OECD GLP QA AUDITOR

**Job Description** **Role Overview:** You will be working as an OECD GLP QA Auditor at Ribosome Research Centre Pvt. Ltd. in Kim. Your primary responsibility will be to conduct study-based, process-based, and facility-based audits to ensure compliance with Good Laboratory Practices (GLP). Additionally, you will review quality tools such as deviation, CAPA, and change control. Your role will also involve facing sponsor and regulatory inspections like OECD GLP, CDSCO, NABL, etc. Ensuring compliance with company standards and regulatory requirements will be crucial in this role. **Key Responsibilities:** - Conducting study-based, process-based, and facility-based audits to ensure compliance with GLP - Reviewing quality tools including deviation, CAPA, and change control - Facing sponsor and regulatory inspections such as OECD GLP, CDSCO, NABL, etc. - Ensuring compliance with company standards and regulatory requirements **Qualifications Required:** - M.Pharm preferably in Pharmacology or M.Sc in Zoology - Experience in Quality Auditing and Quality Assurance - Strong knowledge of Auditing principles and practices - Excellent attention to detail and analytical skills - Ability to work independently and on-site - Compulsory OECD GLP experience (Note: The additional details of the company were not included in the provided job description.),