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    <title>Senior Q&amp;amp;V Specialist - SRG RSS Feed</title>
    <link>https://jobs.co.uk/job/senior-qampv-specialist-srg--87ef8c8b-4a09-4918-b0fe-d15a91150e9c</link>
    <description>RSS feed for Senior Q&amp;amp;V Specialist at SRG.</description>
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    <lastBuildDate>Sat, 05 Sep 2026 02:28:52 GMT</lastBuildDate>
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      <title>Senior Q&amp;amp;V Specialist - SRG</title>
      <link>https://jobs.co.uk/job/senior-qampv-specialist-srg--87ef8c8b-4a09-4918-b0fe-d15a91150e9c</link>
      <guid>https://jobs.co.uk/job/senior-qampv-specialist-srg--87ef8c8b-4a09-4918-b0fe-d15a91150e9c</guid>
      <pubDate>Thu, 03 Sep 2026 23:00:00 GMT</pubDate>
      <description>Location: Falkirk | Salary: Negotiable | Type: Permanent | Senior Qualification &amp; Validation (Q&amp;V) Specialist      Our client is a global pharmaceutical manufacturer with a major GMP-regulated production site in Central Scotland. As part of continued investment in their Quality organisation, they are looking to appoint a Senior Qualification &amp; Validation Specialist to strengthen governance and compliance across site Q&amp;V and Periodic Review activities.   The Role   Reporting into the site Quality function, you will take ownership of key Q&amp;V quality system elements, coordinating, maintaining and promoting Q&amp;V compliance across the site. You will lead and support continuous improvement of related quality and operational systems, ensuring the site and its functions remain compliant with GxP regulations and applicable quality guidelines, including UK/EU/US GMP/GDP, ICH, ISPE and other region-specific requirements.   Key Responsibilities    Provide planning, support and guidance for validation projects, including continuous improvement of validation policies, procedures, templates and working practices.  Oversee project plans and milestones alongside project teams to meet compliance and customer requirements.  Coordinate resourcing and facilitat...</description>
      <category>Permanent</category>
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