEM OPT extensions after graduating from North Carolina universities before transitioning to H-1B sponsorship. Intracompany transferees at multinational firms may use the L-1B for specialized knowledge roles.
How to find software quality assurance visa sponsorship jobs in North Carolina?
Migrate Mate is built specifically for international job seekers and filters software quality assurance roles in North Carolina by visa sponsorship status, saving you from sifting through listings that don't offer sponsorship. You can browse QA openings across Raleigh, Durham, and Charlotte from employers who have previously sponsored work visas. Creating a profile on Migrate Mate and setting up alerts for North Carolina QA roles is a practical starting point for your search.
Which cities in North Carolina have the most software quality assurance sponsorship jobs?
Raleigh and Durham, situated within Research Triangle Park, account for the largest concentration of QA sponsorship roles in the state, driven by the density of technology and life sciences employers in the area. Charlotte is the second major hub, with QA demand coming from financial services technology teams and healthcare IT companies. Smaller clusters exist in Chapel Hill and Cary, particularly near university research partnerships and established tech campuses.
Are there state-specific factors that affect visa sponsorship for QA engineers in North Carolina?
North Carolina's strong university pipeline, including NC State, UNC Chapel Hill, and Duke, produces a steady flow of STEM graduates who pursue OPT and STEM OPT in QA roles before seeking H-1B sponsorship. Employers in Research Triangle Park are experienced with sponsorship processes, which can make the hiring experience smoother than in states with less established tech sectors. Prevailing wage requirements for QA positions are set at the federal level based on the job location's wage data, so RTP and Charlotte roles will reflect those respective metropolitan area rates.
What is the prevailing wage for sponsored software quality assurance jobs in North Carolina?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.