a. Stock keeping of Finished Goods - receipt of stocks , ensuring storage & safe - keeping as per norms and related system transactions & documentation. b. Distribution & sales of Finished Goods - co - ordination for making sales / stock transfers , supervision of loading , related system transactions , documentation & record keeping. c. Raw Materials & Packaging Materials - Co - ordination to ensure sampling for Laboratory Testing , co - ordination with Laboratories for testing against specifications & timely receipt of Reports , checking issue on FMFO basis in compliance with Master Formula , Stock Verification , Monitoring of Shelf Life , co - ordination for return of damaged / non - compliant materials to Vendors , etc. d. Production - Batch Number cross check , maintenance of Log Books , adherence with production schedule , compliance against BMR , BPR & SOP , adherence with Specification Binder , co - ordination for ordering , issue & control over stereos & other consumables. e. Quality - QC and QA adherence , Quality Plan adherence and monitoring of adherence with quality systems (proper work systems , testing of samples for FG clearance , retention of batch - wise samples , etc.). f. Processes & Systems - System entries for issue of materials , compilation of key data & statistics , assisting with validation studies , SOP modifications (as and when required) and co - ordinating audits / inspections by FDA. g. Monitoring of stage wise process wastage & destruction of waste , add back control , defacing of foils and printed material as & when required , etc.