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Remote Biomedical Scientist Jobs in Puerto Rico (NOW HIRING)

Process Development Sr Scientist

Juncos, PR · On-site +1

$89K - $121K/yr

We are looking for a Process Development Sr Scientist for the completion of the cycle development and as a technical resource SUMMARY To independently conceive, design, implement and advance ...

Process Development Sr Scientist

Juncos, PR · On-site +1

$89K - $121K/yr

We are looking for a Process Development Sr Scientist for the completion of the cycle development, documentation and filling validation SUMMARY To independently conceive, design, implement and ...

Remote Biomedical Scientist information

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

To excel as a Remote Biomedical Scientist, you should possess an advanced degree in biomedical science or a related field, strong analytical skills, and experience in laboratory research techniques. Familiarity with digital lab notebooks, data analysis software (such as MATLAB or Python), and compliance certifications like GLP or GCP are often required. Excellent written communication, problem-solving abilities, and self-motivation are essential soft skills for independent remote work. These skills ensure accurate research outcomes, effective collaboration with virtual teams, and adherence to regulatory standards in a remote setting.

What is a Remote Biomedical Scientist job?

A Remote Biomedical Scientist conducts biomedical research, analyzes laboratory data, and supports clinical or scientific studies from a remote location. They may work with digital lab tools, data management platforms, and virtual collaboration systems to assist healthcare, pharmaceutical, or research organizations. Typical duties include interpreting lab results, ensuring data accuracy, and contributing to scientific publications or regulatory compliance. This role is ideal for professionals with expertise in biomedical science who prefer a flexible, remote work environment.

What are the typical daily responsibilities of a Remote Biomedical Scientist?

As a Remote Biomedical Scientist, your daily responsibilities often include analyzing scientific data, designing and interpreting experiments, keeping detailed records of findings, and preparing reports or publications. You may collaborate with other scientists, clinicians, and stakeholders through virtual meetings and project management platforms. Depending on your employer, you might also review literature, contribute to grant proposals, or provide guidance on study design and compliance. Remote roles require strong organization and communication skills to ensure effective integration with the broader research team and timely project delivery.

What are popular job titles related to Remote Biomedical Scientist jobs in Puerto Rico? For Remote Biomedical Scientist jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Remote Biomedical Scientist jobs in Puerto Rico look for? The top searched job categories for Remote Biomedical Scientist jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Remote Biomedical Scientist jobs? Cities in Puerto Rico with the most Remote Biomedical Scientist job openings:
Infographic showing various Remote Biomedical Scientist job openings in Puerto Rico as of July 2026, with employment types broken down into 91% Full Time, and 9% Contract. 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