LivaNova Visa Sponsorship Jobs USA
LivaNova is a global medical device company known for its work in neuromodulation and cardiac surgery. It sponsors both H-1B visa and employment-based Green Cards, making it a viable target for international candidates pursuing long-term careers in the medical technology sector in the U.S.
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Get Access To All JobsAs a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow—because at LivaNova, we don’t just treat conditions — we aspire to alter the course of lives.
ROLE AND RESPONSIBILITIES
The Quality Inspector is responsible for performing incoming inspections on raw components used during manufacturing of in-process subassemblies and finished products. This is a great opportunity for someone who is currently pursuing a degree in engineering and has an interest in the medical device manufacturing industry.
Primary Activities
- Inspects or tests components and raw material according to written inspection procedures
- Inspects electronic or mechanical assemblies, subassemblies, and component parts for compliance with acceptance criteria as defined by specifications, drawings, samples, or illustrations
- Examines units visually, with microscope or other magnifying device, to determine physical defects according to written inspection procedures
- Compares assemblies with drawings, parts lists, illustrations, and/or samples to verify conformance and detect assembly errors
- Examines the alignment of parts and verifies installation of hardware on assemblies and subassemblies
- Measures parts for conformance to specified dimensions using measuring instruments or equipment
- Accepts or rejects materials / product inspected based on conformance to acceptance criteria
- Records inspection data on appropriate forms, logs, and/or in computer databases
- Maintains controlled document files and test records in a timely and accurate manner
- Coordinates calibration of all test equipment and fixtures
- Monitors critical equipment and instrumentation to ensure proper operation and calibration
- Identifies and controls nonconforming material and defective products until the material has been quarantined
- Responsible for identifying, evaluating, recording, and initiating correction or prevention of quality related problems
- Responsible for identifying and controlling nonconforming material and defective products by segregation or product identification
MINIMUM QUALIFICATIONS
- High school graduate or equivalent
- Must be currently enrolled in a college or university program and pursuing a degree in an engineering discipline (e.g. biomedical, mechanical, manufacturing, etc.)
- Exposure to ISO/FDA regulations, Quality Inspection Techniques and Workmanship Standards
- Proficiency in MS Office
- Good verbal and written communication skills
Physical Requirements
- Required to perform the essential duties and responsibilities of the job
- Must maintain near-sight acuity, with or without corrective lenses, adequate to successfully perform the required job functions as defined within the quality-controlled processes
PAY TRANSPARENCY
- A reasonable estimate of the hourly rate for this position is $22 - $25 per hour. Pay ranges may vary by location.
LOCATION AND SHIFT
- This position is located onsite in the Clear Lake area (Southeast Houston)
- Work hours will be between 8:00a and 5:00p, and will be dependent upon your class schedule
- We estimate that this job will require roughly 20 hours per week with a potential increase over the summer (if your schedule allows)
Welcome to impact. Welcome to innovation. Welcome to your new life.
As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow—because at LivaNova, we don’t just treat conditions — we aspire to alter the course of lives.
ROLE AND RESPONSIBILITIES
The Quality Inspector is responsible for performing incoming inspections on raw components used during manufacturing of in-process subassemblies and finished products. This is a great opportunity for someone who is currently pursuing a degree in engineering and has an interest in the medical device manufacturing industry.
Primary Activities
- Inspects or tests components and raw material according to written inspection procedures
- Inspects electronic or mechanical assemblies, subassemblies, and component parts for compliance with acceptance criteria as defined by specifications, drawings, samples, or illustrations
- Examines units visually, with microscope or other magnifying device, to determine physical defects according to written inspection procedures
- Compares assemblies with drawings, parts lists, illustrations, and/or samples to verify conformance and detect assembly errors
- Examines the alignment of parts and verifies installation of hardware on assemblies and subassemblies
- Measures parts for conformance to specified dimensions using measuring instruments or equipment
- Accepts or rejects materials / product inspected based on conformance to acceptance criteria
- Records inspection data on appropriate forms, logs, and/or in computer databases
- Maintains controlled document files and test records in a timely and accurate manner
- Coordinates calibration of all test equipment and fixtures
- Monitors critical equipment and instrumentation to ensure proper operation and calibration
- Identifies and controls nonconforming material and defective products until the material has been quarantined
- Responsible for identifying, evaluating, recording, and initiating correction or prevention of quality related problems
- Responsible for identifying and controlling nonconforming material and defective products by segregation or product identification
MINIMUM QUALIFICATIONS
- High school graduate or equivalent
- Must be currently enrolled in a college or university program and pursuing a degree in an engineering discipline (e.g. biomedical, mechanical, manufacturing, etc.)
- Exposure to ISO/FDA regulations, Quality Inspection Techniques and Workmanship Standards
- Proficiency in MS Office
- Good verbal and written communication skills
Physical Requirements
- Required to perform the essential duties and responsibilities of the job
- Must maintain near-sight acuity, with or without corrective lenses, adequate to successfully perform the required job functions as defined within the quality-controlled processes
PAY TRANSPARENCY
- A reasonable estimate of the hourly rate for this position is $22 - $25 per hour. Pay ranges may vary by location.
LOCATION AND SHIFT
- This position is located onsite in the Clear Lake area (Southeast Houston)
- Work hours will be between 8:00a and 5:00p, and will be dependent upon your class schedule
- We estimate that this job will require roughly 20 hours per week with a potential increase over the summer (if your schedule allows)
Welcome to impact. Welcome to innovation. Welcome to your new life.
Job Roles at LivaNova
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Get Access To All JobsTips for Finding LivaNova Visa Sponsorship Jobs USA
Target engineering and clinical roles first
LivaNova's sponsorship history skews toward technical and clinical functions. If your background is in biomedical engineering, regulatory affairs, or clinical research, you're positioning yourself in the departments most likely to support a visa application.
Understand both H-1B and Green Card pathways
LivaNova sponsors both H-1B visas and employment-based Green Cards. Knowing which pathway fits your timeline, temporary work authorization versus permanent residence, helps you ask the right questions during the hiring process.
Align your experience with medical device industry standards
LivaNova operates in a highly regulated industry. Candidates with FDA compliance, ISO 13485, or neuromodulation or cardiac device experience are more competitive and more likely to receive visa sponsorship consideration for specialty roles.
Search for roles at verified sponsors before applying broadly
Not all medical device employers sponsor visas consistently. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history, helping you focus your search on companies like LivaNova that have a track record of supporting international candidates.
Raise sponsorship early but frame it professionally
With mid-sized medtech companies like LivaNova, recruiters appreciate directness. Confirm sponsorship availability before investing heavily in the interview process, framing it as a logistics question rather than a negotiation point keeps the conversation professional.
Prepare for a structured, multi-stage interview process
Medical device companies typically run thorough interview cycles involving technical panels and compliance-related screening. Building your case around both your specialized qualifications and your understanding of LivaNova's therapeutic areas strengthens your overall sponsorship candidacy.
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Find LivaNova JobsFrequently Asked Questions
Does LivaNova sponsor H-1B visas?
Yes, LivaNova sponsors H-1B visas. The company has a consistent track record of filing H-1B petitions for qualified international candidates, particularly in technical, engineering, and clinical roles. If you're on OPT or transitioning between employers, LivaNova is worth targeting as a sponsor in the medical device space.
Does LivaNova sponsor Green Cards?
Yes, LivaNova sponsors employment-based Green Cards, including EB-2 and EB-3 categories. Green Card sponsorship typically follows a period of H-1B employment and depends on your role, tenure, and business need. It's worth confirming the company's current policy with your recruiter or HR contact during the hiring process.
Which departments at LivaNova are most likely to sponsor visas?
Based on LivaNova's hiring patterns in the medical device industry, sponsorship is most common in engineering, research and development, regulatory affairs, and clinical operations. These are specialized functions where international talent is in demand and where LivaNova has historically supported visa filings for qualifying candidates.
How do I find open visa-sponsored jobs at LivaNova?
Migrate Mate lists roles at verified sponsors like LivaNova, filtered by companies with real sponsorship history, so you're not guessing which employers will support your application. Search for LivaNova directly on Migrate Mate to see current openings and filter by visa type to match your work authorization situation.
How do I approach the LivaNova application process as an international candidate?
Start by confirming sponsorship availability when you first speak with a recruiter, LivaNova's HR teams are familiar with the process. Tailor your application to highlight specialized skills in neuromodulation, cardiac surgery, or medical device compliance. Be prepared for a multi-stage interview and have your work authorization timeline ready to share if asked.
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