Seeking a junior associate to join a leading life sciences and healthcare regulatory team in Brussels. The role focuses on EU regulatory work across medicinal products (including biologics) and medical devices, covering authorisation pathways, clinical trials, manufacturing/import, marketing and promotion, and interactions with European and national regulators.

The team advises on orphan and paediatric rules, pricing, reimbursement and procurement, and supports litigation before EU courts where required. This is an interdisciplinary practice with regular collaboration across competition, white-collar, transactions and IP teams, and the firm provides structured training and mentoring for associates.

1–2 years' post-qualification experience in EU medicinal products and medical devices regulatory regime
Experience in a pharmaceutical company, medical devices manufacturer, or specialised private practice team
Strong legal research, drafting and analytical skills and ability to work independently and in cross-disciplinary teams
Qualified to practise law in the EU and eligible to register as a lawyer in Belgium; work experience at the European Commission (DG SANTE) or European Medicines Agency is advantageous

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