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Regulatory Affairs Associate

£30k - £32k + bens | UK |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:889635

The Role

Regulatory Affairs Associate – Global Medical Devices Company – Remote – £negotiable

The Regulatory Affairs Associate is responsible for submitting and maintaining global regulatory approvals, to support regulatory submissions for new markets and maintaining registrations and licences in existing markets.

 

The Company

This is an exciting time to join an expanding, highly successful global medical devices company based at their site in Cheshire. They develop and manufacture their own products and have an excellent R&D capability ensuring they stay at the forefront of medical devices and associated technology.

  •  Global, leading medical devices company
  • Manufacture and register a range of high-quality devices as well as many more in the pipeline
  • At the forefront of medical devices, particularly within wound care 

 

The Role

The Regulatory Affairs Associate will be responsible for;

  • Submit and maintain global regulatory approvals, supporting regulatory submissions for new markets and maintaining registrations and licences in existing markets.
  • Advising the business regarding any regulatory enquiries
  • Coordinate the preparation, review and submit timely responses to requests for additional information from regulatory authorities on product registrations.

 

You

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

  • Good regulatory experience within medical devices or pharma (6 months-2 years ideally)
  • Good knowledge of MDD/MDR (desirable)
  • Good knowledge of ISO 134585
  • Ideally experienced in managing registrations in EMEA, LATAM & APAC (desirable not essential
  • Science based degree 

 

What should you do next?

This Regulatory Affairs Associate 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 medical devices. 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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