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Graduate Regulatory Affairs / QC Officer

£negotiable | London, North London |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:889595

The Role

Graduate Regulatory Affairs / QC Officer - Leading Consumer Healthcare company - North London - £negotiable

The Graduate Regulatory Affairs / QC Officer is responsible for supporting QC/Regulatory Affairs activities including handling Technical Product Data, e.g. Clinical and Pharmacological Information and handling New Product Development (NPD) projects.

 

The Company

This is an exciting time to join an expanding, highly successful consumer healthcare company based at their site in North London. They offer fantastic training and development as good career development opportunities.

  • Leading consumer healthcare company
  • Excellent research and development function
  • Excellent links with various charities

 

The Role

The Graduate Regulatory Affairs / QC Officer will be responsible for;

  • Handling Technical Product Data, e.g. Clinical and Pharmacological Information
  • Handling New Product Development (NPD) projects
  • Working on standard operating procedures of the Quality Control Dept
  • Quality Control, Customer and Regulatory Issues

 

You

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

  • Pharmacy or biosciences postgraduate
  • Highly organised
  • Accurate with good computer skills and good written and verbal communication skills

 

What should you do next?

This Graduate Regulatory Affairs / QC Officer role is one not to be missed; it encompasses the opportunity to enter a Regulatory Affairs position within a forward thinking company who are at the forefront of consumer healthcare. 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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