Senior Manager, Global Labelling, Regulatory

JR United Kingdom; London; Remote; GBP 70,000 - 90,000; Full time

Job summary

A leading company is seeking a Senior Manager for Global Labelling in London. This role involves developing labelling documents and guiding product teams to align with labelling strategy. Flexible working options are available, making it an attractive opportunity for seasoned Regulatory Affairs professionals.

Benefits

Flexible working options

Qualifications

• Experience developing the CCDS, EU & USPI.
• Strong writing skills for labelling content.
• Ability to influence labelling team decisions.

Responsibilities

• Develop and maintain core labelling documents.
• Provide labelling guidance to product teams.
• Present proposed CCDS to the Executive Labelling Committee.

Skills

Regulatory Affairs

Labelling Strategy

Documentation

Job description

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Senior Manager, Global Labelling, Regulatory, London

Client:

Hays

Location:

London, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

Job Views:

3

Posted:

26.06.2025

Expiry Date:

10.08.2025

Job Description:

Senior Manager, Global Labelling

Your new company

One of my clients is looking for an experienced Regulatory Affairs Labelling Professional to join the team on a 12-month contracting basis. This is a remote contract job outside IR35.

Your new role

The key role as Senior Labelling Manager is to develop and maintain core labelling documents, create EU and USPI, and support local product information throughout the product lifecycle in accordance with processes. You will provide labelling guidance to support product teams and senior management in defining labelling strategy. As a Senior Labelling professional, you will influence labelling team decisions based on precedent labelling negotiations experience and obtain alignment on proposed CCDS wording. Present proposed CCDS and key differences with EU-USPI to the Executive Labelling Committee (ELC) with support from the product team to secure internal approval before submitting major labels. Review scientific data, write effectively, and summarise in the appropriate detail for labelling content. Provide input for the production of high-quality documents supporting changes to labelling content.

What you'll need to succeed

It is essential that applicants have experience developing the CCDS, EU, and USPI.

What you'll get in return

Flexible working options available.

What you need to do now

If you're interested in this role, click 'apply now' to submit an up-to-date CV or contact us directly. If this job isn't quite right but you're seeking a new position, please contact us for a confidential career discussion.