Descripción de la oferta
Experteer Overview
As a QA Auditor, you will support lead auditors in planning, conducting, and reporting quality assurance audits within defined timelines. You’ll manage data entries, track findings in the eQMS, and assist with CAPA and EC plans while maintaining regulatory awareness (GLP/GXP). You will help host customer and regulatory audits, acting as a scribe and ensuring documents and responses are organized. This role combines hands-on audit tasks with quality governance in a hybrid IQVIA Laboratory setting, contributing to data integrity and compliant operations.
Compensaciones / Beneficios
• Assist in planning and conducting quality assurance audits within budget and timelines
• Schedule auditees, perform data reviews, and document audit findings
• Enter and categorize audit findings in the eQMS
• Support closing audits by gathering follow-up information
• Review and approve CAPA and EC plans
• Assist in derogatory status management and provide compliant guidance
• Host customer and regulatory audits as a scribe, review documents, and coordinate interviews
• Maintain knowledge of GLP regulations and auditing techniques
• Support QA consultancy and maintain the eQMS across the audit lifecycle
Responsabilidades
• Bachelor's degree or equivalent
• 1 year of QA experience in pharmaceutical/technical or related area (GXP/QA)
• Knowledge of word processing, spreadsheets, and databases
• Strong knowledge of GXP regulations and auditing techniques
• Excellent interpersonal, problem-solving, organizational, and communication skills
• Ability to work independently and manage multiple projects
• Ability to collaborate with coworkers, managers, and clients
Requisitos principales
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