We are looking for an MES Engineer to support and maintain Manufacturing Execution Systems (MES) for a leading medical device manufacturing environment. This role is ideal for someone with experience in manufacturing automation, system support, and continuous improvement initiatives who enjoys working in a highly regulated environment.
Key Responsibilities
- Provide first-level support for Manufacturing Execution Systems (MES) across lens manufacturing and chemical production.
- Perform system enhancements, change requests, troubleshooting, and bug fixes.
- Monitor system and server health through routine maintenance and preventive checks.
- Support MES-related projects, including:
- User Requirement Specifications (URS)
- Installation & Operational Qualification (IOQ)
- SOP development and review
- Computer System Validation (CSV)
- Ensure compliance with GMP, GDP, HSE, and corporate quality standards.
- Support smart manufacturing and data-driven digitalisation initiatives.
- Maintain high system availability, reliability, and validated system status.
Requirements
- Diploma or Bachelor's Degree in IT, Computer Science, Engineering, or a related discipline.
- 2–5 years of experience within manufacturing or engineering environments.
- Experience in medical device or pharmaceutical manufacturing is highly preferred.
- Hands-on experience with Manufacturing Execution Systems (MES) and SCADA.
- Knowledge of automation technologies including PLC, SCADA, and MES.
- Experience with databases such as Microsoft SQL, Oracle, or Microsoft Access.
- Programming knowledge in one or more of the following:
- C#
- ASP.NET
- Python
- Visual Basic
- Familiarity with IT infrastructure and networking.
- Experience with Computer System Validation (CSV); exposure to Kneat is an advantage.
- Knowledge of 21 CFR Part 11 is preferred.
- Strong analytical and technical problem-solving skills.
- Good communication and stakeholder management skills.
What You'll Be Working On
- Manufacturing Execution Systems (MES)
- Manufacturing Automation
- Digital Manufacturing
- Smart Factory Initiatives
- System Validation & Compliance
- Continuous Improvement Projects
Success in this Role
You will be successful if you can:
- Maintain high MES system uptime and reliability.
- Deliver projects within agreed timelines and budgets.
- Ensure compliance with GMP, GxP, HSE, and company standards.
- Contribute to digital transformation and smart manufacturing initiatives.
Interested? We'd love to hear from you! Apply now or reach out directly to learn more about this opportunity.