Regulatory Affairs Specialist

TN United Kingdom; London; On-site; GBP 40,000 - 70,000; Full time

Job summary

Join a forward-thinking global pharmaceutical company as a Regulatory Affairs Specialist in Central London. This 12-month contract role offers the opportunity to support regulatory compliance and submissions for a diverse range of products. You will ensure adherence to regulatory guidelines, prepare responses for regulatory inquiries, and manage timelines for submissions. Ideal candidates will have a strong background in Cosmetic Regulatory affairs, excellent communication skills, and the ability to work independently on complex projects. This is an exciting opportunity to contribute to a leading company in the pharmaceutical industry.

Qualifications

• Significant experience in Cosmetic Regulatory affairs.
• Strong understanding of UK & EU Cosmetic Product Regulations.

Responsibilities

• Ensure compliance with regulatory agency regulations and guidelines.
• Prepare responses to regulatory agencies' questions and correspondence.

Skills

Regulatory Compliance

Data Analysis

Project Management

Communication Skills

Attention to Detail

Education

B.S. in Chemistry

B.S. in Biology

Job description

Regulatory Affairs Specialist, Central London

Client: Quanta part of QCS Staffing

Location: Central London, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: d89f48117314

Job Views: 5

Posted: 05.05.2025

Expiry Date: 19.06.2025

Job Description:

Regulatory Affairs Specialist - London - 12-Month Contract

Join a forward-thinking global pharmaceutical company with facilities in over 60 countries. We are seeking an experienced Regulatory Affairs Specialist to support our client’s regulatory compliance and submissions.

Responsibilities:

• Ensure compliance with regulatory agency regulations and guidelines.
• Prepare responses to regulatory agencies' questions and correspondence.
• Gather and compile information for submissions according to regulations and guidelines.
• Develop timelines for submissions under supervision of senior regulatory staff.
• Provide solutions for complex problems involving data analysis and intangible variables.
• Advise project teams on regulatory matters.
• Organize and maintain reporting schedules for drug applications and investigations.

Requirements:

• B.S. in Chemistry, Biology, or related field.
• Significant experience in Cosmetic Regulatory affairs, especially with promotional material and artwork review/approval across product lifecycle, managing multiple brands.
• Knowledge of UK ASA, CAP, BCAP Guidance for Advertising, and successful project management of dossiers with ClearCast.
• Strong understanding of UK & EU Cosmetic Product Regulations.
• Excellent leadership, communication, and organizational skills.
• Attention to detail and effective written and oral communication skills.
• Ability to work independently on regulatory projects to meet departmental and company goals.
• Experience in managing key RA projects and strategies aligned with departmental objectives.

If interested, please apply now!