Technical Consultant - MES ASPEN

Advanced Manufacturing Tech Solutions PTE. LTD. (AMTSOL); Singapore; On-site; SGD 120,000 - 190,000; Full time

Job summary

Advanced Manufacturing Tech Solutions PTE. LTD. (AMTSOL) seeks a Senior/Lead MES Technical Consultant with deep Aspen APEM MES expertise for pharmaceutical manufacturing environments in Singapore.

The role requires hands-on design, implementation, and validation of MES in regulated facilities. Candidates must have 9+ years in pharma manufacturing and a proven track record delivering MES projects in GxP settings, including supporting regulatory audits and inspections.

Qualifications

• Minimum 9+ years of total experience in pharmaceutical manufacturing
• Delivered MES implementations for pharma/biotech/API/drug product sites
• Experience in GxP-regulated environments and supporting regulatory audits/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 ISA‑88 / ISA‑95 and global quality standards

Skills

MES expertise

Regulatory compliance

Technical leadership

Aspen APEM

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