Project Engineer (Pharma/Biotech)

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