Regulatory Affairs Specialist

Quanta part of QCS Staffing; London; On-site; GBP 45,000 - 65,000; Full time

Job summary

A leading global pharmaceutical client is seeking an experienced Regulatory Affairs Specialist for a 12-month contract in London. The role involves ensuring compliance with regulatory standards, project management of dossiers, and strategic contributions to the RA Department. The ideal candidate will have a B.S. in a relevant field and significant experience in cosmetic regulations.

Qualifications

• Significant experience in Cosmetic Regulatory affairs.
• Well versed with UK ASA, CAP, BCAP Guidance.
• Strong knowledge of UK & EU Cosmetic Product Regulation.

Responsibilities

• Ensures compliance with regulatory agency regulations.
• Develops timelines for submissions under senior staff direction.
• Provides regulatory advice to project teams.

Skills

Leadership

Communication

Attention to detail

Education

B.S. Chemistry, Biology, or related fields

Job description

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Regulatory Affairs Specialist, Central London

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Client:

Quanta part of QCS Staffing

Location:

Central London, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

d89f48117314

Job Views:

46

Posted:

24.06.2025

Expiry Date:

08.08.2025

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Job Description:

Regulatory Affairs Specialist - London - 12-Month Contract

Do you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring the expertise of an experiencedRegulatory Affairs Specialist.


Responsibilities:

Ensures compliance with regulatory agency regulations and interpretations.

Prepares responses to regulatory agencies' questions and other correspondence.

Gathers and assembles information necessary for submissions in accordance with regulations and relevant guidelines.

Develops timelines for submissions under the direction of senior regulatory affairs staff.

Provides solutions to extreme complex problems in which data analysis requires an evaluation of intangible variables.

Provides regulatory advice to project teams.

Organises and maintains reporting schedules for new drug application and investigations new drug applications.

Requirements:

Minimum B.S. Chemistry, Biology, or related fields

Significant experience in Cosmetic Regulatory affairs mainly with promotional material and artwork review/approval at all stages of life cycle management, with demonstrated accountability of managing multiple brands.

Well versed with UK ASA, CAP, BCAP Guidance for Advertising, proven record of successful project management of dossiers with ClearCast

Strong knowledge and application of the UK & EU Cosmetic Product Regulation

Excellent leadership, communication, and organisational skills

Attention to detail, effective in written and oral communication

Works independently to plan, conduct, and manage regulatory projects to meet department and company objectives

Responsible for identifying, implementing and managing key RA Departmental projects and/or strategies based on both short- and long-term RA Department objectives.

If this role is of interest to you, please apply now!

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