Company Description Dabur Research Foundation (DRF), established in 1979, is an Indian Contract Research Organization offering preclinical services for Drug Discovery and Development. Operating independently since 2008, DRF provides services across In Vitro, Ex-Vivo & In Vivo Pharmacology, Exploratory & GLP Toxicology, and DMPK. With over 30 years of experience, we support global Biotech, Pharma, Phytopharmaceuticals, Cosmeceuticals, and academic sectors through every step of drug discovery and development. Role Description We are looking for a GLP QA Inspector (full-time, on-site, South Delhi). The role involves monitoring and ensuring compliance with Good Laboratory Practices (GLP) in preclinical studies. Responsibilities include conducting audits, reviewing study documentation, ensuring adherence to protocols, and supporting GLP standards across study processes. Qualifications 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 (OECD GLP Guidelines) Experience in audits, inspections, and compliance monitoring Excellent organizational, written, and verbal communication skills Ability to work independently and collaboratively How to Apply Please send your CV to hr@daburresearch.in with the subject line Position_Name .
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.,