As one of the Quality Assurance auditors, you will conduct audits on challenging multi-phase non-clinical studies in an OECD GLP lab environment. Your daily responsibilities are diverse and range from auditing protocols, study data and associated reports to executing process and facility audits to ensure regulatory compliance. In your role as an auditor, you will be liaising with laboratory personnel during on-site study audits and take on an advisory role with respect to the latest requirements of OECD GLP principles and adherence to Charles River’s Standard Operating Procedures.