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1 day ago
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, ₹18,000.00 per month
Work Location: In person
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