Medical Devices Green Card Sponsorship Jobs in Colorado
Colorado's medical devices sector spans the Denver metro, Boulder, and the Front Range corridor, with employers like DaVita, Integra LifeSciences, and Natus Medical among those who have sponsored Green Card petitions. Roles in device engineering, regulatory affairs, and quality assurance are the most common pathways to permanent residency sponsorship in this industry.
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Electromechanical Assembler
Date: Jul 24, 2026
Location: Lakewood, CO, US
Company: Terumo BCT, Inc.
Requisition ID: 35307
At Terumo Blood and Cell Technologies, our 8,000+ global associates proud to come to work each day, knowing that what we do impacts the lives of patients around the world. For Terumo, for Everyone, Everywhere.
We make medical devices and related products that are used to collect, separate, manufacture and process various components of blood and cells. With our innovative technologies and service offerings, we touch a patient’s life every second of every day and are committed to continuing to increase the number of patients we serve. Advancing healthcare with heart.
With some of the best and brightest minds in the industry, an unmatched global footprint, comprehensive benefits and a distinct culture, Terumo Blood and Cell Technologies is a great place to work, grow and be part of a team that is focused on making a difference. Join us and help shape wherever we go next. You create your future and ours.
JOB SUMMARY
The primary functions of this job require accountability for manufacturing procedures and associated documentation and processes. This includes testing, assembling, trouble shooting electronic and mechanical subassemblies and electromechanical medical devices in accordance with applicable regulatory requirements and written procedures.
ESSENTIAL DUTIES
- Takes ownership over all aspects of processes and procedures including training, safety, quality, and efficiencies.
- Applies technique and quality criteria for use of specialized tools and test equipment.
- Assembles, tests, troubleshoots, calibrates and packages highly complex mechanical and electronic sub-assemblies.
- Applies extensive knowledge to adhere to GMP compliance on the manufacturing floor.
- Identifies potential issues that may impact production schedules and is a key contributor in formulating the response to maintain those schedules.
- Detects non-conforming product and dispositions according to company procedure.
- Executes and maintains monthly production schedule.
- Works with and assists engineers, leadership, buyers, planners, material handlers and technicians in problem solving of quality and safety, production process, and raw material issues including prototyping, specialty builds, validations and implementing new materials, designs, maintenance and process improvements.
- Performs area clearance and setup of work stations.
- Performs documentation and regulatory record keeping as defined in the standard operating procedures for manufacturing. This includes but not limited to device history records, work order generation and product labels.
- Provides and receives constructive work direction and feedback without shutting down communication among team members.
- Performs quality control checks on finished products and documentation prior to release. This includes processing and packaging returned goods from customers/vendors and finished goods inventory.
- Ensures efficiency of material loading and unloading for work station.
- Conducts thorough practices with inspecting, packaging, and labeling of product.
- Contributes to resolution and sorting of nonconforming products and processes.
- Requires the ability to work overtime to meet business needs.
- Demonstrates high proficiency with the use of required hand-tools and test equipment.
- Applies technique and quality criteria for soldering as well as use of specialized tools and test equipment.
- Interfaces frequently with computer and understands navigational functions.
MINIMUM QUALIFICATION REQUIREMENTS
Education
- High school diploma or GED.
- Technical background is preferred.
Experience
- Minimum 2 years experience.
- Demonstrated knowledge and maintained competency in all areas required at the assembler level.
- Equivalent experience sufficient to successfully perform the essential functions of the job may be considered.
Skills
- Knowledge and understanding of safety protocols required for operating automated and semi-automated equipment.
- Ability to add, subtract, multiply, and divide whole numbers, decimals and fractions; reason through mathematical word problems; and read tables, scales, graphs, and charts quickly and accurately.
- Understanding usage of the English language; good understanding of words used in business and regulatory environments; ability to memorize different terms and their meanings; and ability to read, comprehend and generate reports, documents, procedures, etc. that may be technical in nature.
- Advanced understanding of manufacturing operating procedures that apply to technical, automated, semi-automated operating systems as well as assembling, testing, and packaging of mechanical and electronic subassemblies and packaging of electromechanical medical devices using safe handling and assembly techniques.
- Understanding of mechanical principles and analysis of mechanical movement. Attention to detail for spotting imperfections or flaws and ability to identify a simple figure that is part of a complete drawing, able to visualize how separate pieces will work as a whole.
- Strong team cooperation and ability to prioritize workload to meet schedule requirements.
- Demonstrated ability to communicate effectively both verbally and in writing.
- Must be able to make decisions based on changes and multiple priorities.
- Knowledge and use of relevant PC software applications and skills to use them effectively.
- Demonstrated ability to assemble, test, calibrate, and troubleshoot mechanical and electronic subassemblies and electromechanical medical devices using safe handling and assembly techniques.
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Ability to continue learning and increase competency in specialty tools such as digital volt meters (DVM), torque wrenches, etc. Demonstrate high proficiency with the use of required hand tools and test equipment.
-
Or -
An equivalent competency level acquired through a variation of these qualifications may be considered.
Physical Requirements
Manufacturing Environment requirements include: use of personal protective equipment, reading, speaking, hearing, walking, bending, standing, stretching/reaching, and hand/finger dexterity.
- Requires ability to lift up to 50 pounds and transport up to 500 pounds via carts, racks or mechanized equipment, up to 1,500 pounds by pallet jack and up to 5,000 pounds by electric pallet jack.
- Requires good manual dexterity and visual acuity including ability to distinguish colors.
- Must be able to maintain pace with the area assigned.
- Requires the ability to regularly perform repetitive motions.
- Must be able to work under fluorescent lighting.
- Requires the ability to sit or stand through the duration of a shift.
The physical demands described here are representative of those that must be met by an associate to successfully perform the essential duties of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential duties.
Target Pay Range: $17.00 to $22.00 - Hourly pay rate to be determined by the education, experience, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data
Target Bonus on Base: 7.0%
We anticipate this requisition will be open for a minimum of five days. We encourage your prompt application.
At Terumo Blood and Cell Technologies, we provide competitive total reward offerings that consist of compensation, benefits, recognition, along with a wealth of other well-being, work-life and recognition programs which support in unlocking the potential for you and your family. Included in our expansive list of benefits offerings are multiple group medical, dental and vision plans, a robust wellness program, life insurance and disability coverages, also a variety of voluntary programs such as group accident, hospital indemnity, critical illness, pet insurance and much more. To help you save for retirement, we offer a 401(k) plan with a matching contribution and for work-life balance we have vacation and sick time programs for associates. For us, it’s about protecting the personal welfare of our associates and their families, helping to achieve personal goals and offering those extra touches for convenience, security and overall peace of mind.
Terumo Blood and Cell Technologies is part of Terumo Group, founded in 1921 and headquartered in Tokyo, Japan.
In 2024, Terumo Blood and Cell Technologies reached $1.5 billion in revenue.
We employ nearly 8,000 associates globally, with global headquarters in Lakewood, CO, U.S., and regional headquarters in Brussels, Buenos Aires, Singapore and Tokyo.
We manufacture devices, disposable sets and solutions at our facilities in Belgium, India, Japan, Northern Ireland, the U.S. and Vietnam. Our global presence enables us to serve customers in more than 130 countries.
Our core values help set our direction, guide our actions and keep us true to our corporate mission of contributing to society through healthcare.
- Respect – Appreciative of others
- Integrity – Guided by our mission
- Care – Empathetic to patients
- Quality – Committed to excellence
- Creativity – Striving for innovation
We contribute to the Leukemia and Lymphoma Society (LLS), raising $2.4 million USD since 2025.
We are proud to be an Equal Opportunity Affirmative Action Employer. All applicants will be afforded equal opportunity without discrimination because of race, color, religion, sex, gender identity or expression, sexual orientation, marital status, order of protection status, national origin or ancestry, citizenship status, age, physical or mental disability unrelated to ability, military status or an unfavorable discharge from military service.
Terumo Blood and Cell Technologies is committed to providing a safe, healthy and secure working environment. Our Colorado campus locations are tobacco-free workplaces, and we maintain a drug-free workplace and perform pre-employment substance abuse testing and detailed background verification.
Green Card Medical Devices Job Roles in Colorado
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Search Medical Devices Jobs in ColoradoMedical Devices Green Card Sponsorship Jobs in Colorado: Frequently Asked Questions
Which medical devices companies sponsor Green Card visas in Colorado?
Several medical devices employers operating in Colorado have documented histories of Green Card sponsorship, including companies in the Denver-Boulder corridor focused on cardiovascular, neurology, and diagnostic imaging devices. Larger manufacturers and multinational device companies are more likely to have established immigration programs. Smaller Colorado-based device startups do sponsor, but less consistently, as the process requires dedicated legal and HR resources.
Which cities in Colorado have the most medical devices Green Card sponsorship jobs?
Denver and its surrounding suburbs, particularly Englewood, Broomfield, and Lakewood, account for the highest concentration of medical devices employers in Colorado. Boulder also has a meaningful cluster of device and life sciences companies. Fort Collins and Colorado Springs have smaller but growing medical technology presences, with sponsorship opportunities tied primarily to manufacturing and engineering facilities in those areas.
What types of medical devices roles typically qualify for Green Card sponsorship?
Roles that most commonly receive employer-sponsored Green Card petitions in medical devices include regulatory affairs specialists, quality engineers, R&D engineers, software engineers working on device software, and manufacturing engineers. These positions generally require specialized degrees in biomedical, electrical, or mechanical engineering, or in regulatory science. Positions requiring niche technical expertise or advanced credentials tend to attract sponsorship more readily than generalist roles.
How do I find medical devices Green Card sponsorship jobs in Colorado?
Migrate Mate filters job listings specifically by visa type, industry, and state, making it straightforward to browse medical devices roles with Green Card sponsorship in Colorado without sorting through positions that don't offer immigration support. Using Migrate Mate, you can identify which Colorado employers are actively hiring internationally and narrow results to the device engineering, quality, and regulatory roles most associated with permanent residency sponsorship.
Are there any Colorado-specific considerations for Green Card sponsorship in medical devices?
Colorado's medical devices sector is closely tied to its broader life sciences and aerospace manufacturing base, which means many employers have experience with employment-based immigration across technical disciplines. The state does not impose additional requirements on top of federal Green Card processes, but Colorado's competitive hiring market for device engineers means employers sometimes initiate the PERM labor certification process earlier to secure talent. Candidates in regulatory affairs and quality roles should be aware that PERM timelines can extend well beyond initial hiring.
What is the prevailing wage for Green Card medical devices jobs in Colorado?
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.