Regulatory Affairs Specialist (Medical Devices)

Regulatory Affairs Specialist (Medical Devices) - Leading Pharmaceutical Company - Lancashire - £Competitive salary and benefits package

The Company

A fantastic company with a great reputation working across new established medical devices.

They offer unique development opportunities and support people to further their career in the UK or globally.

  • Innovative, ideas based company

  • Strong heritage in science

  • Culture of caring both internally and for patients

  • Agile and dynamic despite being a large corporation

The Role

  • This role will lead worldwide product registrations and CE marking activates to ensure timely and systematic approvals are made in accordance with regulatory and business requirements.

  • Regulatory lifecycle management and providing regulatory advice
    Supporting and coordinating regulatory approval for new products and changes to existing products

  • Ensuring that dossiers are created where appropriate in line with local country requirements (incl.

    CE mark and US).

  • Establish and maintain processes for maintenance of registrations.


As a Regulatory Affairs Specialist you will have experience in the following;

End to end regulatory lifecycle management within medical devices

Creating technical dossiers ready for submission

Strong stakeholder management

Global product registrations / CE Marking

What should you do next?

This Regulatory Affairs Specialist job is a great role and won't be around for long! So don't delay.

If you are unsure and need some advice, give me a ring, otherwise just click apply, upload your CV and send, it's really that easy!

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.

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