To perform the Qualification activity coordination with production team.Handling and perform of HVAC Validation.Coordination with water validation in all 3 Phases.Qualification of dry syrup machine made by National Engineering.To check dispensing of raw materials and packaging materials.Collection, storage retrieval and disposal of control sample of Raw Material and Finish Products.To ensure the compliance with cGMP during manufacturing and packing.To ensure Line clearance Type A & B & Approvals to production to further processing.To ensure and maintain the cleaning sanitization records as schedule as respective SOP.To check & maintain environmental condition as required to product.To perform the Process validation of tablet capsule dosage form.To update the Sop with corrective closes.Online BMR/ BPR Review.Issuance of documents with doc. Cell team.Check the art work of primary and secondary packing material.

To perform the Qualification activity coordination with production team.Handling and perform of HVAC Validation.Coordination with water validation in all 3 Phases.Handling of market compliant and Investigation with CQA team.Handling of Planned and Unplanned deviationValidation of Tunnel washing Machine and AutoclaveTo check dispensing of raw materials (Sterile) and packaging materials.Collection, storage retrieval and disposal of control sample of Raw Material and Finish Products.To ensure the compliance with cGMP during manufacturing and packing.To ensure Line clearance Type A & B & Approvals to production to further processing.To ensure and maintain the cleaning sanitization records as schedule as respective SOP.To check & maintain environmental condition as required to product.Online BMR/ BPR Review

To check dispensing of raw materials and packaging materials.Collection, storage retrieval and disposal of control sample of Raw Material and Finish Products.To ensure the compliance with cGMP during manufacturing and packing.To ensure Line clearance Type A & B & Approvals to production to further processing.To ensure and maintain the cleaning sanitization records as schedule as respective SOP.To check & maintain environmental condition as required to product.To perform the Process validation of tablet capsule dosage form.To perform the Hold time study in different stage (Bulk, Intermediate finished product)Online BMR/ BPR Review

To perform the Qualification activity coordination with production team.Handling and perform of HVAC Validation.Coordination with water validation in all 3 Phases.Validation of Tunnel washing Machine and AutoclaveTo check dispensing of raw materials (Sterile) and packaging materials.Collection, storage retrieval and disposal of control sample of Raw Material and Finish Products.To ensure the compliance with cGMP during manufacturing and packing.To ensure Line clearance Type A & B & Approvals to production to further processing.To ensure and maintain the cleaning sanitization records as schedule as respective SOP.To check & maintain environmental condition as required to product.To perform the Process validation of tablet capsule dosage form.To perform the Hold time study in different stage (Bulk, Intermediate finished product)Online BMR/ BPR Review

To check and review the starting and intermediate products during in process of tablets, capsule, oral liquids and external preparation.Line clearance & Approvals are given in production / packaging operations prior to product change over.To check and review dispensing and sampling of starting materials and packaging materials.