Responsibilities

• Ensure adherence to EHS compliance at QC Analytical Laboratory.
• Ensure Good Documentation Practice (GDP) is in place and applied in recording of QC daily activities for easy traceability and facilitate audit requirement.
• Ensure the proper housekeeping and cleanliness is maintained in QC Analytical department
• Preparation and continuous improvement of all relevant SOPs, EOPs, Specifications and ensure those procedures are revised and updated in accordance to stipulated interval and as per cGMP requirement / latest pharmacopoeia.
• Ensure proper safe and regular disposal of laboratory waste such as solvent, reagents and etc. following EHS Department and local regulation.
• Daily monitoring of Drug Product and Drug Substance incoming and retest raw materials, Packing Materials and Consumables in SAP system.
• Coordinate and assign activities to team members for routine test analysis and ensure task...