Job Overview
- Assist in the design, operation, control and optimization of chemical / 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, troubleshooting, deviation investigation, identification and completion of corrective and preventative actions.
- 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.
- To actively seek avenues to improve operational efficiency accruing benefits to the Abbvie businesses in Singapore.
- Actively engaged in developing specifications for process equipment and assist in FAT / SAT of related equipment as part of the new build-outs.
- Participate and lead, when required, in all investigations (contaminations, deviations, and discrepancies) relating to the manufacturing process.
- 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.
- Provide operational support for the successful and uninterrupted operation of manufacturing systems used in manufacture of API and biologic products.
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