Regulatory Affairs Specialist

CK Group- Science, Clinical and Technical
London
11 months ago
Applications closed

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Regulatory Affairs Engineer - Medical Devices - Cambridge

Newton Colmore Cambridge, United Kingdom
Posted
1 Dec 2025 (11 months ago)

CK Group are recruiting for a Regulatory Affairs Specialist to join a fast growing software platform that is simplifying global product compliance. This role will be based in London on a permanent basis.

Company:
The client manage a number of regulatory products designed to support regulatory compliance.

Location:
The role is based in Central London and is hybrid with 3 days a week on site.

Role:

Ensuring all our regulatory products are up to date, these include Regulatory Intelligence, artwork, labelling and SDS tools.
Support in building and managing the regulatory tools.
Codifying regulatory knowledge into the platform.
Acting as a voice of authority around key regulations and regulatory topics.
Create content, webinars and written pieces.Your Background:

Educated to degree level in a relevant life sciences field with experience in Regulatory Affairs.
Experience in a Regulatory Affairs role in food, supplements, pharma or cosmetics and comfortable in learning other Regulations
Flexibility to switch between product categories and markets.
Comfortable acting as the Regulatory face of the company, comfortable in front of the camera and be actively looking to build a profile in the space.
Proficient across excel as there is a significant amount of translating regulatory logic into rules for the system to ingest.Apply:
For more information, or to apply for this Regulatory Affairs Specialist position please contact Mary Bolt on (phone number removed) or email (url removed). Please quote job reference (phone number removed) in all correspondence.
It is essential that applicants hold entitlement to work in the UK

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