Be at the heart of actionFly remote-controlled drones into enemy territory to gather vital information.

Apply Now

Senior Regulatory Affairs Expert - Eastern Europe, Central Asia & Nordics - 12 month fixed term[...]

Bloomberg L.P.
City of London
5 days ago
Create job alert

Senior Regulatory Affairs Expert - Eastern Europe, Central Asia & Nordics - 12 month fixed term contract

Location

London

Business Area

Marketing and Public Relations

Ref #

10046680

Description & Requirements

This is a unique opportunity for a deeply knowledgeable, well-connected regulatory professional to help drive Bloomberg’s engagement on critical policy and regulatory developments. You’ll play a pivotal role across Eastern Europe, the Balkans, Central Asia, and the Nordics, working at the intersection of policy, finance, and technology.

Partnering with Bloomberg’s senior leadership and product experts, you’ll navigate a fast-changing regulatory environment and help shape upstream policy on issues that matter most, for example, digital finance, private markets, market structure, sustainable finance and risk.

What You’ll Do
  • Anticipate and analyse trends in market structure, risk management, digital policy and other key regulatory developments to keep Bloomberg ahead of the curve.
  • Shape regulatory outcomes by driving Bloomberg’s voice in consultations, public comment letters, and direct engagement with authorities across the countries of focus and beyond.
  • Lead senior-level engagement with central banks, regulators, and Bloomberg’s clients.
  • Advise senior leadership through strategic policy briefings and updates that enable sharp, informed decision-making.
  • Collaborate across the business – Legal, Compliance, Product, Risk, Sales – to deliver consistent, well-informed responses to regulatory initiatives.
  • Strengthen Bloomberg’s convening power by contributing to high-impact events that unite policymakers, regulators, and financial leaders.
What You Bring
  • 5+ years of relevant experience, ideally with a financial technology firm, financial institution, or regulatory authority.
  • Deep expertise in market structure, sustainable finance, and regulation across the target regions, plus a broad understanding of global financial markets regulation.
  • Proven track record of shaping policy making and working directly with regulators and policymakers.
  • Exceptional communication skills, with the ability to distil complex regulatory issues into clear, actionable insights.
  • A collaborative, strategic mindset and ease in navigating fast-paced, high-stakes environments.

Bloomberg is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of age, ancestry, color, gender identity or expression, genetic predisposition or carrier status, marital status, national or ethnic origin, race, religion or belief, sex, sexual orientation, sexual and other reproductive health decisions, parental or caring status, physical or mental disability, pregnancy or parental leave, protected veteran status, status as a victim of domestic violence, or any other classification protected by applicable law.

Bloomberg is a disability inclusive employer. Please let us know if you require any reasonable adjustments to be made for the recruitment process. If you would prefer to discuss this confidentially, please email


#J-18808-Ljbffr

Related Jobs

View all jobs

Senior Regulatory Affairs Manager - Strategic leadership role- Medical Devices- Move to south coast

Senior Regulatory Affairs Associate

Senior Regulatory Affairs Consultant - Labelling (home or office based)

Senior Regulatory Affairs Specialist

Senior Regulatory Affairs Specialist

Senior Regulatory Affairs Specialist

Subscribe to Future Tech Insights for the latest jobs & insights, direct to your inbox.

By subscribing, you agree to our privacy policy and terms of service.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Medical Technology Recruitment Trends 2025 (UK): What Job Seekers Need To Know About Today’s Hiring Process

Summary: UK medical technology hiring has shifted from title‑led CV screens to capability‑driven assessments that emphasise regulatory‑aware product delivery (QMS, ISO 13485), software lifecycle & risk (IEC 62304/14971), usability (IEC 62366), clinical & regulatory strategy (MDR/UKCA), device cyber security & privacy, and measurable patient/clinical and commercial impact. This guide explains what’s changed, what to expect in interviews & how to prepare—especially for SaMD engineers, AI/ML in medical devices, product & quality engineers, regulatory/clinical affairs specialists, validation/verification, manufacturing/operations, and digital health roles. Who this is for: Software/firmware engineers in medtech, SaMD/AI engineers, systems & verification engineers, quality & regulatory affairs (QARA), clinical evaluation/PMCF specialists, human factors engineers, medical device cyber security & privacy, test/validation, manufacturing & operations, field/service engineers, and medtech product managers in the UK.

Why Medical Technology Careers in the UK Are Becoming More Multidisciplinary

Medical technology (medtech) is transforming healthcare in the UK — from wearable sensors to AI diagnostic tools, from surgical robots to telemedicine platforms. Advances in hardware, software, data and connectivity are enabling more personalized, efficient and accessible care. But with great power comes great responsibility. As medical devices and health technologies enter hospitals, clinics and consumers’ homes, professionals in this domain must master much more than engineering and algorithms. They must also understand law, ethics, psychology, linguistics & design. That is, medtech careers are now deeply multidisciplinary. In this article, we explore why medical technology careers in the UK are becoming more multidisciplinary, how these five allied fields now intersect with medtech work, and what job-seekers and employers should do to succeed in this evolving ecosystem.

Medical Technology Team Structures Explained: Who Does What in a Modern MedTech Department

Medical technology (MedTech) spans everything from wearable health devices and surgical robots to diagnostic imaging, in-vitro diagnostics (IVD), digital therapeutics, AI-driven triage, and Class I–III medical devices. In the UK, the sector touches NHS care pathways, private providers, and global markets—with stringent expectations for safety, clinical evidence, cybersecurity, and data privacy. As ventures scale from prototype to regulated product, clear team structures become the difference between promising pilots and licensed, market-ready devices. Whether you’re hiring your first clinical specialist or applying for a role in QA/RA, this guide explains who does what in a modern MedTech department, how functions collaborate across the product lifecycle, UK-typical skill sets and salaries, common pitfalls, and best practices for building a resilient team.