Cmc regulatory Work, Jobs (with Salaries)

Sr Associate Regulatory Affairs - CMC
Amgen —London
- Project management
- Organisational skills
- Communication skills
5d
Project Manager, CMC
Iksuda Therapeutics —Newcastle upon Tyne
- £42,000 - £48,000 a year
- Full-time
- Hybrid work
- Master's degree
- Project management
- Presentation skills
- Health & wellbeing programme
- Work from home
Quick apply
12d
Global Change Facilitator – Regulatory CMC
BioPhorum —London
- Full-time
- Project management
- No degree
- Organisational skills
Quick apply
Regulatory Associate - UK Medicines
Reckitt —Slough
- Data analysis skills
- Communication skills
- Employee assistance programme
- Life insurance
1d
Regulatory CMC strategy manager
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Annual leave
- Employee assistance programme
Associate Director, CMC Regulatory Affairs, International
Moderna, Inc. —London
- Full-time
- Engineering
- Master's degree
- Bachelor's degree
- Annual leave
12d
Associate Director, CMC Regulatory Science, International
Moderna, Inc. —London
- Full-time
- Doctoral degree
- Master's degree
- Annual leave
CMC Process Development Manager
SERB Pharmaceuticals —Wales
- Bachelor's degree
- No degree
- Business
5d
Associate Director, CMC Regulatory Affairs (Hematology/Oncology)
Regeneron —Uxbridge
- Bachelor's degree
- IT
- In-person
- Annual leave
1d
Regulatory Affairs Executive
Sandoz —Bracknell
- Full-time
- Project management
- Agile
- Annual leave
17h
CMC Analytical Lead
Engitix —London
- Doctoral degree
- Master's degree
- Project management
Quick apply
9d
Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
Regulatory Affairs Associate/Manager
Transpire BIO Inc. —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Formulation Development Scientist
Immunocore —Oxford
- Doctoral degree
- Master's degree
- Bachelor's degree
Analytical Chemist, Quality Control
Pharmaron —Rushden
- Computer literacy
- Communication skills
- Time management
9d
Compliance Advisory Officer
CMC Markets —London
- Full-time
- Analysis skills
- Communication skills
10d
Associate Analytical Chemist, Quality Control
Pharmaron —Rushden
- Laboratory experience
- Bachelor's degree
- Communication skills
4d
Quality Assurance Advisor (GLP/GCP)
Pharmaron —Rushden
- Communication skills
Quick apply
Senior Analytical Chemist, Quality Control
Pharmaron —Rushden
- Analysis skills
- Communication skills
- Time management
Quick apply
8d
Exec Director, Regulatory Affairs
Gilead Sciences —Uxbridge
- Full-time
- Hybrid work
- Management
- Doctoral degree
- English
11d

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Sr Associate Regulatory Affairs - CMC

Amgen -
London

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Job details

5 days ago

Qualifications

Project management
Product development
Organisational skills
Communication skills

Full job description

United Kingdom - Uxbridge

JOB ID: R-246537 LOCATION: United Kingdom - Uxbridge ; United Kingdom - London; United Kingdom - Cambridge WORK LOCATION TYPE: Flex Commuter / Hybrid DATE POSTED: Jun. 08, 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 – CMC

LIVE

What you will do

In this vital role you will interface with the Amgen global, international, site and biosimilars Regulatory Affairs, Chemistry, Manufacturing and Controls (RA CMC) teams and the device team for specific strategies or activities that impact a product. You will be responsible for varying levels of product support, including leading projects, based upon their experience level.

The RA CMC facilitates product development and global registration by developing and executing regulatory strategies and managing effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle.

Contribute as a key member of the global regulatory CMC product team
Interact with authors/reviewers and subject matter experts with respect to delivery of regulatory documents required for regulatory submissions
Contribute to the organization and preparation of CMC investigational product amendments, post‑market supplements/variations, and new marketing applications
Document and archive CMC submissions and related communications in the document management system
Initiate and maintain CMC product timelines at the direction of product lead
Interface with the regulatory operations team
Train staff on select CMC procedures and systems
Provide report status of activities and projects to teams and department
Participate in cross-functional special project teams

Be part of our team

You be joining a supportive and diverse team, where comprehensive regulatory training is provided, alongside a buddy system and exposure to a wide variety of projects and therapy areas.

The Regulatory Optimization of Technical, Surveillance, and Strategic Support (ROOTS2) group within RA CMC, supports CMC submission execution for Amgen products across phases of development, modality and countries.

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
Background in CMC related functions (e.g., Quality, Manufacturing, etc) with limited or no prior Regulatory Affairs experience.
Curious, proactive, confident in tackling new challenges, and comfortable working collaboratively in a fast-paced learning environment.
Developed project management and organizational skills
Strong and effective oral and written communication skills

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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