We are looking for a Patient Supply Compliance Integration Lead who is collaborative, autonomous and results-driven to join our Patient Supply Strategy & Risk Management team, based at our UCB campus in Braine, Belgium.
About The Role
As the Patient Supply Compliance Integration Lead, you will maximize visibility and anticipation over holistic compliance domains which impact Patient Supply Strategy and Risk & Opportunity profile, by leveraging Regulatory Intelligence Network (RIN) structures and Functional compliance experts. It includes to orchestrate Patient Supply compliance readiness through timely and calibrated solutions.
Who You’ll Work With
You will collaborate with a multidisciplinary team including regulatory and quality assurance experts, sustainability leaders, and supply chain executives. You will also regularly engage with external stakeholders to calibrate and refine our compliance practices based on external dynamics.
What You’ll Do
- You will act as a counterpart for Global QA, Legal, Sustainability teams in defining, maintaining, and continuously improving the corresponding Regulatory Intelligence Network (RIN) processes
- You will conduct an in-depth analysis of the regulatory landscape and identify current pain points within Patient Supply.
- You will lead a comprehensive readiness assessment and develop a compliance framework aligned with our strategic priorities
- You will play a key role in designing and implementing a sustainable and proactive compliance model to ensure our organization is organized to emerging regulatory requirements and keep compliant
- You will lead the centralized orchestration of compliance assessments and recommendations through timely and calibrated solutions
- You will design training and awareness programs to promote compliance
Interested? For this role we’re looking for the following education, experience and skills
- Master’s degree in technical/legal sciences with strong expertise in pharmaceutical regulation and quality.
- Extensive experience in a compliance leadership role, with a focus on model development.
- Strong understanding of regulatory requirements in the pharmaceutical industry.
- Proven skills in risk management and continuous improvement.
- Ability to influence and convince executives to take action
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 around 8,500 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 equitable 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.
As an Equal Opportunity Employer, we are open to all talent, and adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to neurodiversity, race/ethnicity, colour, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
