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UCB S.A.Brussel, Brussel-Hoofdstad, BelgiumMake your mark for patients
To strengthen our Market Quality Europe department, we are looking for a talented profile to fill the position of : Quality Partner Benelux – Brussels, Belgium
About the role
As a Quality Partner Benelux, you will collaborate with the responsible Quality Lead to ensure that global quality practices are integrated within the Benelux area, thereby meeting compliance obligations in line with UCB and local regulations. This role involves maintaining the GDP status of the Belgian and the Dutch affiliates in accordance with both current national and EU GDP and legal requirements, managing the local Quality Management System, and identifying and mitigating issues and risks. Additionally, it highlights improvement opportunities and facilitates the development of solutions. Ensuring all Market Quality deliverables are achieved in a timely manner is a key responsibility. The role involves acting as the delegate of Responsible Person (RP) for UCB Pharma S.A. in the Belgian affiliate, following GDP regulations, local laws, and UCB procedures. There is also an option to be nominated as the RP (and / or QP) for UCB Pharma B.V. in the Netherlands under the same guidelines (+GMP to a limited scope).
You will work with
In this role, you will collaborate closely with the responsible Quality Lead and the local quality team to integrate global quality practices within the Benelux area. You will work together to maintain the GDP status of the affiliates, manage the local Quality Management System, and address issues and risks. The daily interactions are with both internal stakeholders e.g. in market supply, safety, medical, business and UCB global quality, as well as external customers and vendors.
What you will do
- Maintain an effective and compliant local Quality Management System (QMS), which is part of the UCB global QMS
- Ensure the execution of the local QMS : e.g. management of complaints, deviations, change controls and CAPAs according to UCB SOPs, in a timely manner, by using the relevant UCB electronic systems. As well as :
- Ensure quality oversight to local GxP vendors
Support establishment of self-inspection / internal and external audit plans, host GDP / GMP audits in the affiliates
Interested? For this position, you’ll need the following education, experience and skills
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.
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