EU Labeling, Advertising & Promotion Scientist

UCB S.A.

Anderlecht

Hybrid

EUR 70,000 - 100,000

Full time

14 days+

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Benefits offered by this job

Hybrid work model

Job summary

UCB S.A. seeks a Labelling, Advertising and Promotion Scientist to provide EU regulatory expertise for product information and promotional review, ensuring accurate EU labeling across SmPC, Label, PIL, and IFU.

You will translate data into compliant text supporting patient safety and regulatory expectations in a hybrid Brussels office. You will collaborate with EU and Global Regulatory colleagues, Medical, Legal, Commercial, Safety, and Quality teams to align labeling and translations, while

Qualifications

  • Degree in life sciences, pharmacy, healthcare, or a related field.
  • Around 3–5 years of regulatory affairs experience.
  • Clear written and verbal communication skills.
  • Strong collaboration and stakeholder engagement.
  • Ability to manage multiple priorities.
  • High standards of integrity and quality focus.

Responsibilities

  • You will create and maintain EU Product Information aligned with CCDS, RTQs, templates, and SOPs in ECMS.
  • You will be the EU point of contact and represent EU labeling in cross-functional forums.
  • You will coordinate reviews and approvals, tracking changes and timelines.
  • You will manage readability testing end to end.
  • You will coordinate linguistic review, closing sequence, and artwork changes.
  • You will review promotional materials for compliance with EU labeling and regulations.

Skills

Regulatory affairs
Communication skills
Cross-functional collaboration
Prioritization
Attention to detail

Education

Degree in life sciences, pharmacy, healthcare, or a related field

Job description

UCB S.A. seeks a Labelling, Advertising and Promotion Scientist to provide EU regulatory expertise for product information and promotional review, ensuring accurate EU labeling across SmPC, Label, PIL, and IFU.

You will translate data into compliant text supporting patient safety and regulatory expectations in a hybrid Brussels office. You will collaborate with EU and Global Regulatory colleagues, Medical, Legal, Commercial, Safety, and Quality teams to align labeling and translations, while

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