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Regulatory Affairs Manager

£50k - £60k + bonus and bens | Scotland |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:889295

The Role

Regulatory Affairs Manager - EU Post Marketing - Global Pharma - Scottish Boarders - £50k - £60k + bonus and bens

Regulatory Affairs Manager, focusing on EU post marketing activities. Developing regulatory strategies for clinical trials as well as post market compliance for marketed products.

 

The Company

My client is a global R&D based pharmaceutical company focusing on biotechnology and drug discovery. Based in the heart of the Scottish Boarders, this company is at the forefront of technology driven drug discovery.

  • They research and manufacture treatments for Nephrology, Oncology, Immunology and Allergies
  • They use advanced technologies and equipment for all product manufacture
  • Rapidly expanding the business due to continuous success and development

 

The Role

The Regulatory Affairs Manager will be responsible for post market compliance of market products across the EU as well as developing regulatory strategies.

  • Support regulatory activities associated with EU post-licensing activities and development
  • Development of regulatory strategy, regulatory activities for clinical trials, and regulatory activities associated with the maintenance of marketing authorisations
  • Respond to queries from the relevant regulatory authorities

 

You

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

  • 5 years' experience in pharmaceutical regulatory affairs
  • Post marketing experience
  • EU experience
  • Strong stakeholder management
  • Degree educated in life sciences

 

What should you do next?

This Regulatory Affairs Manager role is one not to be missed; it encompasses the opportunity to work with new and exciting products within a company who are at the forefront of technology driven drug discovery. 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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