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Remote Validation Engineer Jobs in Puerto Rico (NOW HIRING)

... data validation, cleansing, and enrichment processes to improve data quality for downstream ... Execution Systems - Senior Engineer Technology: AVEVA PI Historian Experience: 8-12 years Shift:

... validation is not required Required Skills & Experience * 3-6 years of hands-on OT/IIoT engineering ... Based on this role's business requirements, this is a remote position open to qualified applicants ...

This is a primarily remote role supporting enterprise Epic implementation, with minimal travel and ... Validate claim data for demographics, insurance coverage, authorizations, provider information ...

Hospital Billing Operator

San Juan, PR · Remote

$18 - $23/hr

This is a primarily remote role supporting an enterprise Epic implementation, with minimal travel ... Validate claim data for demographics, insurance coverage, authorizations, provider information ...

Remote Validation Engineer information

What are the typical day-to-day responsibilities of a Remote Validation Engineer?

Remote Validation Engineers are responsible for developing and executing test plans, analyzing results, and documenting findings to ensure products meet required standards and specifications. They often collaborate virtually with design, development, and quality teams to identify issues and recommend improvements. Daily tasks may include running automated tests, preparing validation reports, participating in team meetings, and troubleshooting system behaviors. Adapting to shifting project requirements and effectively communicating in a remote setting are also integral parts of the role.

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

To thrive as a Remote Validation Engineer, you need a strong background in engineering or computer science, expertise in validation protocols, and experience with testing methodologies. Familiarity with validation tools such as simulation software, automated test platforms, and knowledge of industry compliance standards (e.g., ISO, FDA, or automotive standards) is typically required, and certifications like ISTQB can be beneficial. Excellent problem-solving skills, attention to detail, and strong written and verbal communication are important for collaborating across distributed teams. These skills ensure the effectiveness and reliability of complex products or systems while supporting seamless teamwork in a remote work environment.

What is a Remote Validation Engineer job?

A Remote Validation Engineer is responsible for testing and verifying that products, systems, or software meet required specifications and function correctly. They develop test plans, run simulations, analyze data, and document results—all while working remotely. This role is common in industries like automotive, semiconductor, and software development, ensuring quality and compliance with standards. Strong technical skills, attention to detail, and proficiency with validation tools are essential.

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What are popular job titles related to Remote Validation Engineer jobs in Puerto Rico? For Remote Validation Engineer jobs in Puerto Rico, the most frequently searched job titles are:
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Sterilization Program Manager (Remote Work)

CIS International LLC

Juncos, PR • On-site, Remote

Full-time

Posted 2 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