Compliance Associate Visa Sponsorship Jobs in Puerto Rico
Compliance associate roles in Puerto Rico are concentrated in financial services, pharmaceuticals, and banking, with employers like Popular Inc., First BanCorp, and major pharma manufacturers on the island actively hiring. San Juan is the primary hub for these positions. International candidates seeking visa sponsorship will find H-1B visa and TN visa pathways most relevant here.
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Get Access To All JobsJOB DESCRIPTION:
Senior Quality Engineer. This position will support the Structural Heart business and will be based in Caguas, Puerto Rico.
On-site position.
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 will provide support to our Medical Devices / Structural Heart business. Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks. Our business purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural heart disease.
As the Senior 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 complex investigations, identifies appropriate corrective and preventive actions without oversight, and trains others in effective CAPA methods.
- Manages quality issues of moderate to high complexity with significant business impact with minimal to no oversight. Responsible for ensuring prompt communication of these issues as they arise and keeping management informed of the investigation status throughout the investigation and resolution lifecycles.
- Leads line support team (QC Supervisor, Mfg. Supervisor, Quality Engineer and Operations) to perform line situation triage and determine if non-conformance present can impact distributed product, determine initial bracketing and containment, and initiate stop ship and escalation process as required. May be responsible for reporting of quality metrics.
- May lead team in developing product quality plans, documents and systems by providing direction for setting product specifications, quality specifications, quality plans, risk analyses, and FMEAs. Responsible for providing support during internal and external audits.
- May be responsible for owning and maintaining product risk analyses and FMEAs. Mentors others in risk management process.
- Proficiently utilizes process monitoring tools and Infinity QS to understand process shifts and aims to reduce process variation. Mentors and trains others in SPC tools and process controls.
- Develops Quality Tools & Training Materials and trains others in use of prevalent tools 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.
- Leads or supports Divisional Product/Process improvement efforts by understanding current quality metric data to enhance sustaining product design, new product development, and compliance.
- Runs complex problem-solving efforts with minimal oversight, and mentors others on best practices.
- Implements complex changes through change management system and provides quality engineering impact assessment for changes implemented by other functional areas and/or sites.
- Works towards reducing site non-conformance index year over year.
- Writes protocols and reports with no oversight to support engineering studies and validations. Can develop complex test strategies, summarize statistical data, and mentor others in best practices. Works with minimal to no oversight.
Required Qualifications
- Bachelor's degree in engineering.
- Minimum 5 years of experience. Relevant experience in Quality and/or Compliance, preferably in medical device industry.
- Knowledge of applicable US & non-US applicable regulations.
- Knowledge and proficiency in the application and principles of Quality Engineering.
- Ability to effectively lead cross-functional teams in resolving Quality issues.
- Excellent written, verbal and interpersonal communication skills in Spanish and English.
- Ability to evaluate complex process.
- Ability to interact effectively with all levels.
- Digital skills, Microsoft office.
LOCATION:
Puerto Rico > Caguas : West Industrial Park Calle B, Lote #20
WORK SHIFT:
Standard
TRAVEL:
Yes, 5 % of the Time
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Keyboard use (greater or equal to 50% of the workday)
The base pay for this position is $66,000.00 – $132,000.00
In specific locations, the pay range may vary from the range posted.
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
JOB DESCRIPTION:
Senior Quality Engineer. This position will support the Structural Heart business and will be based in Caguas, Puerto Rico.
On-site position.
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 will provide support to our Medical Devices / Structural Heart business. Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks. Our business purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural heart disease.
As the Senior 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 complex investigations, identifies appropriate corrective and preventive actions without oversight, and trains others in effective CAPA methods.
- Manages quality issues of moderate to high complexity with significant business impact with minimal to no oversight. Responsible for ensuring prompt communication of these issues as they arise and keeping management informed of the investigation status throughout the investigation and resolution lifecycles.
- Leads line support team (QC Supervisor, Mfg. Supervisor, Quality Engineer and Operations) to perform line situation triage and determine if non-conformance present can impact distributed product, determine initial bracketing and containment, and initiate stop ship and escalation process as required. May be responsible for reporting of quality metrics.
- May lead team in developing product quality plans, documents and systems by providing direction for setting product specifications, quality specifications, quality plans, risk analyses, and FMEAs. Responsible for providing support during internal and external audits.
- May be responsible for owning and maintaining product risk analyses and FMEAs. Mentors others in risk management process.
- Proficiently utilizes process monitoring tools and Infinity QS to understand process shifts and aims to reduce process variation. Mentors and trains others in SPC tools and process controls.
- Develops Quality Tools & Training Materials and trains others in use of prevalent tools 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.
- Leads or supports Divisional Product/Process improvement efforts by understanding current quality metric data to enhance sustaining product design, new product development, and compliance.
- Runs complex problem-solving efforts with minimal oversight, and mentors others on best practices.
- Implements complex changes through change management system and provides quality engineering impact assessment for changes implemented by other functional areas and/or sites.
- Works towards reducing site non-conformance index year over year.
- Writes protocols and reports with no oversight to support engineering studies and validations. Can develop complex test strategies, summarize statistical data, and mentor others in best practices. Works with minimal to no oversight.
Required Qualifications
- Bachelor's degree in engineering.
- Minimum 5 years of experience. Relevant experience in Quality and/or Compliance, preferably in medical device industry.
- Knowledge of applicable US & non-US applicable regulations.
- Knowledge and proficiency in the application and principles of Quality Engineering.
- Ability to effectively lead cross-functional teams in resolving Quality issues.
- Excellent written, verbal and interpersonal communication skills in Spanish and English.
- Ability to evaluate complex process.
- Ability to interact effectively with all levels.
- Digital skills, Microsoft office.
LOCATION:
Puerto Rico > Caguas : West Industrial Park Calle B, Lote #20
WORK SHIFT:
Standard
TRAVEL:
Yes, 5 % of the Time
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Keyboard use (greater or equal to 50% of the workday)
The base pay for this position is $66,000.00 – $132,000.00
In specific locations, the pay range may vary from the range posted.
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
Compliance Associate Job Roles in Puerto Rico
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Search Compliance Associate Jobs in Puerto RicoCompliance Associate Jobs in Puerto Rico: Frequently Asked Questions
Which companies sponsor visas for compliance associates in Puerto Rico?
Financial institutions and pharmaceutical manufacturers are the most active sponsors in Puerto Rico. Popular Inc., FirstBank Puerto Rico, and Oriental Bank have compliance functions that have supported H-1B filings. On the pharma side, companies like AbbVie, Johnson and Johnson, and Amgen operate large manufacturing and regulatory compliance teams on the island and have established sponsorship track records.
Which visa types are most common for compliance associate roles in Puerto Rico?
The H-1B is the most common visa for compliance associates in Puerto Rico, as the role typically qualifies as a specialty occupation requiring a bachelor's degree in finance, accounting, law, or a related field. Candidates from Canada or Mexico may also qualify under the TN visa using the Accountant category if their duties align. L-1 visa transfers apply for candidates relocating from a foreign affiliate of a Puerto Rico-based employer.
Which cities in Puerto Rico have the most compliance associate sponsorship jobs?
San Juan accounts for the large majority of compliance associate openings in Puerto Rico, given its concentration of bank headquarters, insurance companies, and corporate offices. The Guaynabo and Bayamon metro areas also host significant financial and pharmaceutical operations. For pharma-specific compliance roles, the northern corridor between San Juan and Arecibo has notable employer density.
How to find compliance associate visa sponsorship jobs in Puerto Rico?
Migrate Mate filters job listings specifically by visa sponsorship availability, making it easier to identify compliance associate roles in Puerto Rico without sifting through positions that do not sponsor. You can search by role and territory to surface openings at financial institutions and pharma companies on the island. Creating a profile on Migrate Mate also helps you track new sponsorship-eligible postings as they appear.
Are there any Puerto Rico-specific considerations for compliance associate sponsorship?
Puerto Rico follows federal H-1B prevailing wage requirements set by the Department of Labor, so employers must meet wage levels benchmarked to the San Juan metropolitan area, which differ from mainland U.S. metro benchmarks. The University of Puerto Rico and Inter American University produce accounting and finance graduates who enter compliance pipelines locally, meaning employers have a mix of local hiring and sponsorship-track recruitment for specialized roles.
What is the prevailing wage for sponsored compliance associate 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.