Title: Qualified Person 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: 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! Are you passionate about ensuring medicines are safe and meet the highest standards? Join us as a Qualified Person and play a critical role in protecting patients by guaranteeing product quality and compliance. This is your chance to lead with purpose and make a real impact in the pharmaceutical industry. Key Responsibilities: Certify and release finished product batches in line with UK/EU regulations. Ensure compliance with Good Manufacturing Practice (GMP) throughout production. Lead quality initiatives and continuous improvement projects across the site. Provide expert advice on regulatory submissions, audits, and inspections. Act as a mentor and guide for quality matters within the team. Escalate and resolve issues that could impact product quality or timelines. Knowledge, Skills & Experience: Experience in a similar position from a sterile pharmaceutical manufacturing operation Eligible to act as a QP in the pharma industry Solution orientated. Able to propose innovative solutions and deal with ambiguity Strong communicator across all levels Why Join Us? You’ll be part of a collaborative team committed to excellence, innovation, and patient safety. We offer a supportive environment where your expertise truly matters. Apply now and help us deliver medicines that make a difference! 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.