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Line clearance for production operations. Review of BMR, BFR, BPR. In - process QA functions. Control sample management. Collection of In process / Finished product and customer samples. Compilation of APQR data with trend analysis. Participation in process validation, hold time studies etc. Co-ordination for batch release. Routine GMP verification in production and warehouse, production and all other departments. Co-ordination and review of vendor management documents, compilation of vendor assessment reports. Document Archival management as on when required. Issuance and control Formats, SOPs, Specifications and Batch Records.
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