IT Automation Project Specialist

PE Global International

Milton Keynes

On-site

GBP 4,345,000 - 7,389,000

Full time

2 days ago
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Job summary

PE Global International is recruiting for an IT Automation Project Execution Specialist to support critical IT/OT automation and infrastructure projects in a GMP environment. Location: Milton Keynes. Duration: 6 months. Start ASAP. Full-time, Monday–Friday.

The role focuses on delivering, upgrading and lifecycle managing validated systems, interfacing IT and OT, with hands-on work on Rockwell FactoryTalk, EMS, and SCADA. Visa sponsorship is not available.

Qualifications

  • 5+ years delivering IT/OT, automation or infrastructure projects within regulated environments.
  • Experience in pharmaceutical manufacturing is essential.
  • Strong experience administering Windows Server 2022 or later.
  • Solid networking knowledge: VLANs, TCP/IP, switching, routing.
  • GxP documentation and system validation experience.
  • Knowledge of Data Integrity, 21 CFR Part 11 and Annex 1.
  • Experience with Rockwell FactoryTalk/SCADA/EMS is a plus.

Responsibilities

  • Design, develop and maintain automation solutions across IT and OT environments.
  • Administer and support Windows Server 2022 or later environments.
  • Support and integrate automated systems used within pharmaceutical manufacturing.
  • Ensure systems comply with GxP requirements, including validation and documentation standards.
  • Create and maintain GxP documentation (IQ/OQ/PQ, SOPs, risk assessments, validation plans).
  • Support the SDLC within a validated environment.
  • Configure and troubleshoot network infrastructure (VLANs, TCP/IP, routing, switching, firewalls).
  • Work with Quality, Manufacturing and Engineering to maintain system integrity and compliance.
  • Collaborate with Project Manager to deliver upgrades and projects.

Skills

IT/OT project delivery
Stakeholder management
Regulated environments
Networking (VLAN, TCP/IP)
Scripting (PowerShell)
SDLC in validated environments

Education

Degree in IT or Automation

Tools

Rockwell FactoryTalk
Mettler Toledo FormWeigh
EMS/SCADA systems
VMware/Virtualisation

Job description

PE Global is currently recruiting for an IT Automation Project Execution Specialist to join a leading global pharmaceutical organisation, supporting critical IT/OT automation and infrastructure projects.

Location: Milton Keynes

Duration: 6 months

Start Date: ASAP

Working Pattern: Full time, Monday–Friday

Rate: £31.54 - £53.64 per hour PAYE

The Role

We are looking for an experienced IT/OT Automation Engineer with a strong background in pharmaceutical manufacturing and GxP-regulated environments. You will support the delivery, upgrade and lifecycle management of validated automation and infrastructure systems, working at the interface between IT and Operational Technology (OT).

Key Responsibilities
  • Design, develop and maintain automation solutions across IT and OT environments.
  • Administer and support Windows Server 2022 or later environments.
  • Support and integrate automated systems used within pharmaceutical manufacturing.
  • Ensure systems comply with GxP requirements, including validation and documentation standards.
  • Create and maintain GxP documentation, including IQ/OQ/PQ, SOPs, risk assessments and validation plans.
  • Support the Software Development Lifecycle (SDLC) within a validated environment.
  • Configure and troubleshoot network infrastructure, including VLANs, TCP/IP, routing, switching and firewalls.
  • Support industrial and laboratory systems, including:
    • Rockwell FactoryTalk
    • Mettler Toledo FormWeigh
    • Environmental Monitoring Systems (EMS)
    • SCADA systems
  • Work closely with Quality, Manufacturing and Engineering teams to maintain system integrity and compliance.
  • Work alongside the Project Manager to deliver system upgrades and execute project plans.
  • Support system upgrades, migrations and lifecycle activities.
Skills & Experience Required
  • 5+ years' experience delivering IT/OT, automation or infrastructure projects within regulated environments.
  • Previous experience working within pharmaceutical manufacturing is essential.
  • Strong experience administering Windows Server 2022 or later.
  • Solid networking knowledge, including VLAN configuration, TCP/IP, switching and routing.
  • Proven experience working within a GxP-regulated environment such as Pharma, Biotech or Life Sciences.
  • Hands-on experience with GxP documentation, compliance and system validation.
  • Knowledge of Data Integrity, 21 CFR Part 11 and Annex 1.
  • Good understanding of SDLC within a regulated environment.
  • Experience with Rockwell FactoryTalk, Mettler Toledo FormWeigh and/or Environmental Monitoring Systems (EMS).
  • Experience with scripting or automation tools such as PowerShell.
  • Experience with infrastructure automation tools or scripting frameworks.
  • Knowledge of VMware/virtualisation platforms.
  • Understanding of OT cybersecurity principles.
  • Experience working with SCADA and EMS systems.
  • Strong analytical, troubleshooting and problem-solving skills.
  • Experience managing stakeholders and communicating effectively within regulated environments.
  • A degree in IT, Automation or a related discipline, or equivalent practical experience.

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***

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