<?xml version="1.0" encoding="utf-8"?>
<rss version="2.0">
  <channel>
    <title>IT Automation Project Execution Specialist (Pharma) - Room At The Top Recruitment RSS Feed</title>
    <link>https://jobs.co.uk/job/it-automation-project-execution-specialist-pharma-room-at-the-top-recruitment--91765566-d28c-4f3c-b3c9-356dbc1610d2</link>
    <description>RSS feed for IT Automation Project Execution Specialist (Pharma) at Room At The Top Recruitment.</description>
    <language>en-gb</language>
    <lastBuildDate>Wed, 01 Jul 2026 16:23:45 GMT</lastBuildDate>
    <item>
      <title>IT Automation Project Execution Specialist (Pharma) - Room At The Top Recruitment</title>
      <link>https://jobs.co.uk/job/it-automation-project-execution-specialist-pharma-room-at-the-top-recruitment--91765566-d28c-4f3c-b3c9-356dbc1610d2</link>
      <guid>https://jobs.co.uk/job/it-automation-project-execution-specialist-pharma-room-at-the-top-recruitment--91765566-d28c-4f3c-b3c9-356dbc1610d2</guid>
      <pubDate>Wed, 01 Jul 2026 11:52:16 GMT</pubDate>
      <description>Location: Milton Keynes | Salary: 28.67-28.67 Hourly | Type: Contract | Our global pharmaceutical client based in Milton Keynes is seeking a skilled IT/OT Automation Engineer to support the delivery of critical automation and infrastructure projects within a regulated pharmaceutical manufacturing environment. The role focuses on implementing and upgrading validated systems, ensuring compliance with GxP standards, and supporting the full system lifecycle (SDLC). You will work at the interface between IT and Operational Technology (OT), supporting manufacturing systems that are critical to site operations.This is full-time, onsite role working in Milton Keynes. This is initially a 6-month PAYE contract with a possibility of an extension and is paying an hourly rate of £28.67 - £48.77 per hour, plus 25 days holiday pro rata. Duties:Design, develop, and maintain automation solutions for IT and OT systemsAdminister and support Windows Server environments (2022 or later)Support and integrate automated systems used in pharmaceutical manufacturingEnsure systems comply with GxP regulations, including validation and documentationCreate and maintain GxP documentation (IQ/OQ/PQ, SOPs, risk assessments, validation plans)Participate in and support the Software Devel...</description>
      <category>Contract</category>
    </item>
  </channel>
</rss>