Junior CSV Engineer

Principal Contract Consultant: Quality, Validation & Regulatory – EU

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

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

Role Overview

We are seeking a Junior CSV Engineer with 2–3 years of experience to support an upcoming 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

• 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, change controls, and CAPAs
• Assist in ensuring issues are managed and resolved in compliance with GMP and internal quality systems
• 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 environments
• 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

Seniority Level Associate

Employment Type Contract

Job Function Engineering and Quality Assurance

Industries Pharmaceutical Manufacturing and Biotechnology Research