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Compliance Project Coordinator Jobs in Puerto Rico

... management coordination, GMP documentation review, compliance tracking, and quality system support activities associated with engineering and project operations. The role requires strong ...

Compliance Engineer

Juncos, PR · On-site

$70 - $90/hr

... management coordination, GMP documentation review, compliance tracking, and quality system support activities associated with engineering and project operations. The role requires strong ...

... management coordination, GMP documentation review, compliance tracking, and quality system support activities associated with engineering and project operations. The role requires strong ...

This role is responsible for coordinating engineering drawing revisions, maintaining project ... accurate, compliant, and timely documentation throughout the project lifecycle. Position ...

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... This role is responsible for coordinating and supporting engineering activities associated with ...

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... This role is responsible for coordinating and supporting engineering activities associated with ...

Project Engineer

Humacao, PR · On-site

$75 - $100/hr

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... This role is responsible for coordinating and supporting engineering activities associated with ...

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... This role is responsible for coordinating and supporting engineering activities associated with ...

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... This role is responsible for coordinating and supporting engineering activities associated with ...

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... This role is responsible for coordinating and supporting engineering activities associated with ...

Showing results 21-40

Compliance Project Coordinator information

What is a compliance project coordinator?

Compliance Project Coordinators are professionals who oversee and support projects ensuring organizational adherence to legal, regulatory, and internal policy requirements. They coordinate activities between departments, monitor project progress, and help implement compliance strategies. Their role often involves documentation, staff training, and reporting to management or regulatory bodies. By maintaining up-to-date knowledge of applicable laws and standards, they help mitigate risks and keep projects aligned with compliance objectives.

How does a compliance project coordinator typically interact with other departments during a project?

As a Compliance Project Coordinator, you will frequently collaborate with departments such as Legal, Operations, and IT to ensure that projects adhere to relevant regulations and internal policies. This often involves organizing cross-functional meetings, clarifying compliance requirements, and tracking the progress of corrective actions. Building strong relationships and maintaining clear communication with stakeholders in these departments is key to successfully implementing compliance initiatives and addressing any issues that arise.

What are the key skills and qualifications needed to thrive as a compliance project coordinator, and why are they important?

To thrive as a Compliance Project Coordinator, you need strong organizational skills, attention to detail, and a solid understanding of regulatory requirements, typically supported by a bachelor's degree in business, law, or a related field. Familiarity with compliance management software, project management tools like MS Project or Asana, and relevant certifications such as Certified Compliance & Ethics Professional (CCEP) are often required. Outstanding communication, problem-solving abilities, and the capacity to manage multiple priorities help you excel in this role. These skills ensure that compliance initiatives run smoothly, deadlines are met, and organizations adhere to legal and regulatory standards.

What is the difference between Compliance Project Coordinator vs Compliance Analyst?

AspectCompliance Project CoordinatorCompliance Analyst
Required CredentialsCertifications like CCEP, CAMS often preferredCertifications such as CCEP, CAMS common
Work EnvironmentProject-based, cross-departmental teamsData analysis, reporting, policy review
Employer & Industry UsageFinancial, healthcare, manufacturing sectorsFinancial services, healthcare, regulatory agencies

The Compliance Project Coordinator focuses on managing compliance projects, coordinating teams, and ensuring deadlines are met. In contrast, the Compliance Analyst primarily analyzes compliance data, reviews policies, and assesses risks. Both roles require similar certifications and are vital in regulated industries, but their daily tasks and focus areas differ.

What job categories do people searching Compliance Project Coordinator jobs in Puerto Rico look for?

The top searched job categories for Compliance Project Coordinator jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Compliance Project Coordinator jobs?

Cities in Puerto Rico with the most Compliance Project Coordinator job openings:

Compliance Engineer

Pinnaql

Humacao, PR • On-site

Full-time

Re-posted 6 days ago


Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
  • Compliance Engineer

Position Summary
The Compliance Engineer will support capital projects and technical initiatives within regulated pharmaceutical and biotechnology manufacturing environments by supporting quality and compliance activities associated with project execution, engineering operations, and regulated systems.
This role is responsible for supporting investigations, CAPA activities, change management coordination, GMP documentation review, compliance tracking, and quality system support activities associated with engineering and project operations.
The role requires strong organizational skills, attention to detail, technical writing capabilities, and cross-functional collaboration with Engineering, Operations, Quality, Validation, and project teams within highly regulated environments.
Key Responsibilities
  • Support investigations, CAPA activities, and quality system documentation associated with project execution and engineering operations.
  • Support tracking and follow-up of change controls, CAPAs, training activities, and compliance-related metrics.
  • Support document reviews, approvals, document routing, and quality system coordination activities.
  • Assist with onboarding coordination activities, forms, access requests, and related compliance documentation support.
  • Support tracking and organization of quality records, project documentation, and compliance-related deliverables.
  • Participate in project meetings and support communication of compliance activities, documentation status, risks, and action items.
  • Support continuous improvement initiatives related to quality systems, compliance processes, documentation practices, and operational readiness activities.
  • Ensure compliance activities are performed in alignment with applicable GMP requirements, site procedures, and project expectations.

Qualifications & Experience
  • Bachelor's degree in Engineering, Science, Business Administration, or related technical field preferred.
  • Minimum of 2 years of experience supporting compliance, quality systems, investigations, CAPA, change management, validation, or GMP documentation activities within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries.
  • Familiarity with GMP documentation practices, quality systems, investigations, CAPA processes, change controls, and regulated documentation requirements.
  • Experience supporting engineering projects, manufacturing operations, commissioning and qualification activities, or regulated operational environments is preferred.
  • Familiarity with systems such as Kneat, TrackWise, Veeva, Bluebeam, or similar quality and documentation management platforms is preferred.
  • Excellent verbal and written communication skills in both English and Spanish, including technical writing, documentation review, and communication with cross-functional teams.
  • Strong organizational, analytical, and problem-solving skills with attention to detail and the ability to manage multiple priorities simultaneously.

Additional Requirements
  • Ability to work on-site in the eastern region of Puerto Rico.
  • Must be eligible to complete client-required onboarding, training, and site access requirements.
  • Ability to work effectively within fast-paced and highly regulated environments.

The above statements describe the general nature and level of work performed and do not represent an exhaustive list of responsibilities.
At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.