Role & responsibilities
Prepare and review QC documents, test reports, specifications, and SOPs.
Ensure accurate and timely documentation of laboratory activities and test results.
Maintain COA, logbooks, analytical records, and raw data as per GMP requirements.
Review batch-wise analytical documents for completeness and compliance.
Support OOS, deviation, change control, and CAPA documentation.
Ensure proper data integrity and Good Documentation Practices (GDP).
Maintain and archive QC records for traceability and regulatory requirements.
Coordinate with QA, QC, Production, and other departments for document-related activities.

Preferred candidate profile
B.Pharm/M.Pharm/M.Sc./B.Sc. in relevant discipline.
25 years of experience in pharmaceutical QC documentation preferred.
Knowledge of GMP, GLP, GDP, SOPs, and data integrity.
Experience in QC records, COA, logbooks, analytical reports, and documentation.
Valuable MS Office/Excel and ERP skills.
Solid attention to detail, accuracy, and document control.
Valuable communication, coordination, and organizational skills.

📌 Quality Control Documentation Executive Neemrana (India)
🏢 Glowria Lifecare
📍 India