Medical Technology Jobs

13 jobs

Results

Bluetree logo
Featured

Senior Regulatory Affairs & Quality Manager

Last week

Bluetree Cambridge £65,000 – £80,000 pa

Lead regulatory strategy for a cardiology device company expanding into the US, UK, EU and Middle East, owning FDA, CE and UKCA submissions from Class I to Class II/III. Drive an audit-ready QMS (ISO 13485, 21 CFR Part 820, ISO 14971) and advise senior leadership on regulation, quality and clinical governance, working directly with the FDA, MHRA and notified bodies.

Hybrid Permanent
Johnson & Johnson MedTech logo

Post Doc - AI Safety

3 weeks ago

Johnson & Johnson MedTech Maidenhead

Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance, and safety-native architecture. You will design reproducible experiments, prototype layered safeguards, publish results, and work with platform engineers to move validated methods into a GenAI platform.

Hybrid Contract
Johnson & Johnson MedTech logo

Post Doc - AI Safety

3 weeks ago

Johnson & Johnson MedTech Limerick, Ireland

Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance and safety-native architecture. Hands-on work prototyping and validating methods on real GenAI platform workflows, publishing results and handing validated approaches to engineering partners.

Hybrid Contract

Assembly Operative

6 months ago

Pertemps Gloucester Cheltenham £25,000 – £27,000 pa

Assembling precision medical devices within a controlled cleanroom, working to GMP standards and ISO procedures to meet production targets. The role involves handling small components with high accuracy in a fast-paced, high-volume environment, with full training provided. It offers a four-day week, Monday to Thursday, with Fridays off.

On-site Permanent

Clinical Research Administrator

Last week

SPD Development Company Ltd Bedford £30,000 – £35,000 pa

Supports the conduct and monitoring of clinical studies, covering study set-up, sourcing and shipping supplies, volunteer recruitment, tracking study status, administering volunteer payments and maintaining inspection-ready documentation. Works within a clinical programme under GCP, with exposure to IVDR and ISO standards, in a 12-month fixed term contract.

Contract

Head of Operations - Biologics, RNA & MMIC

4 days ago

SRG Darlington £65,000 – £85,000 pa

Senior leadership role overseeing operations across biologics, RNA and medicines manufacturing facilities at two sites. Leads multidisciplinary teams covering operations, engineering, facilities and site services, ensuring GMP, health & safety and quality compliance while driving continuous improvement, capital projects and operational strategy.

Permanent

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Test Technician - Medical & Drug Delivery Devices

3 weeks ago

KO2 Embedded Recruitment Solutions Saffron Walden £25,000 – £28,000 pa

Hands-on testing of medical and drug delivery devices, from injectable and inhalation products to robotics and surgical instruments. Covers mechanical and functional testing, environmental stress conditioning, bespoke test rigs and documentation to SOPs, within a multi-disciplinary project team and under supervision.

On-site Permanent

Postdoctoral Research Assistant in Biomedical Image Analysis

3 weeks ago

University of Oxford Oxford £39,424 – £47,779 pa

Develops cutting-edge machine learning and computer vision methods to analyse multi-omic and biomedical imaging data, identifying disease phenotypes and tissue architecture changes. Works with software engineers and data platform developers to translate research prototypes into robust, reproducible tools, bridging research and implementation.

On-site Contract

Research Assistant - PRECISION-CSF: A Novel Diagnostic Assay for Personalised CNS Therapy in Childhood Leukaemia

Last month

University of Glasgow Glasgow £33,951 – £37,694 pa

Develops a stabilisation fluid added to cerebrospinal fluid samples to preserve leukaemia cells for flow cytometry analysis, optimising the formulation and validating it with patient samples. The role also involves contributing to research publications and proposals and helping manage the project within a university research group.

Contract

PhD Studentship: Development Of Advanced Miniaturised Device Technologies For Point-Of-Care Diagnostics Of Detrimental Diseases

2 weeks ago

University of Birmingham Birmingham

Fully funded PhD studentship in Chemical and Biomedical Engineering, joining the Advanced Nano Materials, Structures and Applications group. The research develops miniaturised point-of-care diagnostic devices, engineering intelligent spectroscopic techniques to non-invasively detect and quantify disease, with clinical validation and applications in monitoring cellular and tissue responses to therapy.

Contract

Assembly Operative

8 months ago

Pertemps Gloucester Cheltenham £25,000 – £27,000 pa

Assembling precision medical devices in a controlled cleanroom, following GMP standards, ISO procedures and strict quality requirements to meet production targets. Working a four-day week within a sociable team, with full training provided for candidates from production or manufacturing backgrounds.

On-site Permanent

New Product Coordinator

3 weeks ago

Response Personnel Bedfordshire £31,000 – £32,000 pa

Coordinate product development projects from sourcing and concept evaluation through to launch, sourcing materials and prototypes for testing. Maintain product and raw material specifications, work with suppliers on technical and quality requirements, and support cost-effective manufacturing. Provide technical product information to sales and marketing teams while ensuring quality, health and safety and regulatory compliance.

On-site Permanent
Johnson & Johnson MedTech logo

Post Doc - AI Safety

3 weeks ago

Johnson & Johnson MedTech Beerse, Belgium

Lead a two-year postdoctoral research program on making agentic AI safe for regulated pharmaceutical R&D, covering provable controls, adversarial assurance, and safety-native architecture. You will design reproducible experiments, prototype layered architectures, and work with platform engineers to move validated methods into a GenAI platform. The role is hands-on research with real systems as the testbed, not frontier model pre-training or production engineering.

Hybrid Contract
Johnson & Johnson MedTech logo

Post Doc - AI Safety

3 weeks ago

Johnson & Johnson MedTech Leiden, Netherlands

Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, continuous adversarial red-teaming, and safety-native architecture. Hands-on work prototyping and validating methods on real GenAI platform workflows, publishing results, and transitioning validated approaches into production with engineering partners.

Hybrid Contract