Future Tech Jobs
Future Tech Jobs
The Senior Financial Analyst role at Medtronic involves leading financial reporting, revenue processes, and digital finance transformation. You will ensure financial accuracy, support margin optimization, and drive automation initiatives across SAP and other systems, collaborating with cross-functional teams.
The Sales Representative role involves developing and maintaining Medtronic's Embolisation, Deep Venous, and Peripheral Vascular portfolios with existing and new customers. Responsibilities include analyzing the marketplace, building sales strategies, and providing technical and clinical support to healthcare professionals.
As a Regulatory Affairs Specialist, you will work across regions and products, preparing global regulatory submissions and maintaining compliance for Smith & Nephew's orthopaedic portfolio. You will collaborate with project teams to develop regulatory strategies, support product changes, and ensure adherence to international regulations.
Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.Are you driven by the opportunity to help shape global marketing strategy in a fast moving, innovation led environment? This is a chance to play a...
The Hips Lifecycle Management Leader role involves leading the lifecycle management of hip joint products within the MedTech Orthopaedics business. Responsibilities include strategic planning, product development, and collaboration with cross-functional teams to drive innovation and improve patient outcomes.
This role involves developing and executing the commercial strategy for a portfolio of hardware and software products in the Cardiovascular space. Responsibilities include leading product launches, creating sales materials, supporting country teams, and tracking performance. The position requires strong strategic thinking, commercial acumen, and cross-functional collaboration.
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. Key responsibilities include coordinating data-driven risk oversight, maintaining clinical quality plans, and communicating risk updates to R&D colleagues through regular review cycles.
The EMEA HEMA Associate Manager supports the regional development and execution of Health Economics & Market Access activities across EMEA. Key responsibilities include coordinating EMEA initiatives, generating evidence, developing value tools, and ensuring compliance with governance and regulatory standards.
The EMEA HEMA Associate Manager supports the regional development and execution of Health Economics & Market Access activities across EMEA. Key responsibilities include coordinating EMEA initiatives, generating evidence, developing value tools, and ensuring compliance with governance standards.
The EMEA HEMA Associate Manager supports the development and execution of Health Economics & Market Access activities across EMEA, working closely with country HEMA Leads. Responsibilities include coordinating EMEA initiatives, generating evidence, developing value tools, and ensuring compliance with governance standards.
The EMEA HEMA Associate Manager supports the regional development and execution of Health Economics & Market Access activities across EMEA. Key responsibilities include coordinating EMEA initiatives, generating evidence, developing value tools, and ensuring compliance with regulatory standards.
The role involves maintaining and ensuring the accuracy of master data across multiple platforms, implementing data governance strategies, and collaborating with various departments to enhance data processes. The position also includes developing analytical reports and supporting the implementation of new MDM systems.
This role involves maintaining and ensuring the accuracy of master data across multiple platforms, implementing data governance practices, and collaborating with various departments to enhance data processes. The position also includes developing analytical reports and supporting the implementation of new MDM systems.
This role involves writing and coordinating clinical documents, such as Phase 1 protocols and clinical study reports, for oncology treatments. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.
This role involves writing and coordinating basic clinical documents such as Phase 1 protocols, Phase 1/2 CSRs, and initial IBs. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.
