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Title:
Quality Assurance SpecialistCompany:
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 quality and innovation in pharmaceutical development? As a Quality Assurance Specialist at Ipsen’s Wrexham site, you’ll be at the forefront of ensuring the safety and efficacy of cutting-edge biologics. You will have the chance to help shape the future of global healthcare by supporting clinical trials and product development across international teams. You’ll collaborate with experts across Europe and the US, influence key quality decisions, and help bring life-changing treatments to patients worldwide.
Key responsibilities:
- Approve semi-finished products and ensure quality standards for clinical trial materials
- Lead and support investigations into quality events, deviations, and change controls
- Manage quality relationships with CDMOs and ensure compliance with operational standards
- Review and approve documentation for batch release and product certification
- Represent Quality in cross-functional development projects and regulatory inspections
- Drive continuous improvement initiatives and contribute to quality training and awareness
Knowledge, skills & experience:
- Degree in a relevant subject or equivalent experience in a similar role from the pharma industry
- GMP knowledge
- Experience with biologics is preferred
If you're driven by quality, inspired by innovation, and excited to contribute to life-changing therapies, we’d love to hear from you. Join us at Ipsen and be part of a global team that’s shaping the future of healthcare. Apply now and help us deliver excellence to patients worldwide.
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IPSEN is committed to equality of opportunity for all staff and applications, individuals are encouraged to apply regardless of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.