Future Tech Jobs
Future Tech Jobs
This role involves shaping the competitive position of bladder and bowel neurostimulation therapies internationally. You will lead product launches, develop marketing strategies, and collaborate with cross-functional teams to drive growth and deliver measurable business impact.
This role involves shaping the competitive position of bladder and bowel neurostimulation therapies internationally. You will lead product launches, develop marketing strategies, and collaborate with cross-functional teams to drive growth and deliver measurable commercial results.
The Senior Clinical Trial Leader will support the planning and execution of clinical trials for medical devices, working closely with cross-functional teams, clinical sites, and external partners. The role involves ensuring quality and compliance while contributing to innovative medical device development that improves patient outcomes.
The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Responsibilities include active participation in study activities, regular risk reviews, maintaining clinical quality plans, and communicating risk updates to stakeholders.
Life Unlimited.At Smith+Nephew we design and manufacture technology that takes the limits off living.TheGlobal Category Manager Utilities “GCM”is responsible for executing the global utilities category strategy across regions and sites. The role manages our global energy portfolio, leads national and...
This role involves designing and leading a global employee listening strategy, translating insights into actionable changes, and refreshing the Employee Value Proposition. The Director will work closely with senior leaders and HR partners to drive cultural and organizational improvements through meaningful feedback and data-driven decision-making.
This role involves leading the Product Marketing team for electrophysiology across EMEA, driving the execution of the regional commercial plan, and developing customer engagement programmes. The position requires deep expertise in MedTech, particularly in electrophysiology and cardiovascular treatments, and a strong track record in product marketing and commercial execution.
The Launch Excellence Lead for Velys Trauma & Data Products is responsible for managing complex projects and processes, coordinating cross-functional teams, and driving process development and simplification. This role ensures the successful implementation of Velys Digital and Capital technologies, supports data-driven decision-making, and aligns project timelines across regional and functional teams.
The Engineering Technician role involves maintaining, fault-finding, and repairing CNC machines in a regulated medical device production environment. Responsibilities include performing preventive maintenance, diagnosing issues, and supporting machine setup and qualification activities. The role also focuses on continuous improvement to increase equipment uptime and process yield.
The Specialist, Clinical Risk Management Oncology, works with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. They actively participate in study activities, maintain clinical quality plans, and communicate risk updates to R&D colleagues through regular review cycles.
This role involves developing evaluation frameworks and rubrics for AI agents in clinical operations and global development. Responsibilities include designing quality dimensions, running human evaluation protocols, and building benchmark datasets. The position requires a strong understanding of clinical operations, regulatory documentation, and AI systems.
The Clinical Trial Leader role involves supporting the planning and execution of clinical trials for medical devices, working closely with cross-functional teams, clinical sites, and external partners. The position focuses on ensuring trials are conducted with quality and compliance, contributing to the development of innovative medical devices that improve patient outcomes.
The Director, 3rd Party RM Program provides strategic leadership for an enterprise-wide third-party risk management program, focusing on anti-bribery and anti-corruption risks. Key responsibilities include setting global standards, developing risk assessment frameworks, overseeing due diligence processes, and partnering with Legal and IT to implement technology solutions.
This role involves managing and shaping the Early Development & Clinical Pharmacology (ED&CP) structure, overseeing trial operations, and ensuring compliance with regulations. Responsibilities include line management, resource allocation, and driving process improvements. The position is hybrid, with 3 days onsite and 2 days remote.
The role involves leading and overseeing regulatory affairs activities for the UK market, ensuring compliance with UK and EU regulations, and managing regulatory risk. The Associate Director will partner with various teams to support product registrations, lifecycle management, and business initiatives, while also leading the UKCA marking strategy and coaching regulatory team members.
