SPECIFIC DUTIES AND RESPONSIBILITIES : 1.Assist the FDA Liaison Officer in the respective division who handles application / renewal of (a) License to operate of International Oil Factory and Cheng Ban Yek & Co., Inc. and (b) Certificate of Production Registration.2.Prepares Q.C. Documentation such as : 2.1Certificate of Analysis2.2Daily documentation of edible oil result of analysis (local and imported) from the filling area.2.3Daily encoding and monitoring of retention sample from incoming delivery and from the production area.2.4Tracking of incoming delivery (Packaging and Raw Materials)3.Prepares standard solution / reagents to be used in the analysis of oil based on the approved work instruction.3.1Documentation of preparation / standardization of reagents3.2Proper labeling of prepared reagents3.3Conducts monthly inventory of reagents and other chemical stocks / supplies.3.4Prepare requisition of all needed chemicals.3.5Cleans all laboratory paraphernalia after use.4.Act as Q.C. Inspector in the production as needed.4.1Filling line inspection during operation.4.2Responsible in the checking of weight and content of the product as per defined frequency.4.3Inspect and weigh packaging materials (cartons / divider, SUP, bottles) during operation.4.4Inspect finished goods before packing.4.5Fortification of Vitamin A.5.Assist in the management of Retention Sample.5.1Ensures proper storage and labeling.5.2Monthly checking and storing of retention samples.5.3Disposal.6.Performs shelf-life testing of raw material and line samples under shelf-life study.7.Conducts inspection of delivery truck, sampling and analysis of incoming delivery of edible oil base on Approved Method.8.Conducts investigation and documentation of out-of-specification results of samples in the laboratory.9.As instructed, brings samples to outside laboratory and act as a liaison officer for third party analysis.10.Provide assistance in checking of packaging materials in the finished goods warehouse when needed.11.Conducts sampling and inspection of packaging materials based on established Sampling Plan.12.Evaluation of backload / returns from MCD.13.As instructed, provide assistance to Asst. Q.C. Head in the spot checking of finished products.14.Assist in the establishment of specifications and standards as needed in the department.15.Establishment / Revision of SOP, WI and other needed documents in the department.16.Inspection and evaluation of packaging materials such as SUP, Labels PET Bottles, plastic and carton, when needed.17.Assigned as the Document Custodian of the department to ensure that documents being used are current and documents / records are controlled and maintained.JOB QUALIFICATIONS :