Quality Control Technician Jobs in USA with Visa Sponsorship
Quality control technicians find the most viable sponsorship at pharmaceutical manufacturers, semiconductor fabs, medical device companies, and food processing facilities where Pfizer, Intel, Medtronic, and Nestle sponsor for roles performing analytical testing, in-process inspection, and batch documentation that require degrees in chemistry, biology, or engineering technology. H-1B visa classification is strongest when positions involve laboratory analysis, SPC methodology, and regulatory compliance under FDA or ISO frameworks, while EB-3 skilled worker green card sponsorship provides experienced certified technicians without bachelor's degrees a direct permanent residency pathway through employers demonstrating domestic recruitment failure.
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Get Access To All JobsINTRODUCTION
QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most – home to hospital, lab to clinic.
Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all.
THE ROLE
As we continue to grow as QuidelOrtho, we are seeking a Quality Control Technician II. The Quality Control Technician II performs a variety of product inspections, generally of finished goods, components, incoming raw materials, or new products, by observing, measuring, and recording data.
This position is in Pompano Beach Florida.
Schedule: This is a 2nd shift position 2:30 pm -10:30 pm
THE RESPONSIBILITIES
- Compare inspection results to defined requirements or specifications and documents differences found.
- Makes accept/reject decision based on established guidelines and documented procedure requirements.
- Ensure that established sampling and statistical process control procedures are followed.
- Performs in process testing and identifies out of specification product.
- Makes accept/reject decision based on established guidelines, documented procedure requirements and knowledge of production.
- Ensures proper disposition of defective products.
- Provides technical support to quality, quality engineering and product support.
- Provides training to new and existing employees as required and reviews work of others.
- Provides support for high priority site projects.
- Possesses strong conflict resolution, change management, communication (written and verbal), organizational management, business ethics and analytical reasoning skills and demonstrates the ability to work in a diverse cross-functional environment.
- Has specialized expertise, typically developed through a combination of job-related training and considerable work experience.
- May participate in internal and external audits as SME (Subject Matter Expert) for the in-coming inspection processes.
- Perform other work-related duties as assigned.
THE INDIVIDUAL
Required:
- High School Diploma/GED with a minimum of 2 years’ experience; or an Associate’s degree and 1 year of experience or a Bachelor’s degree or equivalent combination of education and experience.
Preferred:
- Ability to demonstrate flexibility and adaptability; ability to prioritize within a changing business environment.
- Demonstrates attention detail; ability to stay focused on the task at hand for long periods of time.
- Ability to effectively communicate; demonstrate a sense of urgency to complete production schedule on time; accepts personal responsibility for the quality and timeliness of work.
- Basic computer skills i.e. Microsoft Office (Word, Excel, Outlook).
- Ability to work both independently and within a team environment.
- Be an advocate for a safe work environment and be responsible for my safety and the safety of others.
THE KEY WORKING INTERACTIONS
Internal: Manufacturing, Product Support, Formulations, Engineering, Material Management, Quality Labs, Quality Engineering.
External: Suppliers.
THE WORK ENVIRONMENT
- Protective equipment required: gloves, eyewear, lab coat.
- Biological hazards: blood products.
- Weekends and Overtime may be required.
THE PHYSICAL DEMANDS
- Close Visual Acuity
- Occasional repetitive movements of hands
- Occasional lifting of 10-35 lbs.
- Occasional use of power jack.
- Occasional pushing and pulling.
Equal Employment Opportunity
QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform their duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at recruiting@quidelortho.com.
INTRODUCTION
QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most – home to hospital, lab to clinic.
Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all.
THE ROLE
As we continue to grow as QuidelOrtho, we are seeking a Quality Control Technician II. The Quality Control Technician II performs a variety of product inspections, generally of finished goods, components, incoming raw materials, or new products, by observing, measuring, and recording data.
This position is in Pompano Beach Florida.
Schedule: This is a 2nd shift position 2:30 pm -10:30 pm
THE RESPONSIBILITIES
- Compare inspection results to defined requirements or specifications and documents differences found.
- Makes accept/reject decision based on established guidelines and documented procedure requirements.
- Ensure that established sampling and statistical process control procedures are followed.
- Performs in process testing and identifies out of specification product.
- Makes accept/reject decision based on established guidelines, documented procedure requirements and knowledge of production.
- Ensures proper disposition of defective products.
- Provides technical support to quality, quality engineering and product support.
- Provides training to new and existing employees as required and reviews work of others.
- Provides support for high priority site projects.
- Possesses strong conflict resolution, change management, communication (written and verbal), organizational management, business ethics and analytical reasoning skills and demonstrates the ability to work in a diverse cross-functional environment.
- Has specialized expertise, typically developed through a combination of job-related training and considerable work experience.
- May participate in internal and external audits as SME (Subject Matter Expert) for the in-coming inspection processes.
- Perform other work-related duties as assigned.
THE INDIVIDUAL
Required:
- High School Diploma/GED with a minimum of 2 years’ experience; or an Associate’s degree and 1 year of experience or a Bachelor’s degree or equivalent combination of education and experience.
Preferred:
- Ability to demonstrate flexibility and adaptability; ability to prioritize within a changing business environment.
- Demonstrates attention detail; ability to stay focused on the task at hand for long periods of time.
- Ability to effectively communicate; demonstrate a sense of urgency to complete production schedule on time; accepts personal responsibility for the quality and timeliness of work.
- Basic computer skills i.e. Microsoft Office (Word, Excel, Outlook).
- Ability to work both independently and within a team environment.
- Be an advocate for a safe work environment and be responsible for my safety and the safety of others.
THE KEY WORKING INTERACTIONS
Internal: Manufacturing, Product Support, Formulations, Engineering, Material Management, Quality Labs, Quality Engineering.
External: Suppliers.
THE WORK ENVIRONMENT
- Protective equipment required: gloves, eyewear, lab coat.
- Biological hazards: blood products.
- Weekends and Overtime may be required.
THE PHYSICAL DEMANDS
- Close Visual Acuity
- Occasional repetitive movements of hands
- Occasional lifting of 10-35 lbs.
- Occasional use of power jack.
- Occasional pushing and pulling.
Equal Employment Opportunity
QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform their duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at recruiting@quidelortho.com.
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Get Access To All JobsTips for Finding Visa Sponsorship as a Quality Control Technician
Pharmaceutical QC Laboratories Sponsor at the Highest Volume
Pfizer, Merck, J&J, Abbott, Amgen, and AbbVie sponsor for QC technicians performing HPLC, dissolution, stability, and microbial testing under FDA GMP requirements. Chemistry or biology degrees make H-1B classification viable for laboratory-based QC roles paying $48,000 to $75,000.
Semiconductor QC Technicians Support CHIPS Act Expansion
Intel, TSMC, Samsung, Micron, and GlobalFoundries sponsor for QC technicians performing wafer metrology, defect inspection, and statistical process monitoring at new U.S. fabs. These roles pay $50,000 to $80,000 with cleanroom premiums.
Medical Device QC Requires FDA 21 CFR 820 Knowledge
Medtronic, Stryker, Abbott, Becton Dickinson, and Boston Scientific sponsor for QC technicians performing incoming inspection, final release testing, and complaint sample analysis. Engineering technology or biomedical degrees strengthen H-1B arguments.
Target QC Analyst or QC Engineer Titles for Stronger Classification
Positions titled Quality Control Analyst or QC Engineer at the same companies performing equivalent laboratory and analytical work carry degree requirements supporting H-1B. Always pursue analyst or engineer titles over technician titles when your credentials qualify.
EB-3 Skilled Worker Provides a Green Card Without a Degree
QC technicians with ASQ CQI certification and two or more years of testing and inspection experience qualify for EB-3 skilled worker sponsorship. Processing takes 2 to 4 years but leads directly to permanent residency without requiring H-1B first.
Food and Beverage QC Technicians Also Have Pathways
Nestle, PepsiCo, Tyson, Cargill, and General Mills sponsor for QC technicians performing microbiological testing, chemical analysis, and HACCP verification in food safety laboratories. Food science degrees make H-1B classification viable for laboratory roles.
Quality Control Technician jobs are hiring across the US. Find yours.
Find Quality Control Technician JobsFrequently Asked Questions
Can quality control technicians get visa sponsorship?
Yes, through specific pathways. Pharmaceutical, semiconductor, and medical device QC technicians with chemistry, biology, or engineering technology degrees qualify for H-1B. EB-3 skilled worker green card is available for experienced certified technicians through employers proving domestic recruitment failure.
What is the typical salary for QC Technician roles?
General QC technicians earn $36,000 to $52,000. Pharmaceutical QC lab technicians earn $48,000 to $76,000. Semiconductor QC technicians earn $50,000 to $82,000. Medical device QC technicians earn $44,000 to $70,000. QC analysts and engineers earn $60,000 to $95,000.
Which industries sponsor QC Technicians most frequently?
Pharmaceutical and biotech companies lead for laboratory QC testing roles. Semiconductor manufacturers sponsor for metrology and defect inspection. Medical device companies sponsor for FDA-regulated quality control. Food and beverage manufacturers sponsor for food safety laboratory positions.
How to find Quality Control Technician jobs with visa sponsorship?
To find Quality Control Technician jobs with visa sponsorship, use Migrate Mate, which specializes in connecting international candidates with sponsored positions. Focus your search on manufacturing companies, pharmaceutical firms, food processing plants, and automotive manufacturers that frequently sponsor H-1B, TN, and other work visas for quality control professionals with technical expertise and relevant certifications.
What qualifications improve a QC Technician's sponsorship prospects?
A chemistry, biology, food science, or engineering technology degree opens H-1B pathways. ASQ CQI, CQT, or Six Sigma certifications demonstrate quality methodology expertise. HPLC, GC, dissolution, and CMM instrument proficiency differentiates you from general inspection technicians.
What is the career progression for a sponsored QC Technician?
The path moves from QC technician to senior technician to QC analyst to QC manager to director of quality control. QC managers at pharmaceutical companies earn $90,000 to $130,000. Directors earn $125,000 to $185,000. Some technicians transition into quality assurance, regulatory affairs, or analytical development.
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