Following recent funding, the company is now entering a key growth phase as they scale their product and expand adoption.
Sitting at the intersection of product, engineering, and operations, you will ensure regulatory requirements are met while enabling the company to move quickly and scale effectively.
You will take full ownership of the Quality Management System (QMS), oversee medical device compliance, and act as the internal lead for ISO standards. This role combines strategic oversight with hands-on execution and will be critical in building scalable, audit-ready processes.
There is also a clear pathway to take on (or grow into) a Clinical Safety Officer (CSO) position, contributing to clinical risk management and safety governance as the product evolves.
Own and evolve the company’s Quality Management System (QMS)Ensure ongoing compliance as the product develops (features, integrations, deployments)Maintain audit readiness across documentation, policies, and controlsLead preparation for audits, inspections, and certificationsMaintain relevant certifications and regulatory approvalsSupport clinical safety processes, including risk assessments and governance frameworksAct as a cross-functional partner, translating regulatory requirements into practical business decisions
Experience working within a regulated environment, ideally software as a medical device (SaMD)London-based, with a hybrid working model (3 days in-office)”, “datePosted”: “2026-05-23”, “hiringOrganization”: { “@type”: “Organization”, “name”: “SciPro”, “sameAs”: “https://uk.whatjobs.com/pub_api__cpl__439442526__4861?utm_campaign=publisher&utm_medium=api&utm_source=4861&geoID=33” }, “jobLocation”: { “@type”: “Place”, “address”: { “@type”: “PostalAddress”, “addressLocality”: “London” } } }
We’re working with a fast-growing, venture-backed technology company operating within the healthcare space.
Following recent funding, the company is now entering a key growth phase as they scale their product and expand adoption.
Sitting at the intersection of product, engineering, and operations, you will ensure regulatory requirements are met while enabling the company to move quickly and scale effectively.
You will take full ownership of the Quality Management System (QMS), oversee medical device compliance, and act as the internal lead for ISO standards. This role combines strategic oversight with hands-on execution and will be critical in building scalable, audit-ready processes.
There is also a clear pathway to take on (or grow into) a Clinical Safety Officer (CSO) position, contributing to clinical risk management and safety governance as the product evolves.
Own and evolve the company’s Quality Management System (QMS)Ensure ongoing compliance as the product develops (features, integrations, deployments)Maintain audit readiness across documentation, policies, and controlsLead preparation for audits, inspections, and certificationsMaintain relevant certifications and regulatory approvalsSupport clinical safety processes, including risk assessments and governance frameworksAct as a cross-functional partner, translating regulatory requirements into practical business decisions
Experience working within a regulated environment, ideally software as a medical device (SaMD)London-based, with a hybrid working model (3 days in-office)…