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 In this Senior Embedded Software Engineer role, you’ll develop and refine embedded software for medical devices in a cross-disciplinary team. You’ll collaborate with electronics engineers, scientists, and designers to reimagine...Read More>>.

Overview As a Senior Electronics Design Engineer in our Medical Devices group, you will lead the electronics development of new devices in a regulated environment. You join a multi-disciplinary R&D team in state-of-the-art labs near Cambrid...Read More>>.

Overview In this role you will lead the development of cutting-edge Medical Devices within Health Tech, Biotech and Wearables, ensuring designs meet market and regulatory standards. You will work with a multidisciplinary team to translate i...Read More>>.

Overview In this role you will drive the design and improvement of life-saving medical devices, collaborating with cross-disciplinary experts to tackle complex challenges. You will contribute across the full design lifecycle, ensuring regul...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 Parexel seeks experienced CMC professionals to join as Regulatory Affairs Consultant CMC Author, supporting clients in regulatory affairs and CMC authoring for biologics. The role is remote or office-based across Europe and involve...Read More>>.

Overview In this role, you lead and deliver medical device projects from concept through development in a collaborative, high-caliber lab environment in Cambridge. You combine hands-on mechanical design with cross-functional teamwork, mento...Read More>>.

Overview In this role you will lead electro-mechanical medical device projects in Cambridge, while hands-on electronics work and mentorship are part of the responsibilities. You guide cross-functional teams to deliver life-saving technologi...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 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 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 As a Senior Mechanical Engineer in our Cambridge team, you will help design and mature complex instrumentation for medical devices. You’ll blend hands-on build work with rigorous design to implement gear systems and mechanisms. Y...Read More>>.

Overview In this role you will design and develop groundbreaking medical devices, collaborating with scientists and design specialists to translate concepts into lifesaving technology. You will work across fluid mechanics and biomedical eng...Read More>>.

Overview In this role you will lead multiple electro-mechanical medical device projects from concept through delivery, guiding cross-functional teams and mentoring junior engineers. You will balance hands-on mechanical design work with proj...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 design and develop FPGA-centric electronics for lifesaving medical devices in a Cambridge team. You’ll work alongside mechanical, software, and science specialists to deliver robust, regulated solutions. The role...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 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 Growing Medical Devices company near Cambridge seeks an experienced Mechanical Design Engineer to shape a new device. You will collaborate with a cross-functional team of physicists, electronics engineers, and scientists. You will...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 In this role you drive post-approval regulatory activities for CMC in biological and plasma products, ensuring worldwide submissions stay compliant. You will partner with manufacturing, QA, QC, and other regulatory functions to sha...Read More>>.

A leading pharmaceutical company in the United Kingdom is seeking a Mid-Senior level Regulatory Affairs Specialist to provide regulatory input and support for new Marketing Authorisation Applications. The ideal candidate will have a strong background...Read More>>.

Apsida Life Science are currently partnering with a global biopharmaceutical company recognised for developing innovative medicines that address complex and serious diseases. The organisation combines strong scientific expertise with a patient-...Read More>>.

Do you want to contribute to a safer market while gaining an authentic international experience as a consultant? Obelis is currently looking for a RA Expert Consultant specialized in food supplements! Your role will be:...Read More>>.

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store bran...Read More>>.

Regulatory Affairs and Quality Assurance Assistant – Medical Devices - CambridgeDue to the growth of a medical devices company based in Cambridge, there is need for a new Regulatory Affairs and Quality Assurance Assistant to work with...Read More>>.

About AbbVieAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives a...Read More>>.

Inspiration Healthcare seeks a Head of Quality Assurance and Regulatory Affairs in the UK to lead the Quality Assurance and Regulatory Affairs function, ensuring MDR compliance and regulatory registration across key markets. The role drives a cult...Read More>>.

Job Purpose (Role Definition)The Head of Quality Assurance and Regulatory Affairs:will manage the Quality Assurance and Regulatory Affairs function.is appointed as the person responsible for regulatory compliance,...Read More>>.

Are you tired of pushing paper in a sterile QA office?Or perhaps you're an engineering graduate who loves the hands-on grit of the workshop, but wants a highly lucrative, stable career path in quality?Most Qua...Read More>>.

Senior Regulatory Affairs Specialist - CambridgeAt Hologic, we are committed to enabling healthier lives everywhere, every day. To deliver on that purpose, we need strong regulatory expertise that helps bring new products to marke...Read More>>.

Oxford, UK | Reporting to VP of Operations | Global travel including Boston, USA (Anticipated start date for this role: January 2027) Job Overview The RAQA Director, is responsible for the strategic developm...Read More>>.

BDO UK LLP is seeking a Legal Counsel to join the Office of the General Counsel (OGC) and help protect the firm's practice. You will work closely with Partners and senior members to advise on risk and regulatory matters, and support a range of civ...Read More>>.

Closing Date: 26/10/2026 Group: Strategy and Research Group Management Level: Senior Associate Job Type: Permanent Job Description: Please note that this role will close at 00:01 on Monday 26 October, and therefore we advise getting your applicati...Read More>>.

Ofcom in Edinburgh seeks a Senior Associate to lead Scotland affairs across telecoms, spectrum, and consumer policy. You will build relationships with government, Parliament, and industry, and guide regulatory thinking with a Scotland-focused lens...Read More>>.

MEDICAL TERRITORY MANAGER / MEDICAL ACCOUNT MANAGEREstablished over 35 years with a reputation for excellent customer service and support, this is a fantastic opportunity to join a leading manufacturer of capital equipment used to...Read More>>.

Wolters Kluwer Health seeks a seasoned Lead Project & Program Manager to drive complex, cross-functional initiatives across Operations Enablement, Quality, Regulatory Affairs, Clinical, Operations, Product, Commercial and Technology.You wil...Read More>>.

Elekta is seeking a Lead Software Developer in Test to shape the quality engineering strategy for its radiation therapy systems. You will work closely with software engineers, testers, Product Owners, and architects to drive modern test automation...Read More>>.

Integra LifeSciences Corporation is seeking a Field Service Engineer to ensure the functionality and reliability of medical devices across hospital sites in the UK.You will diagnose, repair, and maintain equipment, travel frequently, and pr...Read More>>.

Elekta is seeking a Manager, User Experience (UX) Research to lead our Global UX Research team in Crawley, ensuring safe, effective, and usable hardware and software. You will collaborate with Product Management, Engineering, Regulatory, and Desig...Read More>>.

AtriCure, Inc. is seeking a Regional Sales Manager to prospect, qualify, and close direct business in cardiac operating and related departments within hospitals. You will train and support the surgeon and staff in procedures and provide in‑O.R....Read More>>.

Can you turn regulatory complexity into commercial success while guiding the launch of tomorrow’s market-leading products?R&D Partners is seeking a Regulatory Affairs Manager to join a leading pharmaceutical company. This role offers a...Read More>>.

Cure Talent are delighted to be partnered with a growing medical device certification organisation that is expanding its scope into a number of additional medical device technologies. As part of this expansion, we are looking to speak with...Read More>>.

Randstad CPE is seeking a 12-month contract role in Cramlington to safely produce single-use medical products in a cGMP cleanroom, following a 4 days on, 4 days off day shift schedule from 6:00 AM to 6:00 PM.You will assemble components, fo...Read More>>.

Integra NeuroSciences Ltd is seeking a Field Service Engineer to ensure the performance and reliability of its medical devices across UK hospitals. You will travel to customer sites, perform diagnostic tests, calibrations, and repairs, and provide...Read More>>.