Quality Engineer Visa Sponsorship Jobs in Florida
Florida's quality engineer roles are concentrated in aerospace and defense around Orlando and the Space Coast, medical device manufacturing near Tampa and Miami, and semiconductor facilities statewide. Major employers including Lockheed Martin, Raytheon, and Johnson and Johnson have sponsored quality engineers here. The state's manufacturing base and growing tech sector create consistent demand for international candidates.
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Get Access To All JobsSenior Scientist, Quality Control Role
About Site
St. Petersburg is the primary softgel development and manufacturing facility in North America. The site has the capability to develop lipid formulations in a dedicated pilot plant which supports rapid transition from laboratory scale to clinical supply. Liquid in bottle, as well as Liquid fill Hard shell capabilities at the facility provide diversification and offerings that increase the speed to clinic. Within the Catalent network, we offer a broad range of integrated formulation and analytical services to solve your most difficult development and manufacturing challenges. Our analytical laboratory provides a full service offering from development of analytical methods to routine QC testing, supporting commercial and development stability studies. With capacity to generate over 18 billion softgels per year and servicing over 100 markets globally, the St. Petersburg site can handle any Over the Counter (OTC), Prescription (Rx), Medical Device, Controlled Substance, or Dietary Supplement manufacturing needs. The facility also contains a segregated hormone manufacturing area that meets current regulatory requirements. In addition to the manufacturing of traditional animal based gelatin softgels, St. Petersburg site manufactures products in non-gelatin based OptiShell® and Vegicaps® to expand the range of molecules that can be encapsulated.
Position Summary
We have an opportunity for a Senior Scientist, Quality Control to join our team. In this role, you will perform testing and release of materials and products in accordance with approved methods and regulatory standards. You will conduct microbiological, environmental, and analytical testing while ensuring compliance with cGMP and data integrity requirements. You will also support method development, validation, and technology transfers, while providing technical guidance and maintaining laboratory operations. This position offers the chance to contribute to high-quality manufacturing and continuous improvement initiatives.
Shift: Standard Hours, Monday through Friday
Location: St. Petersburg, FL
100% Onsite
The Role
- Perform testing and release of raw materials, in-process materials, intermediates, finished products, validation samples, and non-routine products in accordance with approved methods, specifications, and compendial requirements.
- Conduct microbiological testing, including cultivation and identification of bacteria and other microorganisms using selective and non-selective media, Gram staining, API, and other applicable techniques.
- Perform environmental and utility testing, including purified and potable water, compressed gases, manufacturing environmental monitoring, moisture testing, cleaning validation, and process validation support.
- Develop, modify, validate, and implement analytical testing procedures, assays, methods, and technologies; support new product qualifications, method transfers, and technology transfers.
- Analyze, interpret, and document results; perform statistical analyses; maintain laboratory notebooks, logbooks, reports, and LIMS records in compliance with cGMP, SOPs, data integrity standards, and regulatory requirements.
- Review and audit calculations, analytical data, and test results for accuracy and compliance; release samples through LIMS to Quality Assurance for final product disposition.
- Provide technical support, training, and work direction to scientists, analytical chemists, and laboratory technicians; assist with scheduling, internal audits, continuous improvement initiatives, and laboratory operations.
- Maintain laboratory equipment, supplies, cultures, reagents, standards, and media; ensure safe handling of potent and teratogenic compounds, proper hazardous waste disposal, and compliance with FDA, EPA, OSHA, and internal safety requirements.
- Work flexible hours, including evenings and weekends, as needed to support manufacturing and validation schedules.
The Candidate
Minimum Requirements
- Bachelor’s degree in Science or a related field required, preferably Chemistry, Microbiology, or Biology.
- 8 years of analytical laboratory experience required.
- Hands-on experience with UV spectroscopy, infrared spectroscopy, atomic absorption, high-performance liquid chromatography, gas chromatography, and dissolution testing.
- Proficiency in wet chemistry techniques, including titrations, extractions, digestions, and preparation of test solutions; experience with autoclaves and Vitek systems.
- Strong interpersonal, verbal, and written communication skills, with the ability to collaborate effectively with coworkers and maintain organized laboratory records and workflows.
- Individual may be required to sit, stand, walk regularly and occasionally lift up to 15 pounds; no lifting greater than 44.09 pounds without assistance.
- Be accessible to manufacturing, laboratory, and office staff.
- Can use required office equipment.
- Vision requirements include ability to differentiate color, have 20/30 vision with or without corrective lenses, read written documents, and frequent use of a computer monitor.
- Ability to work extended hours or off-hours as required.
Why You Should Join Catalent
- Positive and fast-paced working environment focusing on continually improving processes to remain innovative and dynamic.
- Competitive Paid Time Off plus 8 paid holidays.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition Reimbursement – support to finish your degree or earn a new one.
- Employee Resource Groups focusing on Diversity and Inclusion.
- Environmentally friendly, community engagement green initiatives including regular participation in Beach Clean-up.
- Defined career path and annual performance review and feedback process with potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- WellHub program to promote overall physical and mental wellness.
- Perkspot offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.
Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.
Senior Scientist, Quality Control Role
About Site
St. Petersburg is the primary softgel development and manufacturing facility in North America. The site has the capability to develop lipid formulations in a dedicated pilot plant which supports rapid transition from laboratory scale to clinical supply. Liquid in bottle, as well as Liquid fill Hard shell capabilities at the facility provide diversification and offerings that increase the speed to clinic. Within the Catalent network, we offer a broad range of integrated formulation and analytical services to solve your most difficult development and manufacturing challenges. Our analytical laboratory provides a full service offering from development of analytical methods to routine QC testing, supporting commercial and development stability studies. With capacity to generate over 18 billion softgels per year and servicing over 100 markets globally, the St. Petersburg site can handle any Over the Counter (OTC), Prescription (Rx), Medical Device, Controlled Substance, or Dietary Supplement manufacturing needs. The facility also contains a segregated hormone manufacturing area that meets current regulatory requirements. In addition to the manufacturing of traditional animal based gelatin softgels, St. Petersburg site manufactures products in non-gelatin based OptiShell® and Vegicaps® to expand the range of molecules that can be encapsulated.
Position Summary
We have an opportunity for a Senior Scientist, Quality Control to join our team. In this role, you will perform testing and release of materials and products in accordance with approved methods and regulatory standards. You will conduct microbiological, environmental, and analytical testing while ensuring compliance with cGMP and data integrity requirements. You will also support method development, validation, and technology transfers, while providing technical guidance and maintaining laboratory operations. This position offers the chance to contribute to high-quality manufacturing and continuous improvement initiatives.
Shift: Standard Hours, Monday through Friday
Location: St. Petersburg, FL
100% Onsite
The Role
- Perform testing and release of raw materials, in-process materials, intermediates, finished products, validation samples, and non-routine products in accordance with approved methods, specifications, and compendial requirements.
- Conduct microbiological testing, including cultivation and identification of bacteria and other microorganisms using selective and non-selective media, Gram staining, API, and other applicable techniques.
- Perform environmental and utility testing, including purified and potable water, compressed gases, manufacturing environmental monitoring, moisture testing, cleaning validation, and process validation support.
- Develop, modify, validate, and implement analytical testing procedures, assays, methods, and technologies; support new product qualifications, method transfers, and technology transfers.
- Analyze, interpret, and document results; perform statistical analyses; maintain laboratory notebooks, logbooks, reports, and LIMS records in compliance with cGMP, SOPs, data integrity standards, and regulatory requirements.
- Review and audit calculations, analytical data, and test results for accuracy and compliance; release samples through LIMS to Quality Assurance for final product disposition.
- Provide technical support, training, and work direction to scientists, analytical chemists, and laboratory technicians; assist with scheduling, internal audits, continuous improvement initiatives, and laboratory operations.
- Maintain laboratory equipment, supplies, cultures, reagents, standards, and media; ensure safe handling of potent and teratogenic compounds, proper hazardous waste disposal, and compliance with FDA, EPA, OSHA, and internal safety requirements.
- Work flexible hours, including evenings and weekends, as needed to support manufacturing and validation schedules.
The Candidate
Minimum Requirements
- Bachelor’s degree in Science or a related field required, preferably Chemistry, Microbiology, or Biology.
- 8 years of analytical laboratory experience required.
- Hands-on experience with UV spectroscopy, infrared spectroscopy, atomic absorption, high-performance liquid chromatography, gas chromatography, and dissolution testing.
- Proficiency in wet chemistry techniques, including titrations, extractions, digestions, and preparation of test solutions; experience with autoclaves and Vitek systems.
- Strong interpersonal, verbal, and written communication skills, with the ability to collaborate effectively with coworkers and maintain organized laboratory records and workflows.
- Individual may be required to sit, stand, walk regularly and occasionally lift up to 15 pounds; no lifting greater than 44.09 pounds without assistance.
- Be accessible to manufacturing, laboratory, and office staff.
- Can use required office equipment.
- Vision requirements include ability to differentiate color, have 20/30 vision with or without corrective lenses, read written documents, and frequent use of a computer monitor.
- Ability to work extended hours or off-hours as required.
Why You Should Join Catalent
- Positive and fast-paced working environment focusing on continually improving processes to remain innovative and dynamic.
- Competitive Paid Time Off plus 8 paid holidays.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition Reimbursement – support to finish your degree or earn a new one.
- Employee Resource Groups focusing on Diversity and Inclusion.
- Environmentally friendly, community engagement green initiatives including regular participation in Beach Clean-up.
- Defined career path and annual performance review and feedback process with potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- WellHub program to promote overall physical and mental wellness.
- Perkspot offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.
Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.
Quality Engineer Job Roles in Florida
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Search Quality Engineer Jobs in FloridaQuality Engineer Jobs in Florida: Frequently Asked Questions
Which companies sponsor visas for quality engineers in Florida?
Aerospace and defense contractors such as Lockheed Martin, Raytheon Technologies, and L3Harris Technologies have sponsored quality engineers in Florida, particularly along the Space Coast near Melbourne and Titusville. Medical device companies including Johnson and Johnson and Stryker sponsor roles in the Tampa Bay and Miami corridors. Large manufacturers and regulated-industry employers tend to have established immigration programs, making them more likely candidates for sponsorship.
Which visa types are most common for quality engineer roles in Florida?
The H-1B visa is the most common visa for quality engineers in Florida, as the role typically requires a bachelor's degree in engineering, manufacturing, or a related field, satisfying the specialty occupation requirement. Some candidates with Canadian or Mexican citizenship use the TN visa under the USMCA, which lists engineers as an eligible occupation. Candidates already in the U.S. on F-1 OPT can also work for qualifying employers while an H-1B visa petition is pending.
How to find quality engineer visa sponsorship jobs in Florida?
Migrate Mate is built specifically for international candidates and filters quality engineer roles in Florida by visa sponsorship status, so you are not sorting through listings from employers who do not sponsor. Search by role and state to surface active openings from aerospace, defense, and medical device employers concentrated in Orlando, Tampa, and the Space Coast. Setting up alerts on Migrate Mate for quality engineer positions in Florida helps you respond quickly when new sponsorship roles are posted.
Which cities in Florida have the most quality engineer sponsorship jobs?
Orlando and the Space Coast corridor, including Melbourne and Cape Canaveral, concentrate the most quality engineer sponsorship opportunities due to the density of aerospace and defense contractors. Tampa Bay is a secondary hub driven by medical device and manufacturing employers. Miami sees demand from international companies with Latin American operations, particularly in regulated manufacturing. Jacksonville has a smaller but growing cluster tied to logistics, automotive, and industrial manufacturing.
Are there any Florida-specific considerations for quality engineers seeking visa sponsorship?
Florida's aerospace and defense sector requires security clearances for many senior quality engineer roles, which are generally not accessible to candidates who are not U.S. citizens or permanent residents, narrowing the sponsorship pool. However, commercial manufacturing, medical device, and electronics quality roles do not carry that restriction. Florida has no state income tax, which affects total compensation comparisons. Florida universities such as the University of Florida and the University of Central Florida feed engineering graduates into local manufacturing pipelines, meaning employers are familiar with hiring international graduates.
What is the prevailing wage for sponsored quality engineer 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.