CrawlJobs Logo

EU Affairs Advisor

vodafone.com Logo

Vodafone

Location Icon

Location:
Belgium , Brussels

Category Icon
Category:
Consulting

Job Type Icon

Contract Type:
Employment contract

Salary Icon

Salary:

Not provided
Save Job
Save Icon
Apply Position

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)

Additional Information:

Job Posted:
May 14, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Icon
Vodafone - All Job Offers
Job Link Share:
Copy Link Icon
Facebook Icon Twitter Icon LinkedIn Icon

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for EU Affairs Advisor

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

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

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

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

Regulatory Affairs Consultant - Labelling

As part of Parexel Consulting, you will play a vital role in helping biopharmace...
Location
Location
Australia , Remote
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of a Bachelor’s Degree in a Scientific or Technical Discipline, Advanced Degree Preferred
  • 8 years + experience in an industry-related environment, inclusive of 2+ years of labeling/regulatory experience combined with other global responsibility from Australia including New Zealand.
  • Client-focused approach to work
  • Results orientation
  • Teamwork and collaboration skills
  • Consulting skills
  • Excellent interpersonal and intercultural communication skills, both written and verbal
  • Critical thinking and problem-solving skills
  • Previous experience working in industry in support of Global Labeling, Regulatory (Clinical / Safety), or Medical Writing for labelling updates
  • Use of document management tools (internal systems) and external platforms
Job Responsibility
Job Responsibility
  • Demonstrates the use of the organization’s consulting models and methodologies and uses experience to suggest possible developments/improvements
  • Provides a full range of technical and/or business consulting services within personal area of expertise dealing mainly in areas where policy or precedent is clear
  • Completes activities within project scope and objectives in a timely manner with an understanding of issues which may impact project profitability, quality, and client satisfaction
  • Facilitates client decision making by framing issues, presenting options and providing objective business advice
  • Collaborates with colleagues, as needed, to discuss and facilitate resolution of problems or conflicts. Provides guidance as needed to lower level colleagues on appropriate methods of executing project activities
  • Acts as a trusted advisor to clients and/or project team on technical and/or process issues
  • Supports development of business solutions addressing specific client needs using best practices and knowledge of the client’s business and key industry drivers
  • Interacts professionally at multiple levels including senior management within a client organization
  • Facilitates clients in identifying and addressing their needs and develops processes and solutions to address issues before they become significant problems
  • Completes basic job-related responsibilities, including timesheets, expense reports, maintenance of CVs, project deliverable archiving, participation in internal initiatives/projects or as a mentor as requested by management
What we offer
What we offer
  • Flexible work arrangements
  • Opportunities for career growth
  • Supportive and inclusive environment
  • Diverse and global client exposure
  • Learn from experts
Read More
Arrow Right
New

Onsite Endoscopic Specialist

At KARL STORZ, we are driven by a mission to enhance global health through innov...
Location
Location
United States , Arlington
Salary
Salary:
Not provided
karlstorz.com Logo
KARL STORZ
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • A minimum of high school diploma or equivalent
  • Experience in Sterile Processing, Sales, or other Surgical Technology/Medical role
  • Our successful candidate will have excellent written and spoken English language business communication skills. They will also have demonstrated success working in a collaborative, service-oriented team environment.
  • Effective communicator, collaborative, and effective time management
  • Possess exceptional organizational skills and the ability to multi-task
  • MS Office - proficient user as the role will need to work with Excel spreadsheets and reporting
  • Role requires the completion of a drug screening for safety-sensitive positions
  • Must be able to lift/push/pull up to 25lbs
Job Responsibility
Job Responsibility
  • Face-to-face customer support, including OR, SPD and Biomed
  • Video tower/system set-up and support
  • Inspection, repair, troubleshooting and replacement of KARL STORZ devices
  • Monitoring, reporting, and facilitating repair/ exchange transactions
  • Transporting, cleaning/sterilization and packaging of instruments after use
  • Trouble shoot video and instrument issues in the O.R.
  • Instrument/equipment repair management
What we offer
What we offer
  • Relocation Support
  • Professional Growth & Development
  • Collaborative & Dynamic Work Environment
  • Access to Cutting-Edge Medical Technologies
  • Medical / Dental / Vision including a state-of-the-art wellness program and pet insurance, too
  • 3 weeks vacation, 11 holidays plus paid sick time
  • Up to 8 weeks of 100% paid company parental leave
  • 401(k) retirement savings plan providing a match of 60% of the employee’s first 6% contribution (up to IRS limits)
  • Section 125 Flexible Spending Accounts
  • Life, STD, LTD & LTC Insurance
  • Fulltime
Read More
Arrow Right
New

Pharmacy Technician

We’re building a world of health around every individual — shaping a more connec...
Location
Location
United States , Columbus
Salary
Salary:
17.00 USD / Hour
https://www.cvshealth.com/ Logo
CVS Health
Expiration Date
July 11, 2026
Flip Icon
Requirements
Requirements
  • Must comply with any state board of pharmacy requirements or laws governing the practice of pharmacy, which includes but is not limited to, age, education, and licensure/certification
  • If the state board of pharmacy does not address or mandate a minimum age requirement, must be at least 16 years of age
  • If the state board of pharmacy does not address or mandate a minimum educational requirement, must have a high school diploma or equivalent, or be actively enrolled in high school or high school equivalency program
Job Responsibility
Job Responsibility
  • Living our purpose by following all company SOPs at each workstation to help our Pharmacists manage and improve patient health
  • Following pharmacy workflow procedures at each pharmacy workstation (i.e., production, pick-up, drive-thru, and drop-off) for safe and accurate prescription fulfillment
  • Contributing to positive patient experiences by showing empathy and genuine care: creating heartfelt and personalized moments while serving patients at pick-up, drive-thru, and over the phone
  • keeping patients healthy by offering immunizations and other services at the register and over the phone
  • and demonstrating compassionate care by solving or escalating patient problems
  • Completing basic inventory activities, as permitted by law, and as directed by the pharmacy leadership team, such as accurately putting away medication deliveries and completing cycle counts, returns-to-stocks, waiting bin inventories, etc.
  • Contributing to a high-performing team, embracing a growth mindset, and being receptive to feedback
  • actively seeking opportunities to expand clinical and technical knowledge needed to better assist patients
  • Remaining flexible for both scheduling and business needs, while contributing to a safe, inclusive, and engaging team dynamic
  • voluntarily traveling to stores in the market to work shifts as needed by the business
What we offer
What we offer
  • dental
  • vision
  • wellness resources
  • employee discounts
  • access to certain voluntary benefits
  • other programs
  • Parttime
Read More
Arrow Right
New

Assistant General Manager

Assistant General Manager, at Boston Pizza, one of Canada’s Best Managed Compani...
Location
Location
Canada , Lac La Biche
Salary
Salary:
22.00 - 30.00 CAD / Hour
bostonpizza.com Logo
Boston Pizza
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 1+ year of casual dining experience
  • Previous leadership or supervisory experience is an asset
  • A positive attitude and strong work ethic
  • Excellent communication and team-building skills
  • Ability to thrive in a fast-paced environment
  • A passion for hospitality and guest service
  • Open availability
Job Responsibility
Job Responsibility
  • Support day-to-day operations
  • Lead and motivate the team
  • Ensure an exceptional guest experience
What we offer
What we offer
  • Competitive pay
  • Medical
  • dental benefits
  • Staff accommodations available
  • Flexible scheduling
  • Room to grow within the company
  • Hands-on management training
  • A supportive, close-knit team environment
  • Fulltime
Read More
Arrow Right