Process/Project Engineer (Pharma/Biotech)

NUSANTARA PRIME CONSULTING PTE. LTD.; Singapore; On-site; SGD 70,000 - 90,000; Full time

Job summary

A leading consulting firm in Singapore is seeking a Process Engineer to own the Equipment Package lifecycle, including design, commissioning, and qualification of process equipment. The ideal candidate will have at least 5 years of experience in the pharmaceutical or biologics industry, strong project scheduling skills, and knowledge of cGMP requirements. This role offers a contract length of 12 months, with the option to extend depending on performance.

Qualifications

• 5+ years of experience in process engineering or similar role in a biologics manufacturing plant.
• Experience in pharmaceutical/biologics manufacturing industry.
• Design experience at various stages of the project.

Responsibilities

• Responsible for equipment package ownership, including design and commissioning.
• Coordinate with manufacturing, safety, and quality functions.
• Deliver projects within schedule, budget, and quality constraints.

Skills

Process Engineering

Project Scheduling

cGMP Knowledge

Troubleshooting

Education

Diploma/Degree in Chemical Engineering or Chemistry

Job description

Overview

The role is responsible for Equipment Package Ownership (full lifecycle – Engineering Design, Build, Testing (FAT), Installation and Commissioning), including experience in commissioning and qualification of process equipment.

Responsibilities

• Experience in upstream / downstream / Central services process operation, (experience in equipment design for process equipment will be an advantage).
• Project scheduling and able to come up solutions to keep the schedule on track when there are hiccups.
• Responsible for basic and detailed design, commissioning and qualification activities, including URS development, FAT, SAT, DQ, IQ, OQ and PQ.
• Review industry practices for best-in-class approach.
• Ensure that the appropriate Quality standards are applied consistent with best practice and internal Quality Standards and expectations.
• Deliver the project from conceptual through implementation phase, encompassing support for a wide range of engineering and construction requirements.
• Coordinates with different functions like manufacturing, safety, MSAT, validation and quality for implementation of changes associated with the project.
• Work independently and/or with the project manager to complete the engineering projects within schedule, budget and quality constraints.
• Agile response to equipment issue, troubleshoot and come up with solutions swiftly
• Any other task as assigned by Supervisor/Manager.

About You

• Diploma/Degree in Chemical Engineering, Chemistry or equivalent with at least 5 years' experience in a process engineering role or similar role with a biologics manufacturing plan
• At least 5 years of relevant working experience in the Pharmaceutical / Biologics manufacturing industry with experience in Process Engineer
• In Biologics industry with understanding of cGMP requirement
• Should have Design experience at various stages of project (Base, Detailed design)
• Able to support Installation, Commissioning & Qualification activity at site.
• Must be able to drive projects.
• Any other task given related to Process.

Only shortlisted candidates will be notified.

Contract length: 12 Months. Option to extend depending on performance and business needs.

Location: Tuas