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Flexible Remote Biomedical Engineer Jobs in Puerto Rico

Huntington

Lead ETL Developer

Florida, PR · On-site +1

... flexible work arrangement. We're combining the best of both worlds: in-office and work from home ... Remote roles will also have the opportunity to come together in our offices for moments that matter.

OncoHealth

Case Review Representative

Guaynabo, PR · On-site +1

$13 - $15/hr

Flexible to work rotational shifts inside our office hours from 8:00 a.m. - 8:00 p.m. EST to cover ... Remote/hybrid work experience preferred * A minimum of 2 years of healthcare related administrative ...

OncoHealth

Case Review Specialist - PR

Guaynabo, PR · On-site +1

Flexible to work rotational shifts inside our office hours from 8:00 a.m. - 8:00 p.m. EST to cover ... Remote/hybrid experience preferred * A minimum of 2-4 years' administrative experience and/or ...

All JobsBiomedical Engineer JobsFlexible Remote Biomedical Engineer JobsFlexible Remote Biomedical Engineer Jobs in Puerto Rico

Flexible Remote Biomedical Engineer information

What is the difference between Flexible Remote Biomedical Engineer vs Flexible Remote Medical Device Technician?

AspectFlexible Remote Biomedical EngineerFlexible Remote Medical Device Technician
Required CredentialsBachelor's or Master's in Biomedical Engineering, certifications like IBET or BMETTechnical certifications, training in medical device repair and maintenance
Work EnvironmentDesign, development, testing of medical devices remotelyRemote troubleshooting, installation, and maintenance of medical equipment
Employer & Industry UsageMedical device companies, biotech firms, healthcare tech startupsHospitals, clinics, medical equipment suppliers

While both roles involve remote work in the healthcare industry, a Flexible Remote Biomedical Engineer focuses on designing and developing medical devices, whereas a Flexible Remote Medical Device Technician specializes in troubleshooting and maintaining existing equipment remotely. Understanding these differences helps job seekers find the right fit based on their skills and career goals.

What are popular job titles related to Flexible Remote Biomedical Engineer jobs in Puerto Rico? For Flexible Remote Biomedical Engineer jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Flexible Remote Biomedical Engineer jobs in Puerto Rico look for? The top searched job categories for Flexible Remote Biomedical Engineer jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Flexible Remote Biomedical Engineer jobs? Cities in Puerto Rico with the most Flexible Remote Biomedical Engineer job openings:
Flexible Remote Biomedical Engineer jobs near you
Infographic showing various Flexible Remote Biomedical Engineer job openings in Puerto Rico as of July 2026, with employment types broken down into 1% As Needed, 84% Full Time, 14% Part Time, and 1% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% 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