Coordination with different departments vise (QC, Manufacturing & QA) for material testing. Issuance and release as per the plan. Planning and reviewing of work force availability for material receipts, movements, sampling, Labeling, relocation & dispensing activities.
Reviewing online documentation from all the areas.
Initiating the material write- offs for the rejected as well as non-moving slow moving & expired materials with proper management approval and customs approvals and disposal as per SOPs.
Coordinating with production Head and production planning department to execute daily production schedule requirements.
Monitoring systems / team to follow as per the GMP guidelines;
Monitoring unauthorized movement of people / materials and oversee cleanliness of warehouse.
Monitoring control on rejected and expired materials.
Creating internal dispensing plan and allocating the work in each dispensing area.
Review and approving Change controls, Deviations, Investigations and CAPAs.
Responses to regulatory audits like USFDA , PMDA, ISO ,FSSC , ANVISA internal compliance audits.
