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Responsibilities:
Assist in the design, operation, control and optimization of chemical / biological processes systems used in manufacture of biologics products.
To be part of the commissioning and qualification effort of the process equipment and associated systems.
Assist in 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.
Assist Senior Engineer in proposal and evaluation 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 assisting 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.
Provide operational support for the successful and uninterrupted operation of manufacturing.
Other duties as assigned by manager
Based in Tuas
About You:
Diploma/Degree in Science, Mechanical/Chemical Engineering or a relevant discipline. At least 1-2 years related pharmaceutical experience is preferred. Fresh Graduates or with pharmaceutical internship experience are also welcome to apply.
Good interpersonal and communication skills.
Ability to multitask and hands-on approach
Reliability, responsibility, and personal integrity
Self-motivated and willingness to learn
Creative Thinking
12 months Contract. Extension or conversion subject to performance evaluation.
Based in Tuas.
Job ID: 143540765