MES Engineer (Aspentech)

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

Job summary

A leading technology firm in Singapore is looking for an MES Aspentech Engineer to optimize AspenTech MES in pharmaceutical manufacturing. The role involves deploying and configuring MES, collaborating with clients, and ensuring GxP compliance. Candidates should have a Bachelor's degree and over 5 years of experience with MES implementations. Strong analytical skills and effective communication are essential. This position offers challenges in a fast-paced environment while contributing to continuous improvement.

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 into AspenTech MES solutions.
• Design, configure, and test Aspen MES components for GxP compliance.

Skills

Analytical and problem-solving capabilities

Effective communication

Proactive and self-driven

Team-oriented

Education

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

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.