Regulatory affairs lead Work, Jobs in Potters Bar, Hrt (with Salaries)

European Regulatory Affairs Lead
Amgen —London
- £68,000 - £92,000 a year
- Work from home
19h
Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK
Cepheid —Amersham
- Full-time
- Remote
- Master's degree
- Bachelor's degree
- Annual leave
Regulatory Affairs Knowledge Management Capability Lead
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Hybrid work
- Leadership
8d
Nutrition Specialist (Global Regulatory & Corporate Affairs)
Oatly AB —London
- Part-time
- Hybrid work
- English
- Master's degree
- Travel
Quick apply
Global Value, Access & Government Affairs Lead
Mundipharma —London
- Full-time
- Doctoral degree
- Master's degree
- Business development
Regulatory, Data Protection and Ethics Lead
Foundation Partners —London
- Hybrid work
- AI
- Negotiation
Quick apply
7d
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
1d
Quality and Regulatory Manager
Advanced Healthcare Technology Ltd —Waltham Cross
- £50,000 - £60,000 a year
- Full-time
- No degree
- Organisational skills
- In-person
- Free parking
Quick apply
GB Sr. Manager, Regulatory Affairs - Europe
The Bountiful Company —London
- Writing skills
- Bachelor's degree
- Training & development
Quick apply
Head of Quality Assurance and Regulatory Affairs
Qureight Ltd —London
- Full-time
- Hybrid work
- Project management
- Bachelor's degree
- Continuous improvement
- Annual leave
- Life insurance
Quick apply
14d
Senior ESG Regulatory Operations Associate
Ralph Lauren —London
- Full-time
- Hospitality
- Organisational skills
Director - Regulatory Affairs Lifecycle Management Non-Medicines
Perrigo —London
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Team management
1h
Lead, Licensing & Regulatory Affairs - Africa, Amazon Leo Global Licensing - EMEA
Amazon Kuiper Services Europe SARL, UK Branch —London
- Full-time
- Engineering
- Analysis skills
- Bachelor's degree
Director - Regulatory Affairs Lifecycle Management Medicines
Perrigo —London
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Team management
1h
Senior Medical Director, Global Medical Affairs – Neurosciences (Migraine Lead)
Ipsen Biopharm Ltd —London
- Full-time
- Doctoral degree
- English
- Leadership
South & EE Team Regulatory Affairs Lead
Shell Energy —London
- Full-time
- Engineering
- English
- Supervising experience
Regulatory Market Access Lead
Viasat, Inc. —London
- Full-time
- Communication skills
Associate Director - Regulatory Affairs Operations
Perrigo —London
- Hybrid work
- In-person
- Leadership
Regulatory Scientist
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Bachelor's degree
- Computer skills
Quick apply
Manager Global Scientific Affairs
Sobi —London
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Doctoral degree
Quick apply
7d

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European Regulatory Affairs Lead

Amgen -
London

Apply Now

Job details

£68,000 - £92,000 a year
19 hours ago

Benefits

Work from home

Qualifications

Stakeholder collaboration
Team leadership
Stakeholder liaison
Risk management
Contingency planning

Full job description

United Kingdom - Uxbridge

JOB ID: R-249387 LOCATION: United Kingdom - Uxbridge ; United Kingdom - London; United Kingdom - Cambridge; Portugal - Lisbon WORK LOCATION TYPE: Flex Commuter / Hybrid DATE POSTED: Aug. 05, 2026 CATEGORY: Regulatory

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.

EUROPEAN REGULATORY AFFAIRS LEAD

LIVE

What you will do

In this vital role, you will ensure Amgen obtains and maintains the regulatory licenses required to support clinical development and commercialization of medicinal products. You will represent the region in shaping regulatory strategy, providing regional expertise, and collaborating with stakeholders to ensure regional requirements are effectively incorporated into global plans.

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 local regulatory requirements
Implement product related regulatory strategies, Regulatory Affairs processes and activity planning
Lead development of regional regulatory documents and meetings in accordance with GRT strategy
Provide regulatory direction on regional regulatory mechanisms to optimize product development (e.g. expediting FIH studies, Orphan Drug, Fast Track, compassionate use and paediatric plan)
Participate in the development and execution of regional regulatory product strategies, including precedence, risk management and contingency planning
Consistent with GRT strategy, advise on regulatory implications and requirements related to global clinical development plans and objectives
Lead Health Authority and Agency Interactions and document and communicate outcomes appropriately

Be part of our team

You would be joining the European General Medicine Regulatory team, part of the Global Regulatory Affairs function in Europe. You would 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.

This team is leading the regulatory activities for established products and also development assets in the Metabolic, Cardiology, Inflamation, Endocrine and Bone disease areas, as well as pre-approval filing activities for Biosimilars.

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 in a scientific discipline
Extensive experience in regional regulatory environment
Proven track record of developing and executing regional regulatory strategy
In-depth understanding of the drug life cycle and development process from a regulatory perspective
In-depth understanding of the registration procedures in region for MA, post approval changes, extensions and renewals.
Ability to lead teams and work collaboratively in a dynamic environment
Proactive approach to problem solving
Ability to understand and communicate scientific/clinical information
Ability to anticipate regulatory agency expectations
Strong awareness of the needs of internal and external stakeholders, and the role of Regulatory Affairs in driving successful drug development

THRIVE

What you can expect of us

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

Vast 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 68,000.00 to 92,000.00. Actual pay will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications.

Application due date: 19th of August 2026

Objects in your future are closer than they appear. Join us.

careers.amgen.com

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.

Apply Now

Refine Your Search

regulatory affairs lead jobs in potters bar, hrt

European Regulatory Affairs Lead

Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK

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Nutrition Specialist (Global Regulatory & Corporate Affairs)

Global Value, Access & Government Affairs Lead

Regulatory, Data Protection and Ethics Lead

Quality Assurance & Regulatory Affairs Executive - Maternity Cover

Quality and Regulatory Manager

GB Sr. Manager, Regulatory Affairs - Europe

Head of Quality Assurance and Regulatory Affairs

Senior ESG Regulatory Operations Associate

Director - Regulatory Affairs Lifecycle Management Non-Medicines

Lead, Licensing & Regulatory Affairs - Africa, Amazon Leo Global Licensing - EMEA

Director - Regulatory Affairs Lifecycle Management Medicines

Senior Medical Director, Global Medical Affairs – Neurosciences (Migraine Lead)

South & EE Team Regulatory Affairs Lead

Regulatory Market Access Lead

Associate Director - Regulatory Affairs Operations

Regulatory Scientist

Manager Global Scientific Affairs

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