Medical Devices Jobs in Kentucky with H-1B Sponsorship
Kentucky's medical devices sector spans Louisville, Lexington, and the broader Bluegrass region, with employers like Kindred Healthcare affiliates, Medline, and established device distributors filing H-1B petitions for engineers, regulatory specialists, and quality assurance professionals. The state's manufacturing base and proximity to major health systems create consistent demand for internationally trained talent in this field.
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Get Access To All JobsINTRODUCTION
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.
ABOUT THE JOB
Since 1999, Eurofins Genomics Blue Heron has been a pioneer in the gene synthesis industry and has delivered tens of millions of base pairs of perfectly accurate genes to thousands of customers worldwide using its proprietary GeneMaker® multi-technology platform. We are 100% committed to serving our customers with high quality, strict confidentiality standards, and improved business efficiency. In mid-2019 Blue Heron was acquired by Eurofins Scientific and became a partner of the Eurofins Genomics US division. Blue Heron is searching for manufacturing Manager to join our team. The manufacturing Manager will report to the President of Blue Heron Biotech and lead the day-to-day operations of the gene synthesis operations at the Blue Heron.
RESPONSIBILITIES/ACCOUNTABILITIES
- Oversees, directs, coordinates and prioritizes the daily activities related to Blue Heron GeneMaker® platform including Gene synthesis, plasmid DNA and IVTmRNA production.
- Plan and organize the production schedule while ensuring compliance with safety regulations.
- Recruit, train, develop, and retain staff while ensuring adherence to essential training schedules.
- Identify and analyze problems, develop solutions, and implement corrective actions effectively.
- Act as the primary troubleshooting expert for the production group, identifying and resolving technical and operational issues.
- Manage vendor relationships, negotiate pricing, and oversee the ordering and purchasing of production materials and supplies.
- Support the development, implementation, and optimal use of equipment and systems to enhance efficiency, productivity, and profitability at all levels of manufacturing.
- Implement process controls, validations and metrics for the production equipment to monitor the stability of the manufacturing process while maintaining compliance with ISO 13485:2016 standards.
- Ensure Blue Heron manufacturing group complies with all government regulations and industry standards.
BASIC QUALIFICATIONS
- Bachelor’s degree or higher in a related scientific discipline required; MS or PhD in Molecular Biology preferred.
- Experience working with LIMS and proficiency in molecular biology techniques required.
- 6+ years of direct manufacturing and operations experience, including at least 3 years of managerial and supervisory responsibilities.
- Hands-on, self-motivated, and highly organized, with a demonstrated ability to lead teams effectively.
- Strong communication and interpersonal skills.
- Experience with manufacturing scale up is preferred.
- Experience with ISO or GMP certification and process is a plus.
- Some experiences in lean six sigma is a plus.
SCHEDULE
- 9:00pm - 6:00pm, Monday-Friday, Sunday to Monday or Tuesday to Saturday
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.
INTRODUCTION
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.
ABOUT THE JOB
Since 1999, Eurofins Genomics Blue Heron has been a pioneer in the gene synthesis industry and has delivered tens of millions of base pairs of perfectly accurate genes to thousands of customers worldwide using its proprietary GeneMaker® multi-technology platform. We are 100% committed to serving our customers with high quality, strict confidentiality standards, and improved business efficiency. In mid-2019 Blue Heron was acquired by Eurofins Scientific and became a partner of the Eurofins Genomics US division. Blue Heron is searching for manufacturing Manager to join our team. The manufacturing Manager will report to the President of Blue Heron Biotech and lead the day-to-day operations of the gene synthesis operations at the Blue Heron.
RESPONSIBILITIES/ACCOUNTABILITIES
- Oversees, directs, coordinates and prioritizes the daily activities related to Blue Heron GeneMaker® platform including Gene synthesis, plasmid DNA and IVTmRNA production.
- Plan and organize the production schedule while ensuring compliance with safety regulations.
- Recruit, train, develop, and retain staff while ensuring adherence to essential training schedules.
- Identify and analyze problems, develop solutions, and implement corrective actions effectively.
- Act as the primary troubleshooting expert for the production group, identifying and resolving technical and operational issues.
- Manage vendor relationships, negotiate pricing, and oversee the ordering and purchasing of production materials and supplies.
- Support the development, implementation, and optimal use of equipment and systems to enhance efficiency, productivity, and profitability at all levels of manufacturing.
- Implement process controls, validations and metrics for the production equipment to monitor the stability of the manufacturing process while maintaining compliance with ISO 13485:2016 standards.
- Ensure Blue Heron manufacturing group complies with all government regulations and industry standards.
BASIC QUALIFICATIONS
- Bachelor’s degree or higher in a related scientific discipline required; MS or PhD in Molecular Biology preferred.
- Experience working with LIMS and proficiency in molecular biology techniques required.
- 6+ years of direct manufacturing and operations experience, including at least 3 years of managerial and supervisory responsibilities.
- Hands-on, self-motivated, and highly organized, with a demonstrated ability to lead teams effectively.
- Strong communication and interpersonal skills.
- Experience with manufacturing scale up is preferred.
- Experience with ISO or GMP certification and process is a plus.
- Some experiences in lean six sigma is a plus.
SCHEDULE
- 9:00pm - 6:00pm, Monday-Friday, Sunday to Monday or Tuesday to Saturday
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.
Job Roles in Medical Devices in Kentucky
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Get Access To All JobsFrequently Asked Questions
Which medical devices companies sponsor H-1B visas in Kentucky?
Kentucky-based H-1B sponsors in the medical devices space include manufacturers, distributors, and healthcare technology firms concentrated in Louisville and Lexington. Companies involved in device manufacturing, quality systems, and biomedical engineering have historically filed H-1B petitions in the state. DOL Labor Condition Application disclosure data is publicly searchable and shows which specific employers have sponsored H-1B workers in Kentucky's medical devices industry.
Which cities in Kentucky have the most medical devices H-1B sponsorship jobs?
Louisville is Kentucky's primary hub for medical devices H-1B sponsorship, driven by its concentration of healthcare systems, device distributors, and life sciences firms. Lexington also sees activity, particularly around the University of Kentucky's medical and engineering programs, which attract affiliated employers. Smaller manufacturing communities in northern Kentucky, near the Cincinnati metro, occasionally post device-related H-1B positions as well.
What types of medical devices roles typically qualify for H-1B sponsorship?
Roles that commonly qualify require at least a bachelor's degree in a specific field directly related to the position. In medical devices, this includes biomedical engineers, quality engineers, regulatory affairs specialists, software engineers developing device software, and clinical applications specialists. Positions requiring degrees in biomedical engineering, electrical engineering, computer science, or a life sciences discipline generally meet the H-1B specialty occupation standard more straightforwardly than generalist roles.
How do I find medical devices H-1B sponsorship jobs in Kentucky?
Migrate Mate is built specifically for international job seekers and filters job listings by visa sponsorship type, industry, and state. Searching for medical devices H-1B positions in Kentucky on Migrate Mate surfaces employers actively hiring for sponsored roles, saving time compared to manually screening general job postings. You can also cross-reference DOL OFLC disclosure data to verify which Kentucky employers have previously certified H-1B positions in this industry.
Are there any Kentucky-specific considerations for H-1B sponsorship in medical devices?
Kentucky does not impose state-level visa sponsorship requirements, so H-1B sponsorship follows standard federal USCIS and DOL processes regardless of where in the state you work. However, medical devices roles in Kentucky often intersect with FDA regulatory compliance, meaning employers may prefer candidates with familiarity with 21 CFR Part 820 quality system regulations. Employers near the Louisville medical corridor may also expect experience with Class II or Class III device environments.
What is the prevailing wage for H-1B 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.
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