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

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>>.

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>>.

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>>.

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 companyYou will be joining a growing UK medical device manufacturer based in the Swindon area. The organisation develops and supplies products that improve the everyday lives of patients undergoing chronic and complex medical t...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>>.

Field Service Engineer, Medical Devices Basic Salary £45,000 to £50,000Pension Company Vehicle Private Medical Cover...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 will support the development and continuous improvement of the Quality Management System within a growing medical device business near Fareham. You will help maintain audit readiness, support regulatory compliance,...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>>.

Hologic, Inc. in Cambridge, UK, is seeking a Senior Regulatory Affairs Specialist to support submissions, audits, and documentation for medical devices. You will collaborate with R&D, Quality, Clinical, and international teams to ensure regulatory...Read More>>.

Abbott in Witney is seeking a Senior Specialist Regulatory Affairs to lead regulatory activities for new products and changes across the EMEAP region, coordinating with global teams to ensure timely approvals in Europe, Middle East, Africa and Pak...Read More>>.

Job Title: Regulatory Affairs Manager - IVDs Job Type: Maternity Cover – 12 Month Contract Location: West London, UK – Hybrid/Remote Salary: £60,000 - £76,000 ***Please note that...Read More>>.

Cpl Life Sciences is seeking a Regulatory Affairs Manager - IVDs for a 12-month maternity cover contract. Located in West London with hybrid/remote work options, offering a salary of £60,000 - £76,000.The role sits at the interface of the...Read More>>.

Park Street People Ltd is recruiting a Senior Regulatory Manager for a pharmaceutical company in Europe. The role focuses on leading EMA regulatory affairs strategy, submissions, and regulatory advisory across the European portfolio.The ide...Read More>>.

Hayati is seeking a Regulatory Affairs and Compliance Officer to develop and manage the regulatory framework for e-cigarette products across the UK and European markets. You will monitor regulatory requirements, lead product certification activiti...Read More>>.

Hayati is seeking a Regulatory Affairs and Compliance Officer to develop and manage the compliance framework for e-cigarette products across the UK and European market. You will monitor evolving regulations, lead product certification activities,...Read More>>.

We are supporting a pharmaceutical company committed to delivering innovative therapies that improve patients’ lives in recruiting a Senior Regulatory Manager. Their global teams collaborate to bring cutting-edge solutions from concept to mar...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>>.

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 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>>.

An exciting opportunity for an experienced Regulatory Affairs Manager to take on a new role in a growing generic pharmaceutical company working towards a portfolio of 220 licenses. ++ Please note that this role will be onsite 5 days per...Read More>>.

Moody's in London seeks an AVP, EMEA Regulatory Affairs to support regulatory strategy across the EMEA region through stakeholder engagement, thought leadership, and cross‑functional collaboration.The role manages relationships with regul...Read More>>.

Cure Talent Limited is partnered with an established Medical Device company in Oxfordshire seeking a Regulatory Affairs Manager. The role leads the Regulatory Affairs function, hands-on with technical documentation, submissions and lifecycle activ...Read More>>.

Myn is seeking an experienced Regulatory Affairs Manager for a contract role in London to own UK regulatory strategy and submissions, manage MHRA interactions, and keep a pharma/biotech portfolio compliant across its lifecycle.You will coll...Read More>>.

Senior Regulatory Affairs Specialist - CambridgeAt Hologic, we are committed to enabling healthier lives everywhere, every day. To deliver on that purpose, we need strong regulatory expertise that helps bring new products to marke...Read More>>.

We're recruiting an experienced Regulatory Affairs Manager for a contract role supporting a UK product portfolio. You'll own UK regulatory strategy and submissions, manage MHRA interactions, and keep the portfolio compliant across its lifecycle, w...Read More>>.

Role - International Regulatory Affairs Director Duration - 12 months Inside IR35 Location - Central Cambridge, UK/ Remote The International Regulatory Affairs Director Markets is acc...Read More>>.

Birmingham | National Law Firm | Partner Level An excellent opportunity has arisen for an established Regulatory Partner to take the lead on the development and growth of a regulatory practice in Birmingham for a national law firm....Read More>>.

Shape the Future with Dun & Bradstreet At Dun & Bradstreet, we believe data has the power to create a better tomorrow. As a global leader in business decisioning data and analytics, we help companies worldwide grow, manage risk, and...Read More>>.

Dun & Bradstreet, based in London, seeks a seasoned Regulatory Affairs Specialist to lead regulatory strategy and engagement across Europe and beyond. The role combines policy insight with business impact, reporting to the Senior Director in Londo...Read More>>.

Myn is seeking a Regulatory Affairs Engineer for a contract role in Cambridge to bridge engineering and regulatory oversight. You will build and maintain technical files and ensure products meet UK MDR 2002, UKCA and EU MDR/IVDR requirements throu...Read More>>.

We're looking for a Regulatory Affairs Engineer for a contract role with a medical device manufacturer. This is a technically focused position bridging engineering and regulation. You'll build and maintain technical documentation and make sure pro...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>>.

Regulatory Affairs Specialist Location: West London Hours: 40 hours per week Are you an experienced Regulatory Affairs professional with a strong background in food, beverage or FMCG labelling? I'm recruiting on behalf...Read More>>.

Aurora Lifesciences seeks an experienced Regulatory Specialist to join a medical device organisation and manage regulatory documentation throughout the product lifecycle.You will author, review and maintain Technical Files and regulatory re...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 enga...Read More>>.

We're looking for an Interim Regulatory Affairs Associate you'll support the maintenance and development of our EMEA food supplement portfolio while also providing regulatory support across skincare, cosmetics and medical device categories. We're...Read More>>.

Programme Eligibility To join one of our 12-month Internships you must meet one of the following criteria: You’re currently an undergraduate studying at University and returning to full time education in Autumn 2028...Read More>>.

Are you an ambitious early career professional ready to make a difference? Our client's Regulatory Affairs Early Talent programme offers a two-year rotation across a range of areas. As an early talent Regulatory Affairs graduate you will rotate ac...Read More>>.

Role Summary The Medical Equipment Library Assistant ensures vital medical devices are available, clean, safe, and ready for patient use. They coordinate the management of high-demand equipment, log and process faulty devices, and work al...Read More>>.

Company Description Adi Pharma Limited is a UK-based pharmaceutical and healthcare company specializing in wholesale trading and distribution of branded products. The company operates through three key divisions: branded pharmaceu...Read More>>.

At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedi...Read More>>.

Bayer is seeking a Global Regulatory Affairs Manager in Reading (Hybrid working) to drive regulatory strategies across a diverse Consumer Health portfolio. You will support lifecycle activities, ensure registrations, and maintain marketing authori...Read More>>.

SGS is seeking a Senior Technical Medical Device Coordinator to support the UK Medical Devices Team in Birmingham. This permanent, office-based role runs Monday to Friday 8.30am to 5pm and offers a salary up to £33,000 per annum.You will c...Read More>>.

King's Mill Hospital, part of Sherwood Forest Hospitals NHS Foundation Trust, hosts an in-house Orthotic Service and seeks an Orthotic Technician to join the team. You will manufacture and maintain bespoke orthotic devices, applying craftsmanship...Read More>>.

Carbon seeks a Scientist I - Physical Testing at our Deeside site. This fully on-site role supports medical device development, ensuring physical test methods meet GMP/GLP/GDP requirements and regulatory expectations.You will design, execut...Read More>>.

Getinge is seeking a Field Service Engineer to service medical devices across the South East UK, including London. This field-based role requires a self-starter who can manage workload independently while collaborating with the Service Office and...Read More>>.