regulatory affairs Work, Jobs in cambridge (with Salaries)

Senior Associate Regulatory Affairs
Amgen —Cambridge
- Marketing
- Project management
- Organisational skills
Regulatory Affairs Intelligence Director
AstraZeneca —Cambridge
- Communication skills
7d
Senior Manager, Regulatory Affairs
Hologic —Cambridge
- Engineering
- Analysis skills
- Leadership
Regulatory Affairs Systems and Data Manager
Mundipharma —Cambridge
- Full-time
- Hybrid work
- Communication skills
Scientific Communications and Engagement Lead
Cycle Pharmaceuticals —Cambridge
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Gym membership
- Flexible schedule
8d
Principal Medical Writer - FSP
IQVIA —Cambridge
- Full-time
- Remote
- Microsoft Word
- Doctoral degree
- Master's degree
9h
Compliance Professional Middle East & Africa
Thermo Fisher Scientific —Cambridge
- Full-time
- Hybrid work
- Doctoral degree
- English
- Bachelor's degree
7d
Senior Manager, Market Access Specialty Care
Sobi —Cambridge
- Full-time
- Remote
- Doctoral degree
- English
- Master's degree
Quick apply
12d

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Regulatory Affairs Intelligence Director
AstraZeneca —Cambridge
Proactively Conduct analysis of new drug development and regulatory approaches on e.g. novel clinical trial concepts, RWE, early regulatory access, adaptive/…
7d
Director, Regulatory Affairs, EU Services
Bio Pharma Resourcing —London
The Director, EU Regulatory Services will be expected to direct the EU Regulatory Services team and drive Liquent Direct Outsourcing sales in Europe working…
£60,000 a year

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regulatory affairs jobs near cambridge

Senior Associate Regulatory Affairs

Amgen -
Cambridge

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Job details

Qualifications

Marketing
Project management
Organisational skills
Communication skills

Full job description

United Kingdom - Cambridge

JOB ID: R-242652 LOCATION: United Kingdom - Cambridge ; United Kingdom - Uxbridge WORK LOCATION TYPE: Flex Commuter / Hybrid DATE POSTED: Apr. 22, 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.

SENIOR ASSOCIATE REGULATORY AFFAIRS - UK & IRELAND

LIVE

What you will do

In this vital role you will support and, where appropriate, lead in the local coordination and execution of regulatory submissions in compliance with Amgen corporate standards and national regulatory requirements, as well as Regulatory Affairs processes and deliverables for the UK and Ireland.

Ensure regulatory submissions are made on time and meet Amgen’s corporate and local regulatory requirements and support licence and clinical trials activities
Contribute to and execute local filing plans
Act as a key contact for agency interactions for an assigned portfolio of products
Collate, distribute, exchange and archive regulatory information with colleagues across the business
Participate in regulatory and affiliate process improvements initiatives
Review promotion and non-promotion materials to ensure compliance with local licence, company procedures and Code of Practice

Be part of our team

Reporting to the Director Regulatory Affairs UK & Ireland Affiliate, you would be joining a team of 10 regulatory professionals passionate about delivering the best outcomes for our medicines to patients.

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
Experience in the management of marketing authorisations in the UK and the EU
Experience in/knowledge of developing and maintaining clinical trial documentation in UK and the EU (e.g. IMPDs, IMPD amendments) and ability to work with increasing autonomy
Knowledge and awareness of the relevant regulatory guidelines and legislation
Strong communication skills both oral and written
Organisational skills & developing or demonstrated regulatory project management skills
Experience with Veeva Vault

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: Ability to work flexibly from home with regular office work either from our Cambridge or Uxbridge next generation workspace.

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

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

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regulatory affairs jobs in cambridge

Senior Associate Regulatory Affairs

Regulatory Affairs Intelligence Director

Senior Manager, Regulatory Affairs

Regulatory Affairs Systems and Data Manager

Scientific Communications and Engagement Lead

Principal Medical Writer - FSP

Compliance Professional Middle East & Africa

Senior Manager, Market Access Specialty Care

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