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Remote Medical Affairs Jobs in Puerto Rico (NOW HIRING)

Remote Medical Affairs information

What is a Remote Medical Affairs job?

A Remote Medical Affairs job involves managing scientific and clinical communications between a pharmaceutical, biotechnology, or medical device company and healthcare professionals, regulatory bodies, and internal teams—all while working remotely. Responsibilities may include medical strategy development, reviewing medical content, supporting regulatory submissions, and engaging with key opinion leaders. These roles require a strong scientific background, excellent communication skills, and experience in medical or clinical affairs. Working remotely in this field allows professionals to contribute to medical advancements without being tied to a specific location.

What are the key skills and qualifications needed to thrive in the Remote Medical Affairs position, and why are they important?

To excel in a Remote Medical Affairs role, candidates typically need a strong background in life sciences or pharmacy, in addition to expertise in clinical research and scientific communication. Familiarity with medical information databases, regulatory compliance systems, and certifications such as PharmD, MD, or relevant master's degrees are common requirements. Exceptional soft skills include proactive communication, cross-functional collaboration, and the ability to distill complex information for both scientific and non-scientific audiences. These competencies ensure effective support for medical strategies, compliance with industry regulations, and clear engagement with internal and external stakeholders.

What are some typical challenges faced when working remotely in Medical Affairs, and how can they be addressed?

Remote Medical Affairs professionals often encounter challenges such as coordinating across multiple time zones, maintaining effective communication with cross-functional teams, and staying aligned with rapidly changing regulatory or medical information. Building strong digital collaboration habits—like regular virtual meetings and clear documentation—can help mitigate these challenges. Additionally, setting up a dedicated workspace and leveraging project management tools can enhance productivity and organization. Staying proactive in outreach and knowledge-sharing also helps foster engagement and keeps everyone aligned on shared goals.

What are the most commonly searched types of Medical Affairs jobs in Puerto Rico? The most popular types of Medical Affairs jobs in Puerto Rico are:
What job categories do people searching Remote Medical Affairs jobs in Puerto Rico look for? The top searched job categories for Remote Medical Affairs jobs in Puerto Rico are:
Infographic showing various Remote Medical Affairs job openings in Puerto Rico as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution.
Sterilization Program Manager- Ethylene Oxide (EO) (Remote Work)

Sterilization Program Manager- Ethylene Oxide (EO) (Remote Work)

CIS International LLC

Juncos, PR • On-site, Remote

Full-time

Posted 5 days ago


Job description

Summary:
The Sterilization Program Manager is responsible for leading and managing the sterilization project portfolio, including new product launches, validation and revalidation activities, process improvements, and operational support. This role provides technical oversight for Ethylene Oxide (EO) sterilization processes, drives cross-functional collaboration, manages supplier relationships, and ensures compliance with global sterilization regulations and standards.
Key Responsibilities:
Program & Portfolio Management
  • Lead and manage the full sterilization project portfolio, including:
    • New product launches
    • Sterilization validations and revalidations
    • Process improvement initiatives
  • Develop and maintain integrated project plans, timelines, resource allocation plans, and risk registers.
  • Drive alignment across cross-functional teams including R&D, Quality, Regulatory Affairs, Operations, and Supply Chain.
  • Facilitate portfolio prioritization and support trade-off decisions with senior leadership.
  • Establish, monitor, and report key performance indicators (KPIs), project milestones, and program health metrics.
Technical Oversight
  • Serve as Subject Matter Expert (SME) for EO sterilization processes.
  • Provide technical guidance related to microbiological and chemical sterilization methods.
  • Ensure compliance with applicable international regulations, standards, and industry requirements.
  • Support technical problem-solving and troubleshooting efforts across sterilization-related activities.
  • Collaborate with internal SMEs to resolve complex sterilization challenges.
Sterilization & Service Supplier Management
  • Coordinate with internal stakeholders to manage relationships with contract sterilization providers and laboratory service vendors.
  • Support project scheduling and resource planning with external service suppliers.
  • Ensure supplier activities align with project priorities, timelines, and business objectives.
Stakeholder & Change Management
  • Communicate project status, risks, mitigation plans, and key decisions to executive leadership and cross-functional teams.
  • Lead change control activities associated with sterilization process modifications.
  • Promote continuous improvement initiatives and process optimization opportunities.
  • Drive effective stakeholder engagement throughout the project lifecycle.
Requirements
  • Bachelor’s Degree in:
    • Biomedical Engineering
    • Chemical Engineering
    • Microbiology or related scientific/engineering discipline
  • Minimum 3 years of experience in EO sterilization validation and/or sterilization operations.
  • Strong knowledge of sterilization validation lifecycle activities.
  • Experience supporting validation, compliance, and process improvement projects.
Preferred Qualifications
  • PMP Certification or equivalent project management certification.
  • Experience in medical device, pharmaceutical, or regulated manufacturing environments.
  • Knowledge of international sterilization standards and regulatory requirements.
Required Skills
Sterilization & Validation
  • EO Sterilization Processes
  • Sterilization Validation Lifecycle
  • Revalidation Activities
  • Microbiological Methods
  • Chemical Sterilization Methods
  • Regulatory Compliance
Program Management
  • Portfolio Management
  • Resource Planning
  • Project Scheduling
  • Risk Management
  • FMEA
  • Risk Registers
  • KPI Development & Reporting
  • Cross-Functional Leadership
Software & Tools
  • Microsoft Office Suite
  • Microsoft Project
  • Smartsheet
  • Agile Methodologies
Soft Skills
  • Leadership
  • Strategic Planning
  • Stakeholder Management
  • Communication & Presentation Skills
  • Problem Solving
  • Continuous Improvement Mindset
  • Change Management
Work Methodology
  • Remote work reporting to the Juncos, PR site.
  • Full Time Job 
  • Shift: Administrative Shift, but needs to be available for others.
  • Duration: 1 year (with possible extension or conversion depending on project and performance).
  • Professional services Contract
  • Type of industry: Medical devices