CrawlJobs Logo

EU Affairs Advisor

Belgium, Brussels Employment contract · Job Posted May 14, 2026
Apply Position
Job Link Share

Job Description

The EU Affairs Advisor supports Vodafone's Brussels-based engagement by tracking and interpreting EU policy developments, preparing clear internal briefings and advocacy materials, and helping manage relationships with EU institutions, Member State representations and industry partners. The role works closely with Group and market teams to align positions and ensure Vodafone's priorities are reflected in EU initiatives impacting digital infrastructure and services. Advise and support Vodafone's EU public policy and regulatory engagement, shaping EU legislation and stakeholder relationships to advance Vodafone's strategic priorities.

Job Responsibility

  • Monitor and analyse EU legislative and regulatory developments affecting Vodafone (e.g., connectivity, digital markets, cybersecurity, data, sustainability), translating implications into clear internal advice
  • Support engagement with EU institutions and stakeholders (European Commission, European Parliament, Council, Permanent Representations, regulators, industry associations), including briefings, meeting preparation and follow-up
  • Contribute to the development of Vodafone policy positions, consultation responses and advocacy materials, ensuring consistency with Group strategy and evidence-based messaging
  • Coordinate across Group functions and operating companies to gather inputs, align priorities and maintain a single narrative for EU engagement and external communications
  • Maintain stakeholder and policy intelligence (contact mapping, trackers, briefings, Q&A and data banks) and help deliver events, roundtables and coalition activity in Brussels and key EU capitals

Requirements

  • Strong understanding of EU policy-making processes and institutions, with experience tracking files and engaging stakeholders
  • Ability to turn complex policy developments into concise, actionable advice for senior and non-specialist audiences
  • Drafting skills: briefings, speaking notes, position papers and consultation responses, with attention to evidence and narrative
  • Stakeholder management and coalition-building skills across trade associations, NGOs, think tanks and peer companies
  • Knowledge of telecoms and digital policy issues (connectivity investment, spectrum, competition, cybersecurity, digital platforms and AI) is an advantage
  • Bachelor's degree (or equivalent) in European studies, political science, law, economics, international relations or similar
  • Experience in EU public affairs/public policy (e.g., industry, consultancy, trade association, EU institution), typically 3+ years

Nice to have

Knowledge of telecoms and digital policy issues (connectivity investment, spectrum, competition, cybersecurity, digital platforms and AI)

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Similar Jobs for

EU Affairs Advisor

8 matching positions

Director, EU Public Affairs

Shopify is seeking a senior leader to direct our EU Government Affairs work. Dec...
Location
Location
Belgium , Brussels
Salary
Salary:
Not provided
shopify.com Logo
Shopify
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 15+ years of experience in government affairs, public policy, or regulatory advocacy, with deep expertise in tech policy, digital services, payments, ecommerce, or other highly regulated adjacent sectors
  • Deep understanding of EU institutions and the legislative process, with an established network across the European Commission, European Parliament, Council, and key member state capitals
  • Demonstrated track record of end-to-end ownership and delivery on high-impact EU policy and advocacy outcomes
  • Strong data literacy and ability to use research, analytics, and merchant stories to strengthen advocacy
  • Exceptional written and verbal communication skills in English
  • Working proficiency in additional EU languages is an asset
  • Track record of building durable relationships and coalitions across government, industry, and civil society to move policy outcomes
  • Experience managing trade associations and external advisors
  • Reflexive AI use: you're comfortable leveraging AI tools for drafting, research, and analysis but also know when human judgment, nuance, and stakeholder expertise are essential
Job Responsibility
Job Responsibility
  • Develop, lead, and execute Shopify's EU government affairs and public policy strategy, ensuring our priorities are at the center of EU legislative and political debates
  • Be Shopify's lead voice in Brussels with the European Commission, European Parliament, Council, regulators, trade associations, and industry peers
  • Oversee Shopify's EU trade association memberships and external advisors, keeping advocacy efforts aligned and focused
  • Lead engagement on priority policy areas affecting Shopify and our merchants, including platform regulation, artificial intelligence, payments and fintech, privacy and data protection, consumer protection, digital trade, and emerging digital policy issues
  • Coordinate engagement across priority EU member states, translating EU-level advocacy into relevant national government outreach, coalition building, and consultation responses where appropriate
  • Develop and deliver data-driven policy narratives that translate merchant experience, market realities, and Shopify's strategic priorities into messaging that lands with EU institutions, member-state policymakers, and the press
  • Create opportunities for policymakers to engage directly with Shopify's merchant ecosystem, bringing real-world business experience into policy discussions
  • Anticipate regulatory trends, political risks, and policy opportunities
  • translate them into strategic recommendations that shape product, business, and reputation strategy
  • Brief and advise Shopify's executive team on EU political and regulatory developments
  • Fulltime
Read More
Arrow Right

Qa/ra Manager

Regulatory & Quality Manager (Medical Devices). About the company: We are a rapi...
Location
Location
United Kingdom , London
Salary
Salary:
Not provided
srgtalent.com Logo
SRG
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Degree in a scientific, engineering, or regulatory discipline (or equivalent experience)
  • 7+ years' experience in regulatory and/or quality roles within the medical device industry, ideally including Class I devices
  • Demonstrated experience implementing or improving QMS frameworks to ISO 13485 and/or 21 CFR 820
  • Experience managing teams including coaching and developing remote or hybrid team members
  • Solid knowledge of risk management (ISO 14971), post-market surveillance, and audit management
  • Excellent written and verbal communication skills
Job Responsibility
Job Responsibility
  • Embed QMS to achieve and sustain compliance with ISO 13485 and 21 CFR Part 820
  • Lead the implementation and continuous improvement of a digital EQMS solution
  • Oversee document control, CAPA, supplier management, change control, complaints, and risk management processes
  • Prepare for and lead internal and external audits, ensuring year-round audit readiness
  • Promote a 'right first time' quality mindset across teams
  • Maintain compliance and technical documentation for the company's Class I medical device portfolio
  • Lead regulatory submissions, renewals, and notifications for relevant markets
  • Act as the main point of contact for competent authorities, notified bodies, and regulatory partners
  • Stay current with evolving regulations (EU MDR, UK MDR, FDA, etc.) and proactively adapt internal systems
  • Oversee vigilance and post-market surveillance activities, driving timely investigation and resolution
What we offer
What we offer
  • Competitive salary and performance based incentives
  • Comprehensive insurance
  • Pension scheme with employer contributions
  • Hybrid work option [Monday, Wednesday, Thursday in Office, rest Remote]
  • Inclusive and dynamic work culture with opportunities for career growth
  • Fulltime
Read More
Arrow Right

Senior Regulatory Affairs Specialist

Are you interested in the future of digital health and medical device innovation...
Location
Location
Denmark , Copenhagen
Salary
Salary:
Not provided
3shape.com Logo
3Shape
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s degree within natural sciences, computer science, engineering or similar
  • 5-10+ years in regulatory affairs (preferably both software and hardware medical devices)
  • Global regulatory market experience (e.g. EU, UK, Switzerland and MDSAP)
  • Demonstrated experience applying and interpreting relevant guidance and standards across software and hardware medical devices, including: IEC 60601 series, ISO 14971, IEC 62304, IEC 82304
  • Strong knowledge of cybersecurity and the evolving regulations for digital health and AI/ML devices
  • Adaptable and open to change and adjustments in agile work environments
  • Global mindset and experience with work relations in different cultures
Job Responsibility
Job Responsibility
  • Ensuring that regulatory requirements are in place for our innovative medical device software solutions and intraoral scanner portfolio incl. AI devices
  • Involved in development projects from the start, where your regulatory expertise will be needed as crucial input for the development and market release planning and registration of our devices
  • Ensuring global device registrations
  • Working closely with many stakeholders across R&D, Marketing, Product Management and sales offices around the globe as well as local external advisors and regulatory consultants
  • Active within advocacy and are involved externally in industry organizations and relevant forums influencing policy work and regulatory frameworks
What we offer
What we offer
  • An attractive healthcare package to keep you fit and well
  • Breakfast every day, and a delicious and healthy lunch cooked by our private chefs
  • Good work/life balance e.g., work from home policy for up to 2 days per week
  • Amazing location – our office is located in the heart of Copenhagen, right next to Kongens Nytorv
  • Social clubs, monthly Friday social activities, as well as various in-team activities
  • Fulltime
Read More
Arrow Right

Senior Corporate Counsel

We are looking for a dynamic, highly motivated, and experienced commercial and r...
Location
Location
United Kingdom , London
Salary
Salary:
Not provided
https://www.microsoft.com/ Logo
Microsoft Corporation
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Law degree with relevant academic credentials
  • Practicing certificate in the United Kingdom or any EU member state
  • Extensive experience at a law firm or an in-house legal department
  • Relevant experience leading real estate and other complex commercial transactions in EMEA, ideally with experience in large infrastructure projects, datacenters, real estate lease, purchase and development agreements, and/or international transactions
  • Demonstrable experience developing, negotiating, and documenting complex, multi-party transactions
Job Responsibility
Job Responsibility
  • Drafting and negotiating complex commercial agreements in support of cloud and datacenter infrastructure, including real estate acquisitions and property development agreements, colocation leases, and related transactions
  • Managing outside counsel in colocation leasing, land acquisition, and development, including due diligence, purchase agreements, and post-acquisition development issues
  • Creating new contract models, templates, and process improvements to improve quality, amplify scale, and reduce contract cycle time for datacenter infrastructure expansion
  • Collaborating with team members including zoning and permitting, easements, development agreements, networking and power agreements and across organizational boundaries, including engineering, finance, marketing, government and public affairs, and communications teams
  • Developing trusted advisor relationships with business clients and executives
  • Fulltime
Read More
Arrow Right

Director, European and UK Public Policy

We are looking for an experienced public policy strategist and advocate to lead ...
Location
Location
United Kingdom , London
Salary
Salary:
Not provided
whatnot.com Logo
Whatnot
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 7+ years of public policy or government affairs experience with or in European institutions and national governments
  • Strong policy judgment and subject-matter fluency across issues relevant to Whatnot
  • Experience building and sustaining trusted relationships with policymakers, regulators, industry groups, and civil society
  • Clear, effective written and oral communication skills
  • Comfort moving seamlessly from defining strategy to executing it
  • A collaborative approach to driving outcomes, with experience partnering closely with Legal, Product, Comms, and external consultants
Job Responsibility
Job Responsibility
  • Lead Whatnot’s advocacy across the EU and UK
  • Build and maintain trusted relationships with key policymakers, regulators, and government officials, as well as with business associations, civil society organisations, and other third parties
  • Monitor and interpret policy and regulatory developments across the EU and UK
  • Advise senior leadership on the implications of key policy and regulatory proposals
  • Position Whatnot as a credible, constructive partner on topics such as e-commerce, shipping and customs, product safety, platform liability, and consumer protection
  • Manage and coordinate external consultants and advisors in Brussels, London and key European markets
  • Collaborate closely with the Head of Global Public Policy and cross-functional partners to set priorities, refine narrative, and prepare for emerging issues
What we offer
What we offer
  • Generous Holiday and Time off Policy
  • Health Insurance options including Medical, Dental, Vision
  • Work From Home Support
  • Home office setup allowance
  • Monthly allowance for cell phone and internet
  • Care benefits
  • Monthly allowance for wellness
  • Annual allowance towards Childcare
  • Lifetime benefit for family planning, such as adoption or fertility expenses
  • Retirement
  • Fulltime
Read More
Arrow Right

Vice President, Regulatory Affairs

Reporting to the Chief Medical Officer, the Vice President of Regulatory Affairs...
Location
Location
United States , Philadelphia
Salary
Salary:
Not provided
cabalettabio.com Logo
Cabaletta Bio Inc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced degree in life sciences, pharmacy, or related field (PhD, PharmD, or equivalent preferred)
  • 15+ years of regulatory affairs experience in biopharmaceuticals from pre-clinical to commercialization, with at least 8 years in leadership roles
  • Experience in cell and gene therapy field is preferred
  • Proven track record of successful IND and BLA submissions (prior BLA experience required)
  • Deep knowledge of FDA CBER regulations, EMA ATMP guidelines, GxPs, and global regulatory frameworks
  • Strong leadership, strategic thinking, and negotiation skills
  • Excellent communication and stakeholder management abilities
  • Strong team orientation and passion for continuous self-development
Job Responsibility
Job Responsibility
  • Develop and implement global regulatory strategies for cell therapy programs across clinical development, manufacturing, and commercialization
  • Serve as the primary regulatory advisor to executive leadership, ensuring alignment with corporate objectives and regulatory requirements
  • Anticipate and interpret evolving regulatory trends in cell and gene therapy, including FDA CBER guidance and EMA ATMP frameworks
  • Assess and communicate potential regulatory risks and propose mitigation plans
  • Collaborate with cross-functional teams including clinical and nonclinical development, manufacturing, quality assurance, and medical affairs to develop and implement competitive regulatory strategies that expedite development and maximize the probability of success for cell therapy product development
  • Oversee content preparation and submission of INDs, CTAS, and BLAs/MAAs, and other relevant submissions to regulatory agencies
  • Lead strategy for global expedited pathways (e.g. RMAT, Priority Review, PRIME), orphan designation, and pediatric study plans (US and EU), where applicable
  • Ensure compliance of programs and submission documentation for adherence to GxP, ICH, and regional regulatory requirements throughout development and manufacturing
  • Build and maintain strong relationships with FDA CBER and other regulatory agencies and represent the company in key regulatory meetings and negotiations
  • Ensure timely and high-quality responses to health authority inquiries, including pre-BLA meetings, Type B/C/D meetings, and scientific advice
What we offer
What we offer
  • health and retirement
  • PTO
  • stock option plans
Read More
Arrow Right
New

Lawn Operative

Due to growth and expansion, we have exciting opportunities for Lawn Care Operat...
Location
Location
United Kingdom , Chichester
Salary
Salary:
27248.00 GBP / Year
jobs.360resourcing.co.uk Logo
360 Resourcing Solutions
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Full, UK driving licence for manual vehicles
  • Excellent communication and customer-facing skills
  • A passion for lawn care
  • Want a job where they can work independently, outdoors and keep active
  • Be able to deliver top quality customer service
  • Excellent organisation and timekeeping skills
  • Have the right to work in the UK
Job Responsibility
Job Responsibility
  • Maintaining contact with the customer before a treatment is carried out to inform them when you will be attending
  • To visit a number of designated customers on a daily basis to apply fertiliser and herbicide
  • Where possible, inform the customer before any work commences, that you are there
  • At the conclusion of the work, notify the customer that the treatment has been completed and supply the invoice explaining what work has been carried out
  • Inform the customer of the next treatment date
  • Identify any lawn issues and offer any necessary advice on lawn and mowing practice and any additional treatments which may be required
  • Carrying out essential Spring/Autumn machine work such as Aerators, Scarifiers and lawn top-dressers using a variety of professional lawncare machinery
  • Aeration and scarification is the reduction of moss, thatch and soil compaction which needs to be carried out in a safe and professional manner
  • The use of regular garden tools such as rakes, leaf sweepers and brooms to clear scarification waste
  • Working in a team or alone on machine work which can be physically demanding so good general fitness is required
What we offer
What we offer
  • Starting salary: £27248.00 + £2,000 OTE
  • Annual salary reviews
  • Annual holiday allowance increase, up to 22 days + Bank Holidays
  • Company van and mobile phone
  • New uniform annually
  • Paid training and qualification in the application of pesticides and chemicals
  • Ongoing training and development
  • Medical cash plan
  • Christmas Shutdown
  • Free Lawn Treatments
  • Fulltime
Read More
Arrow Right
New

Lead Applications Analyst (Workday/UKG)

Lead Workday and UKG Applications Analyst, IS Administration, Baptist Health Med...
Location
Location
United States , Jacksonville
Salary
Salary:
Not provided
baptistjax.com Logo
Baptist Health (Florida)
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of 2 years of experience in healthcare, healthcare operations, or information technology required
  • Working knowledge of project management techniques, systems design, and analysis required
  • Bachelor's Degree required
  • Driver's License - DMV
  • Minimum 2 years of related experience
  • Clinical Applications and Systems - design, build, integration, activation
Job Responsibility
Job Responsibility
  • Lead day to day operations, mentors team members, provides the highest level of support
  • Assigns operational tasks and Duties, performs as a Project Lead while also leading in design and support
  • Duties include 24/7 support for information systems within accountability and/or enterprise-wide applications
  • Deep knowledge of Workday modules (HCM, Finance, Payroll, Supply Chain) and UKG Pro WFM (Timekeeping, Scheduling, Accruals, Workforce Analytics)
  • Experience with system configuration, business process design, integrations (APIs, middleware), and reporting/analytics
  • Strong understanding of data governance, security roles, and compliance requirements in healthcare environments
  • Proven ability to lead system implementations, optimizations, and post-go-live stabilization
  • Ability to lead through influence, driving alignment across business and technical stakeholders
  • Strong critical thinking and problem-solving skills, with a focus on root cause analysis and sustainable solutions
  • Effective communicator capable of translating complex technical concepts into business-friendly language
  • Fulltime
Read More
Arrow Right