Job Overview
Location
Costa Rica Remote
Job Type
Full-time
Category
HR & Recruiting
Date Posted
March 27, 2026
Full Job Description
đź“‹ Description
- • As a Quality Assurance Auditor at Clario, you will play a critical role in safeguarding the integrity and compliance of clinical services by leading audits that ensure adherence to global regulatory standards such as GCP, ISO 9001/13485, and 21 CFR Part 11, directly contributing to the delivery of safe and effective medical therapies worldwide.
- • You will perform comprehensive internal audits of operational and technical departments, evaluate vendor quality systems, support client audits and regulatory inspections, analyze findings, and drive corrective and preventive actions (CAPAs) to closure, ensuring continuous improvement across Clario’s quality management system.
- • You will conduct quality reviews of critical documentation throughout the System Development Life Cycle (SDLC), including medical device development, change control, system requirements, testing/validation records, installation qualification, maintenance, migration, and other computer system validation processes to ensure traceability and compliance.
- • You will author and update QA/Regulatory SOPs, deliver annual training programs for staff, provide consulting to external partners, and assist in system testing execution when needed, positioning yourself as a trusted quality advisor across the organization.
- • You will support Clario’s Continuous Improvement program by participating in issue management meetings, identifying trends, and recommending process enhancements that strengthen compliance culture and operational excellence.
- • You will collaborate with cross-functional internal teams, external vendors, and clients in a fully remote environment based in Costa Rica, requiring strong self-management, clear communication, and persistence in follow-up to ensure audit readiness and quality accountability.
- • You will gain deep expertise in global clinical quality standards, regulatory frameworks (GxP, ISO, 21 CFR), and medical device QA while developing leadership, analytical, and documentation skills that advance your career in quality assurance and regulatory affairs.
- • You will contribute directly to Clario’s mission of developing safer and more effective medical therapies by ensuring high-quality endpoint data and analytics through rigorous quality oversight, making a tangible impact on global patient outcomes.
🎯 Requirements
- • High school diploma or associate degree required; Bachelor’s degree or equivalent in Health/Life Sciences, Clinical Sciences, or related field preferred.
- • Minimum 1 year of experience in Quality Assurance (QA) with a demonstrated focus on Good Clinical Practices (GCP).
- • Strong self-management and organizational skills to work independently and effectively in a fully remote work environment.
- • Effective communication skills with the ability to engage internal and external stakeholders, including persistence in follow-up on audit findings and CAPAs.
- • Experience hosting client audits or regulatory inspections is preferred (nice-to-have).
- • Prior experience with GMP and medical device QA is preferred (nice-to-have).
🏖️ Benefits
- • Competitive compensation package aligned with market standards for remote QA roles in Latin America.
- • Private health insurance coverage to support employee well-being and access to medical care.
- • Engaging employee programs designed to foster connection, recognition, and a positive workplace culture.
- • Flexible work schedules enabling work-life balance in a fully remote setting.
- • Attractive paid time off (PTO) plan including vacation, holidays, and personal days.
- • Flex workspace allowance to support a productive and ergonomic home office setup.
Skills & Technologies
GCP
Remote
Degree Required
About Clario
Clario is a global healthcare technology and services company that provides endpoint data solutions for clinical trials. It delivers imaging, cardiac safety, respiratory, eCOA, and precision motion technologies, supported by scientific and regulatory expertise, to help biopharmaceutical sponsors generate high-quality evidence and accelerate drug development.
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