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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Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Job Description
The QC Laboratory Technician 1 is involved in the daily analysis of manufactured product. The position carries the responsibility to release or reject product, and is involved in the maintenance, calibration and validation of equipment used in the analysis. The technician is expected to conduct the duties assigned with sound technical and business judgment and to follow the practices of the laboratory.
Overall Objectives and Responsibilities
- Works and communicates effectively with QC personnel and members of other departments (Manufacturing, Customer Support, Development, Maintenance, and Logistics).
- Understands and follows documents relevant to responsibilities, e.g., Work flows, Work Instructions, Checklists, Batch Records, and Logs.
- Makes Quality Control decisions according to the company's specifications in a time-sensitive manner after completion of training and demonstration of proficiency.
- Is able to multi-task product analysis while paying close attention to detail.
- Ensures proper daily operation of automated equipment.
- Keeps equipment and work environment clean, organized and ready for use.
- Has the ability to troubleshoot and correct commonly encountered issues with laboratory equipment.
- Maintains accurate production records according to requirements and in compliance with established Quality System standards.
- Maintains consistent quality and efficiency in all work processes.
- Follows all relevant company health, safety and regulatory policies, including handling of hazardous materials and wearing of proper PPE (personal protective equipment).
- Completes applicable on-site training programs successfully.
- Performs other related duties as assigned.
Qualifications Requirements
- BS or High School degree or equivalent.
- Proven ability to follow written and oral instructions.
- Ability to perform under pressure in a fast paced environment.
- Is prepared to work overtime during shifts other than the one assigned or weekends, if requested.
- Proven ability to work well in a team with little supervision.
- Ability to lift 35+ pounds.
Preferences
- Previous experience working in an ISO-9000 or cGMP environment.
- Previous experience in MALDI_TOF, mass spectrometry, ESI mass spectrometry, Capillary Gel Electrophoresis, and HPLC is a plus but not necessary.
- Previous experience working with general laboratory equipment.
- Microsoft Windows and Excel proficiency and experience using lab specific software.
- Previous experience working with Hazardous Chemicals.
Additional Information Schedule:
Tues to Sat 3:00 pm - 11:30 pm
What we offer:
- Excellent full time benefits including comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
Eurofins USA Genomic Services is a Disabled and Veteran Equal Employment Opportunity employer.
Company Description
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Job Description
The QC Laboratory Technician 1 is involved in the daily analysis of manufactured product. The position carries the responsibility to release or reject product, and is involved in the maintenance, calibration and validation of equipment used in the analysis. The technician is expected to conduct the duties assigned with sound technical and business judgment and to follow the practices of the laboratory.
Overall Objectives and Responsibilities
- Works and communicates effectively with QC personnel and members of other departments (Manufacturing, Customer Support, Development, Maintenance, and Logistics).
- Understands and follows documents relevant to responsibilities, e.g., Work flows, Work Instructions, Checklists, Batch Records, and Logs.
- Makes Quality Control decisions according to the company's specifications in a time-sensitive manner after completion of training and demonstration of proficiency.
- Is able to multi-task product analysis while paying close attention to detail.
- Ensures proper daily operation of automated equipment.
- Keeps equipment and work environment clean, organized and ready for use.
- Has the ability to troubleshoot and correct commonly encountered issues with laboratory equipment.
- Maintains accurate production records according to requirements and in compliance with established Quality System standards.
- Maintains consistent quality and efficiency in all work processes.
- Follows all relevant company health, safety and regulatory policies, including handling of hazardous materials and wearing of proper PPE (personal protective equipment).
- Completes applicable on-site training programs successfully.
- Performs other related duties as assigned.
Qualifications Requirements
- BS or High School degree or equivalent.
- Proven ability to follow written and oral instructions.
- Ability to perform under pressure in a fast paced environment.
- Is prepared to work overtime during shifts other than the one assigned or weekends, if requested.
- Proven ability to work well in a team with little supervision.
- Ability to lift 35+ pounds.
Preferences
- Previous experience working in an ISO-9000 or cGMP environment.
- Previous experience in MALDI_TOF, mass spectrometry, ESI mass spectrometry, Capillary Gel Electrophoresis, and HPLC is a plus but not necessary.
- Previous experience working with general laboratory equipment.
- Microsoft Windows and Excel proficiency and experience using lab specific software.
- Previous experience working with Hazardous Chemicals.
Additional Information Schedule:
Tues to Sat 3:00 pm - 11:30 pm
What we offer:
- Excellent full time benefits including comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
Eurofins USA Genomic Services is a Disabled and Veteran Equal Employment Opportunity employer.
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.