Singapore-based Senior Pharma Process Engineer – GMP & C&Q

BRUNEL INTERNATIONAL SOUTH EAST ASIA PTE. LTD.; Singapore; On-site; SGD 120,000 - 180,000; Full time

Job summary

Brunel International South East Asia Pte Ltd is seeking an experienced Senior Process Engineer with a pharmaceutical manufacturing background to design, deliver, and qualify process equipment for a GMP-regulated facility.

You will coordinate process design activities, manage interfaces with equipment suppliers, and review C&Q documentation to ensure GMP compliance across IQ/OQ/PQ. Strong knowledge of cGMP and ISPE/BPE standards is essential.

Qualifications

• Bachelor's degree in Chemical Engineering, Process Engineering, or a related engineering discipline.
• 6+ years of process engineering experience within pharmaceutical, biotech, or life sciences manufacturing.
• Strong knowledge of commissioning and qualification practices and validation lifecycle.
• Solid understanding of cGMP requirements and regulatory expectations.
• Familiarity with clean utilities, bioprocessing/API equipment, or sterile systems is an advantage.

Responsibilities

• Coordinate process design activities with the design consultant and key project stakeholders to meet GMP and project timelines.
• Manage process equipment package interfaces between client user team and equipment suppliers.
• Review C&Q documentation for process equipment packages to align with GMP and regulatory expectations.
• Liaise with construction team to confirm equipment readiness and coordinate installation sequencing.
• Facilitate Process Hazard Analysis (PHA) workshops and identify risks.
• Develop site-specific engineering documentation including scopes of work, specs, and standards.
• Provide progress updates and engineering support to the Site Engineering Lead.
• Support troubleshooting of process equipment issues during design, installation, and qualification.
• Ensure deliverables comply with cGMP and industry codes (ISPE, ASME BPE).

Skills

Process design

GMP compliance

C&Q (IQ/OQ/PQ)

Regulatory compliance

Project coordination

Education

Bachelor's degree in Chemical Engineering or Process Engineering

Job description

Brunel International South East Asia Pte Ltd is seeking an experienced Senior Process Engineer with a pharmaceutical manufacturing background to design, deliver, and qualify process equipment for a GMP-regulated facility.

You will coordinate process design activities, manage interfaces with equipment suppliers, and review C&Q documentation to ensure GMP compliance across IQ/OQ/PQ. Strong knowledge of cGMP and ISPE/BPE standards is essential.