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Regulatory Affairs Manager

£negotiable | South East, Berkshire |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:889625

The Role

Regulatory Affairs Manager - Biocides - Global Healthcare company - Slough - £negotiable

The Regulatory Affairs Manager - Biocides is responsible for managing a small team whilst remaining hands on creating technical files / dossiers for biocide products within the UK.

 

The Company

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

  • Global healthcare company
  • Innovative product range covering medicines, medical devices, biocides/chemicals and cosmetics
  • Excellent career progression and training opportunities
  • Fast paced organisation with the opportunity to work on numerous projects concurrently

 

The Role

The Regulatory Affairs Manager - Biocides will be responsible for;

  • Full lifecycle regulatory affairs for a range of biocidal products
  • Managing submissions for the UK
  • Managing a small team
  • Liaising with and advising senior stakeholders on all regulatory matters in relation to the products
  • To be the key interface for the MHRA

 

You

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

  • Proven Regulatory Affairs experience ideally with Biocidal or Chemicals products
  • Good understanding of BPL, CPL, REACH registrations
  • UK submission experience
  • Good managerial skills
  • Strong stakeholder management
  • Science based degree

 

What should you do next?

This Regulatory Affairs Manager - Biocides 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.

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’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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