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Associate Process
2 weeks ago
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 buildouts.
- 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
Requirements:
- Diploma/Degree in Science, Mechanical/Chemical Engineering or a relevant discipline. At least 12 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 handson approach
- Reliability, responsibility, and personal integrity
- Selfmotivated and willingness to learn
- Creative Thinking
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