MES OpCenter Engineer at Advanced Manufacturing Tech Solutions (AMTSOL)

Singapore, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

07 Jul, 26

Salary

0.0

Posted On

08 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

MES OpCenter, Siemens MES, Pharmaceutical Manufacturing, cGMP, Workflow Design, System Validation, Change Control, Troubleshooting, ISA-95, ERP, DCS, PLC, Requirement Gathering, Technical Documentation, System Integration

Industry

Pharmaceutical Manufacturing

Description

We are seeking a talented MES Engineer to join our team in the Life Sciences industry. The successful candidate will collaborate closely with cross-functional teams to ensure the efficient and compliant execution of manufacturing processes. Key Responsibilities: Responsibility during MES implementation phases Collaborate with stakeholders, including manufacturing, quality assurance, and IT teams, to gather requirements and define design specifications. Design and develop manufacturing workflow within the Manufacturing Execution System (MES) platform to support pharmaceutical manufacturing processes. Conduct testing and validation activities to verify the functionality and performance of workflow within the MES environment, in accordance with regulatory requirements. Provide training and support to end-users on functionality, navigation, and troubleshooting within the MES system. Provide Hypercare Responsibility during MES Operational support Support change control process for any changes made to MES system Analyze and troubleshoot any system interface issues related to MES system Analyze and troubleshoot any workflow design related issues Support development of Standard Operating Procedures for MES Participate in continuous improvement initiatives to optimize design processes, enhance system usability, and ensure alignment with evolving business needs and regulatory standards. Support MES system upgrade project. Qualifications and Requirements: Bachelor’s degree in chemical engineering, Bioengineering, Computer Science, or a related field. Experience in designing and configuring batch record within a Manufacturing Execution System (MES), preferably using the Siemens MES OpCenter platform. Strong understanding of pharmaceutical manufacturing processes, cGMP guidelines, and regulatory requirements, with knowledge of industry standards such as ISA-95. Experience in conducting testing, validation, and qualification activities for MES implementations, ensuring compliance with regulatory standards. Strong understanding of MES system interfaces (with ERP, DCS, PCS/PLC) Excellent communication and collaboration skills, with the ability to effectively engage with cross-functional teams and stakeholders to gather requirements and drive project success. Ability to work independently and manage multiple projects simultaneously in a fast-paced, dynamic environment

Responsibilities

The MES Engineer will design and implement manufacturing workflows within the Siemens OpCenter platform to support pharmaceutical production. They are responsible for system validation, troubleshooting interface issues, and providing end-user training and operational support.