• Work alongside experienced QC professionals in the same team 
• Work on one of the largest project for the QC field 
• To prioritise and perform various testing /analysis in a timely manner, in order to support the business requirements 
• Analysis of Bulk product, in-process, raw material or environmental samples according to Standard Operating Procedures and Test Methods. 
• Documentation of results in accordance with current Good Manufacturing Practices (cGMP)
• Problem solving of analytical methods as well as troubleshooting of equipment
• Involvement in method transfers and validation 
• Involved in equipment qualification and technical selection of QC equipment and/or standards and reagents. 
• Assay trend analysis, document revision and update 
• General lab support including housekeeping, equipment maintenance, inventory of supplies, lab supplies ordering, management of glass wares,autoclaving etc 
• Any other duties as assigned by your Supervisor/Manager

Job Requirements: Min Diploma/Degree in Life Science and Min 3 years of relevant HPLC and GC exp in Pharmaceutical industry