Quality Specialist I

Assisting Quality Management in monitoring GCP regulatory compliance, the full-time remote Quality Specialist I will schedule and perform internal assessments, manage quality metrics, and support continuous improvement initiatives in clinical trial operational activities. Key responsibilities Schedule and conduct internal assessments, including audits and equipment validations Update and maintain quality metrics and Key Performance Indicators for management review Participate in root cause analyses and track non-conformance reporting and corrective actions Required qualifications Bachelor's degree (B.S./B.A.) preferred 1-2 years of related experience and/or training, or equivalent combination of education and experience Experience with quality management systems and regulatory compliance in clinical trials Ability to work independently and collaboratively on multiple projects Familiarity with document control and record retention requirements