5 International Relations jobs in the United Kingdom

Description
Join our UK Operations Communications team as a PR Manager based in the Midlands. You'll drive public relations initiatives supporting our fulfillment and logistics network, working remotely while maintaining strong connections with both regional and national media. In this role, you'll develop compelling narratives that showcase Amazon's contributions in the region and support our national PR campaigns.
We're seeking a creative communications professional who can translate complex operational stories into engaging narratives that resonate with diverse audiences. You'll work closely with the Senior PR Manager for UK Operations to shape and deliver communications that highlight Amazon's positive impact on local communities, employment, and the economy.
The ideal candidate brings strategic thinking capabilities, excellent storytelling skills, and the ability to manage both proactive and reactive communications effectively. You should be adaptable, detail-oriented, and capable of building strong relationships with stakeholders at all levels.
This is a remote position with regular travel required throughout the Midlands region. The ideal candidate will be based in the Midlands to facilitate easy access to our various fulfillment centers.
Key job responsibilities
- Lead and execute high-impact external communications programmes across the Midlands while contributing to national initiatives
- Represent Amazon as an official spokesperson, delivering our message with clarity and confidence
- Craft strategic PR campaigns that illuminate Amazon's operational innovations and community investments
- Navigate complex, fast-moving communications challenges with exceptional judgment and poise
- Develop compelling content including news releases, media advisories, and multimedia materials that cut through the noise
- Cultivate and nurture relationships with key journalists and media outlets
- Collaborate across functions to uncover and amplify stories worth telling
A day in the life
Basic Qualifications
- Demonstrated track record in public relations, including social media, content creation, event management and crisis communication
- Experience developing and executing communications plans including strategy, goals, budget and tactics
- Strong writer who crafts clear, compelling copy that resonates with target audiences
- Fluent communicator with professional proficiency in written and spoken English
Preferred Qualifications
- Bachelor's degree in a relevant field
- Communications experience within technology, retail, or logistics/transportation sectors
- Established network of regional and national media relationships
- Demonstrated ability to excel in fast-paced environments while managing multiple priorities
- Creative problem-solver who develops innovative approaches to communications challenges
- Skilled relationship-builder who can manage diverse stakeholders effectively
- Strategic thinker who can analyse complex situations and provide valuable counsel
- Experience collaborating with senior executives and cross-functional teams
Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions based on your experience and skills. We value your passion to discover, invent, simplify and build. Protecting your privacy and the security of your data is a longstanding top priority for Amazon. Please consult our Privacy Notice ( ) to know more about how we collect, use and transfer the personal data of our candidates.
Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status.
Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner.

Description
Project Kuiper is an initiative to launch a constellation of Low Earth Orbit satellites that will provide low-latency, high-speed broadband connectivity to unserved and underserved communities around the world.
Key job responsibilities
Functions include providing strategic direction and executing in the following areas:
· Working with the technical and systems/RF engineering teams to analyze the potential for harmful interference between Kuiper and other satellite networks (both geostationary and non-geostationary) and terrestrial systems, developing the coordination strategy and mitigation techniques, and negotiating favorable coordination agreements.
· Preparing and managing ITU satellite network filings in conformity with the Radio Regulations and applicable deadlines.
· Executing the coordination strategy and reviewing satellite network filings and preserving coordination rights by commenting on filings within the regulatory deadlines.
·Assist with the global licensing strategy by advancing coordination requirements for Kuiper's system.
· Excellent communication skills with the ability to identify tradeoffs, risks, and opportunities; remove bottlenecks; and establish mechanisms to speed progress.
This position may require access to export-controlled information (ECI) subject to EAR and ITAR. Final employment decision is contingent upon satisfactory completion of export control screenings and obtaining any necessary export licenses or approvals, based on nationality, citizenship, and other factors considered by applicable export control regulations.
A day in the life
The Engineer, International Spectrum Management and Strategy will articulate and execute the strategy for enabling and protecting Kuiper's use of radio frequency spectrum and satellite orbits through the ITU filing, coordination, and notification processes. The ideal candidate has strong experiences with RF simulation tools and knowledge of the applicable Radio Regulations, Rules of Procedure, and ITU-R Recommendation.
About the team
The Global Regulatory Affairs team is responsible for enabling and protecting Kuiper's use of radio frequency spectrum at home and abroad, defining and leading the Project Kuiper regulatory agenda. The Regulatory Affairs team operates worldwide, engaging with the International Telecommunication Union (ITU) and regional organizations, coordinating the use of spectrum with other operators, obtaining licenses for Kuiper services, and promoting safety in space. The Global Regulatory Affairs team is also responsible for domestic licensing and collaborates with associations, government agencies, and other satellite operators in order to advocate for rules and regulations in the best interest of our customers. This team works in close collaboration with the Kuiper technical design teams to optimize for spectrum sharing and customer experience as well as with Amazon's public policy and legal teams to enhance the overall regulatory strategy.
Basic Qualifications
- Experience analyzing dynamic interference from satellite systems and/or other radiocommunication systems
Preferred Qualifications
- Masters Degree in Electrical Engineering or related discipline (telecommunications)
- Experience preparing, managing, and coordinating ITU satellite network filings with other satellite operators internationally in conformity with the Radio Regulations
- Experience with non-geostationary satellite systems
- Experience with satellite systems in the 20/30 GHz bands.
- Experience with Visualyse Professional
- Excellent analytical, problem solving, and communication skills.
Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions based on your experience and skills. We value your passion to discover, invent, simplify and build. Protecting your privacy and the security of your data is a longstanding top priority for Amazon. Please consult our Privacy Notice ( ) to know more about how we collect, use and transfer the personal data of our candidates.
Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status.
Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner.

Job Title: Global Associate Director, Regulatory Affairs

Job Type: Full-time permanent position

Location: Hertfordshire, UK – Hybrid (2/3 days per week in the office)

Remuneration: Competitive benefits package

An exciting opportunity to join an established pharmaceutical company that specialises in Oncology and Neurology. The role will be working across both portfolios and will have a heavy focus on regulatory strategy.

Directing the development of submission of Neurology and Oncology clinical trial applications, product registration dossiers, supplements, and amendments. Provides strategic product direction to project teams on interacting and negotiating with regulatory agencies in order to expedite approval of pending registration and answers any questions.

A great opportunity to demonstrate your knowledge in leading regulatory processes for products across the globe, with a focus on oncology and neurology. In this unique position, you will interact with a wide and diverse range of colleagues across the organisation.

Responsibilities:

• Provides strategic product direction to project teams on interacting and negotiating with regulatory agencies in order to expedite approval of pending registration and answers any questions.
• Regulatory Submissions (CTA/MAA): Participating in regulatory submission activities and reviewing regulatory documents prior to submission to ensure overall quality, compliance and timeliness. Partnering with project teams to assess regulatory support needs and align resources (i.e., sub teams) to provide regulatory support. Creation of regulatory documents, working with the cross functional team to create responses per Agency timelines.
• Interfacing with Authorities: Acting as the point of contact with regulatory authorities for assigned product(s). Leading calls or meetings with regulatory authorities. Authoring Scientific Advice requests, leading team strategy.
• Regulatory Strategy Development: Contributing to the development of global regulatory strategies across programs for own functional area and region. Identifying, monitoring and resolving regulatory issues and reporting progress to management
• Serves as a regulatory liaison on the project team throughout the product lifecycle.
• Ensures that clinical trial designs meet regulatory requirements. Ensures rapid and timely approval on of new drugs, biologics/biotechnology and/or medical devices and continued approved status of marketed drugs or medical devices.
• Advice on all aspects of product development from a regulatory perspective.

Requirements:

• Bachelor's degree
• Extensive industry experience with demonstrated experience in direct Regulatory Affairs in the biotech/biopharmaceutical industry.
• Demonstrated track record of interfacing effectively with global regulatory agencies, such as the EMA.
• Experience in Clinical Trial Applications, including submission and maintenance
• Paediatric Investigation Plan experience preferred but not required.
• Strong understanding and practical experience with regulations and guidelines governing pharmaceutical development and registration.

An excellent opportunity to work for a leading pharmaceutical company at the heart of science and neuroscience development. The role comes with some excellent benefits, including a bonus, car allowance life assurance, pension scheme, and private healthcare.

This role does not provide sponsorship, and you must have the Right to Work in the UK.

For more details about this position, please feel free to contact

Job Description

Job Title: Global Associate Director, Regulatory Affairs

Job Type: Full-time permanent position

Location: Hertfordshire, UK – Hybrid (2/3 days per week in the office)

Remuneration: Competitive benefits package

An exciting opportunity to join an established pharmaceutical company that specialises in Oncology and Neurology. The role will be working across both portfolios and will have a heavy focus on regulatory strategy.

Directing the development of submission of Neurology and Oncology clinical trial applications, product registration dossiers, supplements, and amendments. Provides strategic product direction to project teams on interacting and negotiating with regulatory agencies in order to expedite approval of pending registration and answers any questions.

A great opportunity to demonstrate your knowledge in leading regulatory processes for products across the globe, with a focus on oncology and neurology. In this unique position, you will interact with a wide and diverse range of colleagues across the organisation.

Responsibilities:

• Provides strategic product direction to project teams on interacting and negotiating with regulatory agencies in order to expedite approval of pending registration and answers any questions.
• Regulatory Submissions (CTA/MAA): Participating in regulatory submission activities and reviewing regulatory documents prior to submission to ensure overall quality, compliance and timeliness. Partnering with project teams to assess regulatory support needs and align resources (i.e., sub teams) to provide regulatory support. Creation of regulatory documents, working with the cross functional team to create responses per Agency timelines.
• Interfacing with Authorities: Acting as the point of contact with regulatory authorities for assigned product(s). Leading calls or meetings with regulatory authorities. Authoring Scientific Advice requests, leading team strategy.
• Regulatory Strategy Development: Contributing to the development of global regulatory strategies across programs for own functional area and region. Identifying, monitoring and resolving regulatory issues and reporting progress to management
• Serves as a regulatory liaison on the project team throughout the product lifecycle.
• Ensures that clinical trial designs meet regulatory requirements. Ensures rapid and timely approval on of new drugs, biologics/biotechnology and/or medical devices and continued approved status of marketed drugs or medical devices.
• Advice on all aspects of product development from a regulatory perspective.

Requirements:

• Bachelor's degree
• Extensive industry experience with demonstrated experience in direct Regulatory Affairs in the biotech/biopharmaceutical industry.
• Demonstrated track record of interfacing effectively with global regulatory agencies, such as the EMA.
• Experience in Clinical Trial Applications, including submission and maintenance
• Paediatric Investigation Plan experience preferred but not required.
• Strong understanding and practical experience with regulations and guidelines governing pharmaceutical development and registration.

An excellent opportunity to work for a leading pharmaceutical company at the heart of science and neuroscience development. The role comes with some excellent benefits, including a bonus, car allowance life assurance, pension scheme, and private healthcare.

This role does not provide sponsorship, and you must have the Right to Work in the UK.

For more details about this position, please feel free to contact