System Admin

Lorien; Pirbright; On-site; GBP 20,000 - 33,000; Part time

Benefits offered by this job

Job summary

Lorien, Surrey, is seeking a System Administrator (GxP Systems) on a 3-month contract, part-time, Inside IR35. The role involves supporting validated systems in regulated environments (GxP/GMP) and CSV/validation activities.

Key duties include system administration, patch management, testing and validation, change control, audit readiness, and documentation. You will collaborate with Engineering, Manufacturing, Quality and external vendors; working pattern is 2–3 days per week.

Qualifications

• GxP System Validation/CSV experience.
• 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.

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 System Validation

CSV

Change Control

Patch Management

Compliance & Audit Readiness

System Lifecycle Management

CAPA & Risk Management

Vendor & Stakeholder Management

Project Delivery & Coordination

Job description

System Administrator (GxP Systems)

3-Month Contract | part time | 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