Responsibilities: ● Assist in the design, operation, control and optimization of biological processes ●To be part of the commissioning and qualification effort of the process equipment and associated systems. ●Design, install and commission new production units, monitoring modifications and upgrades and troubleshooting existing processes ● Participate in improvement efforts leading to higher process capability and production volume while maintaining and improving quality standards ●In a cGMP environment, lead modifications and changes to processes and equipment. ●Propose and evaluate modifications to equipment, processes and operations to improve safety,increase efficiency and enhance company goals. ●Maintain reliable and safe manufacturing systems while improving production rates, efficiencies, yields, costs and changeovers ●Actively engaged in developing specifications for process equipment and assist in FAT / SAT of related equipment as part of the new build-outs. ●Assist in development of systems that ensure the process works at the optimum level, to the right rate and quality of output, in order to meet supply needs ● Any other tasks and responsibilities as assigned by the reporting manager About You: ● Bachelor’s Degree inEngineering ● At least 7 years of relevant work experience. ●Knowledge of cGMP is required ●Strong technical knowledge coupled with hands-on working experience in a biotech facility. ●Good communication skills ●Able to adhere to tight timeline and schedule. ●Willing to travel to Tuas Duration: 12-month Contract