Sign up with

Already have an account? Log in here

Need some help?
Talk to us at +91 7670800001

MES Engineer (Aspentech) at Advanced Manufacturing Tech Solutions (AMTSOL)

Singapore, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

26 Sep, 26

Salary

0.0

Posted On

28 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

AspenTech MES, Pharmaceutical Manufacturing, GxP Compliance, Electronic Batch Records, Validation Lifecycle, FDA 21 CFR Part 11, GMP, System Architecture, Batch Execution Models, Root Cause Analysis, Process Automation, Data Integrity

Industry

Pharmaceutical Manufacturing

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.

Responsibilities

Support the deployment, configuration, and optimization of AspenTech MES within pharmaceutical manufacturing environments. Design and test MES components and electronic batch records while ensuring GxP compliance and system integration.