Junior CSV Engineer

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

Job summary

A leading life sciences consultancy is seeking a Junior CSV Engineer to join their team on a 9-month contract. The role involves supporting documentation preparation, lifecycle activities, and coordinating with vendors. Ideal candidates will have 2-3 years of experience in Computer Systems Validation, possess a degree in a relevant field, and have knowledge of GMP and GAMP 5. This remote position includes paid travel for client site visits and offers the possibility for fixed-term employment or contract extension after the initial term.

Benefits

Travel and accommodation expenses covered

Opportunity to work on high-impact projects

Flexible employment options

Qualifications

• 2–3 years experience in Computer Systems Validation within regulated environments.
• Degree in Engineering, Computer Science, Life Sciences or related discipline.
• 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, validation plans, protocols, and reports.
• Support the review and documentation of deviations and change controls.
• Coordinate CSV tasks with external vendors and service providers.
• Support tracking of CSV activities, deliverables, and timelines.

Skills

Computer Systems Validation

GMP knowledge

Risk assessment

Collaboration with stakeholders

Education

Degree in Engineering, Computer Science, 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

XHTML - "Collaborate with internal stakeholders (IT, Automation, Engineering, Quality)"
• 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