Senior Regulatory Counsel – Med Devices & Life Sciences

Illumina

Lucca

In loco

EUR 130.000 - 180.000

Tempo pieno

2 giorni fa
Candidati tra i primi
Generatore di candidature

Ottieni una risposta da questo datore di lavoro — un curriculum e una lettera di presentazione perfettamente in linea con ciò che sta cercando.

Supera i filtri ATS

Vantaggi offerti da questo lavoro

Bonus/variable compensation
Equity eligibility
Flexible time off
Private medical insurance (UK)
Pension contribution (UK, 10%)
Life moments support

Descrizione del lavoro

Illumina seeks a senior Regulatory Legal Counsel in Lucca, Tuscany, to guide the lifecycle of medical devices, diagnostics, and life-science products across EMEA and LATAM. You will translate complex rules into actionable guidance for executives and product teams, balancing compliance with innovation.

You will collaborate with Regulatory Affairs, Quality, Commercial Legal, Compliance and IT to ensure submissions, market access, and post-market obligations are met in a fast-paced global setting.

Competenze

  • Legal qualification to practice in the UK, US or EU.
  • Experience advising on regulatory frameworks for medical devices and diagnostics.
  • Strong understanding of EU/UK IVDR and related post-market obligations.

Mansioni

  • Provide regulatory legal advisory across EMEA and Latin America.
  • Interpret EU and UK medical device and IVD frameworks for product teams.
  • Assess regulatory risk and support strategic business decisions.
  • Coordinate with external counsel and cross-functional stakeholders.

Conoscenze

Regulatory expertise
Regulatory strategy
Cross-functional collaboration
EU/UK IVDR
Communication
Regulatory intelligence

Formazione

Law degree
Bar admission (UK/US/EU)

Descrizione del lavoro

Illumina seeks a senior Regulatory Legal Counsel in Lucca, Tuscany, to guide the lifecycle of medical devices, diagnostics, and life-science products across EMEA and LATAM. You will translate complex rules into actionable guidance for executives and product teams, balancing compliance with innovation.

You will collaborate with Regulatory Affairs, Quality, Commercial Legal, Compliance and IT to ensure submissions, market access, and post-market obligations are met in a fast-paced global setting.

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