Title: Manufacturing Execution Systems Designer Company: Ipsen Biopharm Ltd About Ipsen: Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation. Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society! For more information, visit us at https://www.ipsen.com/ and follow our latest news on LinkedIn and Instagram. Job Description: Location: Wrexham, UK Function: Supply Chain, Technical Operations Join Our Award‑Winning Team at Ipsen Wrexham At Ipsen, we are committed to improving the lives of patients, with a special focus on advancing neuroscience therapies. Our Wrexham site is a vital part of this mission, delivering cutting‑edge solutions in a dynamic and collaborative environment. We are proud to be Great Place to Work certified and a Shingo Bronze Medallion holder, reflecting our commitment to excellence, innovation, and continuous improvement. With a recent £24 million investment in the site and a further £86.4 million expansion underway, there has never been a more exciting time to join us. If you are passionate about making an impact and want to be part of a team that values growth, innovation, and excellence, then Ipsen could be where you thrive. Role summary In this role you will: Lead the design, configuration and deployment of Manufacturing Execution System (MES) solutions, supporting recipe testing, validation, and continuous improvement Act as a site champion for MES and automation, working closely with Manufacturing, Quality Assurance, CSV, MS&T, IT/OT and Manufacturing 4.0 teams Take ownership of Master Batch Records (MBR), MES solutions, and master data processes, ensuring they remain accurate, compliant, and optimised Key responsibilities Lead requirements gathering and design for MBR and MES enhancements Design, create, maintain, and improve Master Batch Records within the MES environment Develop and update User Requirement Specifications (URS) and Functional Design Specifications (FDS) Manage master data, state diagrams, and equipment integration within MES Support validation activities, including Operational Qualification and issue resolution Troubleshoot MES and MBR defects during validation and operational use Coordinate MES project scoping and enhancements, including PharmaSuite solutions Design and deliver end‑user training in collaboration with cross‑functional subject‑matter experts About you Essential experience and qualifications: Scientific, Quality, or Engineering background Proven experience working with Manufacturing Execution Systems in a pharmaceutical, GMP‑regulated environment Strong automation expertise and experience integrating MES with ERP systems and manufacturing equipment Solid understanding of cGMP manufacturing operations Strong knowledge of Rockwell FTPS A‑Level or HND in a relevant discipline Fluent written and spoken English Desirable experience: Significant experience with pharmaceutical MES and automation Integration experience with ERP, manufacturing equipment and LIMS Broader Rockwell FTPS exposure Experience supporting change management initiatives Bachelor’s or Master’s degree in Data Science, Engineering, Information Systems, or Life Sciences Additional European language capability Ways of working This role is based at our Wrexham site with hybrid working available in line with Ipsen policy. Travel requirements are minimal (up to 20%). You will collaborate across all Ipsen manufacturing sites and work with stakeholders at all levels of the organisation. Why Ipsen At Ipsen, you will be empowered to take accountability, manage complexity, and deliver high‑quality outcomes in a regulated manufacturing environment. You will be part of a team that values execution excellence, continuous improvement, and collaboration — all driven by a shared commitment to patient impact. LI‑Hybrid LI‑Onsite We are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace “The Real Us”. The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve. This means we also want to help you perform at your best when applying for a role with us. If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application.