Latest Medical Devices Jobs

Spotlight

Senior Clinical Trial Case Manager

This role involves leading safety data review and pharmacovigilance activities within clinical trials, ensuring compliance with international regulations such as GxP. The individual will mentor team members, manage CAPAs, support regulatory inspections, and contribute to safety reporting and risk management. Key responsibilities include MedDRA coding, safety data analysis, and developing pharmacovigilance procedures to support global regulatory requirements.

CSL

On-site Permanent

Spotlight

Senior Computational Chemist, LNP Design

This role involves leading the computational design of lipid nanoparticles for nucleic acid delivery, using chemical and biophysical principles, AI tools, and molecular simulations. You will work closely with the experimental team to translate computational insights into testable strategies and refine formulations iteratively.

CureAge Therapeutics London, ENG, United Kingdom

Hybrid Permanent Part-time

Medical Devices Project Leader - Warwick

Lead the development of medical devices from concept to commercial launch within a multidisciplinary engineering team. Provide technical leadership, mentor junior engineers, and ensure robust design and compliance, particularly for products involving injection-moulded plastic components. Contribute to regulatory strategy and full lifecycle development in a fast-paced environment focused on improving patient outcomes.

Newton Colmore Warwick, United Kingdom

On-site Permanent

Embedded Software Engineer - Medical Devices

This role involves developing embedded C and C++ software for medical devices, ranging from lab and hospital equipment to personal use sensors. You will work through all project stages, from concept to manufacture, and interact closely with clients and team members.

ECM Selection Cambridge, Cambridgeshire, United Kingdom £45,000 – £55,000 pa

Mechatronics Design Expert - Medical Technology

This role involves designing and developing novel mechatronic systems for medical devices and biotechnology applications, working closely with a multidisciplinary team to take ideas from concept to manufacture. Responsibilities include creating intricate mechanisms and overseeing the overall development of complex machines.

Newton Colmore Cambridge, United Kingdom

Firmware Engineer

This role involves designing and developing FPGA functionality using VHDL for high-performance data acquisition and signal processing systems, as well as developing embedded software in C to control hardware and interface with FPGA-based systems. You will collaborate with hardware and software engineers to integrate, test, and optimize new features across complex electronic products.

Platform Recruitment Milton, Cambridgeshire, Cambridgeshire, United Kingdom £35,000 – £45,000 pa

Product Definition Lead

The Product Definition Lead will drive the technical direction and product definition for complex medical device systems, manage a team of systems and requirements engineers, and support the engineering team with technical issue resolution. The role involves close collaboration with interdisciplinary teams to translate business and clinical needs into precise requirements.

Talentmark Calderbank, Lanarkshire, ML6 9TB, United Kingdom £23 – £26 ph

On-site Contract Clearance Required

Senior Electronic Design Engineer

This role involves working from customer requirements to define and develop new products, designing custom electronic circuit boards, and performing board bring-up, verification, and testing. You will also liaise with customers on integration, commissioning, and problem resolution, and occasionally write technical reports.

Platform Recruitment Cambridge, Cambridgeshire, United Kingdom £60,000 – £65,000 pa

Senior Scientist R&D

The Senior R&D Scientist will execute complex experimental workstreams, analyse data, and present findings to stakeholders. They will apply Design for Manufacture (DFM) principles to optimise product formulations and ensure compliance with GLP, GMP, and GDP standards in a laboratory setting.

Talentmark Stirling, Stirling And Falkirk, United Kingdom £25 – £27 ph

On-site Contract Clearance Required

QC Analyst

This role involves testing raw materials, in-process, stability, and finished product samples using approved analytical methods in a busy GMP laboratory. You will work closely with Production, QA, and Technical teams, supporting investigations, method validation, and continuous improvement.

Adepto Technical Recruitment Ltd Watford, Hertfordshire, United Kingdom £33,000 – £35,000 pa

On-site Permanent

Quality Assurance Officer

The QA Officer will work within an experienced team to maintain high quality standards in a GMP manufacturing environment. Responsibilities include controlling quality documentation, developing training programs, investigating GMP breaches, and supporting audits and continuous improvement projects.

SRG Bradwell, Norfolk, NR31 8PS, United Kingdom £30,000 – £37,700 pa

On-site Permanent

Compliance Engineer

The Compliance Engineer will be responsible for creating, reviewing, and maintaining regulatory and technical documentation to ensure products remain compliant and audit-ready. Key responsibilities include authoring technical files, supporting EU MDR and UK regulatory compliance, and assisting with Notified Body and external audit requirements.

Aurora Life Sciences Doncaster, South Yorkshire, United Kingdom £50,000 pa

Senior Mechanical Engineer

This role involves designing and developing complex mechanical products, from concept to manufacture. Responsibilities include 3D CAD modeling, DFMA, prototyping, testing, and working with suppliers. The position is ideal for engineers with a strong background in mechanical design and experience in multidisciplinary environments.

Lynx Recruitment London, United Kingdom £60,000 – £70,000 pa

Regulatory Affairs Manager

The Regulatory Affairs Manager will lead day-to-day regulatory activities, maintaining and developing technical documentation for existing and future medical devices and IVD products. You'll support UKCA and CE marking, regulatory strategies, and collaborate with scientific, data, and technical teams to ensure compliance throughout product development.

Cure Talent Hildersham, Cambridgeshire, United Kingdom £60,000 – £75,000 pa

Senior Regulatory Affairs Specialist UK and Ireland

This role involves leading regulatory strategy and hands-on activities for medicinal products, medical devices, and cosmetics in the UK and Ireland. Responsibilities include managing regulatory submissions, ensuring compliance, and supporting product launches and lifecycle management.

GI Group Tottenham Court Road, London, United Kingdom

Field Service Engineer, Scientific Optical Lasers

This role involves servicing, installing, repairing, and calibrating sophisticated scientific and laboratory systems used in pharmaceutical and research environments. The position requires a background in field service engineering and a qualification in electronics, with experience in high-value capital equipment.

TRS Consulting Sparkbrook, West Midlands (county), B11 1AG, United Kingdom £43,000 pa

Field Service Engineer, Laboratory X-Ray Systems

This role involves servicing, installing, repairing, and calibrating sophisticated laboratory X-ray systems in pharmaceutical and research environments. The position requires a background in field service engineering and a qualification in electronics, with experience in high-value capital equipment.

TRS Consulting Wolverhampton, West Midlands (county), United Kingdom £43,000 pa