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10 hours 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
Pay: ₹12,000.00 - ₹18,000.00 per month
Work Location: In person
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