Title:
Master Batch Record DesignerCompany:
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:
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 winner of 2025 Pharma Company of the Year, 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!
We are seeking a Master Batch Record Designer to join our Technical Operations team in Wrexham. In this role, you will lead the design and continuous improvement of Master Batch Records (MBRs) within our Manufacturing Execution System (MES), ensuring compliance with cGMP standards and supporting operational excellence across manufacturing processes.
Key responsibilities:
- Design and maintain Master Batch Records (MBRs) within our Manufacturing Execution System (MES).
- Gather requirements and collaborate with manufacturing, QA, and technical experts.
- Update master data, state diagrams, and equipment management instructions.
- Troubleshoot and resolve issues during validation and implementation.
- Support MES enhancements and participate in user training.
- Drive continuous improvement and innovation in manufacturing processes.
Knowledge, skills & experience:
- Experience in a similar role or an avid learner with experience from a manufacturing function and some manufacturing systems knowledge.
- Experience with Rockwell FTPS is ideal.
- Enthusiastic and hands-on style, self-reliant with excellent troubleshooting skills
Why Join Us?
You’ll play a vital role in ensuring patient safety and operational excellence, working in a dynamic environment that values innovation and collaboration.
#LI-Hybrid
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.
