Latest Healthcare Jobs

Field Service Engineer, Medical Diagnostic Systems

This role involves servicing and repairing advanced medical diagnostic systems in NHS and private laboratory settings. The engineer will perform on-site maintenance, troubleshoot technical issues, and deliver customer support across pathology and clinical chemistry departments. Full product training is provided, and the role requires a flexible schedule including weekend work.

TRS Consulting Poole, Dorset, United Kingdom £52,000 pa

Field Service Engineer, Medical Diagnostic Systems

Provide on-site service and repair for advanced medical diagnostic systems used in NHS and private laboratories. Troubleshoot complex technical issues and deliver customer support to laboratory managers and technicians. Receive full product training and work across a range of high-value scientific equipment, with a focus on reliability and customer satisfaction.

TRS Consulting Bournemouth, Dorset, United Kingdom £52,000 pa

On-site Permanent

Field Service Engineer - Medical Diagnostics - South Region - Exeter - London - Kent

Perform on-site and remote technical support for Roche’s diagnostic systems, including troubleshooting, preventive maintenance, and customer training across the South Region. Use advanced diagnostic tools to resolve electro-mechanical faults and ensure regulatory compliance. Work within a customer-centric team to maximise system uptime and operational efficiency in clinical environments.

Roche United Kingdom

Field Service Engineer - Medical Diagnostics -Central Region Wales, Wirral and East Anglia

This role involves providing on-site and remote technical support for Roche’s diagnostic systems across medical laboratories and healthcare facilities. You’ll troubleshoot electro-mechanical faults, perform preventive maintenance, and deliver training to ensure optimal system uptime and customer proficiency. The position emphasizes compliance, reporting, and collaboration within a customer-centric field support team.

Roche United Kingdom

Associate Director, CMC Regulatory Affairs, International

This role involves leading CMC regulatory strategies and submissions for international markets, with a focus on mRNA-based products across vaccines, oncology, and rare diseases. The individual will guide global regulatory compliance, interact with health authorities, and support manufacturing and quality teams through regulatory interpretation and change control. It requires deep expertise in CTD-format filings and a proactive approach to managing multi-therapeutic regulatory programs in a fast-paced environment.

Moderna

On-site Permanent

Associate Director, Global Regulatory Science, CMC

This role leads global regulatory CMC strategy for mRNA-based medicines, developing and implementing regulatory plans for international submissions. The individual will guide CMC documentation, interact with health authorities, and provide strategic input across product development stages, ensuring compliance with EU and global regulations. The position plays a key part in advancing Moderna’s pipeline of transformative therapeutics across vaccines, oncology, and rare diseases.

Moderna

Hybrid Permanent

Analytical and Synthetic Chemistry (Multiple Roles) Industrial Placement, 2027

This 12-month industrial placement offers hands-on experience in either Analytical or Synthetic Chemistry within GSK’s R&D environment in Stevenage. In the Analytical role, you’ll use techniques like HPLC, GC, and NMR in a GMP setting to support medicine development. The Synthetic Chemistry role involves designing and running experiments to create new compounds, working alongside experienced scientists in a multidisciplinary team. Both roles emphasize technical skill development, project ownership, and real-world impact in drug discovery.

GSK Stevenage, United Kingdom

Medical Director, Oncology Clinical Development - GU

This role involves providing medical leadership within GSK's oncology clinical development team, focusing on genitourinary (GU) cancers. The Medical Director will lead medical monitoring, ensure patient safety, interpret clinical data, and contribute to study design and regulatory submissions. Working closely with cross-functional teams, the role integrates physician-level insight into clinical strategy and drug development execution.

GSK Stevenage, United Kingdom £472,500 – £787,500 pa

Director, International Value & Access, Immunology

This role involves developing and operationalizing international access strategies for immunology assets, shaping payer value propositions, and collaborating with cross-functional teams to maximize patient access to innovative therapies. The Director will also manage resources, anticipate policy trends, and represent Novartis in internal and external stakeholder engagements.

Novartis London, United Kingdom £87,360 – £162,240 pa

Global Program Safety Lead - Oncology

This role involves leading the end-to-end safety strategy for oncology programs, managing safety signals, and ensuring compliance with regulatory requirements. You will work closely with global teams, health authorities, and internal leaders to drive safety governance and benefit-risk evaluations.

Novartis London, United Kingdom £83,510 – £155,090 pa

Clinical Development Medical Director (MD required)

The Clinical Development Medical Director is responsible for providing medical and scientific oversight for clinical trials, ensuring patient safety, and contributing to the design and execution of clinical studies. They will also participate in safety reviews, interact with healthcare professionals, and support regulatory activities.

Pfizer United States

Clinical Development Medical Director (MD required)

The Clinical Development Medical Director is responsible for providing medical and scientific oversight for clinical trials, ensuring patient safety, and designing clinical studies. They will also participate in committees, review compounds for in-licensing, and support new business development.

Pfizer

Laboratory Team Lead

Lead a laboratory team in a regulated medical device environment, overseeing microbiology and chemistry testing, quality systems, and staff development. Provide technical expertise, drive continuous improvement, and ensure compliance with cGMP and ISO 13485 standards while supporting method validation and leading investigations into deviations.

Aurora Life Sciences Leeds, West Yorkshire, United Kingdom £42,000 – £48,000 pa

Laboratory Technician

Process environmental samples through DNA extraction, normalization, and library preparation pipelines using automated systems and manual techniques. Perform QC checks, maintain LIMS records, and support R&D protocol testing in a high-throughput, CL2-compliant lab environment. Contribute to maintaining a safe, organized workspace and enable scalable data generation for AI-driven biological discovery.

Basecamp Research London, United Kingdom

On-site Permanent

Senior Scientist, R&D

Develops and optimizes metagenomic extraction and sequencing workflows for diverse sample types, focusing on low-biomass and inhibitor-rich matrices. Works end-to-end from DNA/RNA extraction to library prep, with emphasis on high molecular weight recovery and virology applications. Collaborates globally to enhance data quality and scalability for AI-driven biological discovery.

Basecamp Research London, United Kingdom

On-site Permanent