Medical Devices Green Card Sponsorship Jobs in Puerto Rico
Green Card sponsorship jobs in Puerto Rico's medical devices industry are concentrated around major manufacturers in Aguadilla, Juncos, and the San Juan metro area. Companies like Medtronic, Boston Scientific, and Stryker operate significant facilities on the island, regularly sponsoring permanent residence for engineers, quality assurance specialists, and regulatory affairs professionals with specialized expertise.
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Get Access To All JobsINTRODUCTION
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.
Green Card Medical Devices Job Roles in Puerto Rico
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Search Medical Devices Jobs in Puerto RicoMedical Devices Green Card Sponsorship Jobs in Puerto Rico: Frequently Asked Questions
Which medical devices companies sponsor Green Card visas in Puerto Rico?
Puerto Rico hosts a substantial cluster of multinational medical devices manufacturers with documented Green Card sponsorship activity. Companies with major island operations include Medtronic, Boston Scientific, Stryker, Johnson & Johnson (DePuy Synthes), Becton Dickinson, and Abbott. These firms have filed PERM labor certification applications for roles spanning engineering, quality systems, regulatory affairs, and manufacturing operations. Sponsorship patterns are verifiable through OFLC disclosure data.
Which cities in Puerto Rico have the most medical devices Green Card sponsorship jobs?
The greatest concentration of medical devices Green Card sponsorship activity in Puerto Rico falls in the northwestern corridor, particularly Aguadilla, Arecibo, and Manatí, where large manufacturing campuses are established. Juncos and the eastern region also host several device manufacturers. The San Juan metropolitan area supports corporate, regulatory, and quality leadership roles. These municipalities together account for the majority of PERM filings in the island's medical devices sector.
What types of medical devices roles typically qualify for Green Card sponsorship?
Roles requiring specialized degrees and technical expertise are the most commonly sponsored. These include manufacturing engineers, process validation engineers, quality engineers, regulatory affairs specialists, reliability engineers, and R&D scientists. Positions tied to FDA-regulated production, design control, or CAPA systems are especially common in PERM filings. Roles that require a specific bachelor's or advanced degree in engineering, biology, chemistry, or a related field generally meet the specialty occupation threshold required to initiate the Green Card process.
How do I find medical devices Green Card sponsorship jobs in Puerto Rico?
Migrate Mate lists medical devices jobs in Puerto Rico filtered specifically for employers with verified Green Card sponsorship history, saving you from sorting through postings at companies that don't sponsor. You can filter by role type, location within Puerto Rico, and visa category to surface positions where PERM filings have been documented. This is more efficient than general job searches, since employer sponsorship intent for permanent residence is often not stated explicitly in job postings.
Are there Puerto Rico-specific considerations for Green Card sponsorship in medical devices?
Puerto Rico's medical devices industry operates under U.S. federal law, so PERM labor certification, I-140 petitions, and adjustment of status or consular processing timelines follow the same rules as the continental United States. One practical consideration is that Puerto Rico-based roles may involve Spanish-English bilingual requirements, which can affect how employers draft the minimum requirements used in PERM applications. Prevailing wage determinations for Puerto Rico positions are issued by OFLC and may differ from mainland metropolitan area wages for comparable roles.
What is the prevailing wage for Green Card 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.