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Regulatory Affairs Associate (Hybrid/Remote)

JR United Kingdom

London

Hybrid

GBP 40,000

Full time

9 days ago

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Job summary

An established industry player is seeking a Regulatory Affairs Associate to join their dynamic team in London. This role offers the flexibility of hybrid or remote working, allowing you to support innovative product developments and ensure compliance with critical regulatory standards in Europe and the USA. With a competitive salary of up to £40,000 and a vibrant work environment, this position promises a varied and engaging workload, perfect for someone passionate about regulatory affairs in the medical device sector. If you have the required experience and skills, this is an exciting opportunity to make a significant impact.

Qualifications

  • 2+ years of experience in regulatory affairs or a similar role.
  • Working knowledge of regulatory requirements in medical devices.

Responsibilities

  • Support new product developments and regulatory submissions.
  • Ensure compliance with EU and USA regulatory requirements.

Skills

Regulatory Requirements Knowledge
Risk Management
Product Development Support
Market Approval Requirements (EU MDR & 510(k))

Job description

Social network you want to login/join with:

Regulatory Affairs Associate (Hybrid/Remote), London
Client:

AVD Appoint

Location:

London, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

9

Posted:

18.04.2025

Expiry Date:

02.06.2025

Job Description:

Regulatory Affairs Associate - Devon - Up to £40,000 pa + benefits - Ref 1894

Hybrid or remote working

I am currently recruiting for a Regulatory Affairs Associate to work for a multi-national medical device organisation. Salary up to £40,000 pa + benefits.

On a day-to-day basis, you can expect to be supporting new product developments and creation of their submissions in Europe and USA in compliance with regulatory requirements.

Responsibilities:
  • 2+ years within a similar position
  • Working knowledge of regulatory requirements
  • Ideally has experience in key market approval requirements within Europe and USA (EU MDR & 510(k))
  • Understanding of Risk Management within a Medical Device industry

This is a fantastic opportunity for a Regulatory Affairs Associate to work for a leader within their field where the work is continuously varied keeping you engaged and challenged.

This is an immediate requirement so if you have the required skills and experience then please get in touch ASAP with an up-to-date copy of your CV. Either apply direct or contact David on 01183 366 100.

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