<?xml version="1.0" encoding="utf-8"?>
<rss version="2.0">
  <channel>
    <title>Technical Product Owner - New Appointments Group RSS Feed</title>
    <link>https://jobs.co.uk/job/technical-product-owner-new-appointments-group--31c14061-d133-47bb-88b1-3ce08144797c</link>
    <description>RSS feed for Technical Product Owner at New Appointments Group.</description>
    <language>en-gb</language>
    <lastBuildDate>Tue, 28 Jul 2026 18:15:44 GMT</lastBuildDate>
    <item>
      <title>Technical Product Owner - New Appointments Group</title>
      <link>https://jobs.co.uk/job/technical-product-owner-new-appointments-group--31c14061-d133-47bb-88b1-3ce08144797c</link>
      <guid>https://jobs.co.uk/job/technical-product-owner-new-appointments-group--31c14061-d133-47bb-88b1-3ce08144797c</guid>
      <pubDate>Sun, 26 Jul 2026 23:00:00 GMT</pubDate>
      <description>Location: Folkestone | Salary: Negotiable | Type: Temporary | Technical Product Owner    Global Digital Transformation | Veeva RegulatoryOne | Hybrid Working   Our client is seeking an experienced Technical Product Owner to support a major global digital transformation programme focused on Regulatory Information Management.  Working closely with Regulatory, Quality and IT teams, you''ll own the product backlog, gather and define business requirements, support solution delivery and play a key role in implementing Veeva RegulatoryOne across a global organisation.   Responsibilities    Own and prioritise the product backlog  Lead requirements gathering and business analysis  Translate business needs into user stories and acceptance criteria  Support Veeva RegulatoryOne implementation  Collaborate with global stakeholders  Support testing, validation and release activities  Drive continuous process improvement    Requirements    Previous Technical Product Owner or Senior Business Analyst experience  Hands-on Veeva Vault RegulatoryOne experience  Product Lifecycle Management (PLM)  Quality Management Systems (QMS)  Agile methodologies  Computer System Validation (CSV)  GxP/FDA regulated environment experience   This is a fantastic opportunity to j...</description>
      <category>Temporary</category>
    </item>
  </channel>
</rss>