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Company OverviewSkills, Experience, Qualifications, If you have the right match for this opportunity, then make sure to apply today.Heartfelt Technologies is a medical device startup on a mission to transform how we monitor patients with heart failure. Our passive, camera-based technology predicts heart failure events before they happen, enabling earlier intervention and improving lives. As we ramp up production for a major clinical trial, we are looking for a proactive and detail-oriented Quality Control Technician to help us maintain the highest standards of product quality and compliance.The RoleThis is a key role in ensuring our devices meet medical-grade reliability and regulatory expectations. As our Quality Control Technician, you will take ownership of inspection, documentation, and quality procedures. You will work closely with operations and manufacturing, inspecting components and devices, tracking results, and helping refine our quality processes.We are a growing and collaborative team, and in the early months, you will be hands-on with manufacturing to gain a deep understanding of our assembly process and contribute to device builds when needed. ResponsibilitiesPerform inspections of incoming components, subassemblies, and finished devices against defined specificationsAccurately record inspection data using ERPAG and maintain detailed QC records using digital toolsEnsure all inspection and documentation activities comply with applicable quality standards and regulatory requirements, including ISO 13485 and Good Manufacturing Practice (GMP) guidelinesMaintain and support quality procedures and documentationAssist in investigations of defects and non-conformancesEnsure traceability and documentation is complete and audit-readyProvide proactive feedback to manufacturing to support continuous improvementContribute to the development of inspection protocols and assist with training staff on quality proceduresSupport day-to-day manufacturing activities during peak periods or as neededWhat We Are Looking ForHands-on experience in a quality or inspection role - medical device or electronics background preferredFamiliarity with ISO 9001 is essential; knowledge of ISO 13485 and GMP is highly desirableExcellent attention to detail and a methodical, problem-solving mindsetComfortable using digital tools document and track inspections resultsA proactive self-starter who takes ownership of their work and thrives in a fast-paced environmentTeam player with strong communication and collaboration skillsCalm under pressure, flexible, adaptable, and eager to learn new skillsWhy Join Us?Contribute to a life-changing technology during a pivotal growth stageBe part of a growing, friendly, and motivated teamGain hands-on experience across quality and manufacturing, with room to growOffice-based in North Cambridge, with on-site parking and easy cycling distance from the city centre25 days paid holiday plus public holidaysCasual dress and a mission-driven cultureNo recruiters