MES Engineer - PAS -X - Singapore

Advanced Manufacturing Tech Solutions PTE. LTD. (AMTSOL); Singapore; On-site; SGD 120,000 - 180,000; Full time

Job summary

Advanced Manufacturing Tech Solutions PTE. LTD. (AMTSOL) in Singapore seeks an experienced MES specialist to configure and support Werum PAS-X based batch records and MES workflows in a pharmaceutical manufacturing environment.

You will design eBRs, manage configuration, assist SAP integration, and support validation activities (IQ/OQ) while ensuring cGMP and 21 CFR 11 compliance. This role involves hands-on problem solving on shopfloor MES issues and opportunities for continuous improvement.

Qualifications

• 6–8 years MES experience in pharma/biotech.
• Hands-on Werum PAS‑X configuration experience.
• Strong knowledge of eBR design, workflow configuration, and MES support in live manufacturing environments.

Responsibilities

• Configure and develop electronic batch records (eBR) using Werum PAS‑X
• Perform workflow configuration using MBR Designer / PAS‑X tools
• Support FAT, SAT, and validation activities (IQ/OQ)
• Assist in integration with SAP and automation systems (DeltaV / PLCs)
• Provide shopfloor MES support during batch execution
• Troubleshoot workflow, master data, and interface issues
• Support change control, deviations, and SOP documentation
• Participate in system upgrades and continuous improvement initiatives

Skills

MES experience in pharma/biotech

WERUM PAS-X configuration

eBR design

workflow configuration

live manufacturing MES support

cGMP / GAMP 5 / 21 CFR Part 11 / ISA-8

Tools

WERUM PAS-X

MBR Designer

DeltaV

PLC integration

Job description

Roles & Responsibilities

• Configure and develop electronic batch records (eBR) using Werum PAS‑X
• Perform workflow configuration using MBR Designer / PAS‑X tools
• Support FAT, SAT, and validation activities (IQ/OQ)
• Assist in integration with SAP and automation systems (DeltaV / PLCs)
• Provide shopfloor MES support during batch execution
• Troubleshoot workflow, master data, and interface issues
• Support change control, deviations, and SOP documentation
• Participate in system upgrades and continuous improvement initiatives

Requirements

• 6 to 8years of MES experience in pharma/biotech
• Hands‑on experience with Werum PAS‑X configuration
• Strong knowledge of eBR design, workflow configuration, and MES support in live manufacturing environments
• Good understanding of cGMP, GAMP 5, 21 CFR Part 11, ISA‑88 / ISA‑95 fundamentals