Your Role:

At EIT we are seeking an experienced and detailed orientated Laboratory Quality Manager to lead the development, implementation and continuous improvement of our Laboratory Quality Management System (QMS). The post-holder will provide quality direction across laboratory teams, enabling assurance that testing, research, and analytical activities consistently meet regulatory expectations, accreditation requirements and scientific best practice.

Your Responsibilities:

• Quality Management System (QMS) Leadership Develop, implement, and maintain a robust QMS tailored to laboratory operations. Ensure all processes are documented, controlled, and audit-ready. Lead the creation and review of quality policies, SOPs, and manuals to guarantee compliance with regulatory and accreditation standards.

• GLP Compliance Oversight Act as the organisation’s subject matter expert for Good Laboratory Practice (GLP). Monitor study plans, raw data, reports, and sample handling to ensure adherence to GLP principles and data integrity (ALCOA+). Provide guidance to laboratory teams and maintain awareness of regulatory updates from MHRA and other authorities.

• ISO Accreditation Support Drive preparations for ISO 17025 or ISO 15189 accreditation and re-accreditation cycles. Oversee technical quality activities such as method validation, proficiency testing, calibration, and uncertainty of measurement. Serve as the primary contact during external audits.

• Internal Audits & Risk Management
  Design and execute an internal audit programme aligned with GLP and ISO standards. Conduct audits, produce detailed reports, and verify corrective actions. Support risk assessments for change control, equipment, and method implementation, using audit trends to inform continuous improvement initiatives.

• Incident, Deviation & CAPA Management
  Lead investigations into deviations, non-conformances, and complaints using structured root cause analysis tools (e.g., fishbone diagrams, 5 Whys). Develop and track Corrective and Preventive Actions (CAPAs) to ensure sustainable improvements and verify their effectiveness.

• Document Control & Records Management
  Oversee document control systems for SOPs, technical methods, equipment files, and training records. Ensure all data and records are accurate, secure, and traceable, supporting digital QMS implementation for efficiency and compliance.

• Equipment & Method Quality Support
  Ensure equipment qualification, calibration schedules, and maintenance programmes meet regulatory requirements. Support method development and validation by embedding quality considerations into protocols and reviewing technical documentation for compliance.

• Training & Quality Culture Development
  Deliver training on GLP, ISO principles, data integrity, and audit readiness. Conduct competency assessments and promote a proactive quality culture where staff feel empowered to raise issues and contribute to process improvements.

• Quality Governance & Reporting
  Coordinate Laboratory Quality Meetings and Management Review Boards. Prepare and present quality reports, KPIs, and trend analyses to leadership. Provide strategic advice during planning for new methods, facilities, or technologies.

Requirements

Essential Skills, Qualifications & Experience:

• Degree in a scientific discipline (e.g. biology, chemistry, biomedical science, biotechnology).
• Substantial experience working within a GLP-compliant laboratory environment.
• Demonstrable experience with ISO 17025 (preferred) or ISO 15189 QMS requirements, including audit preparation and technical quality processes.
• Practical experience in internal auditing, deviation management and CAPA systems.
• Strong understanding of laboratory data integrity, document control and records management.
• Ability to lead cross-functional teams and collaborate with laboratory staff, study teams and senior management.
• Excellent analytical, organisational and communication skills.

Desirable Knowledge, Skills and Experience:

• Experience interacting with UKAS or regulatory bodies (MHRA, OECD GLP monitoring authority).
• Formal QMS training (ISO 17025/15189 auditor training, GLP advanced courses, ISO lead auditor).
• Experience in a multidisciplinary research or technology environment (e.g. translational research, diagnostics, engineering/biotech labs).
• Experience managing or mentoring junior quality staff.

Benefits

Our Benefits:

• Salary: £50,000 - £60,000 + travel allowance + bonus
• Enhanced holiday pay
• Pension
• Life Assurance
• Income Protection
• Private Medical Insurance
• Hospital Cash Plan
• Therapy Services
• Perk Box
• Electric Car Scheme

Working Together – What It Involves:

• You must have the right to work permanently in the UK.
• You will live in, or within easy commuting distance of, Oxford and can commit to being fully office based. Please note we cannot offer hybrid working for this role.