Our client is a global credit ratings and risk analytics firm.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...Read More>>.

Medical Devices Technician Basic Salary £27,000 to £28,000 Bonus £1,500 Car Allowance £4,500Full Product Training...Read More>>.

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>>.

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>>.

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>>.

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>>.

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>>.

Technical and Regulatory Associate, for a leading materials manufacturer based in the East Yorkshire area.- Are you passionate about chemical regulatory compliance?- Do you want variety including lab and commercial based activitie...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>>.

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 In this role you will lead European regulatory strategy for oncology products, accelerating approvals and securing strong labels. You will represent AstraZeneca with European regulators, steering high-stakes meetings and shaping gl...Read More>>.

Overview In this role you will drive regulatory strategies and submissions for cutting-edge medical devices and IVDs in the EMEAP region. You will collaborate within a global team to accelerate market access and meet regulatory requirements...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>>.

OVERVIEWWorking across both established and emerging product categories, you'll keep up to date on changing regulations, provide expert guidance to cross-functional teams and help ensure our products meet global compliance requirements...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>>.

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>>.

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

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>>.

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>>.

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>>.

This is a Part-time position, between 16-20 hours a week.You’re comfortable working where detail matters. Managing documentation, supporting compliance processes, and keeping quality systems running smoothly behind the scenes. Y...Read More>>.

Welcome to the era of Velsera! Seven Bridges, Pierian & UgenTec have combined to become Velsera.Velsera is the precision engine company. We empower researchers, scientists, and clinicians to drive precision R&D, expand access to, and m...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>>.

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>>.

Sizewell C Limited invites applications for Head of Regulatory Affairs. The role is based in Manchester or London with hybrid working and a minimum of two days on-site, and involves travel to other offices and sites.Reporting to the Safety,...Read More>>.

Job DescriptionGeneral Summary:The Senior Director, Regulatory Strategy International, is a regulatory leader with expert technical and tactical experience in regulatory strategy who will be responsible for overseeing the d...Read More>>.

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collabo...Read More>>.

Revolut is seeking an experienced Regulatory Affairs Manager to lead interactions with external regulators and ensure ongoing compliance as the company expands its regulated fintech operations. You will translate complex regulatory proposals into...Read More>>.

HSBC is seeking an HCIB Regulatory Affairs Senior Manager (MSS) to lead regulatory engagements with UK regulators from London. The role focuses on horizon scanning, regulatory developments, and clear reporting to senior governance bodies.Yo...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...Read More>>.

If you’re looking for a career that will help you stand out, join HSBC, and fulfil your potential - whether you want a career that could take you to the top, or an exciting new direction, we offer opportunities, support and rewards that will tak...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>>.

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>>.

Under the supervision of line management or guidance from an experienced Senior Regulatory Manager, conduct agreed strategic regulatory activities for assigned products and markets to obtain and maintain Marketing Authorizations and support Clinic...Read More>>.

Pfizer Inc. is seeking a Senior Regulatory Manager to drive regulatory strategy for assigned products and markets. You will partner with cross-functional teams to obtain and maintain marketing authorizations and support clinical trial applications...Read More>>.

Regulatory Affairs Engineer - Medical Devices - Cambridge A leading technology and product development organisation in Cambridge is seeking a Regulatory Affairs Engineer to support a diverse portfolio of complex engineering projects. W...Read More>>.

Quality Engineer (Medical Devices)Read all the information about this opportunity carefully, then use the application button below to send your CV and application. £40,000 - £43,000 + Bonus + Sick Pay + Life Assurance + 33 Days Ho...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>>.