embecta Visa Sponsorship Jobs USA
embecta is a medical device company focused on diabetes care, known for sponsoring Green Card pathways for skilled professionals in regulated healthcare and engineering roles. While not the highest-volume sponsor in its sector, it offers a genuine pathway for qualified candidates seeking long-term U.S. employment in medical devices.
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Get Access To All JobsINTRODUCTION
embecta is a global medical device company with a 100-year legacy in insulin delivery and diabetes care. Driven by innovation, purpose, and a commitment to improving lives, we are expanding our portfolio of solutions to serve even more patients, healthcare providers, and communities around the world.
As a Production Operator in our advanced Holdrege manufacturing facility, you’ll help build life-changing insulin delivery syringes that support and positively impact millions globally. This is work that matters—and we’ll make sure you’re supported every step of the way.
The Holdrege manufacturing facility runs 24 hours a day, 7 days a week, producing 2.3 billion medical devices annually. Our team includes approximately 450 people across our operation on both day and night shifts.
We are currently hiring for production operators for a 12 hour night shift.
What’s in it for you?
- Competitive pay & benefits
- Health coverage & retirement plans
- Paid time off to recharge
- Career growth opportunities
- A team that values your impact
- Comprehensive onboarding and training program
Ready to make a difference? Apply now and power the future of diabetes care with embecta.
What Does a Production Operator Do?
As a Production Operator, you’ll be at the heart of our manufacturing process. Here’s what your typical day might look like:
- Gown up with the required PPE (personal protective equipment) and safety shoes.
- Start your shift by checking in with your team and reviewing the day’s goals.
- Depending on whether you work in Molding, Assembly, Packaging or Warehouse, you will set up and operate the relevant machines and equipment that mold, assemble and package our insulin syringes.
- Regularly throughout your shift, you will inspect the products and perform in-process checks to ensure products meet our high quality standards and regulatory requirements.
- Completing inspection and quality documentation is the norm in a highly regulated medical devices facility and will be a critical part of your role.
- At times, you will move raw material supplies and finished products to the necessary locations in the facility.
- You will continually monitor the equipment for output and issues and help problem-solve efficiently and quickly should something go wrong.
- You will work as part of a highly engaged team to keep everything running smoothly and safely, with safety being your highest priority.
Paperwork Matters
In this role, accurate paperwork is essential. It helps us prove our products are safe, meet our regulatory requirements and ensures we can trace and fix any issues quickly. If you're detail-oriented and like doing things right, this is the job for you!
What You Bring:
- High School Diploma or GED
- At least 1 year of experience working with or fixing manufacturing equipment
- Excellent attention to detail in reading and completing product quality checks and documentation.
- Comfortable using computers and basic software like Microsoft Office
- Good communication skills and a team-first attitude
- Reliable, organized, and ready to learn
- An innate focus on safety, naturally integrating safety considerations into your daily work and decision making
Join Us in Making a Difference
If you're ready to play a hands-on role in improving the lives of people with diabetes around the world, we want to hear from you. Apply today to become a Production Operator at embecta and help shape a healthier future.
(04 Packager - D Shift)
embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
INTRODUCTION
embecta is a global medical device company with a 100-year legacy in insulin delivery and diabetes care. Driven by innovation, purpose, and a commitment to improving lives, we are expanding our portfolio of solutions to serve even more patients, healthcare providers, and communities around the world.
As a Production Operator in our advanced Holdrege manufacturing facility, you’ll help build life-changing insulin delivery syringes that support and positively impact millions globally. This is work that matters—and we’ll make sure you’re supported every step of the way.
The Holdrege manufacturing facility runs 24 hours a day, 7 days a week, producing 2.3 billion medical devices annually. Our team includes approximately 450 people across our operation on both day and night shifts.
We are currently hiring for production operators for a 12 hour night shift.
What’s in it for you?
- Competitive pay & benefits
- Health coverage & retirement plans
- Paid time off to recharge
- Career growth opportunities
- A team that values your impact
- Comprehensive onboarding and training program
Ready to make a difference? Apply now and power the future of diabetes care with embecta.
What Does a Production Operator Do?
As a Production Operator, you’ll be at the heart of our manufacturing process. Here’s what your typical day might look like:
- Gown up with the required PPE (personal protective equipment) and safety shoes.
- Start your shift by checking in with your team and reviewing the day’s goals.
- Depending on whether you work in Molding, Assembly, Packaging or Warehouse, you will set up and operate the relevant machines and equipment that mold, assemble and package our insulin syringes.
- Regularly throughout your shift, you will inspect the products and perform in-process checks to ensure products meet our high quality standards and regulatory requirements.
- Completing inspection and quality documentation is the norm in a highly regulated medical devices facility and will be a critical part of your role.
- At times, you will move raw material supplies and finished products to the necessary locations in the facility.
- You will continually monitor the equipment for output and issues and help problem-solve efficiently and quickly should something go wrong.
- You will work as part of a highly engaged team to keep everything running smoothly and safely, with safety being your highest priority.
Paperwork Matters
In this role, accurate paperwork is essential. It helps us prove our products are safe, meet our regulatory requirements and ensures we can trace and fix any issues quickly. If you're detail-oriented and like doing things right, this is the job for you!
What You Bring:
- High School Diploma or GED
- At least 1 year of experience working with or fixing manufacturing equipment
- Excellent attention to detail in reading and completing product quality checks and documentation.
- Comfortable using computers and basic software like Microsoft Office
- Good communication skills and a team-first attitude
- Reliable, organized, and ready to learn
- An innate focus on safety, naturally integrating safety considerations into your daily work and decision making
Join Us in Making a Difference
If you're ready to play a hands-on role in improving the lives of people with diabetes around the world, we want to hear from you. Apply today to become a Production Operator at embecta and help shape a healthier future.
(04 Packager - D Shift)
embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
Job Roles at embecta
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Get Access To All JobsTips for Finding embecta Visa Sponsorship Jobs USA
Target roles in regulated technical and engineering functions
embecta's sponsorship history skews toward specialized roles in medical device development and regulatory environments. Focus your application on positions in R&D, quality engineering, regulatory affairs, or manufacturing science where deep technical expertise justifies the sponsorship investment.
Understand that embecta sponsors Green Card pathways, not H-1B visas
embecta's sponsorship activity centers on permanent residency rather than temporary work visas. If you already hold valid U.S. work authorization, this makes embecta a strong long-term play for candidates looking to secure a Green Card through EB-2 or EB-3 classification.
Position yourself as a long-term hire, not a short-term resource
Companies that prioritize Green Card sponsorship are investing in retention. Frame your application and interviews around long-term contributions, domain expertise in diabetes care or device manufacturing, and your commitment to growing within the regulated medical device space.
Research embecta's core product lines before applying
embecta operates in a narrow, specialized segment of diabetes management. Candidates who demonstrate fluency in the company's product focus and relevant FDA regulatory frameworks stand out significantly in a technical interview process typical of medical device employers.
Confirm active openings before investing in your application
embecta sponsors selectively, so timing your application to an open role aligned with your background matters. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history and identify current openings at embecta without guesswork.
Be prepared for a thorough hiring process given the regulatory environment
Medical device companies like embecta operate under strict FDA oversight, which means hiring timelines are often longer and more structured than in other industries. Expect multiple interview rounds, technical assessments, and compliance-related screening before any sponsorship conversation begins.
Frequently Asked Questions
Does embecta sponsor H-1B visas?
Based on available sponsorship data, embecta does not have a significant history of H-1B visa sponsorship. Its visa activity is concentrated on permanent residency pathways, specifically EB-2 and EB-3 Green Card sponsorship. If you require H-1B sponsorship to maintain current work authorization, embecta may not be the right fit unless you already hold a work-authorized status.
What visa types does embecta sponsor?
embecta sponsors employment-based Green Card categories, primarily EB-2 and EB-3. These pathways suit candidates with advanced degrees or substantial experience in medical device roles. EB-2 typically covers professionals with a master's degree or higher, while EB-3 applies to bachelor's-level professionals and skilled workers in qualifying positions at the company.
Which departments or roles at embecta are most likely to receive visa sponsorship?
Sponsorship at embecta tends to align with technical, scientific, and regulatory functions where specialized expertise is hardest to source domestically. Roles in quality assurance, regulatory affairs, research and development, and manufacturing engineering within the diabetes care device space are the most likely candidates for Green Card sponsorship support.
How do I find open roles at embecta that offer visa sponsorship?
Migrate Mate is the most efficient way to identify current openings at embecta that align with verified sponsorship activity. Rather than sorting through generic job listings, Migrate Mate filters opportunities by real sponsorship history so you can focus your effort on roles where sponsorship has actually been granted, saving significant time in your search.
How do I approach the application process at embecta as a sponsored candidate?
Because embecta sponsors Green Cards rather than H-1B visas, the most practical approach is to apply while holding existing work authorization, then raise sponsorship as a long-term discussion once you have an offer. Be upfront about your immigration status early in the process, and emphasize your expertise in FDA-regulated environments and medical device development to demonstrate the value that justifies the sponsorship commitment.