<?xml version="1.0" encoding="utf-8"?>
<rss version="2.0">
  <channel>
    <title>QC Validation and Systems Lead - Nexus Life Sciences RSS Feed</title>
    <link>https://jobs.co.uk/job/qc-validation-and-systems-lead-nexus-life-sciences--67e25623-19a6-4070-87fa-235808a19391</link>
    <description>RSS feed for QC Validation and Systems Lead at Nexus Life Sciences.</description>
    <language>en-gb</language>
    <lastBuildDate>Wed, 10 Jun 2026 10:30:33 GMT</lastBuildDate>
    <item>
      <title>QC Validation and Systems Lead - Nexus Life Sciences</title>
      <link>https://jobs.co.uk/job/qc-validation-and-systems-lead-nexus-life-sciences--67e25623-19a6-4070-87fa-235808a19391</link>
      <guid>https://jobs.co.uk/job/qc-validation-and-systems-lead-nexus-life-sciences--67e25623-19a6-4070-87fa-235808a19391</guid>
      <pubDate>Fri, 15 May 2026 11:52:21 GMT</pubDate>
      <description>Location: Cheshire | Salary: 40000.00-40000.00 Annual | Type: Permanent | QC Validation and Systems Lead Cheshire £40,000 £50,000 Pharmaceutical / GMP Laboratory The Role We are seeking an experienced QC Validation and Systems Lead to take ownership of QC laboratory equipment lifecycles and computerized systems within a GMP-regulated environment. This senior, hands-on role blends equipment validation, CSV, data integrity, and team leadership, ensuring QC operations remain compliant, efficient and inspection-ready at all times. Key Responsibilities  Own the full lifecycle of QC laboratory equipment, including procurement, qualification, maintenance, change control, and retirement Lead equipment validation activities (IQ/OQ/PQ) and manage site calibration programmes, including oversight of external service providers Manage QC equipment and validation status using electronic systems (e.g. LIMS), ensuring GMP compliance and inspection readiness Lead Computer System Validation (CSV) and administration for QC systems such as Empower and LabX, ensuring data integrity and regulatory compliance Author and approve validation and GMP documentation, and lead deviation investigations, impact assessments, and CAPA related to equipment and systems Provide technical lea...</description>
      <category>Permanent</category>
    </item>
  </channel>
</rss>