About this role
Salary: £40,000 - 80,000 per year
Requirements: Solid operational experience in Quality within a regulated industry such as manufacturing, medical devices, pharmaceuticals, aerospace, automotive, or food and beverageApplied working knowledge of ISO 9001:2015 and at least one sector-specific standard such as ISO 13485, AS9100, IATF 16949, or FDA 21 CFR Part 820, gained through real-world useHands-on experience with non-conformance management, CAPA investigation and review, and audit participation or preparationStrong analytical and written communication skillsAbility to clearly explain why an answer is incorrect and what a compliant, high-quality response should look likeComfortable working through large volumes of detailed evaluation work while maintaining accuracy and consistencyConfident applying professional judgement where standards require interpretation rather than checklist complianceWilling to challenge plausible-sounding but incorrect outputs, prioritising correctness and regulatory integrityInterested in contributing to the development of AI for regulated environments, even if your background is not technical Responsibilities: Apply annotation guidelines for Quality training data set by our AI Domain Lead, ensuring consistent and defensible labelling decisionsLabel Quality datasets at scale, using practitioner-level judgement to classify non-conformances, evaluate CAPA plans, and categorise audit and supplier quality issuesEvaluate AI-generated outputs against expert-defined rubrics, identifying errors, gaps, or unsafe interpretations and clearly documenting what a correct response looks like and whyTest AI capabilities against realistic and complex Quality scenarios, including ambiguous root causes, cross-functional failures, and regulatory edge cases drawn from real experienceContribute to Quality red-team testing by identifying challenging scenarios, complex CAPA chains, and multi-standard regulatory situations that stress-test the modelSupport the curation and validation of Quality regulatory reference materials to ensure accuracy, relevance, and traceabilityParticipate in calibration sessions with other specialists to maintain consistency, resolve interpretation differences, and uphold high evaluation standardsWork closely with our AI engineers and product teams, translating practitioner feedback into actionable improvements in model behaviour Technologies: AISupport More:
We are Ideagen, building AI for regulated industries where correctness is non-negotiable. This is a permanent, hybrid role based in Ruddington, Nottinghamshire, with three days a week in our head office and salary to be discussed at the next stage. We offer benefits at Ideagen, support flexible arrangements, and value work-life balance. We operate globally with offices in America, Australia, Malaysia and India, and our software helps keep airplanes flying, food safe, and patients cared for. We are building a future-ready team and welcome people who are curious, adaptable, and open to using AI to improve how they work.
last updated 36 week of 2026