Top 56 Compliance Jobs in Carolina, Pr

Dossier Excellence Specialist (Regulatory Affairs - Medical Devices)
ECONS —San Juan, PR
- $28 - $30 an hour
- Contract
- Microsoft Excel
- Microsoft Outlook
- Engineering
Quick Apply
3d
Senior Manager Corporate Quality Compliance
Amgen —Municipio de Juncos, PR
- $138,264.40 - $187,063.60 a year
- Doctoral degree
- Up to 50% travel
- Laboratory experience
- Disability insurance
- Health insurance
COMPLIANCE SPECIALIST
MENTOR TECHNICAL GROUP CORP —Caguas, PR
- Mid-level
- 3 years
- Analysis skills
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COMPLIANCE ANALYST
Universal Insurance —Guaynabo, PR
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Compliance Associate
Advantage Life Insurance —San Juan, PR
- Full-time
- Microsoft Word
- English
- Mid-level
Quick Apply
COMPLIANCE OFFICER - BSA COMPLIANCE DEPT (GOVERNANCE & SANCTIONS UNIT) - FIRST BANK PR
FirstBank Florida —San Juan, PR
- Spanish
- Microsoft Outlook
- English
7d
Grant Compliance Senior Associate
BDO —San Juan, PR
- Full-time
- Microsoft Word
- Spanish
- Microsoft Outlook
- Employee stock ownership plan
- Retirement plan
Associate, Grant Management/Grant Compliance Specialist
BDO —San Juan, PR
- Full-time
- Spanish
- Mid-level
- Analysis skills
- Employee stock ownership plan
- Retirement plan
Compliance Associate
Pharmpix —Guaynabo, PR
- Full-time
- Spanish
- Microsoft Excel
- Computer literacy
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Safety Compliance Administrator
Envocore, LLC —San Juan, PR
- $20 - $25 an hour
- Monday to Friday
- Word processing
- Computer literacy
- Bachelor of Science
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6d
Compliance Engineer
Validation & Engineering Group, Inc —Gurabo, PR
- Engineering
- Mid-level
- Organizational skills
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COMPLIANCE ASSISTANT MANAGER-COMPLIANCE REGULATORY TESTING DEPT-FIRSTBANK PR
FirstBank Florida —San Juan, PR
- Spanish
- Microsoft Outlook
- 5 years
Retail Operations Inventory Auditor & Controls
Liberty Latin America Communications, Inc. —Guaynabo, PR
- Full-time
- Background check
- Spanish
- Computer literacy
FRAUD ANALYST - BANKING OPERATIONS FRAUD MNGT - FIRSTBANK PR
FirstBank Florida —San Juan, PR
- Weekends as needed
- Microsoft Word
- Mid-level
- Analysis skills
- Flexible schedule
Compliance Officer & AML Analyst
AGC Consulting —Guaynabo, PR
- Spanish
- English
- Mid-level
Quick Apply
Regulator Reporting Senior Consultant
Deloitte —San Juan, PR
- $118,000 - $130,000 a year
- Full-time
- Computer Science
- Bachelor's degree
- Team management
Quality Control Manager Bilingual for Federal Contract
Allied Universal —Guaynabo, PR
- $72,000.24 a year
- Full-time
- Bilingual
- Military
- High school diploma or GED
- AD&D insurance
- Paid holidays
Quick Apply
4d
IT AUDITOR - INTERNAL AUDIT DEPT - FIRSTBANK PR
FirstBank Puerto Rico —San Juan, PR
- Full-time
- Hybrid work
- Spanish
- Customer service
- English
- Health insurance
- Dental insurance
Quick Apply
Director of Governance, Risk & Compliance (GRC)
Inkit —San Juan, PR
- Full-time
- Continuous improvement
- Senior level
- Leadership
Quick Apply
Sr Business Risk Officer
Popular Bank —San Juan, PR
- Full-time
- Hybrid work
- Spanish
- 7 years
- English

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compliance jobs near carolina, pr

Dossier Excellence Specialist (Regulatory Affairs - Medical Devices)

ECONS
San Juan, PR

Quick Apply

Job Details

Contract
$28 - $30 an hour
3 days ago

Qualifications

Teamwork
Microsoft Excel
Microsoft Outlook
Technical documentation
English
Attention to detail
Organizational skills
Microsoft Teams
Technical writing experience within technology
Achieving project delivery timelines
FDA regulations

Full Job Description

Location: Puerto Rico (Remote)
Employment Type: Full-Time
Industry: Medical Devices / Life Sciences / Regulatory Affairs

About the Opportunity

We are seeking a detail-oriented Dossier Excellence Specialist to support regulatory affairs operations for medical device products in global markets. This position plays a critical role in the preparation, organization, maintenance, and submission readiness of regulatory dossiers while ensuring compliance with applicable regulatory requirements, company procedures, and quality standards.

The ideal candidate is highly organized, skilled in technical documentation management, and capable of working in a fast-paced regulatory environment supporting international submissions.

Key Responsibilities

Gather and compile technical and regulatory documentation required for dossier preparation.
Follow up with cross-functional teams to obtain pending documents and supporting information.
Perform technical writing activities for specific dossier sections and regulatory documentation.
Prepare regulatory dossier packages following established procedures, templates, and quality requirements.
Upload, organize, and maintain documentation in electronic document management systems.
Ensure documentation accuracy, completeness, traceability, and version control.
Support local and global regulatory submissions through effective document management practices.
Participate in regulatory and quality training programs and remain current with evolving regulations and requirements.
Maintain accurate information within MDRIM and other applicable electronic systems.
Collaborate with Regulatory Affairs, Quality, Engineering, Manufacturing, and Product Lifecycle Management teams.
Meet established timelines and performance objectives while maintaining high-quality standards.
Identify documentation gaps and proactively work toward resolution.

Responsibilities include dossier preparation, technical writing, document gathering, document tracking, submission support, electronic records management, training participation, and maintenance of regulatory systems.

Required Qualifications

Bachelor's Degree in Science, Engineering, Life Sciences, Regulatory Affairs, Quality, Technical Writing, or a related discipline.
Minimum 2 years of experience in Regulatory Affairs, Quality Systems, Documentation Control, Medical Devices, Pharmaceuticals, Biotechnology, or a regulated industry.
Experience working with technical documentation and controlled documents.
Strong document management and organizational skills.
Excellent written and verbal communication skills in English.
Proficiency with Microsoft Office Suite (Word, Excel, Outlook, Teams).
Ability to manage multiple projects and deadlines simultaneously.
Strong attention to detail and commitment to quality.

Preferred Qualifications

Experience supporting Medical Device regulatory submissions.
Knowledge of international regulatory requirements.
Experience with Product Lifecycle Management (PLM) systems, document repositories, or regulatory information management systems.
Familiarity with MDRIM, Agile, Windchill, SAP, TrackWise, Documentum, or similar platforms.
Experience in a Johnson & Johnson, FDA-regulated, ISO 13485, or comparable environment.

Key Competencies

Regulatory Documentation Management
Technical Writing
Data Accuracy & Compliance
Attention to Detail
Problem Solving
Time Management
Cross-Functional Collaboration
Continuous Improvement Mindset
Customer Focus

What Success Looks Like

Dossiers are completed accurately and on schedule.
Regulatory documentation is complete, traceable, and submission-ready.
Electronic systems remain current and accurate.
Stakeholders receive timely support for regulatory submission activities.
Documentation quality meets established regulatory and business requirements.

Pay: $28.00 - $30.00 per hour

Work Location: In person

Quick Apply

Refine Your Search

compliance jobs in carolina, pr

Dossier Excellence Specialist (Regulatory Affairs - Medical Devices)

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