Cure Talent are delighted to be partnered with a growing diagnostics company based near Cambridge. As they continue to progress their existing medical devices and move towards the next stage of their IVD development programme, we have an exciting...Read More>>.

Cure Talent are delighted to be partnered with a growing medical device certification organisation that is expanding its UK audit team. With continued growth in demand, the business is now looking to appoint a Medical Device Auditor to support man...Read More>>.

Global Labelling Lead, Regulatory Affairs, hybrid working, contract jobYour new company We are currently seeking an experienced Global Labelling Lead to join a leading global biopharmaceutical organisation on a contract basis. This is an e...Read More>>.

My client is seeking a Regulatory Affairs Associate to join their Global Markets team on a temporary contract basis, supporting regulatory compliance and product registrations across Europe, the Middle East and Africa (EMEA)....Read More>>.

Job DescriptionClinical Specialist – Medical Devices\nOutline:\n This is fantastic opportunity for someone who has some medical or clinical experience and would like to work in a medical training role...Read More>>.

Job DescriptionLocation: South East EnglandPreferred locations: Tunbridge Wells, Hastings, Eastbourne or GillinghamSalary: £50,000 - £65,000 DOEThe Role\nWe...Read More>>.

Job DescriptionMedical Devices Technician\n\n Basic Salary £27,000 to £28,000 \n Bonus £1,500 \n Car Allowance £4,500\n...Read More>>.

Overview In this role you integrate regulatory thinking with engineering to support a diverse portfolio of complex projects in Cambridge. You’ll work closely with design engineers, scientists and project teams to ensure development pathwa...Read More>>.

Overview In this role, you support regulatory activities across the business, collaborating with engineers and scientists to align development with global requirements. You will help operate the quality management system and guide teams thr...Read More>>.

At Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by o...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>>.

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 take...Read More>>.

Company Description About AbbVie AbbVie'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 remarkabl...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>>.

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>>.

Job Description The Director, Structured Content Authoring is a transformational leadership role responsible for accelerating the organisation's evolution from document-centric regulatory operations to a modern, data-driven and compon...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>>.

Arxada is looking for a Regulatory Affairs Specialist based in Manchester, UK. This part-time position offers a hybrid working model and involves delivering regulatory aspects of critical projects, managing post-submission activities, and providin...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>>.

The HCIB Regulatory Affairs Senior Manager will be part of a small team which has broad remit and responsibilities, including and not limited to: identification and oversight of upcoming and in-train material regulatory compliance developments, su...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>>.

Whiteoak Associates is seeking a Senior Regulatory Affairs Manager to lead the UK-based European Regulatory Affairs function for a coatings portfolio. The role involves managing UK and EU regulatory registrations and notifications, and supporting...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>>.

Medical Devices Project Leader - Warwick We're looking for a driven and technically credible Project Leader to take a leading role in our Warwick based medical devices team. This is a chance to shape genuinely impactful technologies gu...Read More>>.

The Director, Structured Content Authoring is a transformational leadership role responsible for accelerating the organisation's evolution from document-centric regulatory operations to a modern, data-driven and component-based operating model....Read More>>.

OverviewMedical Devices Project Leader – CambridgeWe are seeking a dynamic and driven Project Leader to join our innovative medical devices team based in Cambridge. This is a unique opportunity to lead cutting-edge development...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>>.

1 week ago Be among the first 25 applicantsGet AI-powered advice on this job and more exclusive features.Direct message the job poster from Entrust Resource SolutionsFinding Outstanding Talent in the Emerging Scientific Indus...Read More>>.

Vitalograph Limited is seeking an experienced Product Manager to own and evolve the comPAS PFT Solutions portfolio across software and hardware. You will translate clinical workflows and technical considerations into actionable roadmaps and requir...Read More>>.

Select how often (in days) to receive an alert:Manager - Regulatory Affairs Lifecycle Management - MedicinesLocation: London, GB, SW11 7BWAt Perrigo, we are driven by our mission to Makes Lives Better Th...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>>.

Job DescriptionThe Director, Structured Content Authoring is a transformational leadership role responsible for accelerating the organisation's evolution from document-centric regulatory operations to a modern, data-driven and componen...Read More>>.

Regulatory Affairs Specialist (Manchester, UK – hybrid, part‑time) As a Regulatory Affairs Specialist you will play a vital role in enabling Arxada’s continued growth and market access across the EMEA region. Working within the M...Read More>>.

Location City, Belfast Job Type Permanent PostedLocation: Belfast, United KingdomThales is a global technology leader with more than 83,000 employees on five continents. With over 7,500 people in the UK, operating across d...Read More>>.

Job Description 24-Month Regulatory Affairs Graduate Programme featuring rotations in International Regulatory Affairs CMC and UK Regulatory Affairs, with exposure to regulatory strategy, submissions, compliance, and health authority engagement. O...Read More>>.

MSD is offering a 12-month Regulatory Affairs CMC student placement in Moorgate, London, delivering hands‑on exposure to regulatory strategy, submissions management, health authority engagement, and operational excellence projects across the EME...Read More>>.

Job Description 12-Month Regulatory Affairs CMC Student Placement offering exposure to regulatory strategy, submissions management, health authority engagement, and operational excellence projects. Our Regulatory Affairs team...Read More>>.

Job Description24-Month Regulatory Affairs Graduate Programme featuring rotations in International Regulatory Affairs CMC and UK Regulatory Affairs, with exposure to regulatory strategy, submissions, compliance, and health authority engag...Read More>>.

MSD in London offers a 24-month Regulatory Affairs Graduate Programme with rotations in International Regulatory Affairs CMC and UK Regulatory Affairs, exposing you to strategy, submissions, compliance and health authority engagement.Based...Read More>>.

MSD invites applications for a 12-month Regulatory Affairs CMC student placement in London. You will gain exposure to regulatory strategy, submissions management, health authority engagement, and operational excellence projects.The role is...Read More>>.

MSD Malaysia in London invites applications for a 24-month Regulatory Affairs Graduate Programme, with rotations across International Regulatory Affairs CMC and UK Regulatory Affairs, exposure to strategy, submissions, compliance and health author...Read More>>.

Job Description 12-Month Regulatory Affairs CMC Student Placement offering exposure to regulatory strategy, submissions management, health authority engagement, and operational excellence projects. Our Regulatory Affairs team bring new medical adv...Read More>>.

Haemonetics Interventional Technologies is seeking a Field Service Engineer to install, service, repair and maintain a portfolio of devices across South East England and Midlands. You will travel within your region and the UK, providing applicatio...Read More>>.

JOB DESCRIPTION: Medical Device Inventory Coordinator Location: Witney Bring your passion, ideas and purpose to life in a company that can truly help you achieve your full potential Abbott has bee...Read More>>.

Location:Reading (Head Office) Start date: 1st July 2027 Duration: 13 months - Until 31st July 2028 Working Model: Full-time Hybrid position (3 days in office, 2 days working from home) Face to Face Assess...Read More>>.

Sanofi is offering a Head Office placement in Regulatory Affairs for a Life Science undergraduate returning to university after completion. The role provides hands-on regulatory work across UK & Ireland, with opportunities to contribute to product...Read More>>.

NBCUniversal is one of the world's leading media and entertainment companies. We create world-class content, which we distribute across our portfolio of film, television, and streaming, and bring to life through our global theme park destinations,...Read More>>.