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
