Medical Devices TN Sponsorship Jobs in Indiana
Indiana's medical devices sector spans manufacturing hubs in Warsaw, Indianapolis, and Fort Wayne, with employers like Zimmer Biomet, DePuy Synthes, and Cook Medical regularly hiring international professionals. Canadian and Mexican citizens in engineering, scientific, and technical roles can pursue TN visa sponsorship with Indiana-based medical devices companies across a range of qualifying occupations.
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Manufacturing Engineer is a staff level position with responsibility to work with high attention to detail on engineering assignments related to PTS analyzers and manufacturing equipment and processes to produce medical diagnostics devices. This position will be responsible for determining design feasibility, sustainability, and supporting cross-functional departments for order execution. The Manufacturing Engineer will take the lead in electro-mechanical prototype development, equipment repairs and upgrades, design verification, root cause analysis, support of engineering projects, troubleshooting of manufacturing equipment issues, and testing for compliance with medical device design standards. Projects involve the construction, characterization, and troubleshooting of mechanical systems containing electronic, optical, and software controls used in new products, prototypes, test fixtures, and manufacturing equipment. Work includes mechanical design, knowledge of digital and analog electronics, optics, and mechanical manufacturing systems. This position generates formal reports and presentations using applicable software. This position is also responsible for ensuring compliance with regulatory requirements of the Quality System documentation as required for design control.
Essential Duties and Responsibilities
- Interact well with Manufacturing, Engineering, Quality, and R&D personnel
- Daily interfacing with manufacturing staff to ensure manufacturing lines are up and running efficiently
- Exhibit quality of work and documentation habits exceeding the needs of those employed in the medical diagnostics industry
- Generate formal reports and presentations to support Quality System and business needs
- Perform product and process verification and validation activities in a regulated industry
- Work effectively with outside vendors of materials and equipment
- Supervise and perform maintenance to production equipment
- Monitor and analyze mechanical devices for problems
- Perform root cause analysis and work towards resolutions
- Design of experiments approach for assessing mechanical and product-based performance
- Develop and test devices for improvement
- Recommend design changes, cost reductions, warranty improvements, and manufacturing issue resolutions
- Write product specifications, document test results, prepare product operating instructions, and review technical literature
- Participate in Factory Acceptance / Site Acceptance testing activities
Qualifications
- Background in medical diagnostics or devices preferred
- Experience with equipment/process validation
- Experience using risk mitigation tools such as PFMEA and Control Plans
- Strong mechanical aptitude; hands-on capability for troubleshooting and repairs
- Working with analytical software will be required
- Detailed, meticulous application of engineering principles
- Able to provide leadership or mentorship among team members; provides support and encourages collaboration
- Experience with automated assembly lines preferred
- Willingness to travel to supplier / PTS sites as needed
Education and/or Experience
- Bachelor’s degree (B.S.) in Mechanical Engineering or related Engineering discipline
- Minimum of five (5) years hands-on related experience in a design, development, and manufacturing environment
- Working knowledge of the medical diagnostics / medical device industry
Work Environment
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Employee works in a typical office and manufacturing environment.
Equal Opportunity Employer: PTS Diagnostics is an Equal Opportunity and E-Verify employer. Employment decisions for all applicants and employees will be made without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, age, national origin, marital status, veteran status, disability, or other characteristics protected under local, state, or federal law.
Quality Commitment
This position requires compliance with applicable quality system and regulatory requirements. This individual adopts a “quality in everything we do” approach to all aspects of the execution of responsibilities of this position. Through vigilance, this individual remains alert to any potential compliance situations and must report such observations to managers and the Head of Quality.
Statement of Other Duties Disclaimer
This job description in no way states or implies that these are the only duties to be performed by this employee. This employee will be required to follow any other instructions and to perform any other duties requested by their supervisor.
Summary
Manufacturing Engineer is a staff level position with responsibility to work with high attention to detail on engineering assignments related to PTS analyzers and manufacturing equipment and processes to produce medical diagnostics devices. This position will be responsible for determining design feasibility, sustainability, and supporting cross-functional departments for order execution. The Manufacturing Engineer will take the lead in electro-mechanical prototype development, equipment repairs and upgrades, design verification, root cause analysis, support of engineering projects, troubleshooting of manufacturing equipment issues, and testing for compliance with medical device design standards. Projects involve the construction, characterization, and troubleshooting of mechanical systems containing electronic, optical, and software controls used in new products, prototypes, test fixtures, and manufacturing equipment. Work includes mechanical design, knowledge of digital and analog electronics, optics, and mechanical manufacturing systems. This position generates formal reports and presentations using applicable software. This position is also responsible for ensuring compliance with regulatory requirements of the Quality System documentation as required for design control.
Essential Duties and Responsibilities
- Interact well with Manufacturing, Engineering, Quality, and R&D personnel
- Daily interfacing with manufacturing staff to ensure manufacturing lines are up and running efficiently
- Exhibit quality of work and documentation habits exceeding the needs of those employed in the medical diagnostics industry
- Generate formal reports and presentations to support Quality System and business needs
- Perform product and process verification and validation activities in a regulated industry
- Work effectively with outside vendors of materials and equipment
- Supervise and perform maintenance to production equipment
- Monitor and analyze mechanical devices for problems
- Perform root cause analysis and work towards resolutions
- Design of experiments approach for assessing mechanical and product-based performance
- Develop and test devices for improvement
- Recommend design changes, cost reductions, warranty improvements, and manufacturing issue resolutions
- Write product specifications, document test results, prepare product operating instructions, and review technical literature
- Participate in Factory Acceptance / Site Acceptance testing activities
Qualifications
- Background in medical diagnostics or devices preferred
- Experience with equipment/process validation
- Experience using risk mitigation tools such as PFMEA and Control Plans
- Strong mechanical aptitude; hands-on capability for troubleshooting and repairs
- Working with analytical software will be required
- Detailed, meticulous application of engineering principles
- Able to provide leadership or mentorship among team members; provides support and encourages collaboration
- Experience with automated assembly lines preferred
- Willingness to travel to supplier / PTS sites as needed
Education and/or Experience
- Bachelor’s degree (B.S.) in Mechanical Engineering or related Engineering discipline
- Minimum of five (5) years hands-on related experience in a design, development, and manufacturing environment
- Working knowledge of the medical diagnostics / medical device industry
Work Environment
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Employee works in a typical office and manufacturing environment.
Equal Opportunity Employer: PTS Diagnostics is an Equal Opportunity and E-Verify employer. Employment decisions for all applicants and employees will be made without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, age, national origin, marital status, veteran status, disability, or other characteristics protected under local, state, or federal law.
Quality Commitment
This position requires compliance with applicable quality system and regulatory requirements. This individual adopts a “quality in everything we do” approach to all aspects of the execution of responsibilities of this position. Through vigilance, this individual remains alert to any potential compliance situations and must report such observations to managers and the Head of Quality.
Statement of Other Duties Disclaimer
This job description in no way states or implies that these are the only duties to be performed by this employee. This employee will be required to follow any other instructions and to perform any other duties requested by their supervisor.
TN Medical Devices Job Roles in Indiana
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Search Medical Devices Jobs in IndianaMedical Devices TN Sponsorship Jobs in Indiana: Frequently Asked Questions
Which medical devices companies in Indiana sponsor TN visas?
Warsaw is home to a concentration of orthopedic device manufacturers, including Zimmer Biomet and Biomet, that have historically hired international professionals in technical and engineering roles. Cook Medical in Bloomington and employers in the Indianapolis metro also operate at a scale that supports TN visa sponsorship. Sponsorship practices vary by role, location, and hiring cycle, so confirming directly with the employer's HR or immigration team is always advisable.
Which cities in Indiana have the most medical devices TN sponsorship jobs?
Warsaw stands out as one of the most concentrated orthopedic device manufacturing areas in the world, making it the most active city for medical devices hiring in Indiana. Indianapolis offers broader opportunities across device manufacturing, quality, and regulatory functions. Fort Wayne and Bloomington also have employer presence in the sector, particularly in manufacturing operations and research roles that may qualify for TN status.
What types of medical devices roles typically qualify for TN sponsorship in Indiana?
TN status covers specific USMCA-defined occupations, so not every medical devices role qualifies automatically. Roles that commonly align with TN categories include engineers (mechanical, biomedical, electrical, industrial, manufacturing), scientific roles such as chemist or biologist, computer systems analysts, and certain management consultants. The position must require a qualifying degree, and the job duties must correspond to a listed TN occupation. Employers and immigration counsel typically assess this on a case-by-case basis.
How do I find medical devices TN sponsorship jobs in Indiana?
Migrate Mate is built specifically for international job seekers and filters medical devices TN sponsorship jobs in Indiana by visa type, making it easier to identify employers actively open to TN candidates. Because TN sponsorship eligibility depends on the specific role and employer, focusing your search on companies with established hiring in Indiana's device manufacturing corridor, particularly around Warsaw and Indianapolis, increases the likelihood of finding a qualifying position.
Are there any Indiana-specific considerations for medical devices TN sponsorship?
Indiana's concentration of orthopedic and surgical device manufacturers means many open roles involve manufacturing, quality assurance, and regulatory affairs functions. TN applicants should confirm that their specific job title and duties map to a USMCA-listed occupation before applying, as generic manufacturing or operations titles may not qualify. Indiana employers in this sector are generally experienced with work authorization requirements given the area's international workforce, but sponsorship decisions remain employer-specific.