GLP Reviewer-quality control

Job Title: GLP Reviewer – Quality Control (Full-Time) Location: Rau, Indore Experience Required: 1–2 Years Industry: Pharmaceutical / Healthcare Department: Quality Control (QC) Working Days: 6 Days a Week

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

 Experience in pharmaceutical manufacturing setups

 Proficient in MS Office and basic data handling

Job Type: Full-time

Pay: ₹12,000.00 - ₹18,000.00 per month

Work Location: In person