Future Tech Jobs
Future Tech Jobs
Latest UK roles, updated daily.
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...
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...
Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.We’re looking for a driven Account Manager to join our Orthopaedics - Trauma & Extremities team, covering the Birmingham & Coventry area. If you’re passionate about...
Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.We’re looking for a driven Account Manager to join ourSports Medicine team based in the Birmingham and West Midlands area. If you’re passionate about building strong...
The Senior Process Engineer will lead the optimization of manufacturing value streams for medical devices, ensuring safety, compliance, and cost-effectiveness. Key responsibilities include hands-on engineering leadership, process development and validation, quality improvement, and collaboration with cross-functional teams to drive innovation and continuous improvement.
The Lead Local Trial Manager is responsible for managing and overseeing clinical trials in the UK, ensuring compliance with protocols, SOPs, and regulatory standards. Key responsibilities include coordinating trial activities, maintaining high-quality data, and collaborating with internal and external stakeholders to deliver successful trials.
This role leads clinical risk management across therapeutic areas, ensuring trial data integrity, patient safety, and regulatory compliance. The Associate Director drives risk-based oversight, inspection readiness, and quality assurance for clinical trials, working closely with global teams to identify, assess, and mitigate risks. They also support audits, develop quality strategies, and provide expert guidance on GCP and regulatory standards.
This role involves leading clinical risk management across multiple therapeutic areas, focusing on ensuring trial data integrity, patient safety, and regulatory compliance. The individual will drive risk-based oversight, support inspection readiness, and guide cross-functional teams in implementing quality strategies throughout clinical development. A key aspect is providing expert advice on quality issues and leading continuous improvement in clinical trial quality systems.
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 supports inspection readiness, drives risk-based oversight, and collaborates with cross-functional teams to implement effective quality strategies and corrective actions.
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.
