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Regulatory Affairs Associate (Hybrid/Remote)

JR United Kingdom

Bury

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. This role offers the chance to work hybrid or remotely while supporting innovative product developments in the medical device sector. You will be instrumental in ensuring compliance with regulatory requirements across Europe and the USA, making a significant impact in a fast-paced environment. If you have a passion for regulatory affairs and a desire to contribute to groundbreaking projects, this is the perfect opportunity for you to thrive and grow in your career.

Qualifications

  • 2+ years in a regulatory affairs role with knowledge of EU and USA regulations.
  • Experience with medical device submissions and compliance.

Responsibilities

  • Support new product developments and submissions in compliance with regulations.
  • Ensure compliance with EU MDR and 510(k) requirements.

Skills

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

Education

Bachelor's Degree in Life Sciences

Job description

Social network you want to login/join with:

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

AVD Appoint

Location:

bury, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

8

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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