GLP QA Inspector

Role Overview: As a GLP QA Inspector at Dabur Research Foundation (DRF), your main responsibility will be to monitor and ensure compliance with Good Laboratory Practices (GLP) in preclinical studies. This full-time, on-site position located in South Delhi requires you to conduct audits, review study documentation, ensure adherence to protocols, and support GLP standards across study processes. Key Responsibilities: - Monitor and ensure compliance with Good Laboratory Practices (GLP) in preclinical studies - Conduct audits and inspections to review study documentation - Ensure adherence to protocols and regulatory guidelines (OECD GLP Guidelines) - Support GLP standards across study processes - Collaborate with the team to maintain compliance and quality standards in preclinical research Qualifications Required: - Bachelor's or Master's degree in Life Sciences, Biotechnology, Pharmacology, Chemistry, or related field - 2-4 years of QA experience in a GLP environment (preclinical research experience preferred) - Strong understanding of regulatory guidelines and protocols, particularly OECD GLP Guidelines - Experience in conducting audits, inspections, and compliance monitoring - Excellent organizational, written, and verbal communication skills - Ability to work independently as well as collaboratively with the team Please send your CV to hr@daburresearch.in with the subject line Position_Name to apply for this GLP QA Inspector position at Dabur Research Foundation.,