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>>.

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>>.

Your new company An established and growing organisation operating within the Medical Device and Healthcare sector. With a strong commitment to quality, compliance and innovation, the business develops and manufactures products that have a dir...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 kn...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 In this role you will contribute to inventing and developing brand-new medical devices in a fast-growing setting in London. You will collaborate with physicists, mechanical engineers, and scientists to create lifesaving technologie...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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

Progress Sales Recruitment is seeking a Business Development Manager for theatre products and surgical instruments. The role is home based across the North East England and Scotland, covering cities such as Newcastle, Leeds, Sunderland and beyond,...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>>.

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>>.

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>>.

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>>.

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>>.

Abbott Diabetes Care in Witney is seeking a Senior Manager, Design Transfer to lead end-to-end transfer of new products and design changes from R&D into manufacturing across Abbott sites and partners. You will shape strategies, coordinate cross-fu...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>>.

Vertech Group (UK) Ltd in London is seeking a Safety Software Engineer to join a team evaluating software development processes and technical evidence underpinning AI-enabled medical devices. You will review software lifecycle, V&V, configuration...Read More>>.

VERTECH GROUP (UK) LTD in London is seeking a Software Safety Engineer to join a fast-growing technology business operating in a highly regulated, safety-critical environment. The role focuses on assessing software development processes and techni...Read More>>.

Abbott Diabetes Care in the United Kingdom seeks a Senior Manager of Design Transfer to oversee the transfer of glucose monitoring products from R&D into manufacturing. You will collaborate with Quality, Operations, Engineering, Regulatory Affairs...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>>.

Sapien Engineering is assisting a design and manufacturing client in the UK that delivers machinery from concept to inception for medical and pharmaceutical customers. They are expanding and have two vacancies to fill.You will own machinery...Read More>>.