MES Engineer

Advanced Manufacturing Tech Solutions (AMTSOL); Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A leading technology firm is seeking an MES Aspentech Engineer for Pharmaceutical Manufacturing in Singapore. The role involves supporting the deployment and optimization of AspenTech MES, collaborating with clients, and ensuring compliance with industry regulations. Ideal candidates have a Bachelor's Degree and over 5 years of experience with AspenTech MES or similar platforms. Strong analytical skills, effective communication, and team orientation are essential for this dynamic position.

Qualifications

• 5+ years of experience in MES implementations, preferably with AspenTech MES or similar platforms.
• Experience with Aspen MES configuration and integration.
• Familiarity with pharmaceutical batch process automation and data integrity requirements.

Responsibilities

• Support the deployment, configuration, and optimization of AspenTech MES in pharmaceutical manufacturing settings.
• Collaborate with clients to translate operational needs and regulatory requirements into AspenTech MES solutions.
• Design, configure, and test Aspen MES components to align with GxP compliance and manufacturing workflows.

Skills

MES implementations

AspenTech MES

Strong analytical and problem solving

Effective communication

Team-oriented

Education

Bachelor's Degree in Computer Science, Engineering, Information Systems, Life Sciences, or related disciplines

Tools

AspenTech MES

Rockwell PharmaSuite

Werum PAS-X

Siemens Opcenter

Job description

Job Title: MES Aspentech Engineer for Pharmaceutical Manufacturing

Key Responsibilities:

• Support the deployment, configuration, and optimization of AspenTech MES in pharmaceutical manufacturing settings.
• Collaborate with clients to translate operational needs and regulatory requirements into AspenTech MES solutions.
• Design, configure, and test Aspen MES components to align with GxP compliance and manufacturing workflows.
• Provide input on system architecture, batch execution models, and integration requirements.
• Troubleshoot Aspen MES application and integration issues; support root cause analysis and system improvements.
• Participate in the design and development of electronic batch records (EBRs) within Aspen MES.
• Support validation lifecycle activities (IQ, OQ, PQ) in compliance with FDA 21 CFR Part 11 and GMP.
• Deliver on-site and remote support during MES deployment, commissioning, and post-Go Live optimization.

Qualifications and Requirements:

• Bachelors Degree in Computer Science, Engineering, Information Systems, Life Sciences, or related disciplines.
• 5+years of experience in MES implementations, preferably with AspenTech MES or similar platforms (e.g., Rockwell PharmaSuite, Werum PAS‑X, Siemens Opcenter).
• Experience with Aspen MES configuration and integration
• Familiarity with pharmaceutical batch process automation and data integrity requirements.
• Knowledge of industry regulations and practices: GxP, 21 CFR Part 11, Annex 11.
• Strong analytical and problem‑solving capabilities.
• Effective communication with both technical and non‑technical stakeholders.
• Proactive, self‑driven, and able to work in a fast‑paced, client‑facing environment.
• Team‑oriented, with a commitment to quality and continuous improvement.