MES (Manufacturing Execution System) Engineer (Contract)

MES (Manufacturing Execution System) Engineer
(12-month contract)

About the Company:
Our client is a US healthcare and a leading global biopharmaceutical company. They have a revenue of US $40.1 billion, with more than 69,000 employees across 140 countries with a heritage of more than 125 years. Our client is committed to provide patients and customers with a reliable supply of high-quality, safe, and effective medicines and vaccines. Their global supply strategy relies on manufacturing capabilities and expertise to achieve this mission

Primary Responsibilities:
The MES (Manufacturing Execution System) Engineer is responsible for providing technical support in the field of automation. Supports a large spectrum of automated systems within Manufacturing Operations. Responsible for resolution of automation problems, implementation of Automation changes and troubleshooting in compliance with SDLC, GMP, safety, and environmental regulations. Actively support an empowered team culture including significant interaction with manufacturing, quality, pharmaceutical technical operations and engineering groups.

Reporting to the Manager of Manufacturing Operations, the MES Engineer is responsible for providing technical support to the MES system to ensure that production runs smoothly.

In this role, you will be responsible for all or subset of the key responsibilities below:

• Support MES Lead in providing expertise technical knowledge/advice to manufacturing team on MES system.
• Escalate any ongoing MES system related issues to the MES Lead in a timely manner.
• Ensures timely resolution of identified MES system issues and unplanned events identified in the daily walk-through.
• Perform automation change controls to ensure that changes are raised and closed on time following the required quality standards.
• Prepares and performs Automated Installation Qualification (AIQ)/ Automated Operational Qualification (AOQ), test plans, and Software Development Lifecycle (SDLC) documentation, ensuring documentation meets required regulatory standards.
• Develops and updates MES training packages and conducts MES training
• Support for deviation and operation investigation requiring Master Batch Record (MBR) changes and system-level troubleshooting.
• Supports a continuous improvement framework within MES and IPT, and works with Leads to identify and implement improvements.
• Develops Automation SOPs, Job Aids and procedures.
• Support Digitalization, Capital and Site projects and other activities assigned by MES Lead

Requirements:

• Diploma or bachelor's degree in electronic / chemical or any other relevant engineering field
• At least 1 years of experience in process automation engineering
• At least 1 years of relevant working experience in GMP environment within the pharmaceutical/chemical manufacturing.

Reg No: R22104540
EA License no: 94C3609