GMP & CSV Validation Specialist

SLS Services Limited

Northern Ireland

On-site

GBP 25,000 - 38,000

Full time

14 days+

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Job summary

SLS Services Limited is seeking a Validation Analyst to support qualification and validation activities across pharmaceutical facilities in the UK. You will prepare and maintain validation documentation, coordinate commissioning and qualification work, and ensure GMP compliance.

Strong analytical and communication skills are required, with a focus on quality and timely delivery. The role involves working with cross-functional teams, contributing to procedures, and supporting ongoing process

Qualifications

  • Degree in a scientific, engineering or IT discipline or equivalent.
  • GMP knowledge and practical understanding of validation activities.
  • Strong report writing and technical communication skills.
  • Ability to manage multiple priorities and meet milestones.
  • Familiarity with CSV concepts is desirable.

Responsibilities

  • Prepare, review and maintain qualification and validation documentation (protocols, reports, master plans, SOPs).
  • Coordinate and execute qualification and validation activities across equipment, facilities and systems.
  • Manage project schedules, monitor progress and support milestones.
  • Contribute to development and improvement of validation procedures.
  • Work with cross-functional teams and represent Validation in technical discussions.
  • Ensure activities comply with GMP and industry regulations.
  • Perform periodic reviews and support corrective actions.

Skills

GMP knowledge
Written communication
Planning and organisation
Analytical skills
Data interpretation

Education

Science/Engineering/IT degree
A-Levels or equivalent with 12 months experience

Job description

SLS Services Limited is seeking a Validation Analyst to support qualification and validation activities across pharmaceutical facilities in the UK. You will prepare and maintain validation documentation, coordinate commissioning and qualification work, and ensure GMP compliance.

Strong analytical and communication skills are required, with a focus on quality and timely delivery. The role involves working with cross-functional teams, contributing to procedures, and supporting ongoing process

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