Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

At Grifols, we believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment.

Position Summary:

The MES Manager will be responsible for development, configuration and testing of Master Batch Records (MBRs) from initial to final design. The successful candidate will have at least five years’ experience in a pharmaceutical or biotech industry and will have demonstrated competency in leading teams to deliver complex MBR designs in time with project and commercial timelines.

What You Will Do:

Lead and develop a team of MES Specialists and Junior MES Specialists, providing guidance, support, and technical expertise.
Oversee the design, configuration, testing, and implementation of Master Batch Records (MBRs) from initial concept through to deployment.
Lead MBR design reviews and collaborate with cross-functional stakeholders, including Operations, Process Validation, Quality, IT, and R&D.
Manage the creation, execution, and review of testing activities to ensure MBRs are fully validated and fit for use.
Support the ongoing development and enhancement of the MES platform, driving continuous improvement of MES processes and ways of working.
Deliver training and support to Electronic Batch Record (EBR) users, including Supervisors, Operators, Quality, Technical, and Support teams.
Develop, maintain, and update MES-related procedures and documentation to ensure compliance and consistency.
Coordinate and manage MBR change requests, working closely with key stakeholders to ensure timely implementation and documentation.
Ensure adherence to quality systems and established timelines for deviations, change controls, and CAPAs.
Lead equipment and system integration activities, enabling seamless interaction between MES and manufacturing systems such as ERP, OSI PI, Siemens PCS7, Wonderware, Werum, and other shop-floor technologies.
Troubleshoot and resolve MES-related issues, including system interface errors and inventory discrepancies between ERP and MES platforms.
Partner with the global MES team to identify best practices, enhance system capabilities, and implement improved ways of working.
Provide technical guidance and MES expertise to manufacturing and operational teams as needed.

What You Will Bring:

Bachelor’s degree in Engineering or Science or related industry qualification.
5+ years’ experience in an operation’s pharmaceutical environment.
Experience in PAS-X Software and design.
Knowledge of regulation requirements (GMP & IT/System Integration) is desirable.
Experience with OSi Pi software is desirable.
Experience with AIZON software is desirable.
PAS-X Training Certification is desirable.
Project Management Certification is desirable.

Our Benefits Include:

A highly competitive salary package
Group pension scheme - Contribution rates are (3%/ 5%/ 7%) and company will match
Private medical insurance for the employee
Ongoing career development opportunities within a rapidly growing organisation
Strong focus on succession planning and internal promotion
Dedicated education and professional development allowance
Wellness and social initiatives, including activities such as padel and summer events

We understand that self-doubt can hold talented individuals back from applying for opportunities. We encourage everyone who meets the qualifications to apply – we're excited to hear from you!

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Location:Grange Castle International Business Park, Grange, Co. Dublin, D22 K2R3

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MES Manager

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