Latest Healthcare Jobs

Field Service Engineer, Medical Diagnostic Systems

This role involves servicing and repairing advanced medical diagnostic systems used in NHS and private laboratories. The engineer will conduct on-site maintenance, troubleshoot technical issues, and provide expert support to laboratory staff. Full product training is provided, with a strong emphasis on customer service and technical problem-solving in clinical environments.

TRS Consulting Portsmouth, Hampshire, United Kingdom £52,000 pa

On-site Permanent

Field Service Engineer, Medical Diagnostic Systems

This role involves servicing and repairing advanced medical diagnostic systems used in NHS laboratories and clinical chemistry environments. The engineer will visit customer sites to perform maintenance, troubleshoot issues, and deliver technical solutions while working closely with laboratory staff. The position requires a technically skilled individual with experience in high-value capital equipment and offers extensive product training.

TRS Consulting Salisbury, Wiltshire, United Kingdom £52,000 pa

On-site Permanent

Country Study Start-Up Team Leader (cSTL)

Leads and optimises clinical trial start-up operations in the UK for Roche, ensuring regulatory compliance and efficient site activation. Oversees regulatory submissions, contract and budget strategy, and cross-functional collaboration with global teams. Champions innovation, process standardisation, and inclusive leadership within a matrixed environment.

Roche Welwyn Hatfield, United Kingdom

Machine Learning Scientist - Quantum Chemistry

Develop machine learning models grounded in quantum chemistry to accelerate small-molecule drug discovery. Create synthetic datasets using quantum mechanics and build scalable, deployable pipelines integrated into molecular design tools. Collaborate with computational and experimental scientists to advance drug discovery through publications and open-source contributions.

Roche

Hybrid Permanent

Contract Manager

Manages end-to-end contract processes for Investigator Initiated Studies and Supported Collaborative Studies with academic and research institutions. Responsibilities include drafting, negotiating, and finalizing agreements, resolving contractual issues, ensuring timely execution, and supporting clinical development activities within a global biopharma environment.

GSK United Kingdom

Principal Medical Writer

Author and lead the development of high-quality clinical regulatory documents such as protocols, Clinical Study Reports, and CTD submissions. Interpret complex clinical and statistical data to produce accurate, compliant narratives. Collaborate with cross-functional teams and manage complex writing projects across therapeutic areas and global submissions.

GSK CA$118,000 – CA$168,000 pa

Hybrid Permanent

Logistics Manager

Copello have partnered with an established engineering business in the recruitment of an experienced Logistics Manager to lead the setup and operation of a and-new logistics function supporting advanced manufacturing activities in Swindon.The successful candidate will have proven experience leading...

Copello Swindon, Wiltshire, United Kingdom £50,000 – £70,000 pa

Operations Lead

Lead end-to-end manufacturing, logistics, and warehouse operations within a regulated life sciences environment, driving performance in safety, quality, delivery, and cost. Champion lean principles and continuous improvement while developing teams and supporting new product introductions and site expansion initiatives.

Hays Procurement Jobs Llantrisant, Mid Glamorgan, United Kingdom £75,000 – £85,000 pa

On-site Permanent

Graduate Field Sales Representative (Life Science / MedTech)

This role involves demonstrating and selling advanced MedTech devices to healthcare, research, and pharmaceutical clients across a local patch covering South London, Surrey, and Kent. As a Graduate Field Sales Representative, you'll work autonomously from home, building relationships and driving sales after completing comprehensive training. The position offers a structured career path within a globally recognised MedTech organisation.

Ernest Gordon Recruitment Guildford, United Kingdom £30,000 – £34,000 pa

Hybrid Permanent

Field Applications Specialist

Talentmark are recruiting for a Field Applications Specialist to join a company in the pharmaceutical industry on a contract basis for 12 months.Salary:£180 to £230 per day PAYE, or £245.27 to £305.06 per day Umbrella.Field Applications Specialist Role:- Support customers...

Talentmark Devon, United Kingdom £180 – £230 pd

Production maintenance technician

Production Maintenance Technician – Night ShiftLocation: Plymouth, DevonSector: Medical Devices / Advanced ManufacturingEmployment Type: PermanentKinetic Business Solutions are supporting a leading medical devices manufacturer based in Plymouth with the appointment of a skilled Production Technician to join their night shift...

Kinetic Business Solutions Devon, United Kingdom £30,000 – £31,000 pa

(Fixed Term) Manufacturing Associate I

Operate and maintain mRNA vaccine production equipment in compliance with cGMP and safety standards, executing manufacturing processes, troubleshooting equipment and digital systems, and supporting quality documentation and continuous improvement initiatives. Work within a cross-functional team to ensure timely batch release and operational excellence in a fast-paced, highly regulated environment.

Moderna Oxford, United Kingdom

On-site Temporary

(Fixed Term) Manufacturing Associate I

Operate production equipment for mRNA vaccine manufacturing in compliance with cGMP and safety standards. Perform routine maintenance, support deviation investigations, and contribute to continuous improvement in a highly regulated, technology-driven environment. Work collaboratively with QA and cross-functional teams to ensure timely batch disposition and operational excellence.

Moderna

On-site Temporary

Global Safety Lead - Formulation Safety

Leads global safety strategy for formulation safety across the product lifecycle, focusing on clinical safety evaluation, signal detection, and risk management. Oversees production of key pharmacovigilance documents and ensures compliance with regulatory standards. Acts as safety representative in cross-functional teams and drives safety specifications and risk mitigation plans.

CSL

Global Safety Lead - Formulation Safety

Leads global safety strategy for formulation safety within CSL's GSPV department, overseeing clinical safety evaluation across product lifecycles. Responsible for signal detection, risk management planning, and regulatory compliance across clinical development and post-marketing phases. Serves as safety representative in cross-functional teams, ensuring alignment with medical, regulatory, and business objectives.

CSL