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Chemical Legislation Regulatory Manager

£negotiable | Yorkshire & The Humber |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:889486

The Role

Chemical Legislation Regulatory Manager - Global Healthcare Company - Yorkshire - £negotiable

Chemical Legislation Regulatory Manager responsible for leading a small team as well as ensuring the full portfolio remains compliant to relevant chemical legislations.

 

The Company

My client is a global healthcare company covering multiple therapy areas. Based in Yorkshire, this company operate on a global scale and have recently open their new state of the art R&D Centre in Yorkshire.

  • Global, leading healthcare company
  • Covering multiple countries across the globe
  • Flexible working
  • Great career progression
  • Diverse range of projects / products to work on

 

The Role

The Chemical Legislation Regulatory Manager will be responsible for leading a team of Regulatory professionals whilst ensuring all products remain compliant.

  • Ensure product compliance to REACH and other relevant legislation
  • Manage a small team of regulatory professionals
  • Ability to translate complex regulatory information into stakeholder friendly language.
  • Work to refine compliance and post approval maintenance processes and procedures

 

You

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

  • Excellent regulatory affairs experience within chemicals, biocides, REACH etc
  • Degree educated in a scientific field
  • Strong stakeholder management
  • Can work in a fast-paced environment and deliver to strict timescales

 

What should you do next?

This Chemical Legislation Regulatory 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 pharma and biocides. 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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