Junior CSV Engineer

X4 Life Sciences; Remote; GBP 60,000 - 80,000; Full time

Job summary

A specialized recruitment firm is looking for a Junior CSV Engineer with 2–3 years of experience in Computer Systems Validation. This fully remote role requires support for validation documentation and coordination with internal and external teams, with minimal travel needed. Candidates should possess a degree in Engineering, Computer Science, or Life Sciences, plus knowledge of GMP principles. The position offers the opportunity to engage with high-impact projects in the Life Sciences sector.

Benefits

Travel and accommodation expenses covered

Opportunity for contract or FTC

Work on high-impact regulated projects

Qualifications

• 2–3 years’ experience in Computer Systems Validation within pharmaceutical, biotech, or regulated environments.
• Working knowledge of GMP, GAMP 5, and validation lifecycle principles.

Responsibilities

• Assist in the preparation, review, and maintenance of CSV documentation.
• Support the development of validation deliverables including risk assessments and validation plans.
• Collaborate with internal stakeholders and coordinate CSV tasks with external vendors.

Skills

Computer Systems Validation

GMP knowledge

Cross-functional collaboration

Education

Degree in Engineering, Computer Science, or Life Sciences

Job description

Contract Type: 9-Month Contract (FTC or Contract option available)

Location: Fully Remote (2–3 on‑site client visits during the project; expenses paid)

Rate: £200 per day (8 hour day)

Role Overview

We are seeking aJunior CSV Engineer with 2–3 years of experience to support an upcoming буен т? project. The role will focus on documentation support, lifecycle CSV activities, and coordination with internal teams and external vendors. This is an excellent opportunity to gain further exposure to the Life Sciences sector whilst working remotely with limited site presence.

Key Responsibilities

Document Preparation

• Assist in the preparation, review, and maintenance of CSV documentation
• Support the development of validation deliverables including risk assessments, validation plans, protocols, and reports

Deviation & grandchildren

• Support the review and documentation of deviations, change controls, and CAPAs
• Assist in ensuring issues are managed and resolved in compliance with GMP and internal quality systems

CSV Coordination

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• Coordinate CSV tasks with external vendors and service providers
• Support tracking of CSV activities, deliverables, and timelines

Required Experience & Qualifications

• 2–3 years’ experience in Computer Systems Validation within pharmaceutical, biotech, or regulated environmentsժ
• Degree in Engineering, Computer Science, Life Sciences, or a related discipline
• Working knowledge of GMP, GAMP 5, and validation lifecycle principles

What’s on Offer

• Fully remote role with minimal travel (2–3 site visits during the project)
• Travel and accommodation expenses fully covered
• Opportunity to work on regulated, high-impact projects
• Option for fixed‑term employment or contract setup at the end of the initial term