The firm keeps this requirement live for the right practice, rather than to a fixed closing date. We take approaches at any stage in your own timeline.

Senior partner role to lead and expand a life sciences regulatory practice from the firm's Brussels office. The role focuses on advising pharmaceutical, biotech and medical device clients on EU regulatory, product compliance and market access matters.

Candidate will join a cross-border regulatory group and work closely with commercial and litigation teams across Europe. The position offers significant client development scope and the opportunity to build and manage a specialist team.

Portable book of business of €3–4M minimum, ideally €5M+ (EUR)
Extensive life sciences regulatory experience advising pharma/biotech/medical device clients
Proven business development record and ability to originate and grow client relationships in Europe
Experience leading teams and managing cross-border matters in EU regulatory frameworks

Discussions are held in confidence and no detail leaves us without your explicit approval.

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Confidential. We never contact your current employer.