Latest Life Sciences Jobs

System Test Technician

The role involves executing system-level testing of Class 3 medical devices, including functional, performance, safety, and reliability testing across electrical, mechanical, and software domains. The technician will build and maintain test fixtures, document results in compliance with medical device regulations, and support continuous improvement of test procedures within a quality-managed environment.

OrganOx Oxford, United Kingdom

On-site Permanent

Senior Supplier Assurance Engineer

The Senior Supplier Assurance Engineer leads supplier quality activities, ensuring compliance with global regulations and internal QMS processes. Key responsibilities include supplier qualification, performance monitoring, and continuous improvement, with a focus on maintaining high-quality standards across the supply chain.

OrganOx Oxford, United Kingdom

On-site Permanent Flexible

Senior Orthopaedic Sales Specialist

This role involves working as a trusted expert in orthopaedic revision surgery, supporting complex procedures in operating theatres, and driving the adoption of innovative technologies, including robotics. You will develop account plans, collaborate with sales teams, and gather market intelligence to strengthen Smith & Nephew's market position.

Smith & Nephew Cambridge, United Kingdom

Hybrid Permanent

Senior Orthopaedic Sales Specialist

This role involves working closely with surgeons and key accounts to drive the adoption of advanced orthopaedic revision technologies, including robotics. You will lead sales strategies, support complex procedures, and gather market intelligence to strengthen Smith & Nephew's position in the M1 Corridor to the East of England.

Smith & Nephew Chatham, ME4 4NP, United Kingdom

Hybrid Permanent

Sr Director, External Scientific Innovation Transactions

The Sr Director, External Scientific Innovation Transactions leads business development activities, including transactions, research collaborations, licensing, and asset acquisitions. They focus on identifying and securing top scientific innovations, primarily in the APAC region, and work closely with R&D, finance, legal, and IP teams to develop and execute complex deals.

Johnson & Johnson MedTech London, United Kingdom

On-site Permanent

Product Manager Software & Hardware Electrophysiology

This role involves developing and executing the commercial strategy for a portfolio of hardware and software products in the Cardiovascular space. Responsibilities include leading product launches, creating sales materials, supporting country teams, and tracking performance. The position requires strong strategic thinking, commercial acumen, and cross-functional collaboration.

Johnson & Johnson MedTech United Kingdom

Hybrid Permanent

Regulatory Affairs and Quality Assurance Assistant - Cambridge

This role involves supporting quality assurance and regulatory affairs activities within a medical devices R&D environment, ensuring compliance with ISO 13485, FDA 510(k), and 21 CFR Part 820 standards. The assistant will collaborate closely with R&D teams, providing guidance on regulatory requirements during product development and improvement. The position plays a key part in maintaining quality management systems and enabling the delivery of innovative, life-improving medical technologies.

Newton Colmore Cambridge, United Kingdom

On-site Permanent

Clinical Sales Representative (Benelux Region)

This role involves providing clinical and scientific expertise to support customers and internal teams in the medical technology sector, with a focus on promoting products within hospital settings across the Benelux region. The representative will build relationships with key decision-makers and clinical stakeholders, particularly in specialties such as oncology, anesthesia, and intensive care. A strong clinical background and industry experience in medical devices are essential for success in this position.

Hyper Recruitment Solutions Netherlands

Hybrid Permanent

Mechanical Design Engineer

This role involves enhancing and maintaining existing diagnostic product designs within a regulated medical technology environment. The engineer will lead design updates, conduct testing, manage engineering changes, and ensure compliance with quality and regulatory standards. Collaboration with R&D, manufacturing, and suppliers is key to improving product performance and reliability.

ProTech Recruitment Ltd Bath, Somerset, TA7 8PH, United Kingdom £45,000 – £50,000 pa

Hybrid Permanent

Principal Medical Science Liaison

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing...

Medtronic London, United Kingdom

Affera Regional Clinical Educator

The Affera Regional Clinical Educator role involves driving clinical excellence among Affera Mapping Specialists in the UK. Responsibilities include in-field training, coaching, and support for the rollout of the Affera Mapping System and other electrophysiology technologies. The role requires strong expertise in electrophysiology and cardiac mapping, as well as the ability to develop and deliver tailored training programs.

Medtronic Watford, United Kingdom

On-site Permanent

Clinical Research Scientist

This role involves critically reviewing clinical data and preparing high-quality technical and clinical evaluation reports to support regulatory compliance under MDR and IVDR standards. The Clinical Research Scientist will assess scientific literature and post-market data, compile documentation for CE marking, and present findings to cross-functional teams. It offers a chance to deepen expertise in regulatory scientific writing within the medical device sector.

Randstad Delivery Witney, Oxfordshire, United Kingdom £32,500 pa

On-site Contract

Quality Engineer - Medical Devices - Didcot

The role involves managing key Quality Engineering activities across the full Quality Management System, including CAPA, non-conformities, complaints, change control, and internal audits. You will support supplier quality, manufacturing compliance, and collaborate with engineering teams on validation and risk management. The position plays a critical part in maintaining regulatory compliance and driving continuous improvement within a growing medical device environment.

Newton Colmore Didcot, United Kingdom

Hybrid Permanent

Graduate Quality Engineer

This role involves supporting quality management systems in a regulated pharmaceutical environment, with responsibilities including compliance monitoring, documentation review, risk assessment, and collaboration with R&D and Regulatory Affairs. The candidate will act as a quality subject matter expert during audits and contribute to process improvements across the product lifecycle. It's a 12-month graduate contract offering hands-on experience in medical device manufacturing compliance.

Randstad Delivery Witney, Oxfordshire, United Kingdom £33,000 – £45,000 pa

On-site Contract

Clinical Consultant - Radiology Informatics (PACS)

This role involves coordinating and implementing activities for application configuration, user training, and product commercialization in radiology informatics. You will work with a dynamic team to transform healthcare delivery, focusing on VUE PACS solutions and supporting customers across the UK and Europe.

Philips United Kingdom

Hybrid Permanent Clearance Required