Medical Devices Visa Sponsorship Jobs in Texas
Texas leads the nation in medical device innovation, with major hubs in Austin, Houston, and Dallas-Fort Worth. Companies like Medtronic, Abbott, and Boston Scientific maintain significant operations here, creating substantial demand for international talent in engineering, regulatory affairs, and clinical research roles.
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Get Access To All JobsINTRODUCTION
The Label Designer supports the Athens Production Plant by managing controlled documentation and product labeling activities in accordance with applicable Quality System and Regulatory requirements. This role is responsible for processing, distributing, maintaining, creating, revising, verifying, and controlling documentation, labels, and packaging artwork. The position works cross-functionally with Document Control, Regulatory, Quality, Marketing, Engineering, and Production to ensure accurate information is released in an efficient and timely manner to support product development, labeling changes, and ongoing production activities.
ESSENTIAL FUNCTIONS
- Process, copy, distribute, file, and maintain controlled documentation upon release.
- Maintain, issue, and update documents and labels using QAD, label programs, or other approved systems.
- Create and maintain databases necessary to track document distribution and generate reports.
- Create, revise, maintain, and control product labeling documents, including product labels and labeling specifications.
- Generate and update labeling content in accordance with approved specifications, engineering changes, and Quality System requirements.
- Verify label content for accuracy, including part numbers, catalog numbers, lot/batch information, UDI data, symbols, translations, and regulatory requirements.
- Maintain labeling templates and support consistency across product families and product lines.
- Coordinate with Regulatory, Quality, Marketing, Engineering, Production, and Document Control to support labeling changes, product introduction, and ongoing production needs.
- Ensure documentation and labeling projects meet established deadlines.
- Perform other duties as assigned.
COMPETENCIES
- Strong attention to detail and accuracy.
- Excellent written and verbal communication skills.
- Good PC skills in a Windows environment, specifically Word, Excel, and Access.
- Familiarity with graphical manipulation using software programs.
- Knowledge of document control, change management, and revision control processes.
- Understanding of medical device labeling requirements and Quality System regulations.
- Experience creating and maintaining product labeling within a regulated environment.
- Ability to interface with personnel across departments to support efficient product introduction and documentation flow.
- Self-starter with the ability to work with minimal supervision.
- Good time management skills with the ability to prioritize using sound judgment.
SUPERVISORY RESPONSIBILITIES
N/A
REQUIRED EDUCATION AND EXPERIENCE
- High school diploma or higher.
- Experience using QAD or similar MRP software.
- Knowledge of Medical Device Quality Systems.
- Knowledge of BarTender software or equivalent label design software.
PREFERRED EDUCATION AND EXPERIENCE
- Associate degree preferred.
- Experience with medical device labeling and UDI requirements.
- Experience generating and maintaining production labels and labeling specifications.
- Knowledge of FDA, ISO 13485, and other applicable regulatory requirements related to labeling.
PHYSICAL DEMANDS & TRAVEL REQUIRED
Light
No travel required
INTRODUCTION
The Label Designer supports the Athens Production Plant by managing controlled documentation and product labeling activities in accordance with applicable Quality System and Regulatory requirements. This role is responsible for processing, distributing, maintaining, creating, revising, verifying, and controlling documentation, labels, and packaging artwork. The position works cross-functionally with Document Control, Regulatory, Quality, Marketing, Engineering, and Production to ensure accurate information is released in an efficient and timely manner to support product development, labeling changes, and ongoing production activities.
ESSENTIAL FUNCTIONS
- Process, copy, distribute, file, and maintain controlled documentation upon release.
- Maintain, issue, and update documents and labels using QAD, label programs, or other approved systems.
- Create and maintain databases necessary to track document distribution and generate reports.
- Create, revise, maintain, and control product labeling documents, including product labels and labeling specifications.
- Generate and update labeling content in accordance with approved specifications, engineering changes, and Quality System requirements.
- Verify label content for accuracy, including part numbers, catalog numbers, lot/batch information, UDI data, symbols, translations, and regulatory requirements.
- Maintain labeling templates and support consistency across product families and product lines.
- Coordinate with Regulatory, Quality, Marketing, Engineering, Production, and Document Control to support labeling changes, product introduction, and ongoing production needs.
- Ensure documentation and labeling projects meet established deadlines.
- Perform other duties as assigned.
COMPETENCIES
- Strong attention to detail and accuracy.
- Excellent written and verbal communication skills.
- Good PC skills in a Windows environment, specifically Word, Excel, and Access.
- Familiarity with graphical manipulation using software programs.
- Knowledge of document control, change management, and revision control processes.
- Understanding of medical device labeling requirements and Quality System regulations.
- Experience creating and maintaining product labeling within a regulated environment.
- Ability to interface with personnel across departments to support efficient product introduction and documentation flow.
- Self-starter with the ability to work with minimal supervision.
- Good time management skills with the ability to prioritize using sound judgment.
SUPERVISORY RESPONSIBILITIES
N/A
REQUIRED EDUCATION AND EXPERIENCE
- High school diploma or higher.
- Experience using QAD or similar MRP software.
- Knowledge of Medical Device Quality Systems.
- Knowledge of BarTender software or equivalent label design software.
PREFERRED EDUCATION AND EXPERIENCE
- Associate degree preferred.
- Experience with medical device labeling and UDI requirements.
- Experience generating and maintaining production labels and labeling specifications.
- Knowledge of FDA, ISO 13485, and other applicable regulatory requirements related to labeling.
PHYSICAL DEMANDS & TRAVEL REQUIRED
Light
No travel required
Medical Devices Job Roles in Texas
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Search Medical Devices Jobs in TexasMedical Devices Jobs in Texas: Frequently Asked Questions
Which medical devices companies in Texas sponsor visas most frequently?
Major sponsors include Medtronic (Minneapolis-based with Texas facilities), Abbott (headquarters in Abbott Park but major Texas presence), Boston Scientific, Stryker, and Johnson & Johnson subsidiaries. Texas-based companies like Zimmer Biomet and smaller innovation-focused startups in Austin's medical corridor also regularly sponsor H-1B visa and other work visas for engineering and regulatory positions.
How to find medical devices visa sponsorship jobs in Texas?
Use Migrate Mate to browse current medical device openings specifically filtered for Texas and visa sponsorship. Focus your search on Austin's medical device corridor, Houston's Texas Medical Center area, and Dallas-Fort Worth companies. Target roles in biomedical engineering, regulatory affairs, quality assurance, and clinical research where international expertise is highly valued.
What visa types are most common for medical devices roles in Texas?
H-1B visas dominate for engineering positions, regulatory affairs specialists, and clinical research roles requiring specialized degrees. O-1 visas are used for senior scientists and researchers with extraordinary ability. TN visas work well for Canadian and Mexican engineers. L-1 visas are common for transfers between international medical device company locations.
Which Texas cities have the most medical devices visa sponsorship opportunities?
Austin leads with its established medical device ecosystem and university partnerships. Houston follows closely due to the Texas Medical Center and related research institutions. Dallas-Fort Worth offers opportunities with larger corporations. San Antonio has emerging opportunities, particularly in military medical technology and VA hospital partnerships.
Are prevailing wages higher for medical devices jobs in Texas compared to other states?
Texas generally offers competitive wages without state income tax, making total compensation attractive. Austin and Dallas command premium wages due to tech industry competition for talent. Houston wages are competitive but slightly lower than coastal markets. Rural Texas positions may offer lower wages but significantly reduced living costs.
What is the prevailing wage for sponsored medical devices jobs in Texas?
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.