Associate

·         To prepare and implement SOP’s for production area.

·         Ensure and assuring that activities are strictly adhered to cGMP standard.

·          Assist the control of formats, logbooks & SOPs including inventory, issuance, retrieval & submission to QA department.                                                                                            

·          Check that all the cGMP documents are in place.

·         To assist/prepare for documents such as SOPs, Qualification & Validation documents, change controls, deviations, investigations, CAPAs & BMR review.

·         To assist in regulatory inspections.               

·         To assist/prepare investigations for market complaints, LIR, OOS/OOT.

·          Training to subordinates, workmates & superiors (if required)

·         Department Training Co-coordinator for production.