* 12 month contract +
* Immediate interview and start
* New project
We are seeking a detail-oriented MES Quality Engineer to support the implementation, validation, and optimization of Manufacturing Execution Systems (MES) in a highly regulated medical device manufacturing environment. This role plays a key part in ensuring digital manufacturing processes meet quality standards, regulatory requirements, and operational excellence goals.
Key Responsibilities
* Model and configure MES workflows to align with validated manufacturing processes and quality standards.
* Support validation activities for new and modified MES functionalities.
* Ensure MES data integrity and traceability across integrated systems
* Troubleshoot MES-related issues on production lines, ensuring compliance and minimal downtime.
* Collaborate with Quality, Manufacturing, and IT teams to implement compliant process changes.
* Drive continuous improvement initiatives focused on system reliability, audit readiness, and operational excellence.
Ideal Candidate Profile
* Strong understanding of MES platforms (e.g., Critical Manufacturing MES, or other ERP)
* Experience in process validation and quality documentation.
* Proven ability to troubleshoot and optimize MES in regulated environments.
* Excellent communication and cross-functional collaboration skills.
* Passion for quality, compliance, and continuous improvement.