Associate Process/Project Engineer (Pharma/Biotech)

NUSANTARA PRIME CONSULTING PTE. LTD.; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

NUSANTARA PRIME CONSULTING PTE. LTD. is seeking a process engineer in Singapore to assist in the design and optimization of chemical and biological processes for biologics. The role requires 1-2 years of relevant pharmaceutical experience, although fresh graduates with internship experience are welcome. This position offers a 12-month contract with potential for extension based on performance evaluations.

Key responsibilities include monitoring modifications, troubleshooting existing processes, and providing operational support to ensure smooth manufacturing operations.

Qualifications

• At least 1-2 years related pharmaceutical experience preferred, fresh graduates with internship experience welcome.
• Good interpersonal and communication skills.
• Ability to multitask and hands-on approach.
• Reliability, responsibility, and personal integrity required.
• Self-motivated and willingness to learn essential.
• Creative thinking important for role.

Responsibilities

• Assist in design, control, and optimization of chemical/biological processes.
• Participate in commissioning and qualification of process equipment.
• Monitor modifications, upgrades, and troubleshoot existing processes.
• Lead improvements for operational efficiency and quality.
• Troubleshoot deviation investigations and implement corrective actions.
• Maintain reliable manufacturing systems and improve production metrics.
• Develop specifications for process equipment as required.
• Provide operational support for uninterrupted manufacturing operations.

Skills

Good interpersonal and communication skills

Ability to multitask and hands-on approach

Reliability and responsibility

Self-motivated and willingness to learn

Creative thinking

Education

Diploma/Degree in Science, Mechanical/Chemical Engineering or relevant discipline

Job description

Responsibilities

• Assist in the design, operation, control and optimization of chemical/biological process systems used in the manufacture of biologics products.

• Be part of the commissioning and qualification effort of the process equipment and associated systems.

• Assist in design, install and commission new production units, monitor modifications and upgrades and troubleshoot 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, troubleshoot deviation investigations, identify and complete corrective and preventative actions.

• Assist Senior Engineer in proposal and evaluation of 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 engage in developing specifications for process equipment and assist in FAT/SAT of related equipment as part of 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.

12 months contract. Extension or conversion subject to performance evaluation.

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.

Based in Tuas.