EU Regulatory Affairs Manager

Amgen SA; Greater London; Hybrid; GBP 70,000 - 110,000; Full time

Job summary

Amgen seeks an EU Regulatory Affairs Manager to drive submissions for clinical trials and marketed products from a regulatory perspective within the EU region. The role involves developing strategies, providing guidance on regional mechanisms, and supporting label negotiations. Flexible to work from home with periodic presence in UK offices.

The candidate will contribute to regulatory strategy for products in development and lifecycle management, aligning with global plans and EU requirements.

Qualifications

• Degree educated with previous experience in a regulatory role.
• Experience with registration procedures (clinical trials, MA, post-approval changes).
• Experience developing regulatory strategies for products in development and post-marketing.
• Knowledge of EU legislation and regulations for medicinal products.
• Knowledge of policies, procedures and SOPs.
• Strong written and spoken communication skills.
• Ability to anticipate and prevent issues.
• Basic proficiency in using AI tools to support day-to-day work.

Responsibilities

• Plan and manage regulatory submissions for EU region.
• Provide regulatory guidance on regional mechanisms to optimize development.
• Support EU label negotiation activities.
• Develop regional regulatory product strategies.
• Stay aware of new legislation and regulatory guidance.

Skills

Regulatory strategy

Regulatory knowledge

Communication skills

Issue prevention

Conflict resolution

AI tools

Education

Bachelor's degree in life sciences

Tools

AI tools

Job description

If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.

EUREGULATORY AFFAIRS MANAGER

LIVE

What you will do

In this vital role you will work to ensure that Amgenacquiresandmaintainsall the requiredEUlicensesin order tosupport clinical trials for investigational medicinal products as well as marketedmedicinal products.

You will support one or more products fromanEUregulatory perspective.

Strategy and Execution

• Depending on business needs and experience, the role may includeEU Regulatory Leadresponsibilityfor one or more products.

• Plan and manage regulatory submissions (e.g.clinical trial and marketing applications) for products within Amgen's portfolio in compliance with global filing plans andEUregionalregulatory requirements.

• Under general supervision, implement product related regulatory strategies, Regulatory Affairsprocessesand activity planningin accordance withEU regionallegislation and regulatoryrequirements. Providecontent guidance for regional regulatory documents and meetingsin accordance withglobal strategy.

• Provideregulatory guidance on regional regulatory mechanisms tooptimizeproduct development (e.g.expediting FIH studies,scientificadvice,Orphan Drug,MA approvalmechanismsandpaediatricplans).

• SupportEUlabel negotiation activities.

• Under general supervisionparticipatein the development and execution of regional regulatory product strategies.

• Under general supervision, develop predictions for expectations and risks associated with outcomes by regulatory agencies.

Regulatory Research

• Maintain an awareness of new and developing legislation, regulatory policy and technical Regulatory guidance relating to Amgen products.

• Perform regulatory research to obtain relevant histories,precedenceand other information relevant to regional product advancement.

• Under supervision evaluate and communicate impact of relevant regional regulations,guidances, current regulatory environment and competitor labelling.

Be part of our team

We are currently looking for x3EURegulatory Affairs Managers between Portugal and the United Kingdom, joining theEUOncology or General Medicine teams, part of the Global Regulatory Affairs function in Europe.

You will be working with colleagues whoare responsible forleading the European regulatory strategies and submissions for development and marketed products from first-in human clinical trials to marketingauthorisation, and throughout the products lifecycle.

WIN

What we expect of you

We are all different, yet we all use our unique contributions to serve patients.What weseekin you as anexperiencedprofessional, are these qualifications and skills:

• Degreeeducatedandpreviousexperience in a similar role

• Hands-on experience withregistration procedures intheregion, such asclinical trials,pre-MAA regulatory procedures(egscientificadvice, orphanapplicationsorPaediatricInvestigation Plans(PIPs)),MA, post-approval changes,extensionsand renewals

• Experience developing regulatory strategies for products in clinical development and post-marketing phases.

• Knowledge ofEUlegislation and regulations relating to medicinal products

• Working with policies, procedures andSOP’s.

• Strong communicationskills - both oral and written.

• Ability toanticipateand prevent potential issues.

• Ability to resolve conflicts and develop a course of action leading to a beneficial outcome.

• Basicproficiencyin using AI tools to support day-to-day work.

THRIVE

What you can expect of us

As we work to develop treatments that take care of others, we work to care for our teammates’ professional and personal growth and well-being.

• Growth opportunitiestolearnand move up and across our global organization

• Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act

• Generous Total Rewards Plancomprisinghealth, finance and wealth, work/life balance, and career benefits

LOCATION:

Flexibility to work from home with few days per month working from our Cambridge orUxbridgeoffices.

Equal Opportunity Statement

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.