Field Service Engineer, Medical Devices Basic Salary £45,000 to £50,000Pension Company Vehicle Private Medical Cover...Read More>>.

Step into a leadership role where your expertise drives innovation. As a Director, Regulatory Affairs, you'll guide clients through the complexities of drug, biologic, and medical device development. Leading teams, shaping strategies, an...Read More>>.

Location : WitneyAbbott is about the power of health. For more than 130 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network...Read More>>.

Location: Hybrid role, with ideally a few days each week spent at Head Office, in Selby, North Yorkshire Department: Research & Development/Quality Join GBUK and help deliver medical devices that make a difference....Read More>>.

Job Title: Regulatory Affairs Manager - IVDs Job Type: Maternity Cover – 12 Month Contract Location: West London, UK – Hybrid/Remote Salary: £60,000 - £76,000 ***Please note that...Read More>>.

Cpl Life Sciences is seeking a Regulatory Affairs Manager - IVDs for a 12-month maternity cover contract. Located in West London with hybrid/remote work options, offering a salary of £60,000 - £76,000.The role sits at the interface of the...Read More>>.

Ernest Gordon Recruitment is seeking a CNC Programmer for a medical manufacturing role in Redhill, Surrey. You will code and edit CNC programs, test new programs and set, operate and troubleshoot CNC machinery, ensuring documentation is precise....Read More>>.

An exciting opportunity has arisen within this leading manufacturer of medical devices into the global healthcare and Pharmaceutical industries for a Field Service Engineer to be based in the Crewe, Stoke on Trent, Newcastle under lyme, Stone,...Read More>>.

eg technology is seeking a capable project leader to drive complex product development projects from concept through manufacture. You will coordinate software, electronics, mechanical engineering, industrial design and human factors teams, ensurin...Read More>>.

Medical Device Regulatory and Quality Consultant We are seeking a highly skilled consultant with experience in medical device and/or combination product Quality and Regulatory processes to join our Healthcare & Life Sciences (HLS) cons...Read More>>.

This highly regraded Cambridge-based medical technologies company is seeking a proven engineering leader to help guide high-value development programmes from concept through to transfer to manufacture. Your leadership will accelerate developmen...Read More>>.

ECM Selection is seeking a proven engineering leader for a Cambridge-based medical technologies company. You will guide development programmes from concept to transfer to manufacture, accelerating timelines and managing risk to improve patient out...Read More>>.

PA Consulting is seeking an experienced Medical Device Quality Specialist Consultant to support life‑cycle management of medical devices and combination products. You will guide regulatory strategy, risk management and quality systems across div...Read More>>.

Medical Device Quality Specialist Consultant We believe in the power of ingenuity to build a positive human future. As strategies, technologies, and innovation collide, we create opportunity from complexity. Our teams of...Read More>>.

We believe in the power of ingenuity to build a positive human future. As strategies, technologies, and innovation collide, we create opportunity from complexity. Our teams of interdisciplinary experts combine innovative thinking...Read More>>.

PA Consulting seeks an experienced Medical Device Quality Specialist Consultant to support development and lifecycle management of medical devices and combination products. You will navigate regulatory complexity, embed robust quality systems, and...Read More>>.

About the Role We are seeking an experienced and results-driven Manager, Medical Devices Service Centre to lead a critical service operation supporting our medical device portfolio. This role is responsible for delivering exceptional o...Read More>>.

Abbott Laboratories in Sittingbourne, United Kingdom, is seeking a Manager for the Medical Devices Service Centre to direct a multi-disciplinary team of up to 30 people. This leadership role focuses on delivering exceptional service, quality, comp...Read More>>.

Abbott is recruiting for a Field Service Engineer/Junior based in Peterborough/Leicestershire/Northampton area, with flexibility to travel to Ireland, Nordics and Poland. You will install, upgrade, repair and perform preventive maintenance of vasc...Read More>>.

The role reports to the Head of Materials Compliance, supporting the delivery of the broader EMEA regulatory vision and the mitigation of regional legal risks. The Regulatory Affairs Manager leads the application of the regulatory requirements for...Read More>>.

Regulatory Affairs Engineer - Medical Devices - Cambridge A leading technology and product development organisation in Cambridge is seeking a Regulatory Affairs Engineer to support a diverse portfolio of complex engineering projects. W...Read More>>.

An exciting opportunity for an experienced Regulatory Affairs Manager to take on a new role in a growing generic pharmaceutical company working towards a portfolio of 220 licenses. ++ Please note that this role will be onsite 5 days per...Read More>>.

Pure Search partners with an established international financial services business to appoint Head of Compliance & Regulatory Affairs – British Isles. Based in Jersey, you will oversee regulatory compliance and financial crime frameworks across...Read More>>.

We Are The People Who Give Possibilities PurposeBD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passio...Read More>>.

Moody's in London seeks an AVP, EMEA Regulatory Affairs to support regulatory strategy across the EMEA region through stakeholder engagement, thought leadership, and cross‑functional collaboration.The role manages relationships with regul...Read More>>.

Shape the Future with Dun & Bradstreet At Dun & Bradstreet, we believe data has the power to create a better tomorrow. As a global leader in business decisioning data and analytics, we help companies worldwide grow, manage risk, and...Read More>>.

Dun & Bradstreet, based in London, seeks a seasoned Regulatory Affairs Specialist to lead regulatory strategy and engagement across Europe and beyond. The role combines policy insight with business impact, reporting to the Senior Director in Londo...Read More>>.

Myn is seeking a Regulatory Affairs Engineer for a contract role in Cambridge to bridge engineering and regulatory oversight. You will build and maintain technical files and ensure products meet UK MDR 2002, UKCA and EU MDR/IVDR requirements throu...Read More>>.

OrganOx is seeking an Electronics Design Engineer to design, develop and support electronics for medical devices. The role covers full lifecycle from concept through manufacturing handover, with emphasis on regulation and safety compliance....Read More>>.

CamWebDir in Otley, UK is seeking an enthusiastic embedded software engineer to contribute to medical device development. You will work hands-on across the software lifecycle, writing robust C/C++ code and ensuring documentation is clear and thoro...Read More>>.

GXPeople Global Ltd. seeks an experienced Development Manager for a London-based, office-based role focused on medical device development. You will own the integrated development plan, coordinate hardware and software workstreams, and drive regula...Read More>>.

HSBC in London is seeking an experienced HCIB Regulatory Affairs Senior Manager to oversee regulatory engagements and horizon scanning for the MSS business. You will work with UK regulators, senior stakeholders and 2LoD teams to drive a no-surpris...Read More>>.

At Moody's, we unite the brightest minds to turn today’s risks into tomorrow’s opportunities. We do this by striving to create an inclusive environment where everyone feels welcome to be who they are—with the freedom to exchange ideas, think...Read More>>.

HSBC is seeking an HCIB Regulatory Affairs Senior Manager (MSS) to lead regulatory engagements with UK regulators from London. The role focuses on horizon scanning, regulatory developments, and clear reporting to senior governance bodies.Yo...Read More>>.

Moody's Corporation in London seeks an AVP, EMEA Regulatory Affairs to support the governance and execution of Moody's regulatory strategy across the EMEA region. You will engage regulators, governments, and industry partners to advance Moody's re...Read More>>.

If you’re looking for a career that will help you stand out, join HSBC, and fulfil your potential - whether you want a career that could take you to the top, or an exciting new direction, we offer opportunities, support and rewards that will tak...Read More>>.

Albus Health in Oxford is seeking a senior medical-device verification engineer for an initial three-month contract with potential extension. You will strengthen verification evidence and regulatory documentation for FDA submissions.You wil...Read More>>.

About Albus HealthAlbus Health is an Oxford University spin-out transforming how health data is collected and used in clinical trials and drug development.We have developed Albus Home, a contactless multisensory platform that conti...Read More>>.

Stryker is recruiting an Enterprise Accounts Manager for UK Private Groups to manage and grow high-value accounts across the private sector. This field-based role focuses on relationship-building with C-Suite, procurement, and supply chain stakeho...Read More>>.

CMR Surgical Ltd. is seeking a procurement leader to manage supplier relationships and optimise the sourcing function. The role supports the Versius robotic system, with a hybrid work model requiring 3 days in the Ely/Cambridge office, and global...Read More>>.

I'm working with a small, ambitious sponsor company with a late-stage drug-device combination programme. They need someone to take full ownership of the infusion device, reporting straight to the Chief Solutions Officer. Design and manufact...Read More>>.

NNIT is expanding its Regulatory Affairs team in Europe. The Senior Consultant will lead client engagements, contribute to project delivery and business development, and mentor junior staff. A strong background in Regulatory Affairs within life sc...Read More>>.

About Albus Health Albus Health is an Oxford University spin-out transforming how health data is collected and used in clinical trials and drug development. We have developed Albus Home, a contactless multisensory platform that con...Read More>>.

Siemens Healthineers seeks a maintenance engineering leader to direct an engineering team responsible for maintaining medical device manufacturing equipment. You will set day-to-day priorities, manage workload, and ensure high performance across m...Read More>>.

Medtronic is seeking a Senior Program Manager in Digital Technologies R&D to drive the development and delivery of next-generation surgical technology. You will lead global cross-functional teams of engineers, designers and product owners to deliv...Read More>>.

Barrington James is seeking a Medical Device Programme Lead for a late-stage drug-device combination programme in the UK. This hands-on, senior role requires ownership of timelines, risk decisions and end-to-end delivery, with close collaboration...Read More>>.

ECI is seeking a DHF Engineer to join the Regulatory Compliance Work Stream. You will establish Quality Systems aligned with 21 CFR 820 and ISO 13485, while supporting regulatory compliance across multiple client sites and markets.You will...Read More>>.

Enhanced Compliance Inc. is seeking a DHF Engineer to join the Regulatory Compliance Work Stream. You will establish Quality Systems with a focus on 21 CFR 820 and ISO 13485, working with clients in the life sciences sector to ensure robust compli...Read More>>.

Randox Laboratories Ltd in Antrim is seeking a Software Test Manager to lead the Software Test Engineering Team within the Engineering department. You will oversee verification of software for medical devices and supervise testers across projects,...Read More>>.

Roche Holding AG is seeking a senior safety operations professional to lead the intake, processing, and submission of ICSR and medical device safety reports. You will oversee global performance, drive process improvements, and champion AI-augmente...Read More>>.