<?xml version="1.0" encoding="utf-8"?>
<rss version="2.0">
  <channel>
    <title>Senior Regulatory Affairs Manager CMC biologics - Hays Life Sciences RSS Feed</title>
    <link>https://jobs.co.uk/job/senior-regulatory-affairs-manager-cmc-biologics-hays-life-sciences--6a1200d1-b50a-483b-a325-a95787a2b5c6</link>
    <description>RSS feed for Senior Regulatory Affairs Manager CMC biologics at Hays Life Sciences.</description>
    <language>en-gb</language>
    <lastBuildDate>Tue, 30 Jun 2026 19:19:30 GMT</lastBuildDate>
    <item>
      <title>Senior Regulatory Affairs Manager CMC biologics - Hays Life Sciences</title>
      <link>https://jobs.co.uk/job/senior-regulatory-affairs-manager-cmc-biologics-hays-life-sciences--6a1200d1-b50a-483b-a325-a95787a2b5c6</link>
      <guid>https://jobs.co.uk/job/senior-regulatory-affairs-manager-cmc-biologics-hays-life-sciences--6a1200d1-b50a-483b-a325-a95787a2b5c6</guid>
      <pubDate>Mon, 29 Jun 2026 23:00:00 GMT</pubDate>
      <description>Location: London | Salary: &amp;pound;650 - &amp;pound;700/day &amp;pound;650 - &amp;pound;700 daily rate | Type: Contract | Your new company   Our client, a global biotechnology company focused on developing innovative therapies for rare and serious diseases, is seeking an experienced Regulatory Affairs CMC Manager to join their EU Regulatory team.This is an excellent opportunity to contribute to cutting-edge biologics and advanced therapies, supporting global post-approval strategies and new market applications across both EU and US regions.   Your new role   Reporting to the Senior Director, Regulatory Affairs CMC (EU), you will play a key role in delivering global regulatory CMC strategies for commercial products. You''ll collaborate with international teams across Europe and the US to ensure successful execution of regulatory submissions and lifecycle activities.   Act as the Regulatory CMC representative at site and cross-functional meetings, providing clear regulatory guidance.  Lead the planning, coordination, and compilation of high-quality CMC documentation for global post-approval submissions  Ensure all submissions comply with relevant regulatory requirements and guidelines (EU, FDA, and global standards)  Partner with international teams to support change controls and GMP documentation  Cont...</description>
      <category>Contract</category>
    </item>
  </channel>
</rss>