Software Quality Engineer Visa Sponsorship Jobs in Puerto Rico
Software quality engineer visa sponsorship jobs in Puerto Rico are concentrated in San Juan and surrounding tech corridors, where employers in financial services, healthcare IT, and pharmaceutical manufacturing rely on QA talent to maintain compliance-driven software systems. Companies with significant island operations, including major pharmaceutical firms and federal contractors, have sponsored roles at this level.
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Get Access To All JobsJOB DESCRIPTION:
Quality Engineer
About Abbott
Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:
- Career development with an international company where you can grow the career you dream of.
- Health Insurance (starting on Day 1 of employment), Savings Plan (401K) with company match, Life insurance for you and your spouse/children, Short Term Disability, Long Term Disability, Education Assistance, Employee Assistance Program, Vacation, Sick, Personal Days.
- A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
- A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
This position works out of our Barceloneta location in the Abbott Vascular division. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease.
This is an exempt role: 2nd (Second) Shift
As the Quality Engineer, you’ll provide Process/Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer by assisting in the identification and resolution of quality related issues.
What You’ll Do
- Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
- Identifies manufacturing process defects (scrap, nonconforming material, customer complaints), dispositions non-conforming material, leads identification of primary root causes for basic investigations, identifies appropriate corrective and preventive actions.
- Supports line support team (QC Supervisor, Mfg Supervisor, Quality Engineer and Operations) to perform line situation triage and determine if non-conformance is present, determine initial bracketing and containment, and initiate exception management process.
- Owns basic to moderate exception / CAPA activities without oversight.
- May be responsible for working with process owner to bound product stops and document release criteria.
- Can perform lot to lot yield and rework evaluation.
- May be responsible for reporting of quality metrics.
- Understands product quality plans, documents, and quality systems.
- Develops product quality plans, documents and systems by providing input to product specifications, quality specifications, quality plans, risk analyses, FMEAs in conjunction with other product development team members.
- May be responsible for owning and maintaining product risk analyses and FMEAs.
- Monitors process by using process monitoring tools and Infinity QS to reduce process variation.
- Becomes familiar with Product/Process improvement efforts by understanding current quality metric data and learning the various analysis methods used to enhance sustaining product design and new product development.
- Understands Quality Tools & Training Materials and helps others in gaining knowledge of prevalent tools used and available training materials.
- Can lead Product/Process improvement efforts (e.g. scrap, nonconforming product, customer complaints) by systematically gathering quality metric data and by using appropriate analysis methods to enhance sustaining product design.
- Runs routine problem-solving investigation without oversight and use of six Sigma tools.
- Implements minor and major changes through change management system and provides quality engineering impact assessment for changes implemented by other functional areas.
- May write protocols and reports with management oversight to support engineering studies and validations.
Required Qualifications
- B.S. in engineering discipline
- 2 years of experience in Quality and/or Compliance, preferably in medical device industry
Preferred Qualifications
- Knowledge of applicable US non-US applicable regulations.
- Knowledge and proficiency in the application and principles of Quality Engineering.
- Ability to effectively communicate cross-functionally to assist with resolving Quality issues.
- Excellent written, verbal and interpersonal communication skills in both English and Spanish.
- Ability to interact effectively with all levels of employees.
The base pay for this position is
$54,300.00 – $109,000.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY: Operations Quality
DIVISION: CRM Cardiac Rhythm Management
LOCATION: Puerto Rico > Arecibo : Santana Industrial Park Interior Lot A, Road #2, Km 67.5
WORK SHIFT: Standard
TRAVEL: No
MEDICAL SURVEILLANCE: No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
Abbott is an Equal Opportunity Employer, committed to employee diversity.
JOB DESCRIPTION:
Quality Engineer
About Abbott
Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:
- Career development with an international company where you can grow the career you dream of.
- Health Insurance (starting on Day 1 of employment), Savings Plan (401K) with company match, Life insurance for you and your spouse/children, Short Term Disability, Long Term Disability, Education Assistance, Employee Assistance Program, Vacation, Sick, Personal Days.
- A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
- A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
This position works out of our Barceloneta location in the Abbott Vascular division. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease.
This is an exempt role: 2nd (Second) Shift
As the Quality Engineer, you’ll provide Process/Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer by assisting in the identification and resolution of quality related issues.
What You’ll Do
- Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
- Identifies manufacturing process defects (scrap, nonconforming material, customer complaints), dispositions non-conforming material, leads identification of primary root causes for basic investigations, identifies appropriate corrective and preventive actions.
- Supports line support team (QC Supervisor, Mfg Supervisor, Quality Engineer and Operations) to perform line situation triage and determine if non-conformance is present, determine initial bracketing and containment, and initiate exception management process.
- Owns basic to moderate exception / CAPA activities without oversight.
- May be responsible for working with process owner to bound product stops and document release criteria.
- Can perform lot to lot yield and rework evaluation.
- May be responsible for reporting of quality metrics.
- Understands product quality plans, documents, and quality systems.
- Develops product quality plans, documents and systems by providing input to product specifications, quality specifications, quality plans, risk analyses, FMEAs in conjunction with other product development team members.
- May be responsible for owning and maintaining product risk analyses and FMEAs.
- Monitors process by using process monitoring tools and Infinity QS to reduce process variation.
- Becomes familiar with Product/Process improvement efforts by understanding current quality metric data and learning the various analysis methods used to enhance sustaining product design and new product development.
- Understands Quality Tools & Training Materials and helps others in gaining knowledge of prevalent tools used and available training materials.
- Can lead Product/Process improvement efforts (e.g. scrap, nonconforming product, customer complaints) by systematically gathering quality metric data and by using appropriate analysis methods to enhance sustaining product design.
- Runs routine problem-solving investigation without oversight and use of six Sigma tools.
- Implements minor and major changes through change management system and provides quality engineering impact assessment for changes implemented by other functional areas.
- May write protocols and reports with management oversight to support engineering studies and validations.
Required Qualifications
- B.S. in engineering discipline
- 2 years of experience in Quality and/or Compliance, preferably in medical device industry
Preferred Qualifications
- Knowledge of applicable US non-US applicable regulations.
- Knowledge and proficiency in the application and principles of Quality Engineering.
- Ability to effectively communicate cross-functionally to assist with resolving Quality issues.
- Excellent written, verbal and interpersonal communication skills in both English and Spanish.
- Ability to interact effectively with all levels of employees.
The base pay for this position is
$54,300.00 – $109,000.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY: Operations Quality
DIVISION: CRM Cardiac Rhythm Management
LOCATION: Puerto Rico > Arecibo : Santana Industrial Park Interior Lot A, Road #2, Km 67.5
WORK SHIFT: Standard
TRAVEL: No
MEDICAL SURVEILLANCE: No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
Abbott is an Equal Opportunity Employer, committed to employee diversity.
Software Quality Engineer Job Roles in Puerto Rico
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Search Software Quality Engineer Jobs in Puerto RicoSoftware Quality Engineer Jobs in Puerto Rico: Frequently Asked Questions
Which companies sponsor visas for software quality engineers in Puerto Rico?
Pharmaceutical and biotech companies with manufacturing operations in Puerto Rico, including large multinationals with significant island presences, have historically sponsored software quality engineer roles tied to regulatory compliance systems. Federal contractors and financial technology firms in the San Juan metro also appear in sponsorship filings. Because sponsorship activity shifts year to year, checking current Labor Condition Application disclosure data gives the most accurate picture of active sponsors.
Which visa types are most common for software quality engineers in Puerto Rico?
The H-1B visa is the most common visa category for software quality engineers in Puerto Rico, as the role typically qualifies as a specialty occupation requiring a bachelor's degree in computer science, software engineering, or a related technical field. Candidates from Australia may qualify for the E-3 visa. Those with multinational employer relationships may explore the L-1B for specialized knowledge transfers. Each category has distinct employer obligations and processing requirements.
Which cities in Puerto Rico have the most software quality engineer sponsorship jobs?
San Juan and the broader metro area, including Guaynabo and Bayamon, account for the majority of software quality engineer sponsorship activity in Puerto Rico. These municipalities host corporate headquarters, technology service centers, and pharmaceutical operations that generate ongoing QA hiring. Humacao and Manati occasionally appear in filings linked to manufacturing and life sciences facilities, though volume there is considerably lower than in the capital region.
How to find software quality engineer visa sponsorship jobs in Puerto Rico?
Migrate Mate filters job listings specifically by visa sponsorship availability, so you can browse software quality engineer openings in Puerto Rico without manually screening out roles that won't support international candidates. The platform surfaces positions from employers who have indicated sponsorship willingness, which is particularly useful in Puerto Rico where the sponsoring employer pool is smaller than in mainland tech hubs. Searching by role and territory together narrows results meaningfully.
Are there state-specific considerations for software quality engineers seeking sponsorship in Puerto Rico?
Puerto Rico is a U.S. territory, so federal immigration law applies fully, including H-1B prevailing wage requirements set by the Department of Labor. However, the local tech labor market is smaller than mainland metros, meaning fewer employers file LCAs and sponsorship competition can be concentrated among a limited set of industries, primarily life sciences, financial services, and federal contracting. University pipelines from institutions like the University of Puerto Rico contribute local talent but do not reduce employer sponsorship obligations for foreign nationals.
What is the prevailing wage for sponsored software quality engineer 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.