Regulatory affairs manager Work, Jobs in Uxbridge (with Salaries)

EU Regulatory Affairs Manager
Amgen —London
- £48,957 - £66,237 a year
- Remote
- Research
- Conflict management
- AI
- Work from home
Regulatory Affairs Manager
pladis —Chiswick Park Station
- Full-time
GB Sr. Manager, Regulatory Affairs - Europe
The Bountiful Company —London
- Writing skills
- Bachelor's degree
- Training & development
Quick apply
Vice President, Regulatory Affairs – ELMAC
Amgen —Uxbridge
- Doctoral degree
- Master's degree
- Bachelor's degree
Regulatory Affairs Officer
River Manufacturing Ltd —Sunbury
- £21,000 - £25,000 a year
- Part-time
- Analysis skills
- Continuous improvement
- In-person
- Free parking
Quick apply
13h
Professional Veterinary Affairs Manager UK & Ireland (175066)
Colgate-Palmolive —Surrey
- £70,650 - £78,500 a year
- Doctoral degree
- Sales
- Business development
Regulatory Affairs Manager
Vodafone —London
- Full-time
- Analysis skills
- AI
- Leadership
- Annual leave
Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
Global Regulatory Affairs Manager
GlaxoSmithKline —London
- Full-time
- Doctoral degree
- Writing skills
- Bachelor's degree
1d
Medical Affairs Coordinator
Servier —Slough
- Microsoft Office
- Databases
- Administrative experience
Manager - Regulatory Affairs Lifecycle Management - Medicines
Perrigo —London
- Hybrid work
- Marketing
- English
- Continuous improvement
Senior Manager – ESG and Sustainability Regulatory Legal
Pwc UK —London
- Full-time
- Hybrid work
- Business development
- Analysis skills
- Presentation skills
Regulatory Affairs & Quality Manager – Medical Devices / IVD
Mitra Bio —London
- Full-time
7d
Manager, Oncology Regulatory Strategy
Pfizer —Walton-on-Thames
- Full-time
- Hybrid work
- Communication skills
- Negotiation
6d
Quality Assurance & Regulatory Affairs Executive - Maternity Cover
TensCare Ltd —Epsom
- £35,000 - £42,500 a year
- Temporary
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Team management
- Profit sharing
- Work from home
Quick apply
Associate Director, Precision Medicine (Clinical Diagnostics)
Regeneron —Uxbridge
- Doctoral degree
- Annual leave
Executive Director, Global Patient Safety Sciences Delivery
Regeneron —Uxbridge
- Management
- Doctoral degree
- Master's degree
- Annual leave
Financial Crime & Due Diligence Analyst
Centrica —Windsor
- Analysis skills
- Travel
- Communication skills
2d
Regulatory Engagement & Advocacy Manager – UK and France
Nadara —London
- Full-time
- Analysis skills
- Team management
- Communication skills
Regulatory Quality Assurance Manager
Alliance Medical Ltd —Guildford
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Continuous improvement
Quick apply

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regulatory affairs manager jobs near uxbridge

EU Regulatory Affairs Manager

Amgen -
London

Apply Now

Job details

£48,957 - £66,237 a year

Benefits

Work from home

Qualifications

Research
Conflict management
Clinical trials
AI
Communication skills
Negotiation

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: Aug. 13, 2026 CATEGORY: Regulatory

HOW MIGHT YOU DEFY IMAGINATION?

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.

EU REGULATORY AFFAIRS MANAGER

LIVE

What you will do

In this vital role you will work to ensure that Amgen acquires and maintains all the required EU licenses in order to support clinical trials for investigational medicinal products as well as marketed medicinal products.

You will support one or more products from an EU regulatory perspective.

Strategy and Execution

Depending on business needs and experience, the role may include EU Regulatory Lead responsibility for 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 and EU regional regulatory requirements.

Under general supervision, implement product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with EU regional legislation and regulatory requirements. Provide content guidance for regional regulatory documents and meetings in accordance with global strategy.

Provide regulatory guidance on regional regulatory mechanisms to optimize product development (e.g. expediting FIH studies, scientific advice, Orphan Drug, MA approval mechanisms and paediatric plans).

Support EU label negotiation activities.

Under general supervision participate in 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, precedence and 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 x3 EU Regulatory Affairs Managers between Portugal and the United Kingdom, joining the EU Oncology or General Medicine teams, part of the Global Regulatory Affairs function in Europe.

You will be working with colleagues who are responsible for leading the European regulatory strategies and submissions for development and marketed products from first-in human clinical trials to marketing authorisation, 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 we seek in you as an experienced professional, are these qualifications and skills:

Degree educated and previous experience in a similar role

Hands-on experience with registration procedures in the region, such as clinical trials, pre-MAA regulatory procedures (eg scientific advice, orphan applications or Paediatric Investigation Plans (PIPs)), MA, post-approval changes, extensions and renewals

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

Knowledge of EU legislation and regulations relating to medicinal products

Working with policies, procedures and SOP’s .

Strong communication skills - both oral and written.

Ability to anticipate and prevent potential issues.

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

Basic proficiency in 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 opportunities to learn and 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 Plan comprising health, finance and wealth, work/life balance, and career benefits

LOCATION: Flexibility to work from home with few days per month working from our Cambridge, Uxbridge or Lisbon office.

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 patients above 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 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.

Apply Now

Refine Your Search

regulatory affairs manager jobs in uxbridge

EU Regulatory Affairs Manager

Regulatory Affairs Manager

GB Sr. Manager, Regulatory Affairs - Europe

Vice President, Regulatory Affairs – ELMAC

Regulatory Affairs Officer

Professional Veterinary Affairs Manager UK & Ireland (175066)

Regulatory Affairs Manager

Senior Regulatory Affairs Specialist

Global Regulatory Affairs Manager

Medical Affairs Coordinator

Manager - Regulatory Affairs Lifecycle Management - Medicines

Senior Manager – ESG and Sustainability Regulatory Legal

Regulatory Affairs & Quality Manager – Medical Devices / IVD

Manager, Oncology Regulatory Strategy

Quality Assurance & Regulatory Affairs Executive - Maternity Cover

Associate Director, Precision Medicine (Clinical Diagnostics)

Executive Director, Global Patient Safety Sciences Delivery

Financial Crime & Due Diligence Analyst

Regulatory Engagement & Advocacy Manager – UK and France

Regulatory Quality Assurance Manager

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