Medical Devices Visa Sponsorship Jobs in Illinois
Illinois hosts major medical device companies like Abbott Laboratories in Abbott Park, Baxter International in Deerfield, and Stryker operations in Kalamazoo. The state's strong engineering talent pipeline from Northwestern, University of Illinois, and Illinois Institute of Technology supports visa sponsorship across manufacturing, R&D, and regulatory affairs roles.
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Get Access To All JobsINTRODUCTION
Plans, coordinates, and directs quality control programs designed to ensure continuous production of products consistent with established FDA and ISO standards.
ROLE AND RESPONSIBILITIES
- Designs and implements quality control training programs.
- Investigates and adjusts customer complaints regarding quality.
- Serves as project leader on project teams designated to resolve issues and implement solutions.
- Fully versed in Document Control processes and procedures.
- Assists in reviewing and revising processes within the QCBD (Quality Management System).
- Provides inspection activity for product throughout production cycle.
- Applies total quality management tools and approaches to analytical and reporting processes within each department.
- Creates, implements, updates and maintains work instructions, partnering with the Engineering and other departments.
- Creates and directs process/equipment validations.
- Directs workers engaged in inspection and testing activities to ensure continuous control over materials, facilities, and products.
- Works with suppliers to ensure quality of all purchased parts for company use.
- Must work responsibly with or without supervision using effective communication skills; able to collaborate with various departments and all levels of team members.
- Helps reduce scrap/waste, cost, time; drives for continuous improvement.
- Reliable, timely, ethical and consistent attendance.
- Travels to another facility and/or customer/vendor sites based on company needs is required.
- Other duties as assigned.
BASIC QUALIFICATIONS
- Bachelor's degree in applicable technical discipline such as mechanical or bio-medical engineering is strongly preferred or equivalent,
- or five to ten years of experience in medical device manufacturing industry and in the quality engineering role, and/or training,
- or equivalent combination of education and experience.
- Knowledge of the medical device manufacturing industry.
- Knowledge of ISO 13485 Quality Management System & FDA 21CFR 820 Regulations.
- Knowledge of Geometric Dimensioning and Tolerancing per ASME Y14.5M.
- Familiarity with test methods and standards for the design, verification, and validation of medical device products is required.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
INTRODUCTION
Plans, coordinates, and directs quality control programs designed to ensure continuous production of products consistent with established FDA and ISO standards.
ROLE AND RESPONSIBILITIES
- Designs and implements quality control training programs.
- Investigates and adjusts customer complaints regarding quality.
- Serves as project leader on project teams designated to resolve issues and implement solutions.
- Fully versed in Document Control processes and procedures.
- Assists in reviewing and revising processes within the QCBD (Quality Management System).
- Provides inspection activity for product throughout production cycle.
- Applies total quality management tools and approaches to analytical and reporting processes within each department.
- Creates, implements, updates and maintains work instructions, partnering with the Engineering and other departments.
- Creates and directs process/equipment validations.
- Directs workers engaged in inspection and testing activities to ensure continuous control over materials, facilities, and products.
- Works with suppliers to ensure quality of all purchased parts for company use.
- Must work responsibly with or without supervision using effective communication skills; able to collaborate with various departments and all levels of team members.
- Helps reduce scrap/waste, cost, time; drives for continuous improvement.
- Reliable, timely, ethical and consistent attendance.
- Travels to another facility and/or customer/vendor sites based on company needs is required.
- Other duties as assigned.
BASIC QUALIFICATIONS
- Bachelor's degree in applicable technical discipline such as mechanical or bio-medical engineering is strongly preferred or equivalent,
- or five to ten years of experience in medical device manufacturing industry and in the quality engineering role, and/or training,
- or equivalent combination of education and experience.
- Knowledge of the medical device manufacturing industry.
- Knowledge of ISO 13485 Quality Management System & FDA 21CFR 820 Regulations.
- Knowledge of Geometric Dimensioning and Tolerancing per ASME Y14.5M.
- Familiarity with test methods and standards for the design, verification, and validation of medical device products is required.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
Medical Devices Job Roles in Illinois
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Search Medical Devices Jobs in IllinoisMedical Devices Jobs in Illinois: Frequently Asked Questions
Which medical devices companies sponsor visas in Illinois?
Abbott Laboratories leads Illinois medical device sponsorship, particularly for engineers and regulatory affairs specialists at their Abbott Park headquarters. Baxter International in Deerfield sponsors for biomedical engineers and manufacturing roles. Stryker, Boston Scientific, and Medtronic also maintain Illinois operations with active H-1B visa and TN visa sponsorship programs for technical positions.
How to find medical devices visa sponsorship jobs in Illinois?
Migrate Mate specializes in connecting international candidates with Illinois medical device companies offering visa sponsorship. The platform filters specifically for sponsorship-eligible roles at Abbott, Baxter, and other major Illinois employers. Focus on manufacturing engineering, quality assurance, and regulatory affairs positions which have the highest sponsorship rates in Illinois medical devices.
Which visa types are most common for medical devices roles in Illinois?
H-1B visas dominate Illinois medical device sponsorship for engineering and regulatory roles requiring specialized knowledge. TN visas are common for Canadian and Mexican engineers, especially in manufacturing and quality systems. O-1 visas occasionally appear for senior R&D positions at companies like Abbott, while E-3 visas serve Australian engineers in technical roles.
Which cities in Illinois have the most medical devices sponsorship jobs?
Abbott Park leads with Abbott's global headquarters offering the highest concentration of sponsored positions. The Chicago metropolitan area, including Deerfield and Lake Forest, hosts multiple device companies with active sponsorship. Rockford and suburban Cook County also provide manufacturing-focused opportunities, particularly for process and quality engineers.
What prevailing wage considerations apply to Illinois medical devices roles?
Illinois medical device roles typically command higher prevailing wages than general manufacturing due to FDA regulatory requirements and specialized knowledge needs. The Chicago metro area drives wage levels higher, while downstate positions may offer lower prevailing wages but still meet H-1B requirements. Biomedical and regulatory engineers see particularly strong wage premiums.
What is the prevailing wage for sponsored medical devices jobs in Illinois?
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.