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Regulatory Affairs Project Manager

£40k - £45k + benefits | London |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:889184

The Role

Regulatory Affairs Project Manager - Global Pharma - London - £40k - £45k + bens

This is an exciting time to join an expanding, highly successful global pharma in their offices in London. They offer excellent training and development opportunities as well as great career progression opportunities.

  • Excellent career progression opportunities
  • Great training and development
  • Exciting and innovative product / therapy range

 

The Company

This is an exciting time to join an expanding, highly successful global healthcare company based at their London site.

  • Global healthcare company specialising in Rx and Consumer Healthcare
  • Extensive product range covering multiple therapy areas
  • Great location with good public transport links

 

The Role

The Regulatory Affairs Project Manager will be responsible for managing several technical projects, whilst providing technical regulatory expertise to the business.

  • Provide guidance and expertise for variation packages for products / CMC expertise
  • Mentor junior members of the team
  • Manage concurrent technical projects
  • Providing guidance on Modules 1 and 3 of the dossiers

 

You

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

  • Experienced in Regulatory Affairs, mainly with variations of pharmaceutical products / CMC elements of the dossier
  • Experienced manging or mentoring a small team / junior member of the team
  • Have UK/EU experience

 

What should you do next?

This Regulatory Affairs Project Manager role is one not to be missed; it encompasses the opportunity to work in a fast paced environment on new and exciting products. 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.

Consultant

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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 is your greatest fear?

I don’t really have one, but if there’s one thing I’m well not keen for it would be snakes or an army of ants…

 

How would your friends describe you in three words?

Funny, healthy, sporty

 

You’re stranded on a desert island – what one thing could you not live without?

Bear Grylls! He’d have us rescued in no time!

 

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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