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Regulatory Affairs Manager

£negotiable | UK |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:889721

The Role

Regulatory Affairs Manager - Global Medical Devices company - Home based - £negotiable

The Regulatory Affairs Manager is responsible for managing a small team whilst remaining hands on creating technical files / dossiers for medical devices across the EU/US.


The Company

This is an exciting time to join an expanding, highly successful global medical devices company in a home based managerial hands on role. They offer fantastic training and development as good career development opportunities.

  • Global medical devices company
  • Innovative product range covering class I-III medical devices
  • Excellent career progression and training opportunities
  • Fast paced organisation with the opportunity to work on numerous projects concurrently


The Role

The Regulatory Affairs Manager will be responsible for;

  • Managing a small regulatory team
  • Remaining hands on and creating technical files for a range of class I-III medical devices
  • Managing submissions for the EU/US
  • Liaising with and advising senior stakeholders on all regulatory matters in relation to the products
  • Manage multiple projects concurrently



To apply for this role as a Regulatory Affairs Manager our client is hoping for someone with the following skills and experience;

  • Proven Regulatory Affairs experience within medical devices ideally up to class III
  • EU/US submission experience
  • Good managerial skills
  • Strong stakeholder management and project management experience
  • Good experience working with the FDA
  • Science based degree


What should you do next?

This Regulatory Affairs Manager role is one not to be missed; it encompasses the opportunity to manage a small team within a global, well known company as well as remaining hands on. To discuss further, please submit your current CV.

Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there. Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.



Hayley Shayestehroo

Which team and area do you work/specialise in?

I work in the Regulatory Affairs team and recruit for Regulatory Affairs professionals at all levels within Pharma, Medical Devices companies and Regulatory Consultancies

What are some of the typical roles you cover?

I cover Regulatory Affairs positions at all levels within Pharma, Medical Devices and Regulatory Consultancies, these typically include;

Regulatory Affairs Associate jobs, Regulatory Affairs Executive jobs, Regulatory Affairs Senior Associate jobs, Regulatory Affairs Manager jobs, Regulatory Affairs Senior Manager jobs, Regulatory Affairs Director jobs, Regulatory Affairs Consultant jobs, Regulatory Writer jobs and Medical Writer jobs.

What are the hot issues in your sector currently?

Within Medical Devices it is the transition from MDD to MDR in May 2020. A lot of medical device companies are hiring Regulatory professionals to prepare their company for the transition

What’s makes you #DistinctlyDifferent?

I take pride in getting to know my candidates on a personal level as well as professional. Changing jobs is a big decision for most people so I like to ensure I am placing my candidates in a role that not only matches their career aspirations but also suits their personal situation and key motivations.


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