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>>.

Regional Sales Manager – Aesthetic Medical Devices £45 - 50,000 Basic | £100,000–£110,000 OTE | Car Allowance + BenefitsField-Based | B2B Sales | Medical TechAre you a high-performing B2B sales professional...Read More>>.

12-Month Contract | Hybrid Working | Potential to Convert PermanentAbout the RoleI am supporting an Oncology biotechnology organisation seeking an experienced Regulatory Affairs leader to oversee the execution of global regulator...Read More>>.

Cure Talent are delighted to be partnered with a growing medical device certification organisation that is expanding its technical and clinical assessment capability across a number of new medical device categories.We are looking to speak w...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>>.

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>>.

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>>.

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

12-Month Contract | Remote/Hybrid UKWe are seeking an experienced Global Labelling Lead to support global regulatory labelling activities across the US and EU markets.Key Responsibilities:Lead global labelling strategy and e...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>>.

Overview As Regulatory Affairs Lead, you will shape and strengthen our regulatory affairs function for a leading trading and reporting consultancy. You will drive engagement with regulators and market participants across UK, EU, and other j...Read More>>.

Overview In this role you guide clients through drug, biologic, and medical device development, leading regulatory teams and shaping strategy to deliver high-quality submissions. You’ll be the trusted HA liaison and translate complex requ...Read More>>.

Overview As Regulatory Affairs Lawyer at Teya, you steer UK and EU licensing, public policy, and regulatory strategy to support independent local businesses. You’ll lead licensing activities, engage with regulators and policymakers, and s...Read More>>.

Overview As a Senior Electronics Engineer, you will lead electronic design activities for medical devices that meet ISO 13485 standards and help take products to market. You will work within a cross-functional team of engineers and scientis...Read More>>.

Quality Engineer (Medical Devices) £40,000 - £43,000 + Bonus + Sick Pay + Life Assurance + 33 Days Holiday Andover, HampshireAre you a Quality Engineer from a medical devices background, looking to utilise your knowledge an...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>>.

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 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>>.

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>>.

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>>.

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>>.

Your new company Increase your chances of an interview by reading the following overview of this role before making an application.An established and growing organisation operating within the Medical Device and Healthcare sector. With...Read More>>.

Your new companyAny additional information you require for this job can be found in the below text Make sure to read thoroughly, then apply.An established and growing organisation operating within the Medical Device and Healthcare sect...Read More>>.

Beiersdorf UK Ltd. is seeking a senior Quality Management & Regulatory Affairs leader to drive strategy and ensure compliance across Northern Europe. You will lead the QMS, oversee supplier quality and product releases, and manage regulatory regis...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>>.

Hollybank Trustees Ltd seeks a Head of Quality Assurance and Regulatory Affairs to lead the QA and regulatory function in a hybrid role with Croydon, UK. You will shape the QA strategy, oversee compliance with MDR, ISO 13485 and MDSAP, and manage...Read More>>.

Head of Quality Assurance and Regulatory Affairs Location: Hybrid / Croydon, UKjob type: Permanent / Full-timeSector and subsector: Medical & Healthcare | OtherSalary: Competitive salary...Read More>>.

Scarlet, a London-based leader in medical-device certification software, is seeking a Product Designer to turn complex regulatory work into clear, efficient experiences. You’ll own core workflows, prototypes and interfaces, partnering with produ...Read More>>.

Ripple is offering an onsite Operations Manager role in the United Kingdom, leading manufacturing, quality and supply chain as part of the Senior Leadership Team. This hands-on position drives day-to-day operations, health and safety, and collabor...Read More>>.

Vickerstock are working in partnership with a specialist manufacturing organisation on the appointment of a Group Compliance Officer, based in Co. Fermanagh. Reporting to the SHEQ...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>>.

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>>.

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>>.

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>>.

Invibio, part of the Victrex plc group, is a global leader in biomaterial solutions for medical devices. This Quality Engineer role supports design and development, embedding quality across lifecycle, with emphasis on regulatory compliance and des...Read More>>.

McAllister Recruitment are recruiting on behalf of our client a leading company in the Wound Care and Medical Device space. This is an opportunity to represent an innovative healthcare solutions company whose product portfolio is well represented...Read More>>.