We are looking for an R&D Quality Intelligence Lead who is insight‑driven, influential, and rigorous to join our team in Global Quality (QMS & Quality Intelligence), based at our UCB campus located in Braine‑l’Alleud, Belgium
About The Role
You will lead the end‑to‑end Quality Intelligence strategy across R&D (GCP/GLP/GCLP). You’re going to design, implement, and continuously improve how we sense, interpret, and act on regulatory and inspection signals—while building sustainable, organization‑wide knowledge. You will also drive external advocacy to help shape future regulations and ensure UCB stays inspection‑ready and future‑proof.
Who You Will Work With
You will partner closely with the Head of QMS & Quality Intelligence and collaborate with Global Quality, Patient Evidence (Clinical Operations, Global Regulatory Affairs, Patient Safety), and Patient Solutions (including Labs Operations). You’re going to build strong connections with industry bodies (e.g., EFPIA, IFPMA, BioPhorum, Avoca, Impala) to align UCB’s position and amplify our voice.
What You Will Do
You will lead the Regulatory & Inspection Intelligence process across R&D and embed proactive compliance behaviors.
You will be responsible for monitoring global sources, triaging signals, and activating owners to mitigate risks and seize opportunities.
You will manage impact assessments, action plans, and end‑to‑end tracking until timely, auditable closure.
You will align with QMS teams so critical signals translate into plans, controls, and continuous‑improvement priorities.
You will prepare the organization for inspections and support responses to Quality Intelligence‑related queries.
You will shape tool roadmaps, define metrics, and drive adoption, performance, and engagement across the process.
Interested?
For this role, we are looking for the following education, experience, and skills
Master’s degree in a relevant scientific or health discipline.
Deep, current experience in Regulatory and/or Inspection Intelligence for GLP, GCP, and GCLP in biopharma.
Proven advocacy experience and external engagement to influence policy across geographies.
Exceptional communication and presentation skills; you will brief and influence senior leadership.
Strong analytics and problem‑solving; you will turn complex, global signals into clear decisions.
Self‑directed and collaborative; you’re going to mobilize a matrixed, global network to deliver outcomes.
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About Us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.
Why work with us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.
At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.
UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
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