Quality Supervisor Visa Sponsorship Jobs in Florida
Florida's quality supervisor jobs span aerospace manufacturing in Melbourne and Palm Bay, food and beverage processing across Tampa and Orlando, and medical device production in the Miami corridor. Companies like Lockheed Martin, Tropicana, and Medline have sponsored quality roles in the state. International candidates with backgrounds in manufacturing quality systems are actively recruited.
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Job Summary
We are seeking a dedicated and experienced Quality Engineering Supervisor to drive and maintain the highest standards of product quality and regulatory compliance within our medical device manufacturing operations. This role is critical for ensuring adherence to FDA regulations and ISO standards, encompassing responsibilities from design control and supplier management to advanced statistical analysis and quality auditing. The ideal candidate will leverage their expertise to proactively identify and mitigate quality risks, contribute to continuous improvement, and uphold our commitment to excellence in a highly regulated environment.
Responsibilities
- Monitor and test the quality of products and processes in manufacturing environments, ensuring compliance with established standards and specifications.
- Ensure adherence to GMP (21 CFR 820) and ISO 13485 quality system requirements throughout all quality engineering activities.
- Respond to day-to-day production and customer quality issues related to production lines, resolving problems associated with process errors and non-conforming parts.
- Facilitate and promote the use of appropriate problem-solving techniques for effective root cause analysis and successful corrective and preventive actions (CAPA).
- Analyze customer complaints and conduct appropriate investigation to increase customer satisfaction.
- Utilize statistical knowledge, including sampling plans, control charts, Design of Experiments (DOE), and ANOVA, for process monitoring, improvement, and problem-solving.
- Conduct data mining, trend analysis, and present findings to identify areas for quality improvement and risk mitigation.
- Perform and support internal quality audits to ensure compliance with regulatory requirements and company standards.
- Manage and oversee quality aspects of contract manufacturers and other suppliers.
- Develop and maintain excellent technical documentation, including support for CE marking activities.
- Collaborate effectively with cross-functional teams, demonstrating excellent interpersonal skills, self-motivation, and a proactive approach to quality assurance.
- Oversee and mentor a team of Quality Technicians, providing guidance, training, and performance feedback to ensure effective execution of quality control activities and adherence to established procedures.
Qualifications
- Bachelor's degree in engineering preferred.
- Preferred certifications: ASQ CQE, CMQ/OE, CQA/CBA.
- 4+ years of experience preferred.
- Prior medical device manufacturing experience is required.
- GMP (21CFR820) and ISO 13485 knowledge and experience.
- Ability to perform internal quality audits.
- Prior experience in supplier management/contract manufacturing preferred.
- Knowledge of Design control in a FDA regulated industry.
- Statistical knowledge including sampling plans, control charts, DOE, ANOVA etc.
- Experience in data mining, trend analysis and presentation preferred.
- Excellent interpersonal skills, self-starter and self-motivated.
Anticipated salary range: $70,400 - $100,500
Bonus eligible: No
Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being.
- Medical, dental and vision coverage
- Paid time off plan
- Health savings account (HSA)
- 401k savings plan
- Access to wages before pay day with myFlexPay
- Flexible spending accounts (FSAs)
- Short- and long-term disability coverage
- Work-Life resources
- Paid parental leave
- Healthy lifestyle programs
Application window anticipated to close: 5/4/26 if interested in opportunity, please submit application as soon as possible.
The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate’s geographical location, relevant education, experience and skills and an evaluation of internal pay equity.
LI-JB1
Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.
Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.

Job Summary
We are seeking a dedicated and experienced Quality Engineering Supervisor to drive and maintain the highest standards of product quality and regulatory compliance within our medical device manufacturing operations. This role is critical for ensuring adherence to FDA regulations and ISO standards, encompassing responsibilities from design control and supplier management to advanced statistical analysis and quality auditing. The ideal candidate will leverage their expertise to proactively identify and mitigate quality risks, contribute to continuous improvement, and uphold our commitment to excellence in a highly regulated environment.
Responsibilities
- Monitor and test the quality of products and processes in manufacturing environments, ensuring compliance with established standards and specifications.
- Ensure adherence to GMP (21 CFR 820) and ISO 13485 quality system requirements throughout all quality engineering activities.
- Respond to day-to-day production and customer quality issues related to production lines, resolving problems associated with process errors and non-conforming parts.
- Facilitate and promote the use of appropriate problem-solving techniques for effective root cause analysis and successful corrective and preventive actions (CAPA).
- Analyze customer complaints and conduct appropriate investigation to increase customer satisfaction.
- Utilize statistical knowledge, including sampling plans, control charts, Design of Experiments (DOE), and ANOVA, for process monitoring, improvement, and problem-solving.
- Conduct data mining, trend analysis, and present findings to identify areas for quality improvement and risk mitigation.
- Perform and support internal quality audits to ensure compliance with regulatory requirements and company standards.
- Manage and oversee quality aspects of contract manufacturers and other suppliers.
- Develop and maintain excellent technical documentation, including support for CE marking activities.
- Collaborate effectively with cross-functional teams, demonstrating excellent interpersonal skills, self-motivation, and a proactive approach to quality assurance.
- Oversee and mentor a team of Quality Technicians, providing guidance, training, and performance feedback to ensure effective execution of quality control activities and adherence to established procedures.
Qualifications
- Bachelor's degree in engineering preferred.
- Preferred certifications: ASQ CQE, CMQ/OE, CQA/CBA.
- 4+ years of experience preferred.
- Prior medical device manufacturing experience is required.
- GMP (21CFR820) and ISO 13485 knowledge and experience.
- Ability to perform internal quality audits.
- Prior experience in supplier management/contract manufacturing preferred.
- Knowledge of Design control in a FDA regulated industry.
- Statistical knowledge including sampling plans, control charts, DOE, ANOVA etc.
- Experience in data mining, trend analysis and presentation preferred.
- Excellent interpersonal skills, self-starter and self-motivated.
Anticipated salary range: $70,400 - $100,500
Bonus eligible: No
Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being.
- Medical, dental and vision coverage
- Paid time off plan
- Health savings account (HSA)
- 401k savings plan
- Access to wages before pay day with myFlexPay
- Flexible spending accounts (FSAs)
- Short- and long-term disability coverage
- Work-Life resources
- Paid parental leave
- Healthy lifestyle programs
Application window anticipated to close: 5/4/26 if interested in opportunity, please submit application as soon as possible.
The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate’s geographical location, relevant education, experience and skills and an evaluation of internal pay equity.
LI-JB1
Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.
Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.
Quality Supervisor Job Roles in Florida
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Search Quality Supervisor Jobs in FloridaQuality Supervisor Jobs in Florida: Frequently Asked Questions
Which companies sponsor visas for quality supervisors in Florida?
Aerospace and defense contractors such as Lockheed Martin, L3Harris, and Northrop Grumman have sponsored quality roles in Florida's Space Coast corridor. In the Tampa Bay area, food processing companies including Tropicana and Coca-Cola bottling operations have filed LCAs for quality positions. Medical device firms near Miami and Orlando, including Medline and smaller contract manufacturers, also have sponsorship histories for quality supervisor roles.
Which visa types are most common for quality supervisor roles in Florida?
The H-1B is the most common visa for quality supervisors in Florida, provided the role requires a bachelor's degree in a specific field such as industrial engineering, manufacturing engineering, or quality management. Some multinational manufacturers transfer quality supervisors from overseas operations using the L-1A or L-1B. Candidates with extraordinary ability in quality systems or Six Sigma methodology may qualify for the O-1, though that standard is high.
Which cities in Florida have the most quality supervisor sponsorship jobs?
The Melbourne and Palm Bay area on the Space Coast concentrates aerospace and defense manufacturing, making it Florida's strongest market for quality supervisor sponsorship. Tampa and Orlando support food processing, consumer goods, and defense supply chain employers with active quality hiring. Miami's industrial corridor, particularly near Doral and Hialeah, hosts medical device and pharmaceutical manufacturers that regularly recruit quality supervisors from international candidate pools.
How to find quality supervisor visa sponsorship jobs in Florida?
Migrate Mate filters job listings specifically for roles where employers have indicated sponsorship availability, so you can search quality supervisor positions in Florida without manually sorting through listings that won't support a visa. The platform covers openings across Florida's aerospace, food processing, and medical device sectors. Filtering by location and job title on Migrate Mate lets you identify which Florida employers are actively hiring quality supervisors who need sponsorship.
Are there any Florida-specific considerations for quality supervisor sponsorship candidates?
Florida's quality supervisor market is closely tied to aerospace, defense, and regulated manufacturing industries, all of which have well-established H-1B sponsorship processes due to their federal compliance requirements. Florida also has a pipeline of manufacturing engineering and quality management graduates from the University of Florida and Florida Institute of Technology, so employer expectations for international candidates are generally high. Roles tied to defense contractors may also carry security clearance considerations that can affect sponsorship timelines.
What is the prevailing wage for sponsored quality supervisor jobs in Florida?
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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