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Greater London, United Kingdom Sierra 57 Consult Full timeJob Overview Working alongside our client, an established injection moulding manufacturer, we are looking for a Senior Quality Engineer to join their team to support continued business growth. Remit Working within the Operations team as a Senior Quality Engineer you will lead on quality, ensuring quality KPIs are met, and CI goals are achieved whilst...
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Senior Quality Engineer
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London Area, United Kingdom GxPeople Global Full time £60,000 - £120,000 per yearAn innovative MedTech startup in London looking for a Senior Quality Engineer to help build and lead their Quality Management System (ISO and support the development of their first implantable medical device.You'll work closely with the design teams to ensure products are developed in a controlled, compliant, and scalable way contributing directly to the...
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Senior Quality Engineer
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London, Greater London, United Kingdom Kent Full time £60,000 - £80,000 per yearDescriptionAbout the job:Kent is looking for a Senior Quality Engineer to join the UK Engineering Quality team at Kent. The purpose of this position is to provide Quality support to the UK Engineering business and is a full-time role.We follow a hybrid working model that combines office and remote work, with a requirement to be in the Woking office four days...
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Senior Quality Engineer
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Greater London, United Kingdom Balfour Beatty plc Full timeSenior Quality Engineer (MEPH) Balfour Beatty plc – London, England, United Kingdom About The Role HS2’s new £1 billion Old Oak Common station will become the UK’s best‑connected rail station. Balfour Beatty VINCI SYTRA joint venture is responsible for the final design, construction and commissioning of the station in Northwest London. The Senior...
Senior Quality Engineer
4 weeks ago
An innovative MedTech startup in London looking for a Senior Quality Engineer to help build and lead their Quality Management System (ISO 13485) and support the development of their first implantable medical device.You’ll work closely with the design teams to ensure products are developed in a controlled, compliant, and scalable way contributing directly to the company’s mission to transform neurological care through cutting-edge silicon-based technology.What you’ll be doing:Own and maintain QMS processes in line with ISO 13485Lead QMS remediation and eQMS implementation projectsSupport design and development (DHF, FMEA, design reviews)Oversee supplier qualification, goods handling, and documentation complianceChampion quality culture across engineering and operationsWhat you’ll need:4+ years’ experience in Quality Engineering within medical devicesDeep knowledge of ISO 13485 and design controlsEssential: experience working with integrated circuits or silicon-based technologiesStrong documentation, organisational, and process-driven mindsetHands-on approach and comfort in a complex engineering environmentIf you’re a MedTech QA professional who thrives in a hands-on, fast-paced setting — and want to help bring life-changing technology to market please apply to the advert or get in touch for more details.
