Future Tech Jobs
Future Tech Jobs
The role involves providing high-level field service and customer support for a wide range of medical devices, including surgical robotics and monitoring systems. Key responsibilities include repairing equipment, scheduling maintenance, and driving service revenue growth through customer relationships and contract sales.
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 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.
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeThe...
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.
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. Key responsibilities include active participation in study activities, regular risk reviews, maintaining clinical quality plans, and facilitating risk updates to R&D colleagues.
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, maintaining clinical quality plans, and facilitating regular risk reviews and updates.
The Senior Specialist, Clinical Risk Management, collaborates with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include participating in risk assessments, maintaining clinical quality plans, and communicating risk updates to R&D colleagues through regular review cycles.
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 involves collaborating with various stakeholders to ensure successful product launches and commercial performance.
This role involves leading the Product Marketing team for electrophysiology across EMEA, driving the execution of new product launches, developing customer engagement programmes, and ensuring commercial performance. The position requires deep expertise in MedTech, particularly in electrophysiology and cardiovascular treatments, and a strong track record in product marketing and commercial execution.
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 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.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through...
This role involves overseeing clinical risk management for post-approval clinical trials, ensuring data integrity, patient safety, and compliance with regulatory requirements. Responsibilities include leading a team of CRM Representatives, conducting risk assessments, and developing mitigation strategies.
The Specialist, Clinical Risk Management Oncology, works closely 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 risk management activities, maintain clinical quality plans, and communicate risk updates to stakeholders through regular review cycles.
