At a Glance
- Tasks: Provide strategic legal advice on regulatory matters for groundbreaking medical technologies.
- Company: Join Illumina, a leader in genomic technology and health equity.
- Benefits: Enjoy flexible time off, private medical insurance, and stock purchasing options.
- Other info: Dynamic, inclusive workplace with opportunities for career growth and development.
- Why this job: Make a real impact on global health while working with innovative teams.
- Qualifications: Qualified lawyer with experience in medical device regulations and strong communication skills.
The predicted salary is between 80000 - 100000 £ per year.
At Illumina, we are expanding access to genomic technology to realise health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.
Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world-changing projects, you will do more and become more than you ever thought possible.
The Role
As Associate Director, Regulatory Legal Counsel (EMEA & Latin America) here at Illumina in Cambridge, UK, you will be a key member of Illumina’s global Regulatory Legal team, providing strategic and pragmatic legal advice across the full lifecycle of Illumina’s technologies and medical technology products, including both research use only (RUO) and clinical offerings. In this highly visible role, you will partner closely with Regulatory Affairs, Quality, Medical Affairs, Global Compliance, Commercial, Marketing, and other cross‐functional stakeholders to enable compliant product development, commercialization, and post‐market activities across Europe, the Middle East, Africa, and Latin America. You will play a critical role in translating complex, multi‐jurisdictional regulatory frameworks into clear, business‐focused legal guidance in a fast‐paced, matrixed, international environment.
Illumina's employee benefits are industry-leading and include flexible time off, private medical insurance, compassion and care time off, leisure travel insurance, pension, employee stock purchasing program, volunteer time off, and much more!
Why You
You are a seasoned regulatory lawyer with deep expertise in medical device, diagnostics, or life sciences regulation, and you thrive in complex, international environments. You bring strong judgment and the ability to balance regulatory risk with commercial and innovation‐driven objectives. You are comfortable advising on evolving regulatory landscapes, including EU and UK medical device and IVD frameworks, and enjoy working cross‐functionally with regulatory, quality, medical, and commercial teams. Your communication style is clear, confident, and practical, allowing you to engage effectively with senior leaders, regulators, and technical experts alike. You are adaptable, proactive, and motivated by supporting cutting‐edge science and technology that improves human health.
Key Responsibilities
- Regulatory Legal Advisory & Strategy
- Provide legal guidance on regulatory requirements across EMEA and Latin America applicable to medical devices, diagnostics, and life science products
- Interpret and advise on EU and UK medical device and IVD regulatory frameworks, country‐specific requirements, and horizontal regulations impacting the sector
- Assess regulatory risk across diverse jurisdictions and support informed business decision‐making
- Product Lifecycle & Market Support
- Partner with Regulatory Affairs and Quality to support product development, regional and global submissions, market access strategies, and post‐market obligations
- Advise on regulatory considerations for hardware, software, services, digital solutions, and emerging technologies, including AI‐related regulatory requirements
- Support global and regional product lifecycle management activities
- Commercial, Marketing & Contractual Support
- Review and advise on product labeling, promotional and marketing materials, and external communications to ensure regulatory compliance
- Collaborate with Commercial Legal, Compliance, Procurement, IT, and other stakeholders to assess regulatory considerations in contracts, tenders, licensing, distribution, R&D, and procurement activities
- Post‐Market, Inspections & Regulatory Interactions
- Support inspection readiness, regulatory audits, and post‐market vigilance activities
- Advise on recalls, field actions, and other post‐market corrective activities
- Prepare responses to inquiries, inspections, and communications from regional and country‐specific regulatory authorities
- Regulatory Intelligence, Training & Governance
- Monitor and analyze evolving regulatory developments and trends across EMEA and Latin America
- Assist with the development and maintenance of internal policies, SOPs, training materials, and regulatory process improvements
- Deliver regulatory legal training and updates to business and functional teams
- Coordinate and manage engagement with external counsel in foreign jurisdictions, as required
Experience and Education
- Qualified lawyer in the UK, the United States, or an EU Member State
- Significant experience in a regulatory advisory role within the medical device, med tech, biotechnology, or life sciences sector
- Prior in‐house and/or law firm experience advising regulatory clients preferred
- Full professional fluency in English; additional languages are a plus
- Demonstrated experience supporting business clients in a regulated, international environment
Preferred Credentials
- Experience advising on EU and UK medical device and diagnostics regulatory frameworks, including IVDR
- Familiarity with post‐market vigilance, inspections, and regulatory authority interactions
- Experience supporting global or regional product development and lifecycle management
- Experience working closely with commercial teams on regulated products
Additional Information
- Ability to work across time zones in a global organization
- Location in the London / Cambridge area preferred
- Limited regional and international travel may be required
We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information.
Associate Director, Regulatory Legal Counsel in Cambridge employer: Illumina
At Illumina, we are committed to fostering a dynamic and inclusive work environment where every employee can thrive. As an Associate Director, Regulatory Legal Counsel in Cambridge, you will enjoy industry-leading benefits, including flexible time off and comprehensive health coverage, while collaborating with passionate professionals on groundbreaking projects that advance human health. Our culture prioritises personal growth and innovation, ensuring that you not only contribute to meaningful work but also develop your career in a supportive and empowering atmosphere.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director, Regulatory Legal Counsel in Cambridge
✨Tip Number 1
Network like a pro! Reach out to people in your field, especially those at Illumina. A friendly chat can open doors that a CV just can't.
✨Tip Number 2
Prepare for interviews by understanding Illumina's mission and values. Show how your experience aligns with their goal of transforming human health—this will make you stand out!
✨Tip Number 3
Practice your pitch! Be ready to explain your regulatory expertise and how it can benefit Illumina. Confidence is key, so rehearse until it feels natural.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you're genuinely interested in being part of the Illumina team.
We think you need these skills to ace Associate Director, Regulatory Legal Counsel in Cambridge
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the Associate Director role. Highlight your experience in regulatory law, especially in medical devices and diagnostics, to show us you’re the perfect fit!
Showcase Your Expertise:We want to see your deep understanding of EU and UK regulatory frameworks. Use specific examples from your past roles to demonstrate how you've navigated complex regulations and provided strategic legal advice.
Be Clear and Concise:When writing your application, keep it straightforward. We appreciate clarity, so avoid jargon and get straight to the point about your skills and experiences that align with our needs.
Apply Through Our Website:Don’t forget to submit your application through our official website! It’s the best way for us to receive your details and ensures you’re considered for this exciting opportunity.
How to prepare for a job interview at Illumina
✨Know Your Regulatory Stuff
Make sure you brush up on the EU and UK medical device and IVD regulatory frameworks. Be ready to discuss how these regulations impact product development and market access strategies, as this role requires a solid understanding of complex regulatory landscapes.
✨Show Your Cross-Functional Skills
This position involves working closely with various teams like Regulatory Affairs, Quality, and Commercial. Prepare examples of how you've successfully collaborated across departments in the past, highlighting your ability to translate legal jargon into clear, actionable advice for non-legal stakeholders.
✨Be Ready for Real-World Scenarios
Expect situational questions that test your judgement and problem-solving skills. Think about past experiences where you had to balance regulatory risks with business objectives, and be prepared to explain your thought process and the outcomes.
✨Communicate Clearly and Confidently
Your communication style is crucial in this role. Practice articulating complex legal concepts in a straightforward manner. Consider doing mock interviews to refine your delivery, ensuring you can engage effectively with senior leaders and technical experts alike.
