Test Technician - Medical & Drug Delivery Devices Permanent | On-site Location: Great Chesterford area, Cambridgeshire - up to £28,000Are you looking to start or build your career in medical device testing? We're hiring a...Read More>>.

Export Control and regulatory Coordinator Location: Swinton, ManchesterDepartment: Quality & ComplianceSalary: £32,000 – £40,000 per annum About Luxfer Luxfer MEL Technologies is a lea...Read More>>.

Regulatory Affairs Specialist We’re looking for a Regulatory Affairs Specialist to join us, working across multidisciplinary teams to support and enable breakthrough innovation. Cambridge Consultants is a global technology and...Read More>>.

The Regulatory Affairs (RA) Officer is primarily responsible for ensuring the appropriate licensing, marketing and legal compliance of Sun Pharma’s pharmaceutical and medical products in order to control the safety and efficacy of these produ...Read More>>.

Flexi Start Happy Hour Drinks Fridge (Thursdays & Fridays) #TEAMBULK ARE HIRING A REGULATORY AFFAIRS ASSOCIATE Bulk™ is on an incredible journey, with a mission to move the business from a manufacturi...Read More>>.

Commercial · Proximie London Office · HybridPartnerships Manager, Medical DevicesProximie is on a mission to improve healthcare by transfor...Read More>>.

Regulatory Affairs Advisor – Hybrid To c£45,000 + package Worcester, Redditch, Evesham, Warwick, Cheltenham, Tewkesbury, Droitwich Spa, region around WR11.This business is an international leader in manufacturing and raw material...Read More>>.

CoMind develops non-invasive neuromonitoring technology for clinical brain monitoring. Its technology transforms neuro-signals into longitudinal patient insights to improve the diagnosis and treatment of brain disorders.Задачи...Read More>>.

Company DescriptionAbbVie'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...Read More>>.

AbbVie in Maidenhead seeks a senior Regulatory Affairs professional to lead UK regulatory efforts and serve as primary regulatory contact for designated therapeutic areas, guiding MHRA submissions and supporting launches. The role aligns with the...Read More>>.

Adore Recruitment Ltd is seeking a Territory Sales Manager to drive sales of medical devices across the North of the UK. This role suits healthcare professionals transitioning into sales, leveraging clinical insight to engage with key decision-mak...Read More>>.

Burtons Manufacturing Co Ltd is seeking a Senior Software Developer to join our engineering team in Staplehurst, Kent. You will develop Windows and Linux software primarily in C++, with additional C#, .NET, and web languages for UI and device cont...Read More>>.

United States Digital Space LLC is seeking a Software Safety Engineer to assess software lifecycle processes and regulatory documentation for medical device software. You’ll work with our product, engineering and applied machine learning teams t...Read More>>.

United States Digital Space LLC is seeking a Medical Device Auditor to audit manufacturers’ quality management systems against ISO 13485, EU MDR and UK MDR. You will learn our audit methods and deliver clear conclusions to support certification...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 in...Read More>>.

If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global coll...Read More>>.

OverviewAt BioTalent, we are working with a client exclusively to fill their RA Specialist position. They are a fast growing CGT company focused on developing products in the immuno-oncology. This role will focus on supporting their exist...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>>.

Job DescriptionRegulatory Affairs SpecialistLocation: Hybrid – Kent/LondonJob Type: Full-time, PermanentAbout the RoleAn exciting opportunity has arisen for a Regulatory Affairs...Read More>>.

View Rubicon Technical - The Regulatory Compliance Experts Head of Regulatory Affairs (Food Supplement) Company Overview: Rubicon Bridge is a fast-growing SaaS provider to the consumer healthcare and wellness industry. We are...Read More>>.

Senior Regulatory Affairs Manager - Chemicals / Paints / Coatings / ResinsNorthumberland - near Newcastle Upon Tyne | 4 days on siteA rare opportunity has arisen for an experienced Senior Regulatory Affairs Manager to join an inter...Read More>>.

Rubicon Bridge Ltd. is seeking a Head of Regulatory Affairs (Food Supplement) to lead global regulatory strategy for supplements. You will steer regulatory decisions, liaise with product and tech teams to embed compliance, and interact with major...Read More>>.

1 week ago Be among the first 25 applicantsDirect message the job poster from Hartmann YoungHeadhunter | Specialising in Diagnostics & Genomics | Connecting Top Talent across the Industry Associate Director – Regu...Read More>>.

Who we are At Twilio, we’re shaping the future of communications, all from the comfort of our homes. We deliver innovative solutions to hundreds of thousands of businesses and empower millions of developers worldwide to craft persona...Read More>>.

Crux Product Design Ltd. in Bristol is seeking a talented Project Manager to oversee the development of medical and consumer goods devices from concept through production.You will coordinate design and engineering teams, manage timelines, b...Read More>>.

Skills Alliance seeks an SVP Regulatory Affairs / Chief Regulatory Affairs Officer for a leading biotech with a pivotal Phase 3 programme. Lead global regulatory strategy, oversee NDA/MAA submissions and engage with FDA/EMA to drive speed to appro...Read More>>.

Moody's AVP, EMEA Regulatory Affairs leads policy engagement across regulators and governments, shaping regulatory thinking and strategy across the region. You will produce briefing materials, represent Moody's at key industry events, and drive cr...Read More>>.

AND Digital Limited is seeking four Embedded C++ Developers to join an in-house backend team on a highly regulated medical technology product in London. You will own a self-contained area of the application from design through tested, documented c...Read More>>.

Newton Colmore Consulting in Cambridge is seeking an embedded software engineer to work on diagnostics technologies for the Medical Devices and Life Sciences sectors. The role is permanent and full-time, with an excellent starting salary and compr...Read More>>.

Maclivaro Limited is seeking an experienced Operations Manager to lead manufacturing, warehousing, supply chain and QA at our Houghton Regis site. You will drive performance, optimise processes and contribute to the longer-term strategic plan....Read More>>.

ECM Selection (Holdings) Limited seeks an experienced embedded C/C++ developer to join a multidisciplinary engineering team. You will work on medical technology projects, from on-board device software to driven hardware interfaces, with direct cli...Read More>>.

Product Security Specialist for Medical Devices (Cyber Security) We believe in the power of ingenuity to build a positive human future. As strategies, technologies, and innovation collide, we create opportunity from complexity....Read More>>.

Lexington Medical, Inc. in Bedford, Massachusetts, is hiring an Electrical Engineer to design and develop embedded electrical systems for our AEON surgical stapling platform.You will contribute to schematic capture, PCB design, hardware bri...Read More>>.

Baxter International Inc. in the UK, Ireland and Malta seeks a Country Quality Assurance (CQA) & Regulatory Affairs (RA) Manager to lead Quality and Regulatory across the region. Shape regulatory strategies, ensure a robust QMS, and guide cross-fu...Read More>>.

Position DescriptionServe as a Regulatory Chemistry, Manufacturing and Control (CMC) Lead for the synthetic-moiety (Drug-Linker) of assigned antibody-drug conjugate (ADC) and other bio-conjugate programs, providing regulatory lead...Read More>>.

Keeler Ltd, a global eyecare innovator, invites applications for a Technical Support Associate – Products & Software in Windsor. You will deliver first-line technical support for Keeler product range and software, including Keeler Konnect, Accut...Read More>>.

Looking for an embedded development role with variety, client-contact, and a positive real-world impact? This role may be just the ticket: a well-established medical technology company is seeking an experienced C or C++ developer to join their mul...Read More>>.

Keeler, part of Halma, is seeking a Technical Support Associate – Products & Software to deliver first-line technical support for Keeler’s product range and software, including Konnect, Accutome Connect, Kapture and Kinexis. Ideal for a recent...Read More>>.

AND Digital is seeking four Embedded C++ Developers for an in-house backend engineering team working on a highly regulated medical technology product in London. You will own a self-contained area of the application and drive design through to test...Read More>>.

Bluetree Recruits is seeking a Senior Regulatory Affairs & Quality Manager in Cambridge to shape regulatory strategy for the US first and expand globally. You will own FDA, CE and UKCA submissions and lead a robust QMS, partnering with leadership...Read More>>.

ECM Selection (Holdings) Limited seeks an experienced embedded C/C++ developer to join its multi-disciplinary engineering team near Cambridge. The role offers variety, direct client contact, and the chance to impact medical technology used in labs...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>>.

eg technology is seeking a seasoned Project Manager to lead planning, control and delivery of complex product design and development projects from concept to manufacture. You’ll work with clients and motivate multidisciplinary teams across softw...Read More>>.

Senior Manager, Regulatory Submission Locations: King of Prussia, PA | Glattburgg, Switzerland | Maidenhead, UKWork Arrangement: Hybrid - 3 days onsiteReports to: Global Submission Management Lead CSL...Read More>>.

OrganOx Limited is seeking a Senior IP Specialist to define and execute the company’s global IP strategy. The role acts as the internal authority on IP matters and collaborates with R&D, regulatory, and business teams to protect and exploit the...Read More>>.

Gold Group is seeking an Electrical Engineer for medical devices in Cornwall. You will design electrical systems, develop schematics and PCBs, verify and validate devices, and ensure EMC/safety compliance while collaborating with global R&D teams....Read More>>.

Electrical Engineer - Medical Devices (BBBH73810) Falmouth, England Electrical / Electronics Engineer – Medical Devices Cornwall, UK (On-site) Global Healthcare Organisation | Women's Health & Medical Technology An excit...Read More>>.

CV TECHNICAL LTD is seeking a Senior Automation Engineer in Dorset to lead automated assembly projects from concept through commissioning, validation and full production implementation. You will collaborate with Operations, Quality, R&D, Validatio...Read More>>.

CV Technical Limited is seeking a Senior Automation Engineer in Dorset to lead automation projects from concept through commissioning and full production implementation. The role involves collaboration with Operations, Quality, R&D, and external e...Read More>>.