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Eu Commission Jobs (NOW HIRING)

Fipra Public Affairs

WI · On-site

$70 - $90/hr

Ideal candidates will be familiar with, or have experience engaging with, relevant stakeholders, key organisations and authorities within the European Commission, EU Member States and the European ...

Fipra Public Affairs

WI · On-site

$70.86 - $94.47/hr

Ideal candidates will be familiar with and have established networks with relevant stakeholders, key organizations, and authorities within the European Commission, EU Member States, and the European ...

UCB

Director, Agencies & Media - Global

Atlanta, GA · On-site

S. and EU to close gaps in terms and drive cost efficiency, spanning FTE-based, fee-based, media-commission, and performance/outcome-based models * Media Transparency & Value Recovery : Establish ...

UCB

Director, Agencies & Media - Global

Atlanta, GA · Hybrid

S. and EU to close gaps in terms and drive cost efficiency, spanning FTE-based, fee-based, media-commission, and performance/outcome-based models * Media Transparency & Value Recovery : Establish ...

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How much do eu commission jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for eu commission in the United States is $50.06, according to ZipRecruiter salary data. Most workers in this role earn between $34.86 and $51.92 per hour, depending on experience, location, and employer.

What is the European Commission?

The European Commission is the executive branch of the European Union responsible for proposing legislation, implementing EU laws, managing policies, and overseeing the EU budget. It acts as the guardian of the EU treaties and ensures that member states comply with EU law. The Commission also represents the EU internationally and works to promote the interests of the Union as a whole. Its work covers a wide range of policy areas, from climate change and digital innovation to trade and external relations.

What is the typical structure of a team within the European Commission, and how do team members collaborate on projects?

Within the European Commission, teams are often organized into directorates and units that focus on specific policy areas or administrative functions. Team members, including policy officers, legal experts, and administrative staff, work collaboratively by contributing their expertise to draft proposals, analyze policy impacts, and coordinate with other EU institutions. Regular meetings, both in-person and virtual, help ensure alignment and effective communication among team members. Collaboration also frequently extends across departments and sometimes involves stakeholders from other EU bodies or member states, fostering a diverse and dynamic work environment.

What are the key skills and qualifications needed to thrive as a European Commission official, and why are they important?

To thrive as a European Commission official, you generally need a strong academic background (often at least a university degree), multilingual proficiency, and in-depth knowledge of EU policies and law. Familiarity with EU policy-making tools, digital communication platforms, and project management systems is highly beneficial. Excellent interpersonal, negotiation, and analytical skills distinguish successful candidates, enabling effective collaboration in a multicultural environment. These competencies are essential for shaping EU policy, ensuring regulatory compliance, and fostering international cooperation.

What is the difference between Eu Commission vs European Parliament Member?

AspectEu CommissionEuropean Parliament Member
RoleExecutive branch responsible for proposing legislation and implementing EU policiesLegislative branch representing citizens, debating, and passing laws
Required CredentialsTypically higher education, experience in policy or law, and political appointmentUsually elected, with a background in politics, law, or public service
Work EnvironmentEuropean Commission headquarters, Brussels, Brussels-based, internationalEuropean Parliament sessions, Strasbourg and Brussels, political environment
Employer/Industry UsageEU institutions, government, international organizationsEuropean Union legislative process, government, political institutions

The Eu Commission and European Parliament Members play distinct roles within the EU. The Eu Commission acts as the executive body proposing and implementing policies, while European Parliament Members serve as elected legislators shaping laws. Both are essential but differ in responsibilities, credentials, and work environment.

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Eu Commission jobs near you
Infographic showing various Eu Commission job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 9% Part Time, and 6% Contract. Highlights an 69% Physical, 1% Hybrid, and 30% Remote job distribution, with an average salary of $104,126 per year, or $50.1 per hour.

Regulatory Affairs Specialist

Charter Medical LLC

Winston Salem, NC • On-site

Full-time

Medical, Retirement, PTO

Re-posted 21 days ago

Key responsibilities

  • Prepares, compiles, and submits regulatory documents to obtain approval to market new or modified products, including 510(k) premarket notifications and international submissions.

  • Monitors and interprets regulatory requirements from FDA, EU, and international bodies, and communicates updates to ensure compliance.

  • Provides regulatory support to product development teams and performs regulatory assessments for modifications to existing devices.

Job description

What we are looking for:

Plans, organizes and implements strategies and activities required to procure regulatory approval for new and revised product lines. Coordinates and prepares regulatory submissions, including 510(k) premarket notifications, EU MDR Technical Files and other international registrations. Ensure compliance to all US, EU and international requirements and company policies and procedures regarding submissions and other requirements for market approval of medical devices.

1st Shift: Monday-Friday 8:00 am-5:00 pm

What you will do:

Regulatory Submissions & Approvals

  • Authors, compiles, and submits regulatory documents to obtain approval to market new or modified products, including 510(k) premarket notifications and international submissions.
  • Prepares , maintains and submits Technical Documentation and Declarations of Conformity for CE-marked products under EU MDR 2017/745.
  • Prepares and maintains international product registrations.
  • Prepares and updates US FDA product listings and establishment registrations.

Regulatory Intelligence & Compliance

  • Monitors publications and activities of FDA, EU Commission, and international regulatory bodies to identify and respond to new or revised regulatory requirements affecting company products.
  • Interprets existing and emerging regulatory requirements as they relate to company products and procedures; communicates updates to appropriate personnel and management.
  • Identifies and communicates changes to domestic and international regulatory requirements in a timely manner to support proactive compliance planning.
  • Ensures label claims and content of promotional and marketing materials comply with domestic and international regulatory requirements; reviews and recommends appropriate changes.

Product Development & Change Assessment

  • Provides regulatory support to new product development teams to ensure US and international regulatory requirements are incorporated into the development process from design input through commercialization.
  • Performs and documents regulatory assessments for modifications to existing devices, collaborating with marketing, R&D, and operations on proposed changes.
  • Supports marketing and new product development in regulatory assessments of proposed labeling, design, or manufacturing changes.
  • Collaborates with engineering and operations teams on design controls, validation activities, and technology transfers.

Who you are:

  • Bachelor’s degree or higher in a life science, engineering, or related discipline from an accredited institution.
  • Minimum of 3–5 years of regulatory affairs experience in the medical device industry.
  • Solid knowledge of US FDA regulations including 21 CFR Parts 820 (QSR/QMSR), 803, 806, and 807.
  • Working knowledge of EU MDR 2017/745, including Technical Documentation requirements and Declaration of Conformity preparation.
  • Experience with ISO 13485 quality management system requirements.
  • Direct experience with Class II or III EU MDR submissions and Technical Documentation under EU MDR 2017/745.
  • Ability to correctly interpret regulations and apply them to day-to-day business operations.
  • Strong written and verbal communication skills; ability to interact effectively with individuals in scientific, technical, and regulatory fields.
  • International device registration experience (EU, Asia-Pacific, Australia, or other markets).
  • Familiarity with ISO 14971 risk management.
  • Knowledge of 510(k), MDR, and CE Marking requirements with active role in submissions leading to commercialization.
  • Familiarity with global and regional trends in regulatory affairs.
  • Strongly prefer candidates with Regulatory Affairs Certification (RAC) from the Regulatory Affairs Professionals Society (RAPS) or equivalent professional certification.
  • Ability to interact with individuals in scientific and/or technical fields
  • International device registration experience (preferably EU, Asia, Canada etc.)
  • Ability to effectively negotiate and balance the need for regulatory compliance with the needs of the business
  • Ability to correctly interpret regulations as they apply to day to day business operations.

Perks / Benefits:

  • Generous Paid Time Off
  • Paid Breaks
  • Annual Bonuses
  • 401(k) with excellent company match
  • Health Insurance with multiple plans to choose form
  • Paid Short Term and Long Term Disability