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Regulatory Manager Jobs in Puerto Rico (NOW HIRING)

Oversee and manage the capital projects portfolio , ensuring alignment with organizational strategy and regulatory requirements. * Lead project governance , ensuring consistency across global and ...

Porfolio Manager

Gurabo, PR · On-site

$90 - $120/hr

Oversee and manage the capital projects portfolio , ensuring alignment with organizational strategy and regulatory requirements. * Lead project governance , ensuring consistency across global and ...

Ensure compliance with applicable federal, Commonwealth, and local regulations, contractual ... Support change management, quality assurance, risk management, and resource planning activities ...

Ensure compliance with applicable federal, Commonwealth, and local regulations, contractual ... Support change management, quality assurance, risk management, and resource planning activities ...

Your work will help maintain program quality, regulatory compliance, operational efficiency, and ... The Project Manager serves as the Deputy to the Program Manager and provides leadership for the day ...

Your work will help maintain program quality, regulatory compliance, operational efficiency, and ... The Project Manager serves as the Deputy to the Program Manager and provides leadership for the day ...

PR · On-site

Automation, Control Systems Integration, Information Technology, System Integration and Regulatory ... Lead and manage manufacturing capital project consisting of both client and non-client ...

PR · On-site

Validation Manager About Ocyonbio: OcyonBio is a biotechnology CDMO based in Aguadilla, Puerto Rico ... Serve as Validation SME during regulatory inspections and client audits * Lead deviation ...

Audit Manager

San Juan, PR · On-site

$100K - $132K/yr

We manage all ongoing incentives and operational compliance filings required for operating within ... Stay current with Puerto Rico's tax credit regulations, including any changes to Act 60 of 2019, as ...

Audit Manager

San Juan, PR · On-site

$100K - $132K/yr

We manage all ongoing incentives and operational compliance filings required for operating within ... Stay current with Puerto Rico's tax credit regulations, including any changes to Act 60 of 2019, as ...

PR · On-site

General Manager - Luxury Resort Isabela, Puerto Rico | Full-Time | Hospitality & Resort Operations ... Ensure resort compliance with all applicable safety, regulatory, and environmental standards

Payroll Manager

San Juan, PR · On-site

$70 - $95/hr

Maintain up to date knowledge of payroll laws and regulations and advise department managers as to all pertinent payroll information. * Any other tasks assigned by General Manager or Director of ...

New

PR · On-site

$50 - $55/hr

Automation, Control Systems Integration, Information Technology, System Integration and Regulatory ... ABOUT THE ROLE The Facilities Project Manager will oversee and coordinate well-defined, multi ...

PR · On-site

The Restaurant Manager will support the team, manage resources, and ensure compliance with all operational standards and regulations. Key Responsibilities Operational Management: * Supports the GM ...

Ensure that compliance of all regulatory laws and guidelines are met as they relate to the operation of the building's infrastructure. Responsible for alerting management of building discrepancies.

General Manager

San Juan, PR · On-site

$70 - $90/hr

You will also manage payroll, disciplinary actions, and follow up with documentation on internal policies, procedures and regulatory compliance as needed. Follow up with HR when necessary.Assign ...

PR · On-site

$104K - $108K/yr

Track regulatory changes and manage agency inspections, comments, and permit conditions. * Report permitting status, risks, and schedule impacts to the Project Manager, and support government and ...

PR

$95K - $115K/yr

Ensure compliance with safety protocols, environmental regulations, and utility vegetation management standards. * Monitor equipment, fleet, and tool needs for assigned areas and coordinate with ...

Showing results 21-40

Regulatory Manager information

What is a regulatory manager?

A Regulatory Manager is a professional responsible for ensuring that a company complies with all relevant laws, regulations, and guidelines related to its industry. They oversee the preparation and submission of regulatory documents, communicate with regulatory agencies, and keep the organization updated on changes to regulations. Regulatory Managers play a key role in minimizing legal risks and supporting the approval and launch of products or services in various markets. They often work in industries such as pharmaceuticals, medical devices, food and beverages, and chemicals.

What are some common challenges a regulatory manager faces when coordinating compliance across multiple regions?

Regulatory Managers often encounter the challenge of navigating varying and evolving regulatory requirements across different regions or countries. This requires staying up to date with local laws, understanding cultural and business practice differences, and ensuring consistent compliance strategies company-wide. Effective coordination involves frequent communication with cross-functional teams, such as legal, quality assurance, and operations, to align on regulatory expectations and swiftly address compliance gaps. Successfully managing these challenges enhances the organization's ability to enter new markets and maintain product approvals.

What are the key skills and qualifications needed to thrive as a regulatory manager, and why are they important?

To thrive as a Regulatory Manager, you need strong analytical skills, a deep understanding of regulations in your industry, and typically a bachelor's or advanced degree in a relevant field. Familiarity with regulatory submission systems, compliance management software, and certifications such as RAC (Regulatory Affairs Certification) are often required. Excellent organizational, communication, and negotiation skills help build relationships with regulatory bodies and ensure team alignment. These competencies are crucial for ensuring products or services meet legal requirements, minimizing risk, and maintaining organizational reputation.

What is the difference between Regulatory Manager vs Regulatory Affairs Specialist?

AspectRegulatory ManagerRegulatory Affairs Specialist
Required CredentialsBachelor's degree in life sciences, regulatory affairs certification often preferredBachelor's degree in life sciences, regulatory affairs certification beneficial
Work EnvironmentOversees regulatory teams, manages compliance strategies, interacts with regulatory agenciesSupports regulatory submissions, prepares documentation, conducts research
Employer & Industry UsagePharmaceutical, biotech, medical device companiesPharmaceutical, biotech, medical device companies
Search & Comparison IntentUnderstanding managerial roles, career progressionEntry-level to mid-level regulatory roles, daily responsibilities

The Regulatory Manager typically oversees regulatory teams and strategies, requiring leadership skills and experience, while the Regulatory Affairs Specialist focuses on preparing documentation and supporting compliance tasks. Both roles are essential in regulated industries like pharma and biotech, but they differ in scope and responsibilities.

What are the most commonly searched types of Regulatory jobs in Puerto Rico?

The most popular types of Regulatory jobs in Puerto Rico are:

What are popular job titles related to Regulatory Manager jobs in Puerto Rico?

For Regulatory Manager jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Regulatory Manager jobs in Puerto Rico look for?

The top searched job categories for Regulatory Manager jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Regulatory Manager jobs?

Cities in Puerto Rico with the most Regulatory Manager job openings:

Infographic showing various Regulatory Manager job openings in Puerto Rico as of August 2026, with employment types broken down into 91% Full Time, 4% Part Time, and 5% Contract. Highlights an 88% In-person, 6% Hybrid, and 6% Remote job distribution.

Full-time

Re-posted 25 days ago


Job description

Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, PR, Boston, MA & San Francisco, CA and we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.Key Responsibilities
  • Oversee and manage the capital projects portfolio, ensuring alignment with organizational strategy and regulatory requirements.
  • Lead project governance, ensuring consistency across global and site-specific project management processes.
  • Consolidate and monitor project deliverables, timelines, budgets, risks, and performance metrics across all active projects.
  • Develop and maintain the master project plan, integrating all business-owned deliverables.
  • Provide executive reporting and dashboards to leadership, ensuring visibility of portfolio performance and key risks.
  • Coordinate and facilitate global communications among stakeholders, including senior leadership, site teams, and clients.
  • Define, implement, and maintain standardized roles and responsibilities across sites and projects.
  • Drive continuous improvement in project management tools, methodologies, and governance frameworks.
  • Ensure compliance with FDA regulations, GMP standards, and industry best practices.
  • Lead risk management and mitigation strategies across the portfolio.
  • Support resource planning and capacity management across multiple projects.
  • Mentor and guide Project Managers and cross-functional teams.
Qualifications & Requirements
  • Bachelor's Degree in Engineering, Science, Business, or related field.
  • Minimum 8+ years of experience in project and/or portfolio management, preferably in capital projects.
  • Proven experience in Pharmaceutical, Biotechnology, or Medical Device industries.
  • Strong knowledge of FDA regulations, GMP, and compliance frameworks.
  • PMP Certification (preferred).
  • Demonstrated experience managing multi-site or global project portfolios.
  • Excellent leadership, communication, and stakeholder management skills.
  • Ability to manage multiple priorities in a fast-paced, regulated environment.

Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley.
Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.