select * from applications_reporting where candidate_id = '' 4

Regulatory Affairs Associate - Post Market

£Negotiable | Home based, Cheshire |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:890082

The Role

Regulatory Affairs Associate Post Market - Global Medical Devices Company - Cheshire with remote working - £negotiable

The Regulatory Affairs Associate Post Market is responsible for preparing Post Market Surveillance plans for a range of medical devices within their portfolio.

*Remote interview and onboarding process

 

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 art the forefront of medical devices and associated technology.

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

 

The Role

The Regulatory Affairs Associate - Post Market will be responsible for;

  • Preparing Post Market Surveillance plans for a range of medical devices
  • Supporting the team in ensuring MDR compliance
  • Prepare Post Market Surveillance Plans, Reports, Periodic Safety Update Reports (PSURs)
  • Feed back to the business where required

 

You

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

  • Good regulatory experience within medical devices (6 months-2 years ideally)
  • Good knowledge of MDD/MDR
  • Good knowledge of ISO 134585
  • Ideally experienced in post market surveillance of products
  • Science based degree

 

What should you do next?

This Regulatory Affairs Associate Post Market 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

image

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.

More


More jobs like thisSee all