QC Technician
Listed on 2026-07-09
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Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers
Position Overview
The role is based within the Quality Control Restricted (QCR) Department at Pirbright and supports the testing and release of Foot and Mouth Disease antigen and vaccine batches in line with Good Manufacturing Practice (GMP) and regulatory requirements. It requires strict adherence to biosafety and compliance standards in a high‑containment laboratory environment. The successful candidate will contribute to routine laboratory activities, documentation, and continuous improvement initiatives while maintaining high quality and safety standards.
This is a fixed‑term contract until 31st December 2027 and requires a 72‑hour quarantine from animals susceptible to Foot and Mouth Disease virus (FMDV) after working in the facility. The QCR technician must comply with Specified Animal Pathogen Order (SAPO) Level 4 biosafety requirements, including changing clothing upon entry and exit and showering before leaving the area.
Tasks and Responsibilities- Follow established Standard Operating Procedures (SOPs) to perform laboratory and support activities
- Prepare test materials and reagents required for analysis
- Receive, log, and reconcile samples using the Laboratory Information Management System (LIMS)
- Perform routine laboratory testing, which may include:
- Virus Neutralisation Test
- Tissue Culture
- Serotype Identification
- Microcytopathic Infectivity Testing and Inactivation Kinetics
- Physical Chemical Testing
- Innocuity Testing
- Sucrose Density Gradient 146S testing
- Participate in the review and update of documentation, including SOPs
- Support deviation investigations, including OOX and discrepancy processes, and contribute to change control activities
- Maintain laboratory areas, including cleaning and basic equipment maintenance
- Operate laboratory equipment such as autoclaves and formalin locks in accordance with procedures
- Ensure compliance with GMP, EHS, and biosafety regulations at all times
- Contribute to continuous improvement activities and quality initiatives
- Ability to follow procedures accurately and work in a highly regulated environment
- Strong attention to detail and commitment to quality and compliance standards
- Good verbal and written communication skills in a professional setting
- Ability to organise work effectively, manage time, and prioritise tasks
- Proficiency in Microsoft Office and willingness to learn internal systems
- Ability to work both independently and as part of a team
- Professional approach to work, with adherence to company values, policies, and safety requirements
- Willingness to work in a high‑containment laboratory environment
- Experience with biological laboratory techniques (e.g. pipetting, microscopy, aseptic techniques) is advantageous but not essential
- Relevant education in a scientific discipline is preferred
The role is site‑based and requires on‑site presence in Pirbright. Working hours are Monday to Thursday 08:00–16:30 and Friday 08:00–15:30 (37.5 hours per week). A Disclosure and Barring Service (DBS) check will be required for the successful candidate. Any offer of employment will be subject to a satisfactory DBS certificate.
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