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Technical Specialist - Laboratory Information Systems; LIMS

Job in Hatfield, Hertfordshire, HR6, England, UK
Listing for: Reed Specialist Recruitment
Full Time position
Listed on 2026-10-19
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
Salary/Wage Range or Industry Benchmark: 48000 - 68000 GBP Yearly GBP 48000.00 68000.00 YEAR
Job Description & How to Apply Below

Senior Technical Specialist (LIMS Systems)

12-Month Fixed-Term Contract

Hatfield, Herts

An exciting opportunity has arisen for an experienced Senior QC Systems Technical Specialist to join a leading pharmaceutical manufacturing organisation. This role will focus on supporting and maintaining critical electronic laboratory systems used within a Quality Control environment, ensuring compliance, reliability, and continuous improvement.

The Role

You will act as a subject matter expert for laboratory electronic systems, including the LIMS (Laboratory Information Management Systems), providing technical support and helping to drive system enhancements across the QC function.

Key Responsibilities
  • Provide technical support, troubleshooting, and ongoing maintenance for QC laboratory electronic systems.
  • Manage and maintain master data to ensure system performance remains compliant with GMP and data integrity requirements.
  • Support system enhancements, software updates, new module deployments, and change control activities.
  • Assist with the qualification, validation, and implementation of new or replacement laboratory systems.
  • Train and support laboratory personnel in the effective use of specialist QC software.
About You

To be successful in this role, you will possess:

  • A degree in a scientific discipline, or equivalent industry experience.
  • Proven experience supporting laboratory electronic systems within a pharmaceutical GMP environment.
  • Strong working knowledge of LIMS and/or CDS platforms, including master data management.
  • Excellent communication skills with the ability to explain technical concepts to a range of stakeholders.
  • Good knowledge of pharmaceutical Quality Control processes and GMP regulations.
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