Future Tech Jobs
Future Tech Jobs
Regulatory Affairs Specialist - MedTechA growing medical devices company in Cambridgeshire are currently in need of an experienced quality assurance and regulatory affairs specialist.This is an excellent opportunity for a QARA specialist to join this team of experts and work...
This role involves designing and developing medical devices as part of a multidisciplinary engineering team. The engineer will work on life-saving and life-improving products, contributing to full product development cycles within a regulated environment. The company emphasizes innovation, staff growth, and career progression.
As a Van Driver at Movianto, you will deliver pharmaceutical products efficiently and safely, ensuring compliance with health and safety regulations. You will operate company vehicles, perform daily maintenance checks, and maintain a professional image while adhering to legal requirements and company policies.
As a Van Driver at Movianto, you will deliver pharmaceutical products efficiently and safely, ensuring compliance with health and safety standards. You will operate company vehicles, perform daily maintenance checks, and maintain a professional image while adhering to legal requirements and customer service standards.
This role involves serving as a clinical specialist for advanced wound care, providing hands-on support and education to healthcare professionals in the community setting. The specialist will drive appropriate use of complex wound therapies, build clinical relationships, and ensure patients receive timely, effective treatments across North Wales and the Midlands. A field-based position combining clinical expertise with sales and training responsibilities.
Leads a strategically important manufacturing site for wound care products, driving long-term strategy, operational excellence, and large-scale transformation within a highly regulated environment. Champions cultural change, compliance, and innovation while leading cross-functional teams in manufacturing, quality, R&D, and regulatory. Plays a key role in global operations leadership, influencing supply chain strategy beyond the site.
This role involves driving consultative sales of medical devices and equipment within critical care and respiratory medicine across a large UK territory. The representative will manage both new and existing hospital accounts, lead tenders, conduct clinical workshops, and collaborate with clinical and technical specialists to support customer adoption. Extensive travel and relationship-building with key stakeholders in ICU and emergency settings are central to the position.
This role involves driving consultative sales of medical devices and equipment within critical and intensive care settings across a large UK territory. The representative will manage both new business development and existing accounts, supported by clinical and technical specialists. Key activities include leading tenders, organizing educational workshops, and promoting innovative respiratory medicine technologies to healthcare professionals.
This role involves ensuring product quality on the manufacturing floor by monitoring production processes, implementing Statistical Process Control (SPC), and leading root-cause analysis of defects. The Quality Engineer will drive continuous improvement through corrective actions and support compliance with ISO 9001 and electronic-specific standards like IPC. Close collaboration with engineering teams is required during product transitions from prototype to full production.
This role involves leading all quality operations at a precision manufacturing site, ensuring compliance with stringent regulatory standards, and driving continuous improvement across processes. The Quality Manager will manage audits, lead root cause investigations, and work closely with production and engineering teams to embed quality and safety into daily operations. The position plays a critical role in maintaining certifications and supporting global customer requirements in a highly regulated environment.
This role involves hands-on quality inspection within a precision engineering environment, focusing on medical device manufacturing. You'll conduct first-off, in-process, and final inspections using CMM and precision measuring tools, ensuring compliance with engineering drawings and quality standards. The position supports continuous improvement and operates within a small, collaborative team.
ABOUT ORGANOX:OrganOx is a commercial stage organ technology company dedicated to developing technologies to improve outcomes for patients with acute or chronic organ failure. The company was established as a spin out of the University of Oxford in 2008 and...
This role involves leading quality assurance throughout the New Product Introduction (NPI) process, from design to production launch, within a regulated high-tech manufacturing environment. The engineer will manage APQP/PPAP workflows, lead cross-functional quality initiatives, conduct risk assessments, and ensure compliance with safety and regulatory standards. They will also oversee supplier quality, lead root cause investigations, and drive continuous improvement across NPI processes.
This role involves managing commercial quality processes within a regulated medical devices environment, focusing on distribution activities such as loan kits, kit builds, and service operations. The specialist ensures compliance through CAPA, non-conformance, change control, and complaint systems, supports audits and inspections, and drives continuous improvement across quality functions at the Leeds distribution centre.
Senior NPI Quality EngineerElectronics & Medical DevicesCompetitive Salary plus Bonus & BenefitsRelocation Assistance Provided (If Required)Step into a pivotal leadership role as a Senior NPI Quality Engineer and help bring high-quality, regulated products to life from first design through to...
