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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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 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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

This job is with AstraZeneca, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.Job Title: Regulatory Affairs Director - Oncology...Read More>>.

Your new company Increase your chances of an interview by reading the following overview of this role before making an application.An established and growing organisation operating within the Medical Device and Healthcare sector. With...Read More>>.

Your new company Read on to find out what you will need to succeed in this position, including skills, qualifications, and experience.An established and growing organisation operating within the Medical Device and Healthcare sector. Wi...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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.