Explore pharmaceutical jobs in 21 Pharmaceutical jobs in London
Engineer,International Spectrum Management and Strategy,Project Kuiper,International,Kuiper Regul...
Posted 20 days ago
Job Viewed
Job 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 Kuiperu2019s 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 Kuiperu2019s 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 Kuiperu2019s 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 Amazonu2019s public policy and legal teams to enhance the overall regulatory strategy.
Basic Qualifications
- Master's degree in Electrical Engineering or related discipline (telecommunications)
- Experience analyzing dynamic interference from satellite systems and/or other radiocommunication systems
Preferred Qualifications
- 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 youu2019re applying in isnu2019t listed, please contact your Recruiting Partner.
Engineer,International Spectrum Management and Strategy,Project Kuiper,International,Kuiper Regul...
Posted 20 days ago
Job Viewed
Job 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 Kuiperu2019s 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 Kuiperu2019s 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 Kuiperu2019s 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 Amazonu2019s public policy and legal teams to enhance the overall regulatory strategy.
Basic Qualifications
- Master's degree in Electrical Engineering or related discipline (telecommunications)
- Experience analyzing dynamic interference from satellite systems and/or other radiocommunication systems
Preferred Qualifications
- 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 youu2019re applying in isnu2019t listed, please contact your Recruiting Partner.
Associate Principal Medical Writer - London (Hybrid)
Posted 19 days ago
Job Viewed
Job Description
We are excited to be supporting a leading UK-based MedComms agency in their search for an Associate Principal Medical Writer . This is a fantastic opportunity for an experienced medical writer with a strong background in MedComms agency work who is ready to take on greater responsibility in client strategy, leadership, and team development.
Key Responsibilities:
- Deliver strategic scientific insight to shape client programmes across publications and medical affairs.
- Review and monitor content to ensure accuracy, compliance, and high-quality delivery.
- Act as a primary point of contact for clients , building strong partnerships and driving projects forward.
- Provide direct and indirect line management , mentoring junior and mid-level writers to support their development.
- Lead on the creation of scientifically robust, impactful materials that align with client strategy.
Requirements:
- Proven experience within a UK MedComms agency (essential).
- Solid track record in medical writing , with expertise in publications and/or medical affairs.
- Strong client-facing skills and the ability to provide scientific leadership.
- Experience managing, mentoring, or supporting other writers.
- Ability to combine scientific accuracy with strategic insight.
What’s on Offer:
- Competitive salary and benefits package.
- Hybrid working model based in London .
- A clear career pathway, with opportunities to grow into a Principal Medical Writer position.
- The chance to lead impactful projects for high-profile clients in a collaborative and supportive environment.
If you are ready to take the next step in your MedComms career and want to play a key role in driving client success, we’d love to hear from you.
Pharmaceutical Procurement Specialist - Unlicensed Medicines
Posted today
Job Viewed
Job Description
We are exclusively supporting our client, a market-leading Pharmaceutical business to hire a Procurement Specialist within Unlicensed Medicines (ULM) to join their team and play a key role in supporting their continued growth.
About the company you are joining:
- A very reputable and values driven Pharmaceutical business that has seen tremendous results in recent years - they really are pushing the boat in terms of establishing themselves as a market leader within their respective field, and have continued to invest heavily in growing the business.
- Our client distributes a large range of Pharmaceutical products both domestically and internationally to their ever growing customer base.
- A diverse and inclusive culture of family, where individuals are encouraged to bring ideas to the table, innovate in their own roles, and highlight improvements.
- A fantastic opportunity to join a company that prides itself on investing into your personal growth and professional development
About the role:
If you want to take on the challenge of working in a role that puts you right at the coalface of a business, where you will have the autonomy and gravitas to drive positive change. then this opportunity is for you!
The Pharmaceutical Procurement Specialist is responsible for the competitive sourcing and procurement of products within the Unlicensed Medicine (ULM) department, servicing customers in the the UK. It will involve working at a strategic and operational level to deliver the global procurement and logistic requirements, thus enabling the business to capitalise on new and existing opportunities.
The goal is to obtain the best quality products or services and to meet the needs of the organisation compliantly, efficiently, and effectively. You need to be innovative and be a competent negotiator using risk management to cost save and deliver every time.
You will will be responsible at both a strategic and commercial level for the company's procurement and sourcing activities into the market, so will work cross-functionally to enable you to succeed in this role.
Some of the key responsibilities for the Pharmaceutical Procurement Specialist will involve:
- Developing and leading the Unlicensed Medicines (ULM) procurement strategy and activities to maximise sales opportunities and achieve the overall growth objectives for the business.
- Driving innovation within procurement by identifying and implementing new thinking and practice in procurement strategies and supplier partnerships.
- Competitive procurement of products to ensure cost-effective, timely and quality sourcing to meet patient needs.
- Accurate and timely forecasting to ensure correct products and volumes of products are always in stock and communicated to wider business.
- Identify and communicate any supply issues of regularly purchased products, working with the ULM team to successfully execute a plan to minimise impact on customers.
We are looking for candidates for the Pharmaceutical Procurement Specialist who can demonstrate the following:
- Extensive experience working in a Procurement, Sourcing or Buying role within the Unlicensed Medicines/Specials and/or wider Pharmaceutical field.
- A forward-thinking, outside the box thinker, who can find solutions where others see problems.
- Strategic outlook on procurement activities, and is prompt to market movements.
- Natural relationship builder, who is comfortable and confident in negotiating with stakeholders at all levels.
- Financially literate, with excellent business acumen - having a good grasp of margins, costs, etc. is key in succeeding in this role.
Keywords: Pharmaceutical Procurement Specialist, Procurement Specialist, Sourcing Manager, Buyer, Buying Manager, Pharmaceutical Procurement, Purchasing Specialist, Unlicensed Medicines, Specials, ULM
Our client is an equal opportunities employer and we encourage applicants from all backgrounds. For a full job description and more detailed overview of the opportunity, please apply or reach out directly to hear more. This is an exclusively managed recruiting process by Radar Recruitment. All applicants (including third party/unsolicited approaches) will be sent on and vetted by Radar Recruitment.
Clinical Research Associate
Posted today
Job Viewed
Job Description
Job Title: Junior Clinical Research Associate (CRA)
Location: London, UK (Field-based with regular site visits)
Employment Type: Full-time
About the Role:
We are seeking a motivated Junior Clinical Research Associate (CRA) with a minimum of 2 years of independent monitoring experience to join our London-based team. The successful candidate will play a vital role in ensuring the quality and integrity of clinical trials across multiple therapeutic areas. You will conduct 4–6 monitoring visits per month , providing oversight of study sites while maintaining compliance with ICH-GCP, local regulations, and study protocols.
Key Responsibilities:
- Perform routine monitoring visits (site initiation, interim, and close-out) across assigned sites in London and surrounding regions.
- Ensure adherence to protocol, ICH-GCP, and applicable regulatory requirements.
- Verify accuracy and completeness of case report forms (CRFs) against source data.
- Identify and resolve data discrepancies and protocol deviations in collaboration with site staff.
- Maintain effective communication with investigators, site personnel, and internal study teams.
- Prepare and submit timely monitoring reports and follow-up documentation.
- Support investigators and sites in resolving queries and ensuring readiness for audits and inspections.
- Contribute to trial start-up activities when required (e.g., site feasibility, essential document collection).
Requirements:
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
- Minimum 2 years of independent monitoring experience within a CRO, pharmaceutical, or biotech environment.
- Strong knowledge of ICH-GCP and UK clinical trial regulations.
- Excellent organizational and time management skills with the ability to manage multiple sites.
- Willingness to travel frequently (4–6 site visits per month).
- Strong interpersonal and communication skills, both written and verbal.
What We Offer:
- Competitive salary and benefits package.
- Professional development opportunities within a growing clinical operations team.
- Exposure to diverse therapeutic areas and phases of clinical development.
- Supportive work environment with mentorship from senior CRAs.
Associate Director, AI Data Scientist - Mid-sized pharmaceutical company - Fully remote across UK
Posted today
Job Viewed
Job Description
Planet Pharma is seeking an Associate Director, AI Data Scientist to lead the design and implementation of innovative AI/ML/GenAI solutions that will transform clinical trial execution and digital healthcare. This is a highly visible, strategic role with the opportunity to impact patient recruitment, real-world data generation, and next-generation digital tools across global R&D.
What you’ll do:
Lead AI/ML/GenAI initiatives to optimize clinical trial operations (patient recruitment, retention, data monitoring, automation).
Develop GenAI applications for automated clinical trial documentation (protocols, study reports, medical reports, patient narratives).
Create Digital Healthcare applications to support medical/scientific tools, patient engagement, and real-world evidence generation.
Design predictive models and generative AI solutions leveraging diverse healthcare data (clinical trials, EHRs, wearables, PROs, HEOR, Phase IV).
Collaborate with clinical, data science, RWE, and medical affairs teams to deliver AI-driven business value.
Build relationships with external experts (researchers, regulators, technology partners) to align solutions and stay at the forefront of innovation.
Ensure compliance with data privacy and regulatory standards while promoting knowledge sharing across teams.
What we’re looking for:
️ Advanced degree (MS/PhD) in Data Science, Computer Science, Biostatistics, or related field
️ 7–10 years’ experience, with 3+ years applying AI/ML to healthcare or clinical research data
️ Expertise in Python, R, TensorFlow, PyTorch, and modern ML frameworks
️ Hands-on experience with LLMs, generative AI, and natural language processing for medical text
️ Familiarity with AWS, MLOps, and cloud-based platforms
️ Proven ability to partner with stakeholders and adapt AI solutions to complex healthcare challenges
️ Experience in digital healthcare tool development (advantageous)
This is a unique opportunity to help shape the future of digital healthcare and clinical research by delivering AI solutions that improve patient outcomes and accelerate therapeutic innovation. At Planet Pharma, we connect top talent with impactful roles that drive innovation in life sciences — and this is one of them.
For more information on this position, please apply now and one of our consultants will get in touch to discuss the opportunity with you in more detail.
Associate Director, AI Data Scientist - Mid-sized pharmaceutical company - Fully remote across UK
Posted today
Job Viewed
Job Description
Planet Pharma is seeking an Associate Director, AI Data Scientist to lead the design and implementation of innovative AI/ML/GenAI solutions that will transform clinical trial execution and digital healthcare. This is a highly visible, strategic role with the opportunity to impact patient recruitment, real-world data generation, and next-generation digital tools across global R&D.
What you’ll do:
Lead AI/ML/GenAI initiatives to optimize clinical trial operations (patient recruitment, retention, data monitoring, automation).
Develop GenAI applications for automated clinical trial documentation (protocols, study reports, medical reports, patient narratives).
Create Digital Healthcare applications to support medical/scientific tools, patient engagement, and real-world evidence generation.
Design predictive models and generative AI solutions leveraging diverse healthcare data (clinical trials, EHRs, wearables, PROs, HEOR, Phase IV).
Collaborate with clinical, data science, RWE, and medical affairs teams to deliver AI-driven business value.
Build relationships with external experts (researchers, regulators, technology partners) to align solutions and stay at the forefront of innovation.
Ensure compliance with data privacy and regulatory standards while promoting knowledge sharing across teams.
What we’re looking for:
️ Advanced degree (MS/PhD) in Data Science, Computer Science, Biostatistics, or related field
️ 7–10 years’ experience, with 3+ years applying AI/ML to healthcare or clinical research data
️ Expertise in Python, R, TensorFlow, PyTorch, and modern ML frameworks
️ Hands-on experience with LLMs, generative AI, and natural language processing for medical text
️ Familiarity with AWS, MLOps, and cloud-based platforms
️ Proven ability to partner with stakeholders and adapt AI solutions to complex healthcare challenges
️ Experience in digital healthcare tool development (advantageous)
This is a unique opportunity to help shape the future of digital healthcare and clinical research by delivering AI solutions that improve patient outcomes and accelerate therapeutic innovation. At Planet Pharma, we connect top talent with impactful roles that drive innovation in life sciences — and this is one of them.
For more information on this position, please apply now and one of our consultants will get in touch to discuss the opportunity with you in more detail.
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Associate Director, AI Data Scientist - Mid-sized pharmaceutical company - Fully remote across UK
Posted today
Job Viewed
Job Description
Planet Pharma is seeking an Associate Director, AI Data Scientist to lead the design and implementation of innovative AI/ML/GenAI solutions that will transform clinical trial execution and digital healthcare. This is a highly visible, strategic role with the opportunity to impact patient recruitment, real-world data generation, and next-generation digital tools across global R&D.
What you’ll do:
Lead AI/ML/GenAI initiatives to optimize clinical trial operations (patient recruitment, retention, data monitoring, automation).
Develop GenAI applications for automated clinical trial documentation (protocols, study reports, medical reports, patient narratives).
Create Digital Healthcare applications to support medical/scientific tools, patient engagement, and real-world evidence generation.
Design predictive models and generative AI solutions leveraging diverse healthcare data (clinical trials, EHRs, wearables, PROs, HEOR, Phase IV).
Collaborate with clinical, data science, RWE, and medical affairs teams to deliver AI-driven business value.
Build relationships with external experts (researchers, regulators, technology partners) to align solutions and stay at the forefront of innovation.
Ensure compliance with data privacy and regulatory standards while promoting knowledge sharing across teams.
What we’re looking for:
️ Advanced degree (MS/PhD) in Data Science, Computer Science, Biostatistics, or related field
️ 7–10 years’ experience, with 3+ years applying AI/ML to healthcare or clinical research data
️ Expertise in Python, R, TensorFlow, PyTorch, and modern ML frameworks
️ Hands-on experience with LLMs, generative AI, and natural language processing for medical text
️ Familiarity with AWS, MLOps, and cloud-based platforms
️ Proven ability to partner with stakeholders and adapt AI solutions to complex healthcare challenges
️ Experience in digital healthcare tool development (advantageous)
This is a unique opportunity to help shape the future of digital healthcare and clinical research by delivering AI solutions that improve patient outcomes and accelerate therapeutic innovation. At Planet Pharma, we connect top talent with impactful roles that drive innovation in life sciences — and this is one of them.
For more information on this position, please apply now and one of our consultants will get in touch to discuss the opportunity with you in more detail.
Principal Statistical Programmer FSP
Posted 18 days ago
Job Viewed
Job Description
Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.
**Position Overview:**
This position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Principal Statistical Programmer works independently with only concept level instruction and very little supervision, tracks progress, and provides expert technical support to team members. We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials.
**As a Principal Statistical Programmer, your responsibilities will include:**
+ Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies
+ Develop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs
+ Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs' needs
+ Participate in overseeing CRO's statistical programming deliverables for multiple clinical studies to ensure high-quality and meet the pre-specified timelines
+ Support the preparation of clinical study reports, regulatory submissions, publications, annual DSUR, and exploratory analyses
+ Understand and follow FDA regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions.
+ Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros
+ Participate in the development of CRFs, edit check specifications, and data validation plans
+ Provide review and/or author data transfer specifications for external vendor data
+ Collaborate with internal and external functions (e.g. CROs, software vendors, clinical development partners, etc.) to ensure meeting project timelines and goals
+ Provide review and/or author SOPs and/or Work Instructions related to statistical programming practices
**Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:**
+ At a minimum bachelor's degree in computer science, data science, mathematics, or statistics major preferred
+ 7+ years of experience as a Statistical Programmer on a Biotech/Pharma Clinical Development Biometrics Team or with a similar team and experience supporting drug development, medical device development, or intervention studies
+ Exceptional SAS programming skills and expertise in the development and implementation of statistical programming procedures and processes in a clinical development environment
+ Extensive applied experience of CDISC standards (SDTM, ADaM, and Define.xml), medical terminology, clinical trial methodologies, and FDA/ICH regulation
+ Experience supporting regulatory submissions, interacting with the FDA and/or global regulatory authorities
+ Must be able to work independently
+ Outstanding communication skills (written and verbal) and strong leadership skills
**Preferred Qualifications (nice to have)**
+ Prior work experience with pharmacokinetic data and the neuroscience field,
+ proficiency in languages or tools other than SAS (e.g., R, Python, and Java, Shiny, Markdown, Unix/Linux and git)
Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.
Engineer, International Spectrum Management and Strategy, Project Kuiper, International, Kuiper R...
Posted 20 days ago
Job Viewed
Job 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
- Master's degree in Electrical Engineering or related discipline (telecommunications)
- Experience analyzing dynamic interference from satellite systems and/or other radiocommunication systems
Preferred Qualifications
- 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.