Process/Project Engineer (Pharma/Biotech)

NUSANTARA PRIME CONSULTING PTE. LTD.; Singapore; On-site; SGD 20,000 - 60,000; Full time

Job summary

A leading consulting firm in Singapore is seeking an experienced Process Engineer to take ownership of the Equipment Package lifecycle. The role involves supporting engineering design, commissioning, and qualification activities within the Pharmaceutical/Biologics sector. Ideal candidates will have at least 5 years of relevant experience, a degree in Chemical Engineering or Chemistry, and a deep understanding of cGMP requirements, contributing to ensuring quality standards are met throughout the project stages.

Qualifications

• At least 5 years of experience in a process engineering role or similar in a biologics manufacturing plant.
• Experience in the Pharmaceutical/Biologics manufacturing industry.
• Understanding of cGMP requirements.

Responsibilities

• Responsible for Equipment Package Ownership including lifecycle phases.
• Coordinate with various functions for project implementation.
• Deliver engineering projects within schedule and budget.

Skills

Process engineering experience

Project scheduling

Troubleshooting skills

Agile response to equipment issues

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