Quality Assurance Lead - Scientific Testing & Anti-Doping Laboratory

LGC Limited; Fordham; Remote; GBP 60,000 - 90,000; Full time

Job summary

LGC ASSURE, part of LGC Limited, seeks an experienced Quality Assurance Lead for our Fordham laboratory in Cambridgeshire. You will shape and strengthen quality across scientific operations, focusing on ISO/IEC 17025 accreditation and continuous improvement.

As a hands-on leader, you’ll drive audits, manage risk, and develop the QMS, collaborating with scientific and operational teams to balance compliance with practical workflows.

Qualifications

• Substantial experience leading an ISO/IEC 17025‑accredited QMS.
• Strong understanding of accreditation requirements and practical processes.
• Experience leading audits, root cause analysis, corrective and preventive actions, risk assessments and change control.
• Excellent project management and organisational skills with the ability to coordinate across teams.
• Ability to balance compliance requirements with operational needs.

Responsibilities

• Lead quality across the business as a trusted partner for accreditation and continuous improvement.
• Own and strengthen the QMS to remain compliant across different areas of the business.
• Drive accreditation and compliance by interpreting ISO/IEC 17025 requirements and supporting framework development.
• Lead audits, investigations, non-conformances, corrective actions and change control.
• Collaborate with teams to resolve quality issues and simplify processes.
• Support development of electronic QMS and SharePoint-based tools.

Skills

Quality management

ISO 17025

Audits

Risk assessments

Change control

Stakeholder management

Communication

Tools

eQMS

SharePoint

Job description

Quality Assurance Lead - Scientific Testing & Anti-Doping Laboratory

• Full-time
• Work Arrangement: On-site
• Department: Quality Assurance and Regulatory Affairs

Location: Fordham, Cambridgeshire | On-site

At LGC ASSURE, everything we do is driven by one purpose: Science for a Safer World.

As part of our Sports & Specialised Analytical Services (SSAS) team, you’ll be joining an internationally recognised scientific testing business working across animal sports medication, human drug testing and dietary supplement certification. Our work supports the integrity of sport, protects public health and helps ensure products meet the highest standards.

We’re looking for an experienced Quality Assurance Lead to help shape, strengthen and continuously improve quality across our scientific operations.

This is an on-site role based at our Fordham laboratory in Cambridgeshire. A regular on-site presence is essential to the role, working directly with our scientific and operational teams.

The opportunity

This is more than a traditional quality compliance role. You'll work across a diverse range of scientific and operational teams, each with different processes, priorities and accreditation requirements. You'll need to understand those differences, build strong relationships and find practical solutions that maintain compliance without creating unnecessary barriers.

We're looking for someone who can turn “we can't do that” into “how can we make that work?”

You'll bring the technical credibility to challenge existing practices, the judgement to manage risk proportionately, and the people skills to bring others with you. Alongside maintaining a robust quality framework, you'll have the opportunity to improve systems, simplify processes and make better use of technology.

If you enjoy solving complex problems, influencing change and helping teams find better ways of working, this is an opportunity to make a meaningful impact.

What you'll be doing

Lead quality across the business: Act as a trusted quality partner to scientific and operational teams, providing expert guidance on accreditation, compliance, risk and continuous improvement.

Own and strengthen the QMS: Maintain and develop our Quality Management System, ensuring it remains effective, compliant and fit for purpose across different areas of the business.

Drive accreditation and compliance: Interpret ISO/IEC 17025 requirements, support the ongoing development of our accredited quality framework and deputise for the ISO 17025 Quality Manager as required.

Lead audits and investigations: Manage audit activity, root cause investigations, non-conformances, corrective actions, risk assessments and change control, ensuring actions address underlying issues and deliver lasting improvements.

Turn challenges into solutions: Work collaboratively with teams to resolve quality issues, balance compliance requirements with operational needs and influence decisions at all levels.

Improve systems and processes: Lead improvement initiatives, identify opportunities to simplify processes and support the development of our electronic Quality Management System (eQMS), including digital tools and SharePoint-based solutions.

Coordinate projects and stakeholders: Work with internal teams and external accreditation bodies to plan and deliver accreditation activities, manage competing priorities and achieve successful outcomes.

Develop capability: Coach and support colleagues, helping embed a positive quality culture and build confidence in quality practices across the organisation.

You’ll be an experienced quality professional with a strong understanding of laboratory accreditation and the confidence to operate independently in a varied, fast-moving environment.

You’ll have:

Substantial experience managing or leading a Quality Management System within an ISO/IEC 17025-accredited laboratory environment.

A strong understanding of accreditation requirements and how to translate them into effective, practical working processes.

Experience leading audits, root cause analysis, corrective and preventive actions, risk assessments and change control.

The ability to assess quality risks, prioritise effectively and focus on improvements that deliver meaningful results.

Experience improving quality systems, processes or ways of working, ideally including eQMS, SharePoint or other digital quality tools.

Strong project management and organisational skills, with the ability to coordinate activities across multiple teams and stakeholders.

Excellent communication and influencing skills, with the confidence to challenge constructively, build credibility and bring people along with you.

You’ll be someone who:

Finds solutions, not just problems. You can challenge a decision while working collaboratively to find a compliant way forward.

Builds relationships and credibility. You understand different perspectives and adapt your approach to the people and teams you’re supporting.

Enjoys variety. You’re comfortable switching between different scientific disciplines, operational challenges and competing priorities.

Improves how things work. You question established practices, identify opportunities to simplify and turn ideas into practical improvements.

Brings structure to ambiguity. You’re proactive, comfortable working autonomously and able to create clarity where processes or responsibilities aren't always clearly defined.

Makes quality meaningful. You help colleagues understand not just what is required, but why it matters and how to achieve it effectively.

Our Values

• Passion
• Integrity
• Brilliance
• Respect

Equal opportunities

We are committed to ensuring that every job applicant and employee is valued for their individual talents. We strictly prohibit discrimination on the basis of age, disability, race, colour, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or parental status, religion, or belief. We proudly support an inclusive work environment where everyone can compete and succeed based on their merits.

For more information about us, please visit our website: https://www.lgcassure.com/

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