System Administrator

Lorien; Pirbright; On-site; GBP 28,000 - 41,000; Part time

Job summary

Lorien in the United Kingdom is hiring a System Administrator for a 3-month contract (part-time) based at Pirbright, Surrey. The role covers supporting validated systems in regulated environments (GxP/GMP) with CSV, change control, and release activities.

Expect responsibilities across system administration, testing/validation, implementation, change control, audit readiness, and collaboration with Engineering, Manufacturing, Quality, and external vendors on a regular basis.

Qualifications

• GxP CSV validation experience.
• Change control & patch management.
• Compliance & audit readiness.
• System lifecycle management.
• CAPA & risk management.
• Vendor & stakeholder management.
• Project delivery & coordination.

Responsibilities

• System administration, maintenance, and patch management.
• Testing and validation activities (CSV/GxP).
• System implementation and release support.
• Change control and compliance activities.
• Audit readiness and documentation.
• Root cause analysis and issue resolution.
• Collaborate with Engineering, Manufacturing, Quality, and external vendors.

Skills

GxP Validation/CSV

Change Control

Audit Readiness

Lifecycle Management

CAPA & Risk Management

Vendor & Stakeholder Mgmt

Project Delivery & Coordination

Job description

3-Month Contract | part time | Pirbright, Surrey | Inside IR35

We're looking for a System Administrator with experience supporting validated systems in regulated environments (GxP/GMP).

Key Responsibilities:

• System administration, maintenance, and patch management
• Testing and validation activities (CSV/GxP)
• System implementation and release support
• Change control and compliance activities
• Audit readiness and documentation
• Root cause analysis and issue resolution
• Collaborate with Engineering, Manufacturing, Quality, and external vendors

Required Experience:

• GxP System Validation/Computer System Validation (CSV)
• Change Control & Patch Management
• Compliance & Audit Readiness
• System Lifecycle Management
• CAPA & Risk Management
• Vendor & Stakeholder Management
• Project Delivery & Coordination

Desirable:

• GMP, GxP, FDA 21 CFR Part 11, Annex 11

Working Pattern:

2-3 days per week