Biotech & Pharma Visa Sponsorship Jobs in Puerto Rico
Puerto Rico's biotech and pharmaceutical sector offers strong visa sponsorship opportunities, particularly in the San Juan metropolitan area where companies like Amgen, Bristol Myers Squibb, and Janssen maintain manufacturing operations. The island's status as a U.S. territory provides unique advantages for international professionals seeking biotech careers.
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Get Access To All JobsABOUT ABBVIE
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio.
PURPOSE:
The Commissioning and Qualification (C&Q) Manager will be responsible for leading and executing commissioning and qualification activities for new and existing facilities, utilities and process equipment systems in compliance with regulatory, local and industry standards. This role is to ensure that all systems are installed, tested, and operate according to the design intent and user requirement specifications. The C&Q manager must work with site core functional teams on integrated schedules, resourcing management, and C&Q execution. They must onboard and manage a team of highly skilled C&Q subject matter experts to drive the project in line with the schedule. This role will be based at the AbbVie Barceloneta site (ABL) to support an aseptic fill finish program delivered by Global Engineering.
Responsibilities:
- Lead, motivate, supervise and drive the commissioning and qualification team, providing technical guidance and leadership throughout the project lifecycle.
- Support onboarding of C&Q subject matter experts with the Global Engineering program leads.
- Develop and implement commissioning and qualification strategies, ensuring adherence to company policies and regulatory guidelines (e.g., FDA, GMP).
- Planning and coordination of C&Q activities in line with a risk-based approach (RBV).
- Deliver program updates to both senior management and senior leadership as required.
- Articulate and incorporate all C&Q deliverables into project scheduling tools and delivery outputs. Manage metrics on a weekly basis to ensure C&Q earned value (EV) week on week is tracked.
- Coordinate with engineering, quality, operations, maintenance, and external vendors to ensure project deliverables are met on time and within budget.
- Drive risk assessment consistency ensuring a well-defined risk-based approach is developed and maintained throughout the project lifecycle.
- Participate in team meetings and workshops as required.
- Provide expert support with deviation or non-conformance management.
- Review and approve documentation as necessary ensuring project documentation is always right first time.
- Support internal or external inspections as required and provide subject matter expertise on qualification activities.
- Stay current with changes in regulatory requirements and industry best practices.
QUALIFICATIONS
- Bachelor’s degree in engineering, Science, Life Sciences, or related field.
- 10+ Years’ experience in commissioning, qualification, and validation within the pharmaceutical, biotechnology, or related regulated industry.
- Strong knowledge of relevant regulations (FDA, GMP, ICH Q8/Q9/Q10) and industry standards.
- Experience leading cross-functional project teams and proven ability to drive and motivate a team is essential.
- Must have previous experience in a C&Q project management role.
- Knowledge of a wide range of C&Q disciplines including CSV (Computer System Validation), Utility, Facility & Equipment qualifications.
- Excellent written and verbal communication skills.
- Expert understanding of risk-based commissioning and qualification in line with ISPE C&Q (2019).
- Self-directed, self-motivated with an ability to represent the C&Q function in a high paced project environment.
- Ability to work closely with key project stakeholders to maintain project delivery schedules and limit any potential delays.
ADDITIONAL INFORMATION
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our long-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
ABOUT ABBVIE
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio.
PURPOSE:
The Commissioning and Qualification (C&Q) Manager will be responsible for leading and executing commissioning and qualification activities for new and existing facilities, utilities and process equipment systems in compliance with regulatory, local and industry standards. This role is to ensure that all systems are installed, tested, and operate according to the design intent and user requirement specifications. The C&Q manager must work with site core functional teams on integrated schedules, resourcing management, and C&Q execution. They must onboard and manage a team of highly skilled C&Q subject matter experts to drive the project in line with the schedule. This role will be based at the AbbVie Barceloneta site (ABL) to support an aseptic fill finish program delivered by Global Engineering.
Responsibilities:
- Lead, motivate, supervise and drive the commissioning and qualification team, providing technical guidance and leadership throughout the project lifecycle.
- Support onboarding of C&Q subject matter experts with the Global Engineering program leads.
- Develop and implement commissioning and qualification strategies, ensuring adherence to company policies and regulatory guidelines (e.g., FDA, GMP).
- Planning and coordination of C&Q activities in line with a risk-based approach (RBV).
- Deliver program updates to both senior management and senior leadership as required.
- Articulate and incorporate all C&Q deliverables into project scheduling tools and delivery outputs. Manage metrics on a weekly basis to ensure C&Q earned value (EV) week on week is tracked.
- Coordinate with engineering, quality, operations, maintenance, and external vendors to ensure project deliverables are met on time and within budget.
- Drive risk assessment consistency ensuring a well-defined risk-based approach is developed and maintained throughout the project lifecycle.
- Participate in team meetings and workshops as required.
- Provide expert support with deviation or non-conformance management.
- Review and approve documentation as necessary ensuring project documentation is always right first time.
- Support internal or external inspections as required and provide subject matter expertise on qualification activities.
- Stay current with changes in regulatory requirements and industry best practices.
QUALIFICATIONS
- Bachelor’s degree in engineering, Science, Life Sciences, or related field.
- 10+ Years’ experience in commissioning, qualification, and validation within the pharmaceutical, biotechnology, or related regulated industry.
- Strong knowledge of relevant regulations (FDA, GMP, ICH Q8/Q9/Q10) and industry standards.
- Experience leading cross-functional project teams and proven ability to drive and motivate a team is essential.
- Must have previous experience in a C&Q project management role.
- Knowledge of a wide range of C&Q disciplines including CSV (Computer System Validation), Utility, Facility & Equipment qualifications.
- Excellent written and verbal communication skills.
- Expert understanding of risk-based commissioning and qualification in line with ISPE C&Q (2019).
- Self-directed, self-motivated with an ability to represent the C&Q function in a high paced project environment.
- Ability to work closely with key project stakeholders to maintain project delivery schedules and limit any potential delays.
ADDITIONAL INFORMATION
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our long-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
Biotech & Pharma Job Roles in Puerto Rico
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Search Biotech & Pharma Jobs in Puerto RicoBiotech & Pharma Jobs in Puerto Rico: Frequently Asked Questions
Which biotech & pharma companies sponsor visas in Puerto Rico?
Major pharmaceutical manufacturers in Puerto Rico include Amgen, Bristol Myers Squibb, Janssen, AbbVie, and Merck. These companies operate large-scale manufacturing facilities primarily in the San Juan area and Mayagüez, regularly sponsoring H-1B and other work visas for specialized roles in manufacturing science, quality assurance, regulatory affairs, and process engineering.
How to find biotech & pharma visa sponsorship jobs in Puerto Rico?
Migrate Mate specializes in connecting international professionals with visa-sponsoring biotech and pharma employers in Puerto Rico. Focus your search on manufacturing operations in San Juan and Mayagüez, where most pharmaceutical companies maintain facilities. Manufacturing science, quality control, and regulatory compliance roles typically have the highest sponsorship rates.
Which cities in Puerto Rico have the most biotech & pharma sponsorship jobs?
San Juan and its surrounding metropolitan area host the majority of Puerto Rico's pharmaceutical operations, including Amgen's large manufacturing facility in Juncos. Mayagüez on the western coast also has significant pharma presence. Arecibo and Barceloneta feature additional manufacturing sites, though San Juan remains the primary hub for biotech opportunities.
What visa types are most common for biotech & pharma roles in Puerto Rico?
H-1B visas dominate for specialized roles like manufacturing scientists, quality engineers, and regulatory specialists. L-1 visas are common for transfers from mainland operations or international facilities. TN visas work well for Canadian and Mexican professionals in engineering and scientific roles, while O-1 visas apply to senior research professionals.
Are there unique considerations for biotech visa sponsorship in Puerto Rico?
Puerto Rico's status as a U.S. territory means federal visa regulations apply identically to the mainland, but prevailing wage determinations may differ. The concentration of manufacturing operations means process engineering and quality roles are particularly in-demand. Many positions require bilingual capabilities given the local workforce and regulatory environment.
What is the prevailing wage for sponsored biotech & pharma 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.
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