Quality Control Technician Visa Sponsorship Jobs in Minnesota
Minnesota's quality control technician jobs span medical devices, food manufacturing, and precision manufacturing, with major employers like Medtronic, General Mills, and 3M operating large facilities across the Twin Cities, Rochester, and St. Cloud. International candidates with backgrounds in inspection, testing, and compliance will find active hiring in a state known for its manufacturing depth and technical workforce.
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Get Access To All JobsINTRODUCTION
Anteris is a science-driven structural heart company that is redefining expectations and advancing the field through cutting-edge solutions focused on restoring native-like physiology versus treating symptoms of structural heart disease. We are currently developing a new class of TAVR designed to mimic the performance of a healthy aortic valve. With offices in Minneapolis, MN, US; Geneva, Switzerland; and Brisbane and Perth, Australia, we have a growing and inclusive team.
The Quality Control Inspection team plays a key role supporting our manufacturing operations at the Maple Grove site. This role is involved in a wide range of inspection tasks, where the primary goal is to assure that the products we produce are conforming to specifications and properly evaluated for compliance to visual, dimensional, functional, and various other specified requirements.
The QC Inspector will be responsible for performing inspections in a highly regulated medical device development and manufacturing environment across all areas of standard work for the team (receiving inspection, first article inspections, label verifications, valve inspections, tissue inspections, pre-sterile product inspections, and sterile product inspections). This is a high visibility role with daily interactions across a wide range of peer groups in the Maple Grove site.
Shift: Day Shift, Monday through Friday, 6:00 a.m. - 2:00 p.m.
At Anteris Technologies, you'll be part of a team dedicated to enhancing the quality of life for patients with aortic stenosis through groundbreaking medical devices. Join us in our mission to revolutionize structural heart solutions.
PRIMARY DUTIES AND RESPONSIBILITIES
Perform all duties listed below in strict compliance with the Anteris Quality Management System including Good Documentation Practices.
- Responsible for performing receiving inspection on material/products supplied to Anteris to ensure conformance to requirements and specifications.
- Perform microscope and other aided visual inspections on biological tissue based medical device products to ensure conformance to processing requirements and specifications.
- Perform machine/software-controlled inspections on products to ensure conformance to processing requirements and specifications.
- Perform inspections, as required by procedure, in support of first article inspections and label verifications.
- Perform physical and visual inspections on material, products, and/or packaging being processed for sterilization.
- Make an informed decision, based on training to tasks assigned, on the acceptance of materials, products, and inspected features, requirements, and specifications in all standard work tasks.
- Complete and maintain accurate records of inspection activities, including measurements, observations, results, conclusions, nonconformance issues, and full completion of quality record fields in support of standard work tasks.
- Collaborate with peers in Operations to effectively stay on plan, be mutually organized to goals, and communicate effectively through escalation channels as required.
- Other tasks assigned by group lead or designee.
SKILLS, KNOWLEDGE, EXPERIENCE & QUALIFICATIONS
Required Skills and Knowledge:
- High School diploma or equivalent.
- 4+ years’ overall experience in Medical Device (ISO 13485, FDA QSR) manufacturing environment.
- 2+ years’ equivalent work experience directly applicable to Primary Duties and Responsibilities listed above.
- Strong attention to detail and experience in reading, interpreting, and comprehending product requirement documents and specifications.
- Experience in learning and cross-training on widening set of responsibilities in a team-based environment.
- Experience working directly with computers to input data, perform electronic based work tasks, complete training, and manage email communications.
- Effective verbal and written communication.
- Ability to work in a fast-paced environment.
- Effective problem-solving and troubleshooting skills.
Preferred Skills and Knowledge:
- Vocational or technical training in assembly, sewing, or inspection of biological tissue based medical devices.
- Vocational or technical training in the use of microscopes, including the use of specialized reticles and/or tappi charts.
- Vocational or technical training in the use of MicroVu optical inspection systems.
- Vocational or technical training in Lean or 5S principles.
- Vocational or technical training in GD&T principles and specification designs.
WHAT WE OFFER
- Opportunity to make a significant impact on the healthcare industry by advancing groundbreaking therapies.
- Collaborative and dynamic work environment with a culture of innovation and excellence.
- Competitive compensation package, including salary, performance-based bonuses, and stock options.
- Career development opportunities and a chance to be part of a growing company that values its employees.
HEALTH AND WELLNESS OFFERINGS
- Medical, Dental, and Vision Plans
- Flexible Spending Account (FSA)
- 401k + Company Match
- Life, AD&D, Short Term and Long-Term Disability Insurance
- Bonus Plan Eligibility
- Employee Equity Program
- Paid Holidays & PTO
- Employee Assistance Program
- Inclusive Team Environment
Note: We may require proof of COVID-19 vaccination to comply with the state, local municipality, and/or travel regulations.
PAY
Pay: $28.00 - $31.00 per hour
BENEFITS
- 401(k)
- 401(k) matching
- Dental insurance
- Employee assistance program
- Flexible spending account
- Health insurance
- Paid time off
- Referral program
- Vision insurance
APPLICATION QUESTIONS
- Are you willing to work the 6am - 2pm shift?
- Do you now or at a future date require visa sponsorship to work in the United States?
- How many years' experience do you have working for a Class III medical device company?
- How many years' experience do you have handling and inspecting tissue biologics?
Education
High school or equivalent (Required)
Experience
Medical device quality inspection: 1 year (Required)
ABILITY TO COMMUTE
Maple Grove, MN 55369 (Required)
WORK LOCATION
In person
Anteris Technologies recruits, employs, trains, compensates and promotes regardless of race, religion, color, national origin, sex, disability, age, veteran status, and other protected status as required by applicable law. We have a clear vision: to be a place of belonging for all humans by promoting diversity, multiculturism and inclusion, as a goal and reflection across the organization. Diversity is more than a commitment - it is part of our mission to deliver the best structural heart products on a global scale.
INTRODUCTION
Anteris is a science-driven structural heart company that is redefining expectations and advancing the field through cutting-edge solutions focused on restoring native-like physiology versus treating symptoms of structural heart disease. We are currently developing a new class of TAVR designed to mimic the performance of a healthy aortic valve. With offices in Minneapolis, MN, US; Geneva, Switzerland; and Brisbane and Perth, Australia, we have a growing and inclusive team.
The Quality Control Inspection team plays a key role supporting our manufacturing operations at the Maple Grove site. This role is involved in a wide range of inspection tasks, where the primary goal is to assure that the products we produce are conforming to specifications and properly evaluated for compliance to visual, dimensional, functional, and various other specified requirements.
The QC Inspector will be responsible for performing inspections in a highly regulated medical device development and manufacturing environment across all areas of standard work for the team (receiving inspection, first article inspections, label verifications, valve inspections, tissue inspections, pre-sterile product inspections, and sterile product inspections). This is a high visibility role with daily interactions across a wide range of peer groups in the Maple Grove site.
Shift: Day Shift, Monday through Friday, 6:00 a.m. - 2:00 p.m.
At Anteris Technologies, you'll be part of a team dedicated to enhancing the quality of life for patients with aortic stenosis through groundbreaking medical devices. Join us in our mission to revolutionize structural heart solutions.
PRIMARY DUTIES AND RESPONSIBILITIES
Perform all duties listed below in strict compliance with the Anteris Quality Management System including Good Documentation Practices.
- Responsible for performing receiving inspection on material/products supplied to Anteris to ensure conformance to requirements and specifications.
- Perform microscope and other aided visual inspections on biological tissue based medical device products to ensure conformance to processing requirements and specifications.
- Perform machine/software-controlled inspections on products to ensure conformance to processing requirements and specifications.
- Perform inspections, as required by procedure, in support of first article inspections and label verifications.
- Perform physical and visual inspections on material, products, and/or packaging being processed for sterilization.
- Make an informed decision, based on training to tasks assigned, on the acceptance of materials, products, and inspected features, requirements, and specifications in all standard work tasks.
- Complete and maintain accurate records of inspection activities, including measurements, observations, results, conclusions, nonconformance issues, and full completion of quality record fields in support of standard work tasks.
- Collaborate with peers in Operations to effectively stay on plan, be mutually organized to goals, and communicate effectively through escalation channels as required.
- Other tasks assigned by group lead or designee.
SKILLS, KNOWLEDGE, EXPERIENCE & QUALIFICATIONS
Required Skills and Knowledge:
- High School diploma or equivalent.
- 4+ years’ overall experience in Medical Device (ISO 13485, FDA QSR) manufacturing environment.
- 2+ years’ equivalent work experience directly applicable to Primary Duties and Responsibilities listed above.
- Strong attention to detail and experience in reading, interpreting, and comprehending product requirement documents and specifications.
- Experience in learning and cross-training on widening set of responsibilities in a team-based environment.
- Experience working directly with computers to input data, perform electronic based work tasks, complete training, and manage email communications.
- Effective verbal and written communication.
- Ability to work in a fast-paced environment.
- Effective problem-solving and troubleshooting skills.
Preferred Skills and Knowledge:
- Vocational or technical training in assembly, sewing, or inspection of biological tissue based medical devices.
- Vocational or technical training in the use of microscopes, including the use of specialized reticles and/or tappi charts.
- Vocational or technical training in the use of MicroVu optical inspection systems.
- Vocational or technical training in Lean or 5S principles.
- Vocational or technical training in GD&T principles and specification designs.
WHAT WE OFFER
- Opportunity to make a significant impact on the healthcare industry by advancing groundbreaking therapies.
- Collaborative and dynamic work environment with a culture of innovation and excellence.
- Competitive compensation package, including salary, performance-based bonuses, and stock options.
- Career development opportunities and a chance to be part of a growing company that values its employees.
HEALTH AND WELLNESS OFFERINGS
- Medical, Dental, and Vision Plans
- Flexible Spending Account (FSA)
- 401k + Company Match
- Life, AD&D, Short Term and Long-Term Disability Insurance
- Bonus Plan Eligibility
- Employee Equity Program
- Paid Holidays & PTO
- Employee Assistance Program
- Inclusive Team Environment
Note: We may require proof of COVID-19 vaccination to comply with the state, local municipality, and/or travel regulations.
PAY
Pay: $28.00 - $31.00 per hour
BENEFITS
- 401(k)
- 401(k) matching
- Dental insurance
- Employee assistance program
- Flexible spending account
- Health insurance
- Paid time off
- Referral program
- Vision insurance
APPLICATION QUESTIONS
- Are you willing to work the 6am - 2pm shift?
- Do you now or at a future date require visa sponsorship to work in the United States?
- How many years' experience do you have working for a Class III medical device company?
- How many years' experience do you have handling and inspecting tissue biologics?
Education
High school or equivalent (Required)
Experience
Medical device quality inspection: 1 year (Required)
ABILITY TO COMMUTE
Maple Grove, MN 55369 (Required)
WORK LOCATION
In person
Anteris Technologies recruits, employs, trains, compensates and promotes regardless of race, religion, color, national origin, sex, disability, age, veteran status, and other protected status as required by applicable law. We have a clear vision: to be a place of belonging for all humans by promoting diversity, multiculturism and inclusion, as a goal and reflection across the organization. Diversity is more than a commitment - it is part of our mission to deliver the best structural heart products on a global scale.
Quality Control Technician Job Roles in Minnesota
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Search Quality Control Technician Jobs in MinnesotaQuality Control Technician Jobs in Minnesota: Frequently Asked Questions
Which companies sponsor visas for quality control technicians in Minnesota?
Medtronic, Boston Scientific, and Smiths Medical are among the larger Minnesota employers with established visa sponsorship programs for quality control technicians in medical device manufacturing. In food and beverage, General Mills and Land O'Lakes have sponsored technical roles. 3M's operations across the Twin Cities and Maplewood also generate QC technician openings. Sponsorship availability varies by facility, headcount, and hiring cycle, so confirming directly with employers is advisable.
Which visa types are most common for quality control technician roles in Minnesota?
The H-1B visa is the most common visa for quality control technicians whose roles require at least a bachelor's degree in a relevant field such as engineering, chemistry, or materials science. Roles structured around an associate degree or technical certification may not qualify as H-1B specialty occupations. Some candidates with Canadian or Mexican citizenship use the TN visa under the USMCA if their role fits a qualifying professional category. Each situation depends on how the employer structures the position.
Which cities in Minnesota have the most quality control technician sponsorship jobs?
The Twin Cities metro, encompassing Minneapolis and St. Paul, concentrates the highest volume of quality control technician openings given its density of medical device and food manufacturing headquarters. Rochester sees QC demand tied to healthcare and precision manufacturing. St. Cloud and Mankato have active food and industrial manufacturing sectors with recurring technician needs. Smaller cities like Arden Hills and Maple Grove also host major employer campuses with quality assurance functions.
How to find quality control technician visa sponsorship jobs in Minnesota?
Migrate Mate filters job listings specifically by visa sponsorship availability, making it easier to identify quality control technician roles in Minnesota where employers are open to sponsoring international candidates. Rather than sorting through general job boards, you can browse Minnesota QC technician postings on Migrate Mate knowing sponsorship is already a stated or likely requirement. Setting up role-specific alerts helps you respond quickly when new listings appear in medical device, food production, or industrial manufacturing.
What should international quality control technicians know about Minnesota's hiring environment?
Minnesota's medical device industry is one of the largest in the country, and many QC roles require familiarity with FDA regulatory frameworks, ISO 13485, or Good Manufacturing Practices. Employers in this sector often expect candidates to demonstrate hands-on experience with specific inspection or testing equipment. The University of Minnesota and Minnesota State system produce engineering and science graduates that QC teams draw from, so international candidates benefit from aligning their credentials and experience with these technical benchmarks when applying.
What is the prevailing wage for sponsored quality control technician jobs in Minnesota?
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.