Our client is a global credit ratings and risk analytics firm.We unite the brightest minds to turn todays risks into tomorrows opportunities. We do this by striving to create an inclusive environment where everyone feels welcome to be who t...Read More>>.

Regulatory Affairs Senior Specialist - InternationalLocation: BedfordThe VacancySwiss Precision Diagnostics (SPD) is a world leader in the research, design and supply of advanced consumer diagnostic products. SPD...Read More>>.

Build your career while making a difference in healthcareAt Vitalograph, weve spent more than 60 years developing innovative respiratory diagnostic solutions that help healthcare professionals detect...Read More>>.

Division / Function Global Regulatory Affairs, Regulatory Operations Job Title Director, Regulatory Affairs, Labelling Summary & Purpose Of The Position Responsible for leading the development and...Read More>>.

Join Eye2Gene as our Quality and Regulatory Affairs Manager (SaMD/ AIaMD) Applicants must already have the right to work in the UK. Eye2Gene is a VC-funded, AI-powered precision ophthalmology platform combining imagi...Read More>>.

Ensera Design in Bristol is seeking an experienced Senior Mechanical Engineer to join our world-class team and contribute to delivering innovative solutions for clients in medical devices and consumer health.You will lead electromechanical...Read More>>.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to...Read More>>.

Roche is seeking a Principal for Medical Device safety operations to lead end-to-end case processing and process design across the global network. You will own post-market incident reporting and pre-market clinical investigation safety reporting,...Read More>>.

ECM Selection (Holdings) Limited in Cambridge seeks an engineering leader to guide high-value development programmes from concept through transfer to manufacture. You will accelerate timelines, manage risk, and deliver results that improve patient...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>>.

GB69 (FCRS = GB069) Sandoz Ltd. is seeking a skilled professional to lead project management in the medical device field in Cambridge, England. You will be responsible for overseeing design processes and ensuring compliance with ISO standards....Read More>>.

Sizewell C is entering an exciting phase of growth as we mature into an independent organisation and continue building one of the UK's largest and most important energy projects. We are now recruiting the below position: Head of Regulat...Read More>>.

CMR Surgical is seeking a senior electronics contractor in the UK to join the Versius Plus Ultimate program. You will work with the electronics team to interpret requirements, capture schematics in Altium, and support PCB layout and test in the sy...Read More>>.

Director Quality Assurance and Regulatory Affairs This range is provided by Metric Bio. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range Direct message...Read More>>.

Enterprise Recruitment Ltd is seeking an experienced systems engineer to work on a cutting-edge medical devices project within a world-leading system rollout. Based in a state-of-the-art Surrey facility, you will collaborate with electronics, soft...Read More>>.

This is a fantastic chance for an experienced systems engineer to work on cutting-edge technology within the world of medical devices, supporting the rollout of a brand-new world-leading system. Based out of a purpose-built, state-of-the-art fa...Read More>>.

Steris is seeking a Systems Engineer within the Infection Prevention Technology (IPT) division. The role focuses on technical leadership, translating stakeholder requirements into system level designs, and leading cross-discipline feasibility and...Read More>>.

I’m supporting a UK-based clinical-stage biotechnology company with the appointment of a Senior Manager, Regulatory Affairs. This is a senior, hands‑on regulatory role supporting a development programme as it progresses into late-pha...Read More>>.

Paxman, a global leader in scalp cooling technology, is seeking a Technical Engineering Manager in Huddersfield (hybrid) to own the Technical Files for all Paxman products and ensure regulatory compliance worldwide. You will lead a senior technica...Read More>>.

London, GB, EC2R 7BP Manchester, GB, M1 4HNHead of Regulatory AffairsSizewell C is entering an exciting phase of growth as we mature into an independent organisation and continue building one of the UK’s largest and most impor...Read More>>.

Ready to lead global regulatory strategy and influence the development of innovative oncology therapies on a worldwide scale? Proclinical is seeking an Associate Director of Regulatory Affairs to join a dynamic team in the oncology and p...Read More>>.

Energy Jobline ZR seeks a Senior Mechanical Engineer in Cambridge to drive design from early concepts through high‑volume manufacture for next‑generation medical devices. You will work within a multidisciplinary team to develop precision mecha...Read More>>.

Droplet Scientific Ltd. is seeking a Senior Electronics & Embedded Systems Engineer to lead electronics and firmware development for next‑gen portable biochemical analysers.You will own system design, verification, compliance testing and...Read More>>.

Ready to lead global regulatory strategy and influence the development of innovative oncology therapies on a worldwide scale?Proclinical is seeking an Associate Director of Regulatory Affairs to join a dynamic team in the oncology and ph...Read More>>.

Location Primsdown Industrial Estate, Worcester Road,Chipping Norton, Oxfordshire, OX7 5XP,United KingdomEmployee Type Contractor or FT EmployeeRequired Degree 4 Year DegreeAbout ECIECI’s mission i...Read More>>.

Location Primsdown Industrial Estate, Worcester Road,Chipping Norton, Oxfordshire, OX7 5XP,United Kingdom Employee Type Contractor or FT Employee Required Degree 4 Year Degree Description About EC...Read More>>.

Moderna is seeking an experienced CMC Regulatory Affairs professional to lead global CMC strategies and oversight for international submissions in London. The role requires coordinating regulatory filings, ensuring health authority compliance, and...Read More>>.

HCIB Regulatory Affairs Senior Manager (MSS) Location: London, GB, E14 5HQ Brand: HSBC Area of Interest: Risk and Compliance Role Workstyle: Hybrid Worker Date: 3 Oct 2026 If you’re looking for a caree...Read More>>.

HSBC in London is seeking an HCIB Regulatory Affairs Senior Manager to oversee regulatory engagements and developments within MSS. The role is hybrid, based in London, with a comprehensive pay and benefits package and a focus on regulatory change...Read More>>.

Alnylam Pharmaceuticals in the United Kingdom seeks a Senior Manager, Regulatory Affairs to lead planning and delivery of regulatory submissions to EU and international health authorities. You will work across programs to support product developme...Read More>>.

Level Zero Health in the United Kingdom seeks a Senior Mechanical Design Engineer to own the mechanical architecture of our body-worn medical devices, from concept through to manufacture. You will collaborate with electronics, sensing and industri...Read More>>.

AbbVie seeks an experienced International Regulatory Affairs professional to provide position and guidance on advertising and promotion. You will collaborate with Commercial, Medical, Legal, and Compliance teams to ensure compliant, effective comm...Read More>>.

ARCA Consulting Ltd seeks an experienced Mechanical Engineering Manager for Medical Devices to lead cross-disciplinary product development programs. You will own technical direction, delivery, budgets and schedules while guiding mechanical, electr...Read More>>.

Corin Group is seeking a Senior Software Quality Engineer to oversee software and system development activities across its Global Technology Team. You will ensure compliance with FDA, ISO, and European Medical Device standards and drive quality im...Read More>>.

HSBC is seeking a Regulatory Affairs Senior Manager to lead engagements with UK regulators and oversee regulatory developments across HCIB. The role involves close collaboration with 2LoD, global functions and senior management to ensure timely, w...Read More>>.

About ECI ECI’s mission is to be the global leader of professional consulting services for the life sciences industry. Our clients lean on our diverse perspectives and decades of expertise to tackle their toughest challenges, and we tak...Read More>>.

Consult is seeking a senior Cybersecurity Regulatory Affairs Consultant for a fully remote contract with a UK medical device company. The role focuses on software and cybersecurity regulatory submissions and documentation.You will work auto...Read More>>.

Afferent Medical Solutions Ltd. in Cardiff seeks a skilled Software Architect to design a new software system for a ground-breaking medical treatment. You will work within a small team across research, design, implementation, release and post-rele...Read More>>.

SAVA Technologies Ltd in the United Kingdom is seeking a Senior Mechanical Engineer to join our multi-disciplinary team and drive the mechanical design of a next-generation biosensing device.You will develop tests, verify performance across...Read More>>.

JAM Recruitment Ltd in Leeds is seeking a Customer Service Beeston (Transition) representative on a permanent, full-time basis. The role operates a hybrid model with 37 hours weekly and rotating office/remote days, starting at £13.85 per hour and...Read More>>.

This role will be based in our Belfast site.Throughout the placement, you will be an integral part of Stryker's 2027 Cooperative cohort.Stryker HeartSine AED Regulatory Affairs & Compliance Engineering maintain market access f...Read More>>.

Study Start Up and Regulatory Affairs Specialist Full-timeDepartment: Study Start up and Regulatory Unit Medicine moves forward here. So willyou. Ergomedis a specialist clinical research organization focu...Read More>>.

Ergomed is a specialist clinical research organization focused on rare disease and oncology trials. The Study Start Up and Regulatory Affairs Specialist leads and coordinates all activities related to achieving site initiation readiness and regula...Read More>>.

Roche Products Ltd. in Welwyn Garden City, UK invites you to a two-year One Product Development Regulatory (PDR) Early Talent program that builds foundational regulatory knowledge through hands-on projects and tailored learning.You will wor...Read More>>.

Kenvue is currently recruiting for a:Regulatory Affairs Industrial PlacementWhat we doAt Kenvue , we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the hous...Read More>>.

Kenvue is recruiting for a 12-month Regulatory Affairs Industrial Placement based at the UK HQ in Reading. The role is full-time (37 hours per week) and reports to the Director, Regulatory Affairs, Self Care Lead.It offers practical busines...Read More>>.

TRS Consulting in the United Kingdom is seeking a Medical Devices Technician to set up and support surgical camera systems, inspect and troubleshoot medical devices, and provide on-site client support to ensure equipment functionality for patient...Read More>>.

Elekta is seeking a Lead Software Developer in Test to shape quality engineering for radiation medicine software. You will lead automation framework design, mentor SDETs, and build scalable test strategies for safety-critical systems.The ro...Read More>>.

SRG is seeking a Scientist II to support physical testing within the Medical Devices division. The role involves designing, planning and executing tests to assess physical properties, and developing new testing methods aligned with industry standa...Read More>>.

Abbott's Witney production facility seeks an Medical Device Inventory Coordinator to oversee the booking in and internal movement of product packs, maintain stock records, and support lab colleagues with batch provisions.The role requires s...Read More>>.