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>>.

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>>.

CY Partners are excited to be supporting a global organisation in recruiting an enthusiastic, scientifically minded scientist to join their experienced regulatory team. This is an excellent opportunity to work in chemical regulatory affairs, wo...Read More>>.

Select Pharma Limited provided pay rangeThis range is provided by Select Pharma Limited. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay rangeDirect messa...Read More>>.

Select Pharma Recruitment provided pay range This range is provided by Select Pharma Recruitment. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range Di...Read More>>.

Responsible for developing and managing the company's compliance framework for e-cigarette and medical device products across the UK and European market. This role monitors evolving UK and European regulatory requirements, leads product certifi...Read More>>.

The Regulatory Affairs (RA) Officer is primarily responsible for ensuring the appropriate licensing, marketing and legal compliance of Sun Pharma’s pharmaceutical and medical products in order to control the safety and efficacy of these produ...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>>.

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>>.

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>>.

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>>.

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 in...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>>.

Director Quality Assurance and Regulatory Affairs This range is provided by Metric Bio. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range Direct message...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>>.

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>>.

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>>.

Senior Manager, Regulatory Submission Locations: King of Prussia, PA | Glattburgg, Switzerland | Maidenhead, UKWork Arrangement: Hybrid - 3 days onsiteReports to: Global Submission Management Lead CSL...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>>.

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>>.

Skills Alliance seeks an SVP Regulatory Affairs / Chief Regulatory Affairs Officer for a leading biotech with a pivotal Phase 3 programme. Lead global regulatory strategy, oversee NDA/MAA submissions and engage with FDA/EMA to drive speed to appro...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>>.

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>>.

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>>.

Position DescriptionServe as a Regulatory Chemistry, Manufacturing and Control (CMC) Lead for the synthetic-moiety (Drug-Linker) of assigned antibody-drug conjugate (ADC) and other bio-conjugate programs, providing regulatory lead...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>>.

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>>.