Medical Devices Visa Sponsorship Jobs in Puerto Rico
Puerto Rico's medical devices industry offers significant visa sponsorship opportunities, particularly in San Juan and the central manufacturing corridor. Major employers like Medtronic, Abbott, and Boston Scientific operate substantial facilities across the island, creating demand for engineers, regulatory specialists, and manufacturing professionals with specialized expertise.
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Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake lifesaving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible.
ROLE AND RESPONSIBILITIES
The Quality Engineering Specialist is responsible for providing primary Quality Operations support to Filtration and D&M units at the Fajardo site, ensuring compliant and timely manufacturing activities, documentation, data review, and issue resolution. Also supports cross functional execution, serves as RTC backup, and assists with complaint handling and minor investigations to maintain continuity and compliance. This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance Engineering Team located in Fajardo, Puerto Rico and will be an on-site role.
What You Will Do
Provide day-to-day Quality Operations support for Filtration and D&M manufacturing areas, including manufacturing floor support, documentation review, quality issue triage, and timely escalation of compliance or product quality risks.
- Support customer complaint handling by reviewing complaint information, coordinating sample receipt and analysis, documenting investigation activities, and preparing clear, evidence-based inputs for interim and final customer responses.
- Lead or support investigations and nonconformance assessments, including problem statement development, impact and risk evaluation, root cause analysis, containment, disposition, and timely closure in accordance with applicable procedures.
- Partner with Manufacturing, Engineering, Laboratory, Product Engineering, and Quality teams to drive cross-functional issue resolution, ensure accurate record documentation, and maintain continuity of compliant operations.
- Identify, support, and execute continuous improvement opportunities using DBS and quality system data, including complaint trends, recurring nonconformances, process gaps, and investigation outcomes to improve quality performance and prevent recurrence.
BASIC QUALIFICATIONS
- Bachelor’s degree in Biology, Microbiology, Engineering, or a related scientific or technical discipline.
- Long-standing experience (Minimum of 5-10 years) in regulated life sciences, medical device, pharmaceutical, biotechnology, or manufacturing environments.
- Demonstrated experience supporting cleanroom or controlled environment operations, including environmental controls, contamination control practices, or cleanroom-related quality oversight.
- Demonstrated experience leading or supporting quality investigations, customer complaints, nonconformances, root cause analysis, CAPA, risk assessments, or change control within a Quality Management System.
- Proficiency using electronic quality systems and digital tools, with experience applying AI-enabled tools, data analysis, or automation to support investigation quality, prioritization, metrics, or continuous improvement activities.
PREFERRED QUALIFICATIONS
It would be a plus if you also possess previous experience in:
- DBS, Lean Six Sigma, Toyota Lean System
- Cleanroom Management and Controlled Environments
- Life Sciences, Pharmaceuticals and Medical Devices
Travel, Motor Vehicle Record & Physical/Environment Requirements:
- Ability to travel – list specifics 2% travel, overnight, within territory or locations
- Must have a valid driver’s license with an acceptable driving record
- Ability to lift, move or carry equipment up to 10lb, any other physical requirements
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here. For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer please click here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: 1-202-419-7762 or applyassistance@danaher.com.
INTRODUCTION
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake lifesaving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible.
ROLE AND RESPONSIBILITIES
The Quality Engineering Specialist is responsible for providing primary Quality Operations support to Filtration and D&M units at the Fajardo site, ensuring compliant and timely manufacturing activities, documentation, data review, and issue resolution. Also supports cross functional execution, serves as RTC backup, and assists with complaint handling and minor investigations to maintain continuity and compliance. This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance Engineering Team located in Fajardo, Puerto Rico and will be an on-site role.
What You Will Do
Provide day-to-day Quality Operations support for Filtration and D&M manufacturing areas, including manufacturing floor support, documentation review, quality issue triage, and timely escalation of compliance or product quality risks.
- Support customer complaint handling by reviewing complaint information, coordinating sample receipt and analysis, documenting investigation activities, and preparing clear, evidence-based inputs for interim and final customer responses.
- Lead or support investigations and nonconformance assessments, including problem statement development, impact and risk evaluation, root cause analysis, containment, disposition, and timely closure in accordance with applicable procedures.
- Partner with Manufacturing, Engineering, Laboratory, Product Engineering, and Quality teams to drive cross-functional issue resolution, ensure accurate record documentation, and maintain continuity of compliant operations.
- Identify, support, and execute continuous improvement opportunities using DBS and quality system data, including complaint trends, recurring nonconformances, process gaps, and investigation outcomes to improve quality performance and prevent recurrence.
BASIC QUALIFICATIONS
- Bachelor’s degree in Biology, Microbiology, Engineering, or a related scientific or technical discipline.
- Long-standing experience (Minimum of 5-10 years) in regulated life sciences, medical device, pharmaceutical, biotechnology, or manufacturing environments.
- Demonstrated experience supporting cleanroom or controlled environment operations, including environmental controls, contamination control practices, or cleanroom-related quality oversight.
- Demonstrated experience leading or supporting quality investigations, customer complaints, nonconformances, root cause analysis, CAPA, risk assessments, or change control within a Quality Management System.
- Proficiency using electronic quality systems and digital tools, with experience applying AI-enabled tools, data analysis, or automation to support investigation quality, prioritization, metrics, or continuous improvement activities.
PREFERRED QUALIFICATIONS
It would be a plus if you also possess previous experience in:
- DBS, Lean Six Sigma, Toyota Lean System
- Cleanroom Management and Controlled Environments
- Life Sciences, Pharmaceuticals and Medical Devices
Travel, Motor Vehicle Record & Physical/Environment Requirements:
- Ability to travel – list specifics 2% travel, overnight, within territory or locations
- Must have a valid driver’s license with an acceptable driving record
- Ability to lift, move or carry equipment up to 10lb, any other physical requirements
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here. For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer please click here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: 1-202-419-7762 or applyassistance@danaher.com.
Medical Devices Job Roles in Puerto Rico
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Search Medical Devices Jobs in Puerto RicoMedical Devices Jobs in Puerto Rico: Frequently Asked Questions
Which medical devices companies sponsor visas in Puerto Rico?
Major medical devices companies with Puerto Rico operations that sponsor visas include Medtronic (cardiovascular devices), Abbott (diagnostics and medical devices), Boston Scientific (interventional medical solutions), Covidien (surgical instruments), and Johnson & Johnson subsidiary companies. These multinational corporations maintain significant manufacturing and R&D facilities across the island and regularly sponsor H-1B visa, TN visa, and other work visas for qualified professionals.
How to find medical devices visa sponsorship jobs in Puerto Rico?
Use Migrate Mate to search specifically for medical devices positions in Puerto Rico with visa sponsorship. The platform filters jobs by industry and location, showing which companies actively sponsor work visas. Focus on manufacturing hubs in San Juan, Manatí, and Las Piedras where major medical devices companies operate production facilities and research centers requiring specialized talent from international professionals.
Which cities in Puerto Rico have the most medical devices sponsorship jobs?
San Juan leads with the highest concentration of medical devices visa sponsorship opportunities, followed by Manatí and Las Piedras in the central manufacturing corridor. Aguadilla and Humacao also host significant medical devices operations. These cities benefit from established industrial infrastructure, proximity to Luis Muñoz Marín International Airport, and tax incentives that attract major medical devices manufacturers requiring specialized international talent.
What visa types are most common for medical devices roles in Puerto Rico?
H-1B visas dominate medical devices sponsorship in Puerto Rico for engineering, regulatory affairs, and quality assurance positions requiring specialized knowledge. TN visas serve Canadian and Mexican professionals in similar roles. L-1 visas facilitate transfers within multinational medical devices companies operating both mainland U.S. and Puerto Rico facilities. O-1 visas occasionally apply for professionals with extraordinary ability in medical device innovation or research.
Are prevailing wages different for medical devices jobs in Puerto Rico?
Yes, prevailing wages in Puerto Rico are generally lower than mainland U.S. rates, which can affect H-1B applications requiring minimum wage thresholds. However, major medical devices companies often pay competitive rates to attract specialized talent. The Department of Labor sets specific prevailing wage determinations for Puerto Rico based on local market conditions, and companies must meet these requirements for successful visa sponsorship applications.
What is the prevailing wage for sponsored medical devices jobs in Puerto Rico?
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.