Future Tech Jobs
Future Tech Jobs
Latest UK roles, updated daily.
The Principal Systems Engineer will lead the development of innovative intraoperative support solutions, collaborating across Medtronic's R&D teams. Responsibilities include technical planning, system integration, and defining requirements for advanced surgical systems, with a focus on regulatory compliance and product design.
As a Service Program Manager at Medtronic, you will lead and manage complex projects and programs across the Digital Technologies Business Unit, focusing on business process improvement and the development of service-wide systems. You will work closely with cross-functional teams to enhance service delivery, develop global service strategies, and drive customer satisfaction through effective communication and project management.
As a Production Team Member, you will be part of a close-knit team responsible for running and maintaining complex manufacturing equipment. Your role involves preparing and setting up machines, conducting in-process checks, and ensuring accurate documentation to maintain high-quality standards in a safety-first environment.
This role involves leading and shaping the global OT cybersecurity strategy for a medical technology company. You will define governance, manage risks, and provide technical oversight across OT environments, ensuring alignment with industry standards and supporting secure modernisation initiatives in manufacturing.
The Technology Director, Make (EMEA) is a senior IT leader responsible for shaping and delivering manufacturing technology solutions across DePuy Synthes operations in the EMEA region. This role involves leading the EMEA manufacturing technology strategy, overseeing the delivery and lifecycle management of manufacturing systems, and ensuring compliance with regulatory requirements. The position also focuses on driving standardization, cybersecurity, and continuous improvement across manufacturing systems while leading regional teams and influencing global strategy.
This role involves leading the privacy program for DePuy Synthes in the EMEA region, ensuring compliance with data protection laws and embedding privacy-by-design principles across various business functions. The Director will advise on privacy risks, conduct impact assessments, and partner with multiple teams to manage data protection and innovation.
This role involves leading clinical risk management across therapeutic areas in Johnson & Johnson’s R&D organization, focusing on ensuring data integrity, patient safety, and regulatory compliance in clinical trials. The Associate Director will drive risk-based oversight, support inspection readiness, and provide expert guidance on quality issues and corrective actions. They will collaborate with cross-functional teams to identify, assess, and mitigate risks throughout the trial lifecycle.
This role involves leading clinical risk management activities across therapeutic areas, ensuring trial data integrity, patient safety, and regulatory compliance. The Associate Director drives risk-based oversight, supports inspection readiness, and advises on quality issues and corrective actions within global clinical trials. They collaborate with cross-functional teams to implement robust quality systems and continuous improvement in clinical development.
This role involves leading clinical risk management across multiple therapeutic areas, focusing on identifying, assessing, and mitigating quality risks in clinical trials to ensure patient safety, data integrity, and regulatory compliance. The position drives risk-based oversight, supports inspection readiness, and provides expert guidance on quality issues and corrective actions within a global, cross-functional environment.
This role involves leading clinical risk management across therapeutic areas in Johnson & Johnson's R&D Quality team. The individual will identify, assess, and mitigate quality risks impacting clinical trial data integrity, patient safety, and regulatory compliance. They will drive risk-based oversight, support inspection readiness, lead quality investigations, and provide expert guidance on GCP and regulatory standards across global trial teams.
This role involves managing the end-to-end execution of global clinical trials, including oversight of trial-specific documentation, vendor management, budget control, and regional coordination. The Manager ensures alignment of feasibility strategies, conducts risk reviews, and supports compound training and compliance. They work across matrixed, global teams to mitigate risks and ensure smooth trial delivery within the MedTech and pharmaceutical development environment.
This role involves managing the end-to-end execution of global clinical trials, including vendor oversight, trial documentation, budget management, and regional coordination. The Manager ensures compliance, mitigates risks, and supports compound training while working across matrixed, multinational teams. A key focus is aligning local operational delivery with global trial strategy to ensure timely and successful study outcomes.
This role involves managing the end-to-end delivery of global clinical trials, with responsibility for trial-specific documentation, vendor oversight, budget management, and regional coordination. The position ensures alignment of feasibility strategies, conducts risk reviews, and supports compound training across multi-functional, global teams. It plays a key role in maintaining compliance, driving process improvements, and preparing for health authority inspections.
This role involves managing the execution of clinical trials, including creating trial-specific documentation, overseeing vendors, and coordinating country-level operational delivery. The manager ensures alignment of feasibility strategies, conducts risk reviews, and supports compound training development. It requires strong project management and leadership skills within a global, matrixed environment.
This role involves managing the execution of clinical trials, including creating and updating trial-specific documentation, overseeing vendor activities, and ensuring compliance with operational strategies. The Manager coordinates country and regional trial activities, conducts risk assessments, and supports compound training development. They also mentor team members and contribute to process improvements within a global, matrixed environment.
