Project Engineer

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

Duration: 1 year