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
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