Quality Assurance Inspector Jobs in USA with Visa Sponsorship
Quality Assurance Inspectors can qualify for H-1B sponsorship when the role requires specialized engineering or technical knowledge, particularly in regulated industries like pharmaceuticals, medical devices, or aerospace where quality systems expertise is essential for compliance. For detailed occupation requirements, see the O*NET profile.
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Get Access To All JobsWould you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
This position is on-site only at our Clayton, NC Facility.
Hours: 1st shift Monday - Friday 5:00am - 1:30pm
Summary
Quality Assurance Inspectors work with manufacturing operations during the production process, by approving the raw materials and associated documentation for incoming plasma shipments from donor collection centers and the in-process production batches (Production Units - PUs) at the Plasma Logistics Center (PLC). Quality Assurance Inspectors identify and document deviations of both materials and the manufacturing process and ensure these deviations are corrected to ensure a better finished product for prospective customers.
Primary Responsibilities
- Approves incoming plasma shipment documentation and raw materials by confirming specifications, rejects and returns unacceptable materials as directed by QA Supervisor.
- Generates and documents non-conformance of plasma units or procedures associated with plasma shipments, PUs or final plasma lots.
- Approves PUs by confirming customer and regulatory specifications and communicating required adjustments to the QA Supervisor.
- Responsible for inspecting final outgoing plasma lot shipments to ensure all pallets are properly packaged and loaded for sales and distribution.
- Investigates and reports in-process/final product and processes that do not meet quality specifications and document in a deviation report.
- Participates in the writing or revision of policies and standard operating procedures related to Source Plasma and quality systems at GPLC.
- Executes repetitive functions with strict adherence to procedures and maintains record accountability.
- Documents approval activities in the organizations computer system.
Knowledge, Skills, And Abilities
- Good communication skills with the ability to express ideas with clarity and thoroughness in both verbal and written communications.
- Proactive, results oriented with a strong attention to detail.
- Strong interpersonal skills to interface with manufacturing operators and various levels of management as well as with support and service departments.
- Ability to work in a team-oriented environment and follow safety guidelines.
- Must be computer literate with experience in the use of Microsoft applications.
- Able to perform basic arithmetic functions including addition, subtraction, multiplication, division and using decimals.
Education And Experience
- High School diploma or GED.
- Typically requires a minimum of 1 year of Quality Assurance related experience and 2 years working in pharmaceuticals. Experience in the pharmaceutical, plasma/blood banking or medical device industry is ideal and working knowledge of cGMP helpful.
- Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level typically requires an Associate’s degree plus 2 years of experience, an equivalent could include 4 years of experience or a Bachelor's degree.
This position is eligible to participate in up to 5% of the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, PTO, up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us!
Third Party Agency And Recruiter Notice
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.
Location: NORTH AMERICA : USA : NC-Clayton:USNC0002 - Clayton
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
This position is on-site only at our Clayton, NC Facility.
Hours: 1st shift Monday - Friday 5:00am - 1:30pm
Summary
Quality Assurance Inspectors work with manufacturing operations during the production process, by approving the raw materials and associated documentation for incoming plasma shipments from donor collection centers and the in-process production batches (Production Units - PUs) at the Plasma Logistics Center (PLC). Quality Assurance Inspectors identify and document deviations of both materials and the manufacturing process and ensure these deviations are corrected to ensure a better finished product for prospective customers.
Primary Responsibilities
- Approves incoming plasma shipment documentation and raw materials by confirming specifications, rejects and returns unacceptable materials as directed by QA Supervisor.
- Generates and documents non-conformance of plasma units or procedures associated with plasma shipments, PUs or final plasma lots.
- Approves PUs by confirming customer and regulatory specifications and communicating required adjustments to the QA Supervisor.
- Responsible for inspecting final outgoing plasma lot shipments to ensure all pallets are properly packaged and loaded for sales and distribution.
- Investigates and reports in-process/final product and processes that do not meet quality specifications and document in a deviation report.
- Participates in the writing or revision of policies and standard operating procedures related to Source Plasma and quality systems at GPLC.
- Executes repetitive functions with strict adherence to procedures and maintains record accountability.
- Documents approval activities in the organizations computer system.
Knowledge, Skills, And Abilities
- Good communication skills with the ability to express ideas with clarity and thoroughness in both verbal and written communications.
- Proactive, results oriented with a strong attention to detail.
- Strong interpersonal skills to interface with manufacturing operators and various levels of management as well as with support and service departments.
- Ability to work in a team-oriented environment and follow safety guidelines.
- Must be computer literate with experience in the use of Microsoft applications.
- Able to perform basic arithmetic functions including addition, subtraction, multiplication, division and using decimals.
Education And Experience
- High School diploma or GED.
- Typically requires a minimum of 1 year of Quality Assurance related experience and 2 years working in pharmaceuticals. Experience in the pharmaceutical, plasma/blood banking or medical device industry is ideal and working knowledge of cGMP helpful.
- Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level typically requires an Associate’s degree plus 2 years of experience, an equivalent could include 4 years of experience or a Bachelor's degree.
This position is eligible to participate in up to 5% of the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, PTO, up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us!
Third Party Agency And Recruiter Notice
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.
Location: NORTH AMERICA : USA : NC-Clayton:USNC0002 - Clayton
How to Get Visa Sponsorship in Quality Assurance Inspector
Target regulated industries for stronger H-1B cases
Focus on pharmaceutical, medical device, aerospace, or automotive companies where QA roles require specialized technical knowledge and regulatory compliance expertise that clearly meets specialty occupation requirements.
Highlight technical degree relevance in applications
Emphasize how your engineering, chemistry, or life sciences degree directly relates to quality systems, statistical analysis, and regulatory standards required for the specific inspection role.
Emphasize regulatory knowledge and certifications
Showcase expertise in ISO standards, FDA regulations, Six Sigma, or industry-specific quality frameworks that demonstrate the specialized knowledge needed for the position.
Consider alternative visa paths for entry-level roles
If QA positions don't require a degree, explore E-3 (Australians), TN (Canadians/Mexicans), or O-1 visas based on your nationality and experience level.
Document complex quality system experience
Prepare detailed examples of quality management system implementations, process validations, or regulatory audits that demonstrate the technical complexity of your work.
Research employer sponsorship history carefully
Check OFLC disclosure data for companies that have sponsored QA roles successfully, as not all employers understand how these positions can qualify for H-1B.
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Get Access To All JobsFrequently Asked Questions
Do Quality Assurance Inspector positions qualify for H-1B sponsorship?
QA Inspector roles can qualify for H-1B sponsorship when they require specialized technical knowledge, typically in regulated industries like pharmaceuticals or medical devices. The position must require a bachelor's degree in engineering, chemistry, or related technical field. Basic inspection roles that only need general training typically don't qualify as specialty occupations.
What degree do I need for H-1B sponsorship as a Quality Assurance Inspector?
Most successful H-1B cases for QA Inspectors require a bachelor's degree in engineering, chemistry, biology, or related technical field. The degree must directly relate to the technical aspects of the role, such as understanding manufacturing processes, statistical analysis, or regulatory compliance requirements specific to the industry.
Which industries offer the best sponsorship opportunities for QA roles?
Pharmaceutical, medical device, aerospace, and automotive industries offer the strongest H-1B sponsorship opportunities for QA roles. These regulated industries require specialized technical knowledge of quality systems, regulatory compliance, and process validation that clearly demonstrates the need for a degreed professional rather than general training.
Can Quality Assurance Inspectors get sponsored without prior U.S. experience?
Yes, international candidates can get sponsored for QA Inspector roles, especially if they have experience with international quality standards like ISO 9001, ISO 13485, or regulatory frameworks. Employers value candidates who understand global quality systems and can help with international compliance requirements.
What alternatives exist if my QA role doesn't qualify for H-1B?
If your QA role doesn't meet H-1B specialty occupation requirements, consider the E-3 visa (Australians), TN visa (Canadians/Mexicans), or O-1 for extraordinary ability in quality management. Some candidates also pursue roles with greater technical complexity or regulatory responsibility that better support H-1B petitions.
What is the prevailing wage requirement for sponsored Quality Assurance Inspector jobs?
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.
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