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Regulatory Affairs Manager

Phaidon EPM London · Dundee, United Kingdom · On-site · Senior

  • Dundee, United Kingdom · On-site
  • 12 months

Indexed (6 days ago) · refreshed constantly

Start
date 1/2027
Duration
12 months
Work mode
On-site
Contract
Freelance / B2B
Seniority
Senior
Reference
3063321

Required skills

Job description

Project overview

Regulatory Affairs Consultant | Contract

Responsibilities

Required Experience:

If you're an experienced Regulatory Affairs professional with a background in combination products, or a strong mix of pharmaceutical and medical device regulations, please apply now.

  • Develop and execute global regulatory strategies
  • Build and maintain regulatory dossiers and submission packages
  • Lead interactions with regulatory authorities
  • Support UK, European and future FDA submissions
  • Provide regulatory guidance across development and commercial programmes
  • Work closely with Clinical, R&D, Quality and Operations teams
  • Support products progressing from development through to market
  • Experience with drug device combination products is highly preferred
  • Candidates without combination product experience should demonstrate a strong background across both pharmaceutical and medical device regulatory environments
  • Experience with MHRA, EU and ideally FDA regulatory pathways
  • Proven experience developing regulatory strategies and managing health authority interactions
  • Experience supporting innovative or early-stage product development
  • Previous experience within start ups, scale ups or fast growth environments would be advantageous
  • Comfortable operating in a hands on role with high visibility and influence

Project details

Must be based in the UK or Ireland

12 Month contract opportunity

High impact role with significant influence on future regulatory and development strategy

An innovative life sciences organisation is looking for an experienced Regulatory Affairs Consultant to support the development and commercialisation of a growing product portfolio.

This is a strategic role focused on defining regulatory pathways, preparing submissions, building regulatory dossiers, and leading interactions with regulatory authorities. The position will support both near term commercial activities and longer term development programmes, including innovative combination product technologies.

  • Start: date 1/2027
  • Duration: 12 months
  • Remote: onsite
  • Location: Dundee, United Kingdom, GB

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