Technical Consultant - MES ASPEN

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

Job summary

Advanced Manufacturing Tech Solutions (AMTSOL) in Singapore seeks a senior MES Aspen APEM Technical Consultant to lead pharmaceutical MES projects. You will design, implement and validate Aspen APEM solutions within GxP environments, ensuring compliant, auditable manufacturing operations.

This role requires 9+ years in pharma manufacturing, extensive ISA-88/95 knowledge, and a proven record delivering end-to-end MES deployments.

Qualifications

• Minimum 9+ years of total experience in the pharmaceutical manufacturing industry.
• Must have delivered MES implementations for pharma / biotech / API / drug product manufacturing sites.
• Must have worked in GxP-regulated environments and supported regulatory audits and inspections.

Responsibilities

• Lead end-to-end Aspen APEM MES implementations for pharmaceutical manufacturing sites.
• Act as primary MES SME for batch manufacturing, EBR, genealogy, deviation handling, and controlled execution.
• Define MES architecture aligned to pharma processes, ISA‑88 / ISA‑95, and global quality standards.

Skills

MES Aspen APEM

Pharma manufacturing

GxP compliance

Regulatory audits

ISA-88 / ISA-95

Tools

Aspen APEM

Job description

Job Title :Senior / Lead MES Technical Consultant – Aspen APEM (Pharmaceutical MES)

Experience: 5+
Industry: Pharmaceutical / Life Sciences ONLY (Mandatory)
Location: Singapore

Role Overview

We are seeking a senior-level MES Aspen APEM Technical Consultant with deep, hands‑on experience in pharmaceutical manufacturing environments.
This role is strictly open to professionals who have designed, implemented, and validated MES systems within regulated pharmaceutical facilities.

Candidates without pharmaceutical / life sciences MES experience will NOT be considered.

Mandatory Industry Requirement (Critical)

• Minimum 9 + years of total experience, with significant and proven experience in the pharmaceutical manufacturing industry
• Must have delivered MES implementations for pharma / biotech / API / drug product manufacturing sites
• Must have worked in GxP-regulated environments and supported regulatory audits and inspections

Key Responsibilities

MES Technical & Solution Leadership (Pharma Focused)

• Lead end‑to‑end Aspen APEM MES implementations for pharmaceutical manufacturing sites
• Act as primary MES SME for batch manufacturing, EBR, genealogy, deviation handling, and controlled execution
• Define MES architecture aligned to pharma processes, ISA‑88 / ISA‑95, and global quality standards