Future Tech Jobs
Future Tech Jobs
This role involves leading global regulatory strategies for AI-enabled medical technologies, preparing high-quality submissions, and ensuring compliance with evolving regulations. The specialist will manage multiple projects, collaborate with cross-functional teams, and guide regulatory pathways for innovative digital health solutions. It is a strategic position requiring deep expertise in software, cybersecurity, and AI/ML regulatory frameworks.
Lead end-to-end operational transformation programs in healthcare organizations across EurAsia, translating strategy into measurable improvements in patient outcomes and operational efficiency. Work closely with hospital leaders and cross-functional teams to design and implement sustainable solutions, leveraging expertise in healthcare systems, process optimization, and change management. Contribute to the development of scalable consulting offerings and support capability building across regions.
This role involves leading the assessment and reporting of serious breaches in Johnson & Johnson's sponsored clinical trials to ensure compliance with global regulatory requirements. The Manager, Serious Breach Office will coordinate cross-functional stakeholders, develop performance metrics, and drive continual improvement in breach detection and reporting processes. The position emphasizes data-driven decision-making, process optimization, and strong collaboration across clinical quality, legal, and regulatory functions.
This role involves leading the operational intake of adverse events, product quality complaints, and safety data within Johnson & Johnson's Global Safety System. The scientist ensures compliance, manages vendor partners, and drives process improvements in pharmacovigilance operations. Key responsibilities include oversight of case receipt, due diligence follow-up, regulatory inspection support, and cross-functional collaboration to enhance safety reporting efficiency and accuracy.
Lead a strategically important manufacturing site within a global medical technology company, driving long-term strategy, operational excellence, and large-scale transformation across multi-functional teams. Champion a culture of innovation, compliance, and continuous improvement in a highly regulated environment. Play a key role in the global operations leadership team, influencing broader supply chain strategy while ensuring performance, safety, and regulatory standards are consistently met.
Lead a strategically important manufacturing site within a global medical technology organization, driving long-term strategy, operational excellence, and large-scale transformation across manufacturing, quality, R&D, and regulatory functions. Champion a culture of innovation, compliance, and continuous improvement in a highly regulated environment. Play a key role in the global operations leadership team, influencing broader supply chain strategy while developing a high-performing, multi-functional leadership team.
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 customer support across clinical environments. Full product training is provided, and the role requires occasional weekend work with a five-days-a-week schedule.
This role involves on-site service and repair of advanced medical diagnostic systems used in NHS and private laboratories. The engineer will diagnose and resolve technical issues, provide customer support, and ensure equipment uptime. Full product training is provided, and the role requires regular weekend work due to a five-day, seven-day working pattern.
Lead the design, testing, and improvement of electromechanical systems in medical diagnostic devices, focusing on reliability and production transfer. Own technical projects from concept through verification, conduct root cause analyses, and collaborate with cross-functional teams to integrate new technologies. Work within a regulated environment, ensuring robust system performance and thorough technical documentation.
This role involves designing and optimizing manufacturing processes for medical devices, with a focus on instrumentation and electromechanical systems. The engineer will lead process improvements, support verification and validation at contract manufacturing organizations (CMOs), and ensure compliance with quality standards. Key responsibilities include driving design for manufacturability, managing technical projects, and maintaining rigorous documentation within a regulated environment.
Design and develop custom electrical and pneumatic control systems for bespoke automation machinery used in high-tech industries such as medical devices, aerospace, and advanced manufacturing. Translate client requirements into detailed schematics, safety documentation, and technical specifications, collaborating with cross-functional engineering teams and supporting manufacturing and testing phases. Work spans concept to customer acceptance, with a focus on compliance with machinery safety standards and CE regulations.
This role involves performing calibration, verification, and preventive maintenance of equipment used in medical device manufacturing and testing. The engineer will ensure compliance with regulatory standards, develop calibration schedules, troubleshoot issues, and support quality audits. Collaboration with cross-functional teams and training of technicians are key aspects of the position.
Manages controlled documentation and quality records throughout their lifecycle in a regulated medical device manufacturing environment. Supports change control, audit readiness, and compliance with ISO13485, while ensuring accurate, traceable, and timely document availability. Provides operational support for product release by reviewing batch records, device history files, and manufacturing documentation, and may supervise junior team members.
The role involves manufacturing high-accuracy calibration and reference gases using gravimetric methods, preparing gas cylinders, and ensuring strict adherence to quality and safety standards. The chemist will work within a production team to meet customer specifications and support logistics, maintaining compliance with ISO 6142 and ISO 17034. The position offers structured training and career progression within a global industrial gases company.
This role involves selling MedTech devices to healthcare, research, and pharmaceutical clients across South London, Surrey, and Kent. The successful candidate will work autonomously, managing a local patch with a 60/40 split between new business development and account management. After comprehensive training, they will demonstrate equipment, generate leads, and drive sales within a globally respected biomedical laboratory equipment company.
