Job Description
As a MES Engineer, you will be working on-site with a key client to support the use of the Manufacturing Execution System (MES) in the production environment. Your primary responsibility will be to ensure the site delivers safe and effective products while maintaining compliance.
This includes collaborating with the operations team to provide subject matter expertise on the MES system, ensuring output targets are met in line with the production plan. You will also work closely with Operations, Supply Chain, Engineering, IT, and Quality functions to deliver efficient and effective MES site support during operational hours.
Your role will involve coaching and mentoring the operations team on the use of the MES system, upskilling operations staff on troubleshooting basics, and leading MES activities in the support of validation of new processes.
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Required Skills and Qualifications
* A strong understanding of cGMP requirements, including 21 CFR 11 and Annex 11.
* Excellent knowledge of GAMP principles, systems implementation, and validation concepts.
* Demonstrated analytical and problem-solving capabilities.
* Strong technical writing skills.
* A degree in Computer Science/IT/Pharmaceutical Manufacturing or a related field.
* At least 3 years of experience working with pharma/life sciences manufacturing software systems.
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About Us
We are a publically listed company specializing in IT solutions for life sciences internationally. Our focus is on high-complexity industries where regulatory demands and complexity are high. We advise on and build sustainable digital solutions that benefit patients, citizens, employees, end-users, and customers.
We celebrate diversity and strive to create an inclusive environment for all employees. All candidates are encouraged to apply regardless of their background, age, or personal characteristics.
In our pursuit of fairness and unbiased recruitment, we kindly request candidates to refrain from including pictures in their applications.