jobsPosted 5 days ago
Associate Director, Regulatory Legal Counsel (EMEA & Latin America)
I
Illumina
📅Primary
last date
Open Access
📍
Location/Place/Mode
Cambridge, England, United Kingdom (Hybrid)
🔖
Eligibility
Qualified lawyer in the UK, US, or EU with significant regulatory advisory experience in medical devices, med tech, biotech, or life sciences.

Opportunity
Title: Associate Director, Regulatory Legal Counsel (EMEA & Latin America)
Category: Jobs
Organiser: Illumina
Location: Cambridge, England, United Kingdom (Hybrid)
Eligibility: Qualified lawyer in the UK, US, or EU with significant regulatory advisory experience in medical devices, med tech, biotech, or life sciences.
Deadline: Not specified
Fees: None
Description: Illumina is seeking an Associate Director, Regulatory Legal Counsel for EMEA & Latin America. This hybrid role based in Cambridge, UK, involves providing strategic and pragmatic legal advice across the full lifecycle of Illumina's technologies and medical technology products, including research use only (RUO) and clinical offerings. The counsel will partner closely with Regulatory Affairs, Quality, Medical Affairs, Global Compliance, and Commercial teams to translate complex, multi-jurisdictional regulatory frameworks into business-focused legal guidance.
Key Responsibilities:
Contact Email: accommodations@illumina.com (for accommodation requests)
Category: Jobs
Organiser: Illumina
Location: Cambridge, England, United Kingdom (Hybrid)
Eligibility: Qualified lawyer in the UK, US, or EU with significant regulatory advisory experience in medical devices, med tech, biotech, or life sciences.
Deadline: Not specified
Fees: None
Description: Illumina is seeking an Associate Director, Regulatory Legal Counsel for EMEA & Latin America. This hybrid role based in Cambridge, UK, involves providing strategic and pragmatic legal advice across the full lifecycle of Illumina's technologies and medical technology products, including research use only (RUO) and clinical offerings. The counsel will partner closely with Regulatory Affairs, Quality, Medical Affairs, Global Compliance, and Commercial teams to translate complex, multi-jurisdictional regulatory frameworks into business-focused legal guidance.
Key Responsibilities:
- Provide legal guidance on regulatory requirements for medical devices, diagnostics, and life science products across EMEA and Latin America.
- Interpret EU and UK medical device and IVD regulatory frameworks (including IVDR).
- Support product development, regional/global submissions, market access, and post-market obligations.
- Review product labeling, promotional materials, and external communications for compliance.
- Support inspection readiness, regulatory audits, and post-market vigilance.
Contact Email: accommodations@illumina.com (for accommodation requests)