<?xml version="1.0" encoding="utf-8"?>
<rss version="2.0">
  <channel>
    <title>Regulatory Affairs Manager IVD - Hays Life Sciences RSS Feed</title>
    <link>https://jobs.co.uk/job/regulatory-affairs-manager-ivd-hays-life-sciences--3ce6ff91-da58-4500-a621-f8626bb4457d</link>
    <description>RSS feed for Regulatory Affairs Manager IVD at Hays Life Sciences.</description>
    <language>en-gb</language>
    <lastBuildDate>Mon, 25 May 2026 04:25:08 GMT</lastBuildDate>
    <item>
      <title>Regulatory Affairs Manager IVD - Hays Life Sciences</title>
      <link>https://jobs.co.uk/job/regulatory-affairs-manager-ivd-hays-life-sciences--3ce6ff91-da58-4500-a621-f8626bb4457d</link>
      <guid>https://jobs.co.uk/job/regulatory-affairs-manager-ivd-hays-life-sciences--3ce6ff91-da58-4500-a621-f8626bb4457d</guid>
      <pubDate>Wed, 13 May 2026 23:00:00 GMT</pubDate>
      <description>Location: Hertfordshire | Salary: &amp;pound;45.00 - &amp;pound;55.00/hour &amp;pound;45 - &amp;pound;55 per hour | Type: Contract | Regulatory affairs manager IVD, remote contract job Your new company   Our client, a global leader in life sciences and diagnostics, is seeking an experienced Regulatory Affairs Manager to support their expanding IVD portfolio on a contract basis. This is a fantastic opportunity to work at the forefront of diagnostic innovation, ensuring regulatory compliance across key markets.  Your new role     Lead and support regulatory activities for IVD products across global markets (EU, UK, and potentially US/ROW)  Prepare, review, and submit regulatory documentation (e.g., IVDR technical files, submissions, change notifications)  Provide strategic regulatory guidance throughout the product lifecycle  Collaborate cross-functionally with R&amp;D, Quality, Clinical, and Commercial teams  Ensure compliance with IVDR (EU 2017/746) and other applicable regulations  Support audits, inspections, and interactions with notified bodies and regulatory authorities.    What you''ll need to succeed     Proven experience in Regulatory Affairs within IVD or medical devices  Strong working knowledge of IVDR requirements (essential)  Experience preparing and managing regulatory submissions and technical documen...</description>
      <category>Contract</category>
    </item>
  </channel>
</rss>