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>>.

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>>.

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 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>>.

Regulatory Officer Remote - UK Based Monday to Friday Global Travel - Fully Funded £40,000+ Bonus, Healthcare, 25 Days Holiday + Bank Holiday (Options to increase), p...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>>.

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>>.

Cambridge, Cambridgeshire, United KingdomSenior Regulatory Affairs Specialist - CambridgeAt Hologic, we are committed to enabling healthier lives everywhere, every day. To deliver on that purpose, we need strong regulatory...Read More>>.

Allucent is seeking a Director of Regulatory Affairs to guide clients through drug, biologic and medical device development. You will lead regulatory teams, shape strategies, and ensure high-quality submissions while Interacting with Health Author...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>>.

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>>.

Nuneaton and Bedworth Borough Council is seeking an experienced and dynamic leader to oversee key front-line and enforcement services within a broad portfolio, delivering meaningful outcomes for residents and communities.You will provide st...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 Senior Manager, Regulatory Affairs will work with EU regulatory lead(s) and/or directly with global regulatory lead(s) and within cross‑functional teams to facilitate submission of applications to EU and International health agencies (HA)...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>>.

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>>.

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>>.

SVP Regulatory Affairs / Chief Regulatory Affairs OfficerLocation: UK, Germany or United StatesConfidential search | Late-stage biotechnologyThe opportunityA late-stage biotechnology company developing nov...Read More>>.

Baxter International Inc. in the UK, Ireland and Malta seeks a Country Quality Assurance (CQA) & Regulatory Affairs (RA) Manager to lead Quality and Regulatory across the region. Shape regulatory strategies, ensure a robust QMS, and guide cross-fu...Read More>>.

Select Pharma Recruitment is seeking an experienced Regulatory Affairs Manager for a growing generic pharmaceutical company in the UK. The role is onsite five days per week, focusing on post-approval compliance, variations, license transfers and M...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>>.

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>>.

Pure Search partners with an established international financial services business to appoint Head of Compliance & Regulatory Affairs – British Isles. Based in Jersey, you will oversee regulatory compliance and financial crime frameworks across...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>>.

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>>.

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>>.

Amgen Inc. in the United Kingdom (Uxbridge/Cambridge hybrid) seeks an EU Regulatory Affairs Manager to lead submissions for clinical trials and marketed products.You will craft regional regulatory strategies, provide guidance for regulatory...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>>.

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>>.