GLP Reviewer – Quality Control

Job Description

Key Responsibilities:  Review analytical raw data, reports, and logbooks to ensure compliance with GLP and internal SOPs  Verify the accuracy and completeness of QC documentation before final approval  Maintain proper documentation and archival of reviewed records  Communicate non-conformities or discrepancies to the concerned team for correction and resolution  Ensure adherence to regulatory and quality standards (e.g., WHO, GMP, GLP)  Coordinate with QC analysts and QA teams for timely closure of documentation review  Assist in internal audits and regulatory inspections when required Required Qualifications:  B.Sc. / M.Sc. in Chemistry, Pharmaceutical Sciences, or a related discipline  1–2 years of experience in a GLP environment within a Quality Control department  Familiarity with regulatory requirements related to GLP and GMP  Good documentation and communication skills  Strong attention to detail and analytical ability Preferred Skills:  Hands-on knowledge of QC instruments and procedures Job Type: Full-time Pay: ₹18,000.00 - ₹20,000.00 per month Work Location: In person