Medical Devices OPT Jobs in Kentucky
F-1 OPT medical devices jobs in Kentucky are concentrated around Louisville, where major employers like Kindred Healthcare and Humana intersect with a growing medtech supply chain, and Lexington, home to several biomedical manufacturing and R&D operations. Kentucky's medical devices sector spans surgical equipment, diagnostics, and implantable device manufacturing, giving OPT candidates multiple entry points across engineering, quality, and regulatory functions.
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Get Access To All JobsCompany Description
SGS is the world's leading inspection, verification, testing and certification company. SGS is recognized as the global benchmark for quality and integrity. With more than 97,000 employees, SGS operates a network of over 2,600 offices and laboratories around the world.
Job Description
- Drive quality strategy and objectives for areas of responsibility using appropriate reporting tools.
- Lead Good Manufacturing Practices and Risk Assessments, develop corrective actions based on incident investigations. Attend seminars and keep updated.
- Maintain training materials and train associates in microbiology procedures and hygiene processes.
- Monitor quality KPIs and report monthly on the status of KPIs.
- Work with operations staff to define quality procedures and establish and maintain control and documentation procedures.
- Pest control own and manage the overall process and documentation.
- Effectively manage customer and supplier complaints and actively monitor supplier quality complaints and issues.
- Own reporting, trending, and analysis of micro results and metrics. Take appropriate actions on trends.
- Develop and lead design solutions and influence operational solutions.
- Develops and maintains the quality strategy in line with KPIs and global initiatives.
- Raise awareness of customer requirements across the manufacturing site and lead cross-functional quality improvement teams/projects.
- Support global audit management including leading internal audits, and Hygiene audits (system, process, product, customer and external certification audits). Ensure compliance.
- Instruct and organize quality training for stakeholders and local quality organization.
- Manage the quality control lab, develop continuous improvement plans for the plant and production line.
- Input requirements the design of new plant systems. Verify and validate for hygienic design requirements and outcomes.
- Interface with R&D and others on new innovation, trials, and analytical method development.
- Lead the investigation of out of specification microbiological and related results. Culture and identify microorganisms and lead corrective action development.
Qualifications
- Bachelor’s degree in Microbiology, Biology, Chemistry, Pharmaceutical Sciences, or a related scientific field.
- Master’s degree is a plus.
- 3–7+ years of experience in a pharmaceutical, biotech, or other GMP-regulated environment.
- Hands-on experience with microbiological testing, environmental monitoring, and contamination control.
- Experience supporting FDA inspections and regulatory audits.
- Proven experience investigating out-of-specification (OOS) or environmental excursions.
- Experience working in cleanroom or controlled environments.
- Strong knowledge of:
- cGMP (Current Good Manufacturing Practices)
- FDA regulations (21 CFR Parts 210/211)
- Environmental Monitoring (EM) programs (air, surface, personnel)
- Aseptic processing and contamination control strategies
- CAPA, deviation, and root cause investigation processes
Additional Information
SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.
This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company’s rights to assign or reassign duties and responsibilities to this job at any time.
If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call 201-508-3149 for assistance and leave a message. You will receive a callback. Please note, this phone number is not for general employment information but is only for individuals who are experiencing difficulty applying for a position due to a disability.
Company Description
SGS is the world's leading inspection, verification, testing and certification company. SGS is recognized as the global benchmark for quality and integrity. With more than 97,000 employees, SGS operates a network of over 2,600 offices and laboratories around the world.
Job Description
- Drive quality strategy and objectives for areas of responsibility using appropriate reporting tools.
- Lead Good Manufacturing Practices and Risk Assessments, develop corrective actions based on incident investigations. Attend seminars and keep updated.
- Maintain training materials and train associates in microbiology procedures and hygiene processes.
- Monitor quality KPIs and report monthly on the status of KPIs.
- Work with operations staff to define quality procedures and establish and maintain control and documentation procedures.
- Pest control own and manage the overall process and documentation.
- Effectively manage customer and supplier complaints and actively monitor supplier quality complaints and issues.
- Own reporting, trending, and analysis of micro results and metrics. Take appropriate actions on trends.
- Develop and lead design solutions and influence operational solutions.
- Develops and maintains the quality strategy in line with KPIs and global initiatives.
- Raise awareness of customer requirements across the manufacturing site and lead cross-functional quality improvement teams/projects.
- Support global audit management including leading internal audits, and Hygiene audits (system, process, product, customer and external certification audits). Ensure compliance.
- Instruct and organize quality training for stakeholders and local quality organization.
- Manage the quality control lab, develop continuous improvement plans for the plant and production line.
- Input requirements the design of new plant systems. Verify and validate for hygienic design requirements and outcomes.
- Interface with R&D and others on new innovation, trials, and analytical method development.
- Lead the investigation of out of specification microbiological and related results. Culture and identify microorganisms and lead corrective action development.
Qualifications
- Bachelor’s degree in Microbiology, Biology, Chemistry, Pharmaceutical Sciences, or a related scientific field.
- Master’s degree is a plus.
- 3–7+ years of experience in a pharmaceutical, biotech, or other GMP-regulated environment.
- Hands-on experience with microbiological testing, environmental monitoring, and contamination control.
- Experience supporting FDA inspections and regulatory audits.
- Proven experience investigating out-of-specification (OOS) or environmental excursions.
- Experience working in cleanroom or controlled environments.
- Strong knowledge of:
- cGMP (Current Good Manufacturing Practices)
- FDA regulations (21 CFR Parts 210/211)
- Environmental Monitoring (EM) programs (air, surface, personnel)
- Aseptic processing and contamination control strategies
- CAPA, deviation, and root cause investigation processes
Additional Information
SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.
This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company’s rights to assign or reassign duties and responsibilities to this job at any time.
If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call 201-508-3149 for assistance and leave a message. You will receive a callback. Please note, this phone number is not for general employment information but is only for individuals who are experiencing difficulty applying for a position due to a disability.
OPT Medical Devices Job Roles in Kentucky
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Search Medical Devices Jobs in KentuckyMedical Devices OPT Sponsorship Jobs in Kentucky: Frequently Asked Questions
Which medical devices companies sponsor F-1 OPT visas in Kentucky?
Kentucky-based medical devices employers that have sponsored international workers include operations tied to surgical and implantable device manufacturing in the Louisville metro, along with contract manufacturers and distributor networks across the state. Companies with established international hiring processes, particularly those with dedicated HR or legal teams, are most likely to support F-1 OPT authorization. Reviewing employer OPT sponsorship history through DOL disclosure data can help narrow your search.
Which cities in Kentucky have the most medical devices F-1 OPT sponsorship jobs?
Louisville is Kentucky's primary hub for medical devices employment, supported by its large healthcare infrastructure and proximity to distribution networks along major logistics corridors. Lexington has a secondary cluster, particularly in biomedical research and manufacturing roles tied to the University of Kentucky's health sciences programs. Smaller pockets of medical devices activity exist in Bowling Green and northern Kentucky, near the Cincinnati metro border.
What types of medical devices roles typically qualify for F-1 OPT sponsorship?
Roles in quality assurance, regulatory affairs, manufacturing engineering, biomedical engineering, and R&D are among the most common medical devices positions that align with F-1 OPT work authorization. These roles typically require a relevant degree in engineering, life sciences, or a related technical field, which supports both the OPT employment eligibility and the employer's ability to later pursue H-1B visa sponsorship if needed. General administrative or sales-only roles are less commonly tied to OPT pathways.
How do I find medical devices F-1 OPT sponsorship jobs in Kentucky?
Migrate Mate is built specifically for international students and professionals seeking visa-sponsored roles, and filters directly for F-1 OPT medical devices jobs in Kentucky. Rather than sorting through general job boards where sponsorship status is often unclear, Migrate Mate surfaces employers who have demonstrated willingness to work with OPT candidates in the medical devices industry. Filtering by Kentucky and the medical devices category gives you a focused, relevant results set.
Are there any state-specific or industry-specific considerations for F-1 OPT in Kentucky's medical devices sector?
Kentucky's medical devices manufacturing environment means many roles involve hands-on lab or production floor work, which is fully compatible with STEM OPT extensions for eligible degree holders in engineering or life sciences. Students pursuing STEM OPT extensions should confirm their degree program appears on the official STEM-designated degree program list maintained by DHS. Employers in regulated manufacturing environments also tend to require E-Verify enrollment, which is a standard requirement for all OPT employment regardless of state.