Medical Devices Visa Sponsorship Jobs in Kentucky
Kentucky's medical devices sector centers around Louisville's established medical technology hub, with companies like Humana, KentuckyOne Health, and Medtronic's regional operations. The state's proximity to major healthcare markets and lower operational costs attract both established manufacturers and emerging medtech startups seeking skilled international talent.
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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.
Medical Devices Job Roles in Kentucky
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Search Medical Devices Jobs in KentuckyMedical Devices Jobs in Kentucky: Frequently Asked Questions
Which medical devices companies sponsor visas in Kentucky?
Major sponsors include Humana's health technology division in Louisville, Medtronic's Louisville facility, and ResMed's operations in the region. Smaller medtech companies like Appriss Health and healthcare IT firms also sponsor visas, particularly for software engineers, biomedical engineers, and regulatory affairs specialists with medical device experience.
How to find medical devices visa sponsorship jobs in Kentucky?
Use Migrate Mate to search specifically for medical devices positions in Kentucky that offer visa sponsorship. The platform filters roles by industry and visa sponsorship availability, showing opportunities at both large medical device manufacturers and emerging health technology companies throughout Louisville and Lexington metro areas.
Which visa types are most common for medical devices roles in Kentucky?
H-1B visas dominate for engineering positions like biomedical engineers, software developers, and quality assurance specialists. O-1 visas are used for senior researchers and regulatory experts with specialized medical device expertise. TN visas serve Canadian and Mexican professionals in engineering and clinical research roles.
Which cities in Kentucky have the most medical devices sponsorship jobs?
Louisville leads with the highest concentration, hosting major medical device operations and health technology companies. Lexington follows with University of Kentucky research partnerships and smaller medtech firms. Northern Kentucky near Cincinnati also offers opportunities due to proximity to Ohio's medical device corridor.
What prevailing wage considerations apply to medical devices jobs in Kentucky?
Kentucky's lower cost of living translates to competitive prevailing wages that are often 10-20% below coastal markets. This benefits employers filing H-1B petitions while still offering attractive compensation packages. Biomedical engineers and regulatory specialists typically see the strongest wage premiums in the Louisville market.
What is the prevailing wage for sponsored medical devices jobs in Kentucky?
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.