Quality Assurance Auditor I

Role: Quality Assurance Auditor within GLP-regulated environments, focusing on audits of studies, facilities, and compliance with FDA, EPA, and international GLP standards. Responsibilities: conduct facility and process audits review documentation prepare audit reports support validation assessments assist with regulatory inspections Requirements: Bachelor’s degree in chemistry, life sciences, or related field 2-4 years of experience in GLP or similar regulated settings, preferably with auditing expertise strong understanding of regulatory requirements, data integrity, and quality systems proficiency with electronic data systems and SOPs preferred qualifications include knowledge of Part 11 compliance, risk assessments, and vendor evaluations High-Value: GLP compliance, audit execution, FDA/EPA standards, validation oversight, electronic data systems, and regulatory inspection support. Work setup: Office or laboratory environment; travel is expected for inspections and client interactions; physical activity includes moderate movement and laboratory safety protocols. #J-18808-Ljbffr