GLP QA AUDITOR

The position of OECD GLP QA Auditor at Ribosome Research Centre in Kim is a full-time on-site role. As the GLP QA Auditor, your primary responsibility will be to conduct quality audits, ensure compliance with GLP regulations and guidelines, prepare audit reports, and recommend corrective actions. Your day-to-day tasks will involve reviewing study protocols, performing study-based inspections, facility-based inspections, and carrying out quality assurance activities. Additionally, you will collaborate with research staff to enhance quality management practices. To excel in this role, you must have prior experience in an OECD GLP environment. Proficiency in quality auditing, auditing skills, and quality management practices is essential. Strong written and verbal communication skills are also crucial for effective performance. A Master's degree in any life sciences field (e.g., Biotechnology, Pharmacology) is a mandatory qualification. Furthermore, your ability to work efficiently in a team-oriented environment will be key to succeeding in this position.,