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Nexus Life Sciences

Validation Officer

Preston
£33k – £42k/yr
Posted 1 day ago
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Validation Officer 📍 Preston | 💷 £33,000– £42,000K | 🧪 GMP Manufacturing | 📍100% site based

Are you an experienced Validation professional looking to take the next step in your career within a fast-paced, highly regulated manufacturing environment? We’re supporting a growing life sciences manufacturer in Preston who are looking for an experienced Validation Officer to join its growing Quality team.

Role Overview

Reporting to the Validation Manager, you’ll play a key role in delivering the site’s Validation Master Plan, ensuring robust validation standards are upheld across processes, equipment, cleaning, analytical methods, and new product introduction activities.

Key Responsibilities

  • Generating, reviewing, and executing validation protocols and reports to support successful validation activities.
  • Managing process and engineering change controls to ensure validated systems remain compliant post-change.
  • Reviewing analytical/method validation data (including chromatography outputs) to support validation decisions.
  • Conducting risk impact assessments aligned with ICH Q10 principles (including ICH Q3D).
  • Assessing process deviations, root causes, and CAPAs from a validation perspective.
  • Supporting cleaning validation activities including swab recoveries, clean/dirty hold times.
  • Delivering process validation for mixing, filling, and re-validation of existing products.
  • Supporting equipment validation and lifecycle management in line with Annex 15.
  • Providing validation input for regulatory submissions and NPD/NPI projects.
  • Assisting with GMP inspection readiness and cross-functional validation support.

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  • Minimum 3 years’ experience in a pharmaceutical manufacturing validation role.
  • Strong understanding of Quality and Validation principles within GMP environments.
  • Degree in Science or Engineering (Analytical Chemistry background advantageous).
  • Ability to interpret technical data, manage multiple priorities, and work to tight timelines.
  • Confident communicator with the ability to influence and collaborate across departments.
  • A proactive, continuous-improvement mindset suited to a dynamic manufacturing setting.

Note

This is a permanent position. Only apply if you already have permanent, unrestricted right to work in the UK, as sponsorship is not available for this role.

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Skills

Validation Protocols
GMP Manufacturing
Change Control
Analytical Method Validation
Risk Impact Assessment
ICH Q10
ICH Q3D
CAPA
Cleaning Validation
Process Validation
Annex 15
NPI Projects
GMP Inspection Readiness
Technical Data Interpretation
Cross-functional Collaboration

Location

Preston, England, United Kingdom

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