QC Technician - Temp/Contract

Cranleigh Scientific Ltd; Bracknell; On-site; GBP 23,000 - 29,000; Part time

Job summary

BioChek (UK) Limited in Bracknell is seeking a Quality Control Technician to join the GMP‑regulated QA team and support testing and documentation for veterinary diagnostic products used worldwide.

This temporary contract runs until the end of December 2026, with potential extension. You will perform QC assays, prepare reagents, record results, maintain controlled documentation and help investigate any anomalies in a team‑based laboratory environment.

Qualifications

• Previous laboratory experience in life sciences or diagnostics.
• Good practical lab skills including accurate pipetting.
• Follow written procedures and test methods carefully.
• Strong attention to detail and data integrity.
• Organise and prioritise work as testing requirements change.
• Knowledge of GMP/GLP or controlled quality documentation is beneficial.

Responsibilities

• Carry out QC assays in line with approved test methods.
• Prepare reagents, standards, controls and samples for testing.
• Inspect and test finished products, diagnostic kits and materials.
• Record test results and maintain controlled documentation.
• Review data and escalate unusual results; assist investigations.
• Maintain stock of reagents and keep areas clean and organized.

Skills

Lab experience

Pipetting

Documentation

Data integrity

GMP/GLP knowledge

Communication skills

Education

Science-based degree / HNC / HND / BTEC

Job description

We’re recruiting for a Quality Control Technician to join BioChek (UK) Limited in Bracknell, supporting the testing and quality control of veterinary diagnostic products used by customers worldwide. This is a hands‑on laboratory role suited to someone with previous lab experience who is comfortable following controlled procedures, carrying out accurate testing and maintaining high standards of documentation. The position will run on a temporary/contract basis until the end of December 2026. There is potential for extension/being made permanent but no guarantee.

The role

Working within BioChek’s Quality Control team, you’ll help ensure products and materials meet the required quality, regulatory and technical standards before they are released.

Your day-to-day work will involve laboratory testing, preparing samples and reagents, recording and reviewing results, checking equipment and supporting investigations where required. You’ll work within established GMP, GLP and Quality Management System procedures, with training provided on relevant methods and systems.

What you’ll be doing

• Carrying out Quality Control assays in line with approved test methods and procedures
• Preparing reagents, standards, controls and samples for laboratory testing
• Inspecting and testing finished products, diagnostic kits, components and incoming materials
• Accurately recording test results and maintaining controlled documentation
• Reviewing routine test data and escalating unusual or out‑of‑specification results
• Operating laboratory equipment and completing routine checks and calibrations
• Supporting the manufacture, testing and monitoring of internal controls
• Assisting with investigations, repeat testing and corrective actions
• Maintaining appropriate stocks of laboratory reagents, consumables and materials
• Keeping laboratory areas and equipment clean, safe and organised
• Working in accordance with GMP, GLP, quality and health & safety requirements
• Contributing to continuous improvement and wider Quality Control activities

What we’re looking for

You’ll need previous experience working in a laboratory environment, ideally gained within life sciences, diagnostics, pharmaceuticals, manufacturing or another relevant setting.

You’ll also bring:

• Good practical laboratory skills, including accurate pipetting
• The ability to follow written procedures and test methods carefully and consistently
• Strong attention to detail and a methodical approach to your work
• Good record-keeping and an understanding of the importance of data integrity
• The ability to organise and prioritise work as testing requirements change
• Confidence using basic computer systems to record and review information
• Good communication skills and a willingness to raise questions or potential quality issues
• The ability to work effectively both independently and as part of a team

Knowledge of GMP, GLP or controlled quality documentation would be beneficial. Previous ELISA experience and a science‑based qualification such as a degree, HNC/HND or BTEC would also be advantageous, but relevant practical laboratory experience will be considered.

Interested?

If you have laboratory experience and are looking for an opportunity to build on your Quality Control skills within a regulated diagnostics environment, we’d be pleased to hear from you.