Deputy Qppv

**Make your mark for patients**

We are looking for a **Deputy QPPV** to join us in our **Patient Safety** team, based in either of our Braine or Brussels, Belgium offices

**About the role**

The Deputy EEA/UK QPPV is - in support of the QPPV - responsible for the establishment and maintenance of UCB’s pharmacovigilance system in accordance with the legal framework for pharmacovigilance of medicinal products for human use in the EU

**Who you’ll work with**

You will report into the Head of Pharmacovigilance & QPPV office, who is the UCB global and EEA/UK QPPV

**What you’ll do**
- Together with the QPPV and other Deputy QPP, act as a Pharmacovigilance contact point for the EEA/UK competent authorities and the EU Agency on a 24-hour basis and as a contact point for Pharmacovigilance inspections.
- In relation to the Pharmacovigilance system, together with the QPPV, is responsible for the establishment and maintenance of the UCB Pharmacovigilance system in accordance with the legal framework for pharmacovigilance of medicinal products for human use in the EEA and in the UK.
- This implies that the (Deputy) QPPV has the authority to influence the performance of the company Pharmacovigilance system and its related quality system to promote, maintain and improve compliance with the legal requirements
- Member of the pharmacovigilance Quality Council to regularly receive outcomes on quality trends, performance and compliance of the pharmacovigilance system and to provide strategic direction on quality performance and improvement area
- Is informed of all Pharmacovigilance audit findings identified by PVQA and their associated CAPAs
- Has access to the UCB PSMF and is in a position of authority to ensure and verify that the information contained in the PSMF is accurate and up to date

I**nterested? For this position you’ll need the following education, experience and skills**:

- Bachelor’s degree required, Medical Degree is strongly preferred
- Several years experience within the Pharma Industry (medical or clinical development) with the majority of the experience in pharmacovigilance.
- Adequate theoretical and practical knowledge for the performance of pharmacovigilance activities.
- Expertise or access to expertise in relevant areas such as medicine, pharmaceutical sciences, as well as epidemiology and biostatistics.
- In-depth knowledge of EEA/UK pharmacovigilance regulations and pharmacovigilance methods with influential skills

If you are interested to learn more about R&D within UCB, please find more information here R&D at UCB.

RANDATUCB

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.