Overview In this on-site Cambridge role, you design functional parts for complex medical devices and collaborate with industrial design and human factors teams. You’ll work on projects ranging from solo efforts to large, cradle-to-grave d...Read More>>.

Overview In this role you will develop embedded C software for highly complex medical devices within a growing medical devices organization. You’ll often be solving challenging problems, sometimes solo, applying strong engineering fundame...Read More>>.

Overview In this role you will help invent and design brand-new medical devices in a multidisciplinary team. You will work on both embedded software and hardware electronics as part of a cross-functional group of engineers and physicists. T...Read More>>.

Overview In this role you design and develop optical systems for life-improving medical devices in Cambridge, collaborating with mechanical, electronics and software engineers. You apply optical design tools to prototype and test novel tech...Read More>>.

Overview In this role you will contribute to inventing lifesaving and life-improving medical devices within a growing division. You’ll work on multiple projects, sometimes leading them, alongside a team of engineers and experts. You’ll...Read More>>.

Overview As Director, Regulatory Affairs, Labelling you will lead global labelling strategy for Ipsen’s products across development and lifecycle management. You will shape early labeling input with development teams and ensure USPI, EU l...Read More>>.

Overview Join Moody’s Government, Public and Regulatory Affairs to guide insurance regulatory strategy across EMEA. You will shape policy positions, engage with regulators, and apply AI-driven approaches to improve regulatory workflows. T...Read More>>.

Overview In this role you will lead Voy’s Government & Regulatory Affairs to shape policy, engage regulators and policymakers, and translate business priorities into actionable workstreams. You’ll build proactive relationships with bodi...Read More>>.

Overview In this role you will help invent life-changing medical devices from Cambridge, collaborating with physicists, engineers and industry experts. You’ll work across imaging, surgical systems, electro-medical and other complex techno...Read More>>.

Overview In this role you will design and develop electronics for cutting-edge medical devices, contributing to life-saving technologies. You will join a dedicated medical devices team on-site in Cambridgeshire, tackling complex design chal...Read More>>.

Overview In this role you ensure quality across medical device projects in a growing Cambridge-based team. You will focus on quality assurance under ISO 13485, with advantageous knowledge of EN 60601, and contribute to technical files and t...Read More>>.

Overview In this role, you will assess and improve quality management systems for software-based medical devices, ensuring regulatory compliance and robust processes. You’ll work within a cross-functional context to strengthen QMS and sup...Read More>>.

Overview In this role you will contribute to the design and development of implantable medical devices in a Cambridge team. You’ll collaborate with engineers, physicists, scientists and clinicians to advance breakthrough implants. The pos...Read More>>.

Overview In this role you act as Ofcom’s lead contact for Scotland across consumer, telecoms, spectrum and postal duties. You will build relationships with senior government, Parliament, and industry stakeholders, and coordinate cross-tea...Read More>>.

Overview In this role you will lead cutting-edge development projects within a multidisciplinary medical devices team in Cambridge, driving from concept to commercialization. You will oversee cross-functional groups, ensuring timelines and...Read More>>.

Overview In this role you will drive adoption and growth of innovative minimally invasive women’s health technologies across a UK territory. You will educate clinicians, provide product expertise and training, and work with cross-function...Read More>>.

Overview In this role you will help invent and improve Medical Devices within a collaborative, multi-disciplinary environment in Cambridge. You’ll translate inventive ideas into practical devices across drug delivery, diagnostics, wearabl...Read More>>.

Overview In this role you contribute to the design and development of cutting-edge medical devices, working within a multidisciplinary design team to deliver safe, reliable products. You will join a growing part of the business with clear c...Read More>>.

Overview In this remote, contract-based role you lead global regulatory strategy and submissions for oncology development programs. You will serve as Global Regulatory Lead, guiding cross-functional teams and aligning with corporate objecti...Read More>>.

Overview In this role you will help invent and design lifesaving medical devices within a multidisciplinary team. You’ll contribute to the development and improvement of products in a regulated ISO 13485 environment, with EN 60601 knowled...Read More>>.

Overview In this role you will lead international CMC regulatory activities to support global product development. You’ll manage agency communications, ensure quality CMC sections, and influence submissions across multiple programs. You w...Read More>>.

Overview In this role, you shape and execute the Global Regulatory Affairs strategy for the IVD and life sciences portfolio, guiding regulatory pathways and milestones across the product lifecycle. You will lead regulatory submissions with...Read More>>.

Overview In this role, you will collaborate with engineers and scientists in Cambridge to invent and advance new medical devices. You work across multiple projects, solving complex problems while keeping pace with evolving Technologies and...Read More>>.

Overview As a Mechanical Engineer, you will help develop new Medical Devices to ISO 13485 standards in a collaborative, state-of-the-art lab setting. You will join a multidisciplinary team of engineers and scientists to push the design and...Read More>>.

Overview In this Electronics Engineer role, you will contribute to inventing and designing lifesaving medical devices within a Cambridge-based team of medical devices experts. You will work on brand-new products, focusing on design, testing...Read More>>.

Overview In this role you will lead the development and execution of global regulatory strategies for international markets, shaping regulatory input across multiple programs. You will collaborate with regional teams to align clinical and c...Read More>>.

Overview As a Medical Device Quality Specialist Consultant, you support development and lifecycle management of medical devices and combination products, navigating regulatory complexity, embedding robust quality systems, and ensuring produ...Read More>>.

Overview In this role you contribute to EU regulatory strategies for Amgen’s biosimilar portfolio, guiding submissions from development to launch and lifecycle management. You will collaborate with global and regional teams to prepare MAA...Read More>>.

Overview As Senior Manager, Regulatory Affairs you will shape and execute global regulatory strategy for a late-stage biotech program. You will work closely with senior stakeholders and external partners to navigate major markets, including...Read More>>.

Overview In this role you will lead and shape medical device research programmes from concept through to manufacturing. You will manage a multi-disciplinary team of engineers and collaborate across cross-functional partners to deliver compl...Read More>>.

Overview In this role you lead the Medical Devices Service Centre to deliver exceptional service, quality, and compliance within a regulated environment. You will manage up to 30 staff, drive financial and operational performance, and partn...Read More>>.

Overview As Senior Manager, Regulatory Affairs at Alnylam, you will drive EU and global regulatory submissions for RNAi therapeutics, collaborating with EU/regulatory leads and cross-functional teams to shape strategy and submissions across...Read More>>.

Overview In this EU Regulatory Affairs Manager role, you help secure and maintain EU licenses for clinical trials and marketed products, supporting one or more products from an EU regulatory perspective. You may lead regulatory activities f...Read More>>.

Overview In this role you will drive the design and development of innovative medical devices within a multidisciplinary team. You will turn concept ideas into robust, manufacturable hardware through hands-on mechatronics work. You’ll col...Read More>>.

Overview In this role you will support Moody's Government, Public and Regulatory Affairs strategy for the EMEA region, engaging with regulators, governments and industry groups. You will help expand insurance regulatory coverage, prepare st...Read More>>.

Overview As Regulatory Affairs Lead, you will shape and strengthen our regulatory affairs function for a leading trading and reporting consultancy. You will drive engagement with regulators and market participants across UK, EU, and other j...Read More>>.

Overview In this role you guide clients through drug, biologic, and medical device development, leading regulatory teams and shaping strategy to deliver high-quality submissions. You’ll be the trusted HA liaison and translate complex requ...Read More>>.

Overview In this role you will contribute to inventing and developing brand-new medical devices in a fast-growing setting in London. You will collaborate with physicists, mechanical engineers, and scientists to create lifesaving technologie...Read More>>.

Overview As Regulatory Affairs Lawyer at Teya, you steer UK and EU licensing, public policy, and regulatory strategy to support independent local businesses. You’ll lead licensing activities, engage with regulators and policymakers, and s...Read More>>.

Overview As a Senior Electronics Engineer, you will lead electronic design activities for medical devices that meet ISO 13485 standards and help take products to market. You will work within a cross-functional team of engineers and scientis...Read More>>.