Future Tech Jobs
Future Tech Jobs
In this role, you will shape the competitive strategy for bladder and bowel neurostimulation therapies, driving international product launches and marketing plans. You will collaborate with sales, market development, and global marketing teams to ensure successful execution and measurable business impact.
This role involves shaping the competitive position of bladder and bowel neurostimulation therapies internationally. Responsibilities include leading product launches, developing marketing strategies, and collaborating with sales, market development, and global marketing teams to drive growth and ensure successful go-to-market execution.
Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.We’re investing in the future of Surgical intervention and Negative Pressure Wound Therapy (NPWT), and this is your opportunity to be part of something truly impactful....
Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.We’re investing in the future of Surgical intervention and Negative Pressure Wound Therapy (NPWT), and this is your opportunity to be part of something truly impactful....
The Medical Affairs Specialist supports the use of Intraocular Lenses (IOLs) through proctoring, case analysis, and managing Medical Information Requests (MIR). They ensure optimal clinical outcomes by providing expert-level support to healthcare professionals and collaborating with various teams to analyze and improve patient outcomes.
The Medical Affairs Specialist supports the clinical use of Intraocular Lenses (IOLs) through case analysis, proctoring, and managing Medical Information Requests (MIRs). They ensure optimal patient outcomes by providing expert-level clinical support, analyzing sub-optimal results, and collaborating with various stakeholders to improve product performance and clinical practices.
The Validation Specialist role involves enhancing validation practices, supporting compliance with regulatory inspections, and streamlining processes. You will identify risk areas and implement mitigation strategies to meet standards set by bodies like the MHRA and FDA.
This role involves installing, maintaining, and repairing clinical diagnostic equipment in hospital settings across London and the Southeast. You will manage service spares, ensure documentation is up-to-date, and perform routine maintenance tasks. The position requires travel and a strong customer service ethic.
Want a 3D Career? Join Norgine.At Norgine, our colleagues Dare themselves to be different and try new things, Drive to achieve their goals and beyond, and Develop themselves and their community.We call it the 3D career at Norgine and it...
Business Development ManagerRevolutionary SaaS | Electronic Health Records | Clinical Trials & Drug DevelopmentSalary: £50,000–£60,000 (negotiable) + uncapped commission + excellent benefitsLocation: Home-based with access to Manchester offices (1–2 days per month)The OpportunityThis is not just another sales role.You’ll be...
The Scientist role involves reviewing clinical data, writing technical reports, and ensuring medical devices meet regulatory requirements for CE marking and global approval. You will collaborate with a scientific and clinical team, prepare high-quality reports, and manage changing priorities in a fast-paced environment.
The role involves installing, commissioning, and maintaining specialist electrical equipment at healthcare and commercial sites across the South of England. You'll perform fault diagnosis, electrical testing, and preventative maintenance in clean, professional environments, primarily hospitals. The position requires regular travel and emphasizes technical documentation and customer support.
The Installation Manager will oversee site operations, coordinate subcontractors, and ensure projects meet safety and quality standards in highly regulated sectors like pharmaceuticals and healthcare. The role involves leading a team, managing compliance, and acting as the primary on-site contact for project success.
The Production Scheduler will plan, coordinate, and monitor production activities across multiple projects in a regulated medical device manufacturing environment. Key responsibilities include developing realistic schedules, working closely with cross-functional teams, and supporting continuous improvement initiatives.
This role involves designing medical devices from concept to production, using SolidWorks to create 3D models and detailed drawings. The engineer will support prototyping, testing, and regulatory compliance while collaborating with manufacturing and cross-functional teams. The work contributes to life-changing healthcare products used globally.
