Job Description

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 Travel may be required based on project needs

About You:

Bachelor's Degree in Engineering At least 5 years of relevant work experience. Knowledge of cGMP is required Strong technical knowledge coupled with hands-on working experience in a biotech facility and Single-use systems Working experience in start-ups, commissioning & qualification of process systems in an operating plant is a plus Good communication skills Ability to work well with teams including external contractors Excellent team player willing to work for the common goal Willing to travel to Tuas
Job Type: Contract
Contract length: 12 months

Pay: $6,000.00 - $10,000.00 per month

Experience:

commissioning and qualification : 5 years (Preferred) Single-use systems: 5 years (Preferred) * FAT / SAT: 5 years (Preferred)