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Quality Systems Manager Remote Jobs in Puerto Rico

Amgen

Senior Specialist, Quality Risk & Governance

Juncos, PR · On-site +1

$80K - $110K/yr

... System through proactive risk management and effective governance practices. This role combines a ... Remote will be considered if applicable. Quality Risk Management (60%) In this role, you will ...

Jj

Global MT SC ERP Quality Manager

Guaynabo, PR · On-site +1

... remote work. Caring for the world, one person at a time has inspired and united the people of ... Collaborate with System Quality and Business Quality teams to develop, implement, and maintain ...

Cognizant Technology Solutions

... efficiency, quality, and sustainability. Responsibilities • Design robust AVEVA PI Historian ... and stakeholder management skills. • Ability to work effectively in a hybrid model with ...

Deloitte

Technical Program Manager

San Juan, PR · Remote

$126K - $163K/yr

... store systems, and enterprise platform deployments across thousands of locations. Define and ... Meticulous attention to detail and quality of work product * Ability to build and sustain ...

Veterans Health Administration

$89K - $116K/yr

... system. * Demonstrates the ability to assess data needed, design data collection procedures ... Facilitates planning and implementation of new Quality Management procedures and policies for ...

ICF

Project Manager - (Puerto Rico)

San Juan, PR · On-site +1

Ensure that project deliverables meet quality standards and business requirements. * Maintain ... Remote role based in Puerto Rico; Must be able to travel to visit clients, stakeholders and ...

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Quality Systems Manager Remote information

What is the difference between Quality Systems Manager Remote vs Quality Assurance Specialist?

AspectQuality Systems Manager RemoteQuality Assurance Specialist
CredentialsISO certifications, quality management trainingISO, GMP, or industry-specific certifications
Work EnvironmentRemote, office, or hybrid; overseeing quality systemsPrimarily on-site or lab-based; focused on product testing
Employer & IndustryManufacturing, healthcare, or tech companiesPharmaceuticals, manufacturing, or food industries
Search & Comparison IntentUnderstanding roles, responsibilities, and remote optionsJob duties, certifications, and industry focus

The main difference is that a Quality Systems Manager Remote oversees the entire quality management system remotely, focusing on compliance and process improvement, while a Quality Assurance Specialist primarily conducts product testing and inspections, often on-site. Both roles require relevant certifications and are common in manufacturing and healthcare industries, but their responsibilities and work environments differ.

What are some common challenges faced by a remote Quality Systems Manager, and how can they be effectively addressed?

A remote Quality Systems Manager often encounters challenges such as ensuring consistent communication across dispersed teams, maintaining oversight of compliance documentation, and driving engagement in quality initiatives without in-person interactions. Leveraging digital collaboration tools, setting clear expectations, and establishing regular check-ins are key strategies to address these challenges. Proactively building relationships with cross-functional teams and utilizing cloud-based quality management systems can also help maintain transparency and accountability in a remote environment.

What are the key skills and qualifications needed to thrive as a Quality Systems Manager (Remote), and why are they important?

To thrive as a Quality Systems Manager (Remote), you need expertise in quality management systems (such as ISO 9001), regulatory compliance, and process improvement, typically supported by a relevant degree and experience in quality assurance. Familiarity with digital quality management software, document control systems, and certifications like Six Sigma or ASQ Certified Quality Auditor are commonly required. Strong analytical thinking, communication, and leadership skills are essential for influencing teams and driving quality initiatives remotely. These competencies ensure robust compliance, continuous improvement, and effective oversight of quality standards across distributed teams.

What are Quality Systems Managers (Remote)?

Quality Systems Managers (Remote) are professionals responsible for developing, implementing, and maintaining an organization's quality management systems while working from a remote location. They ensure that processes comply with industry standards and regulations, such as ISO 9001 or FDA guidelines, to maintain product or service quality. Their duties often include conducting audits, managing documentation, training staff on quality procedures, and analyzing data to drive continuous improvement. Working remotely, they use digital tools to collaborate with teams, coordinate quality initiatives, and report to leadership.
What are popular job titles related to Quality Systems Manager Remote jobs in Puerto Rico? For Quality Systems Manager Remote jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Quality Systems Manager Remote jobs in Puerto Rico look for? The top searched job categories for Quality Systems Manager Remote jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Quality Systems Manager Remote jobs? Cities in Puerto Rico with the most Quality Systems Manager Remote job openings:
Quality Systems Manager Remote jobs near you

Sterilization Program Manager (Remote Work)

CIS International LLC

Juncos, PR • On-site, Remote

Full-time

Posted yesterday

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