Preparation of Batch Manufacturing Record, Batch Packing Record and Master Formula Record and Master Packing records.
SAP related Activities.(Process order Creation, Stock verification, MRP Updation)
Issuance of Batch Manufacturing Record and Batch Packing Record. Checking, issuances and retrieval of Artworks and shade cards.
Creation and Review of Item codes and Maintenance of Item Code List. Review and approval of export order copy and product pack specifications in SAP.
Creation of Bill of Materials.
Preparation and Review of SOP & QAP.
Preparation & review of APQR, Graphical and statistical evaluation by Minitab-18 software.
Implement the quality management system procedure such as Change control, Deviation & CAPA etc.
Adherence to all the policies of the company and current Positive Manufacturing Practices Issuance, retrieval and maintenance of documents and log sheets of the QC department
Review of method validation, Process validation,
stability study protocols and reports
Review of Computer system validation Report.
Preparation of Validation Master Plan, Site Master File and Quality Manual. Handling of cleaning validation activities.
Preparation and evaluation of QRM.
Handling of market complaints. T
o provide the support to regulatory affairs activities.
Review of Completed batch records and Responsible for Batch Release. To perform internal and external audit management and audit compliance.
To perform Self Inspection.
Preparation and evaluation of risk assessment report.
Review and approval of master documents like MFR,MPR etc. investigation , review and closure of OOS ,OOT and Lab Deviations.
To adhere Quality Policy, Ornamental Policy ,EHS Policy and Data Integrity Policy.
To complete the routine training in LMS.