Job Description

Responsibilities:

• Assist in the design, operation, control and optimization of chemical / biological processes systems used in manufacture of API and biologic 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 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.
• Provide operational support for the successful and uninterrupted operation of manufacturing.
• Other duties as assigned by manager

• Diploma/Degree in Science, Mechanical/Chemical Engineering or a relevant discipline. At least 1-2 years related Pharmaceutical experience preferred. Fresh graduates or with pharmaceutical internship 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