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>>.

Commercial · Proximie London Office · HybridPartnerships Manager, Medical DevicesProximie is on a mission to improve healthcare by transfor...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>>.

CoMind develops non-invasive neuromonitoring technology for clinical brain monitoring. Its technology transforms neuro-signals into longitudinal patient insights to improve the diagnosis and treatment of brain disorders.Задачи...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>>.

Crux Product Design in Bristol, UK is seeking an Advanced Human Factors Engineer to lead usability work across medical device programs. You will plan, run and report on studies, ensuring user needs are integrated early and throughout development t...Read More>>.

Adepto Technical Recruitment Ltd is assisting a large CDMO in Hampshire, UK, to recruit a Quality Assurance Specialist for pharmaceutical and Medical Device products. The role focuses on investigating customer quality issues, non-conformities, and...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>>.

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>>.

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>>.

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>>.

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>>.

Keeler Ltd, a global eyecare innovator, invites applications for a Technical Support Associate – Products & Software in Windsor. You will deliver first-line technical support for Keeler product range and software, including Keeler Konnect, Accut...Read More>>.

Looking for an embedded development role with variety, client-contact, and a positive real-world impact? This role may be just the ticket: a well-established medical technology company is seeking an experienced C or C++ developer to join their mul...Read More>>.

Keeler, part of Halma, is seeking a Technical Support Associate – Products & Software to deliver first-line technical support for Keeler’s product range and software, including Konnect, Accutome Connect, Kapture and Kinexis. Ideal for a recent...Read More>>.

Develop embedded C and C++ software to bring new medical technology to life Looking for an embedded development role with variety, client-contact, and a positive real-world impact? This role may be just the ticket: a well-established medi...Read More>>.

ECM Selection (Holdings) Limited seeks an experienced embedded C/C++ developer to join its multi-disciplinary engineering team near Cambridge. The role offers variety, direct client contact, and the chance to impact medical technology used in labs...Read More>>.

OrganOx seeks a Senior IP Specialist to define and execute its global IP strategy, aligning with R&D and business objectives. This role holds autonomy as the primary internal authority on IP matters and guides decisions across product development...Read More>>.

Salary: £45,000 - 85,000 per year Requirements: We require experience as an Embedded Software Engineer, with a strong track record of problem solving using C and other software languages. We prefer experience...Read More>>.

National Highways is seeking an Assistant Lawyer to join the Legal Services team. Reporting to the Team Leader within the General Counsel - Legal function, you will provide pragmatic and effective legal advice across a broad range of disciplines,...Read More>>.

The Medical Devices Safety Officer (MDSO) will provide Trust-wide leadership, oversight and assurance in relation to the safe management, governance and regulatory compliance of medical devices across The Walton Centre NHS Foundation Trust. The po...Read More>>.

Pratap Partnership Ltd is seeking a Quality Control Officer - Medical Devices to support the day-to-day operation of the QMS in a hybrid role. You will work closely with the Quality Assurance Manager on QMS coordination, internal audits, CAPA, com...Read More>>.

Johnson & Johnson in Leeds, West Yorkshire seeks an Import/Export Operations Specialist to manage compliant, timely cross-border movement of DePuy Synthes products. You will handle trade docs, customs, and regulatory requirements in a regulated me...Read More>>.

FlexMedical Solutions, a growing medical device development and manufacturing organisation based in Livingston, seeks an experienced Project Manager to own customer programmes from contract through design, development and manufacture. You will coo...Read More>>.

Guided Solutions is supporting an established medical device business expanding its UK commercial team. The NHS Territory Manager role offers a commercially minded sales professional the chance to own a territory and progress within healthcare sal...Read More>>.

Alliance Pharma PLC in Chippenham, Wiltshire, offers a hybrid Regulatory Affairs Associate role (VMS/Food Supplements) for a 9-month maternity cover starting November 26. The post supports maintenance and development of an EMEA portfolio across VM...Read More>>.

This is a 12-month paid internship starting September 2027. The role is head office based requiring a minimum of 2 days a week to be worked from our office in Winnersh. INTRODUCING THE OPPORTUNITY Joining Boehringer Ingelheim in September 2027, yo...Read More>>.

STADA UK Thornton & Ross in Huddersfield invites applications for a 12-month Regulatory Affairs placement student commencing July 2027. You will gain hands-on experience with submissions, registrations, packaging and product updates under close su...Read More>>.

STADA UK Thornton & Ross invites applications for a Regulatory Affairs Placement Student in Huddersfield. This year‑long, full‑time placement offers hands‑on experience supporting submissions, registrations, packaging and product updates und...Read More>>.

Stryker Belfast is hiring a Manufacturing Operator for the night shift to help build life-saving medical devices in a fast-paced, quality-focused environment. You will work on a production line, assemble, test and package products to meet daily ta...Read More>>.

Manpower UK is seeking a Customer Service Representative for a world-leading healthcare company in Leeds. The role is full-time and hybrid, 37 hours per week, with a two-week rotating schedule and pay starting at £13.85 per hour, rising to £15.0...Read More>>.

Matchtech is assisting a medical device business near Fareham, Hampshire, to recruit a Quality Engineer focused on quality systems, compliance and audits. The role is permanent and hybrid, emphasizing audit readiness, CAPA, and embedded quality pr...Read More>>.

Ernest Gordon Recruitment is seeking a Quality Engineer for a medical devices manufacturer in Andover, Hampshire. The role focuses on maintaining and developing the QMS within a high-end cleanroom and ensuring ISO 9001/13485, AS9100 compliance....Read More>>.

Tangerine Search is seeking a field-based Medical Devices Sales professional to cover East Midlands, Lincolnshire, and Bedfordshire. You will engage NHS and private sector stakeholders, manage key accounts, and lead contract and pricing negotiatio...Read More>>.

Our client is a fast-growing, well-funded company authorised to assess and certify medical devices, combining clinical, technical and regulatory expertise with modern technology to help ambitious health-tech companies bring safe products to market...Read More>>.

Forest Hospitals NHS Foundation Trust invites applications for an Orthotic Technician at King's Mill Hospital. You will join our in-house orthotic manufacturing facility to manufacture and maintain bespoke orthotic devices.We seek a motivat...Read More>>.

Sherwood Forest Hospitals NHS Foundation Trust in Sutton-in-Ashfield is seeking an Orthotic Technician to join our in-house orthotic manufacturing facility. You will manufacture and maintain bespoke devices, with opportunities to develop skills in...Read More>>.

Keeler, a global eyecare leader and Halma member, is based in Windsor and seeks a Technical Support Associate to deliver first-line support for Keeler’s products and software, including Keeler Konnect, Accutome Connect, Kapture and Kinexis....Read More>>.

SGS UK Ltd in the Birmingham area is seeking a Senior Technical Medical Device Coordinator to support the UK Medical Devices Team. You will coordinate Technical Documentation Reviews, monitor KPI reports and drive actions to resolve issues....Read More>>.

Stryker Belfast is seeking a Manufacturing Operator on a permanent basis to help build life-saving medical devices in a quality-focused, supportive environment. This onsite role offers a clear career path within a world-leading medical device comp...Read More>>.