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.,
As a Quality Assurance Inspector, your primary responsibility will be to perform various inspections based on studies, facilities, and processes. You will also be required to participate in regulatory inspections conducted by organizations such as NGCMA, CDSCO, NABL, and USFDA. Your role will involve reviewing Standard Operating Procedures (SOP) and quality tools such as deviation, Corrective and Preventive Actions (CAPA), incidents, and change control. Additionally, you will be responsible for reviewing documents related to computerized system validation and instrument qualification.,