Regulatory Affairs Consultant

CK Group- Science, Clinical and Technical; Flackwell Heath; Hybrid; GBP 100,000 - 125,000; Full time

Job summary

A leading healthcare consulting firm is seeking a Regulatory Affairs Consultant for their High Wycombe site. The role involves developing regulatory strategies across the EMEA region, coordinating regulatory deliverables, and preparing submissions. Candidates should have a relevant degree and experience in regulatory affairs, along with strong knowledge of regulatory frameworks. The position allows hybrid work with 2-3 days on-site each week.

Qualifications

• 5+ years of experience in regulatory affairs, particularly with medicines and food supplements.
• Strong communication skills for cross-functional teams.
• Ability to develop and execute regulatory strategies.

Responsibilities

• Develop regulatory strategies across EMEA.
• Coordinate regulatory deliverables for medicines and food supplements.
• Prepare and submit regulatory submissions as per guidelines.

Skills

Regulatory knowledge

Regulatory frameworks understanding

Development of regulatory strategies

Education

Relevant Bachelor's Degree in Life Sciences, Chemistry, Pharmacy

Job description

Overview

Group are recruiting for a Regulatory Affairs Consultant, to join a company in the Pharmaceutical industry, at their site based in High Wycombe, on a contract basis initially for 6 months.

Salary: 59.18 per hour PAYE or 80.33 per hour Umbrella

Regulatory Affairs Consultant Role

• The Regulatory Affairs Consultant EMEA (Self Care) is responsible for the development of regulatory strategies across the EMEA region, and globally as relevant, providing regulatory input and technical guidance on regulatory requirements to product development teams within the Self Care franchise.
• Evaluates and coordinates the regulatory deliverables for medicines and food supplements, within their geographical and/or brand area of responsibility.
• Prepares and submits regulatory submissions according to applicable regulatory requirements and guidelines.
• Tracks the status of applications under regulatory review and provides updates to the regulatory team.
• Works with local and regional regulatory colleagues to develop global and/or regional regulatory strategies, coordinating regulatory actions and results and develops global/regional dossiers to support local review processes

Your Background

• Relevant Bachelor's Degree or higher in Life Sciences, Chemistry, Pharmacy
• Expertise across a broad spectrum of Regulatory classifications in particular medicine and food supplements in EMEA region
• Strong knowledge of regulatory frameworks and external environments, and the ability to apply these to regulatory solutions throughout the product lifecycle.
• Solid understanding of regulatory/medical/safety/quality requirements in the markets of relevance.
• In-depth knowledge of the business, organizational goals, Regulatory Affairs function, and cross functional business partners to make informed business decisions and create and execute business strategies. Ability to represent RA function on cross-functional teams and governance forums.

Company

Our client is the largest and most broadly-based healthcare company. They strive to improve access and affordability, create healthier communities, and put a healthy mind, body and environment within reach of everyone, everywhere.

Location

This role is based at our clients site in High Wycombe until December 2025, then in Reading from January 2026. This is a hybrid role with 2-3 days expected on site.

Apply

It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only).

Please note

This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

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