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>>.

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>>.

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>>.

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>>.

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>>.

Our client is a global credit ratings and risk analytics firm.We unite the brightest minds to turn todays risks into tomorrows opportunities. We do this by striving to create an inclusive environment where everyone feels welcome to be who t...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>>.

Cure Talent are delighted to be partnered with a global medical device company recognised for its life-saving technologies. As they continue to expand their portfolio, we have an opportunity for a Senior Regulatory Affairs Specialist to join th...Read More>>.

Arevna Cambridge, England, United KingdomRegulatory Affairs Manager (IVD)Arevna Cambridge, England, United Kingdom2 days ago Be among the first 25 applicantsDirect message the job poster from ArevnaOverview...Read More>>.

Parexel is seeking an experienced Regulatory Affairs Consultant CMC Author to support our client. The role focuses on CMC authoring for initial submissions and lifecycle management, with emphasis on biologics.The position can be home or off...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>>.

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>>.

Global Innovation and Technology Centre, Back Lane, Melbourn, Hertfordshire, SG8 6DP, United Kingdom, Melbourn SG8 6DP, GBPA works with many of the world’s most innovative pharmaceutical, medical device and life sciences companies. Bas...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>>.

Contract Type: Unlimited / Full-Time Country / City: United Kingdom / Birmingham Company: Beiersdorf UK Ltd. Job Function: Quality Management Your Tasks Strategy & Compli...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>>.

Location Primsdown Industrial Estate, Worcester Road,Chipping Norton, Oxfordshire, OX7 5XP,United KingdomEmployee Type Contractor or FT EmployeeRequired Degree 4 Year DegreeAbout ECIECI’s mission i...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>>.

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>>.

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>>.

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>>.

Senior Regulatory Affairs & Quality Manager - Cambridge, Cambridgeshire Are you the person regulators, notified bodies and leadership teams turn to when the answer really matters? Bluetree are working with an innovative cardiology me...Read More>>.

BD is seeking a Regulatory Affairs professional to manage regulatory activities for combination devices and pharmaceuticals. You will lead NDA/ANDA/PAS/CBE submissions, interact with FDA CDER, and drive regulatory strategies across R&D, Quality, M...Read More>>.

We Are The People Who Give Possibilities PurposeBD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passio...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>>.

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>>.

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>>.

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>>.

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

About the Role 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 en...Read More>>.

Advanced Medical Solutions in Winsford, England, United Kingdom, is seeking a Regulatory Affairs Associate to manage regulatory documentation for EU and US markets and other territories. You will support submissions, maintain DHF, review risk mana...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>>.

STADA UK Thornton & Ross is on an exciting growth journey with more than 700 employees being fully committed to our purpose of Caring for People’s Health as a Trusted Partner. Together we are shaping the future of Thornton & Ross by living our v...Read More>>.

Role: Regulatory Affairs Associate (Early Talent) Contract: 2 years Office- Maidenhead (and various flexibility required) Join our clients R&D Regulatory Affairs Early Talent Programme...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...Read More>>.

As a Complaints Investigation Engineer, you will play a key role in evaluating, investigating, and resolving customer complaints related to medical devices. You will perform technical investigations, root cause analyses, and product testing to det...Read More>>.

Our client, an innovative medical device business based near Fareham in Hampshire, is seeking a Quality Engineer to support the development and continuous improvement of its Quality Management System. Working within a growing medical technolo...Read More>>.

Noble Futures is seeking a Regulatory Affairs Executive to influence product development, innovation and commercial decisions within an animal health business. You will provide regulatory guidance across the full lifecycle for UK, EU and internati...Read More>>.

Are you a regulatory professional looking for a role where your advice genuinely influences products, innovation and commercial decisions?We’re working with an exciting and growing animal health business to recruit a Regulatory Affairs Ex...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>>.

Alaska Support Industry Alliance is seeking an Interim Regulatory Affairs Associate to support the EMEA food supplement portfolio and provide regulatory guidance across skincare, cosmetics and medical devices. The role emphasizes strong VMS regula...Read More>>.

Vertage Group Portfolio is offering an Regulatory Affairs Early Talent programme in the UK. This two-year rotation spans UK Affiliate Regulatory Affairs and Europe Area Regulatory Strategy, designed to accelerate development for graduates starting...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>>.

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>>.