Regulatory affairs manager Work, Jobs in London, Gtl (with Salaries)

EU Regulatory Affairs Manager
Amgen —London
- £48,957 - £66,237 a year
- Remote
- Work from home
Senior Manager Regulatory Affairs Lifecycle Management Medical Devices
Perrigo —London
- Hybrid work
- Bachelor's degree
- In-person
- Leadership
Senior Regulatory Affairs Manager (UK/Ireland)
Perrigo —London
- Hybrid work
- In-person
- Leadership
1d
Manager - Regulatory Affairs Lifecycle Management - Medicines
Perrigo —London
- Hybrid work
- Marketing
- In-person
- Leadership
2d
Regulatory Affairs Manager
Vodafone —London
- Full-time
- Analysis skills
- Leadership
- Communication skills
- Annual leave
GB Sr. Manager, Regulatory Affairs - Europe
The Bountiful Company —London
- Bachelor's degree
- Leadership
- Communication skills
Quick apply
Senior Manager/Associate Director, Government and Regulatory Affairs
Access Partnership —London
- Hybrid work
Quick apply
Senior Manager – ESG and Sustainability Regulatory Legal
Pwc UK —London
- Full-time
- Hybrid work
- Analysis skills
- Presentation skills
Regulatory Affairs Manager
pladis —Chiswick Park Station
- Full-time
Regulatory Affairs Knowledge Management Capability Lead
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Hybrid work
- AI
- Leadership
3d
Head of Licensing and Regulatory Authorisations
Tether Operations Limited —London
- Full-time
- Remote
- English
- Supervising experience
- Project management
Senior Regulatory Specialist
Androlabs —London
- £85,000 - £108,000 a year
- Full-time
- Hybrid work
- IT
- Annual leave
Quick apply
Account Manager (Public Affairs)
Hanbury Strategy —London
- Hybrid work
- Project management
- Mentoring
- Leadership
- Health & wellbeing programme
- Annual leave
Associate Director - Regulatory Affairs Operations
Perrigo —London
- Hybrid work
- In-person
- Leadership
Sr Manager, Nordics& NECAD, International Patient Engagement
Vertex Pharmaceuticals —Paddington
- Full-time
- English
- Project management
12d
Regulatory Engagement & Advocacy Manager – UK and France
Nadara —London
- Full-time
- Analysis skills
- Communication skills
Manager Global Scientific Affairs
Sobi —London
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
2d
Single Sponsor Clinical Project Manager II (Virology) - 1-2 days in Uxbridge (offices moving to London in May26)
Syneos - Clinical and Corporate - Prod —London
- Full-time
- PMP
- Project management
- Bachelor's degree
Scientific Affairs Manager, UK - London
Rhythm Pharmaceuticals —London
- Full-time
- Doctoral degree
- Presentation skills
- Communication skills
REACH Regulatory Manager
ERM Group —London
- Full-time
- English
- IT
- Leadership

I want to receive the latest job alerts for regulatory affairs manager in london, gtl

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

regulatory affairs manager jobs near london, gtl

EU Regulatory Affairs Manager

Amgen -
London

Apply Now

Job details

£48,957 - £66,237 a year

Benefits

Work from home

Full job description

United Kingdom - Uxbridge

JOB ID: R-239862 LOCATION: United Kingdom - Uxbridge ; United Kingdom - Manchester; United Kingdom - Remote; Portugal - Lisbon; Portugal - Remote; United Kingdom - London; United Kingdom - Cambridge; United Kingdom - Edinburgh WORK LOCATION TYPE: Flex Commuter / Hybrid DATE POSTED: Jul. 13, 2026 CATEGORY: Regulatory

HOW MIGHT YOU DEFY IMAGINATION?

If you feel likeyou’repart of something bigger,it’sbecause you are. AtAmgenour 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,manufacturingand delivering ever-better products that reachover10 million patientsworldwide.It’stime 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 froman EUregulatory 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 anexperienced professional, are these qualifications and skills:

Degreeeducatedandpreviousexperience in a similar role

Hands-on experience withregistration procedures intheregion, such asclinical trials,pre-MAA regulatory procedures(egscientificadvice, orphanapplicationsor PaediatricInvestigation 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,Uxbridgeor Lisbonoffice.

The expected gross pay range for this role in Portugal is EUR 48,957.00 to 66,237.00. Actual pay will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications.

for a career that defies imagination

In our quest to serve patientsabove all else, Amgen is the first to imagine, and the last to doubt. Join us.

careers.amgen.com

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

We will ensure that individuals with disabilities are provideda reasonableaccommodation toparticipatein the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to requestan accommodation.

Apply Now

Refine Your Search

regulatory affairs manager jobs in london, gtl

EU Regulatory Affairs Manager

Senior Manager Regulatory Affairs Lifecycle Management Medical Devices

Senior Regulatory Affairs Manager (UK/Ireland)

Manager - Regulatory Affairs Lifecycle Management - Medicines

Regulatory Affairs Manager

GB Sr. Manager, Regulatory Affairs - Europe

Senior Manager/Associate Director, Government and Regulatory Affairs

Senior Manager – ESG and Sustainability Regulatory Legal

Regulatory Affairs Manager

Regulatory Affairs Knowledge Management Capability Lead

Head of Licensing and Regulatory Authorisations

Senior Regulatory Specialist

Account Manager (Public Affairs)

Associate Director - Regulatory Affairs Operations

Sr Manager, Nordics& NECAD, International Patient Engagement

Regulatory Engagement & Advocacy Manager – UK and France

Manager Global Scientific Affairs

Single Sponsor Clinical Project Manager II (Virology) - 1-2 days in Uxbridge (offices moving to London in May26)

Scientific Affairs Manager, UK - London

REACH Regulatory Manager

I want to receive the latest job alerts for regulatory affairs manager in london, gtl

Related Searches

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected