Future Tech Jobs
Future Tech Jobs
Analyse ECG data from Holter recordings to ensure clinical accuracy and support physician decision-making. Focus on quality assurance, rhythm interpretation, and adherence to diagnostic protocols within a structured healthcare technology environment.
The Lead Local Trial Manager is responsible for managing and overseeing clinical trials in the UK, ensuring compliance with protocols, SOPs, and regulatory standards. Key responsibilities include coordinating trial activities, maintaining high-quality data, and collaborating with internal and external stakeholders to deliver successful trials.
This role involves managing and improving content compliance and copy review processes across EMEA markets for MedTech promotional materials. The specialist ensures regulatory adherence, supports audit readiness, and drives process efficiency through digital tools, AI, and automation. They provide guidance to submitters, maintain documentation, and contribute to system enhancements in a multilingual, cross-regional environment.
The Supplier Quality Engineer will focus on evaluating and onboarding suppliers, ensuring compliance with ISO 13485, and leading CAPA activities. The role involves significant quality expertise in design-for-manufacture and supports the company's growth in the Femtech sector, with a focus on women's health and transformative technology.
This role involves providing regulatory guidance across the full product development lifecycle, supporting multidisciplinary teams in a technology-driven environment. You will interpret global regulations including ISO 13485, ISO 9001, and FDA 21 CFR 820, ensuring compliance while enabling innovation. The position is embedded in project work, offering real-time input on regulatory strategy and contributing to quality management systems across medical and non-medical sectors.
Life Unlimited.At Smith+Nephew we design and manufacture technology that takes the limits off living.We're on a mission to push the boundaries of innovation, and we need a dedicated expert to help us achieve our goals. We are currently searching for...
In this role, you will create robust clinical evidence documentation to support the CE registration of medical devices, working closely with cross-functional teams to ensure product safety and performance. You will act as a subject matter expert, engaging in regulatory interactions and strategic business decisions.
Biomedical Scientist | Pathology | Full Time | Perm | ManchesterWe're looking for a motivated Biomedical Scientist to join our Pathology team at Manchester Hospital. This full‑time, role offers the chance to work in a supportive, well‑equipped laboratory while playing...
Senior Biomedical Scientist Training Lead | Pathology | Full Time | Permanent | ManchesterJob PurposeTo assist in the organisation, management and development of services within a specialised area of the pathology service, or across a range of services provided by...
This role involves conducting precision measurements, preparing inspection reports, and supporting the sales team with technical demonstrations and customer applications. You will also install metrology systems, train operators, and provide technical support to customers and distributors, both in the UK and internationally.
The Quality Engineer will manage and coordinate customer complaints for medical instruments and orthopaedic products, conduct internal audits, and maintain quality procedures. The role involves working independently, leading meetings, and ensuring regulatory compliance in a growing SME.
As a Quality Engineer, you will lead the investigation and resolution of quality issues, champion ISO9001 certification, and drive continuous improvement across the production environment. You will work closely with production and engineering teams to ensure high standards of quality and compliance.
This role involves ensuring quality standards in a sterile, regulated manufacturing environment, with a focus on data analysis, process improvement, and root cause investigation. The Quality Engineer will work closely with production and engineering teams to resolve non-conformances, support process validation, and strengthen quality control across the product lifecycle. It is a hands-on position within a team-based clean-room setting, emphasising compliance and continuous improvement.
As a Q&RA Engineer, you will support quality and regulatory compliance across operations, working closely with cross-functional teams to maintain and improve quality systems. Key responsibilities include leading deviation investigations, managing change control, and supporting audits and inspections.
Quality Engineer, Medical DevicesBasic Salary £40,000 to £50,000HealthcarePensionThe Role - Quality Engineer, Medical DevicesFollowing expansion, they seek to recruit a Quality Engineer responsible for all aspects of quality management including:Drafting processes, procedures and documentationPerforming internal auditsManaging and resolving complaintsYour Background...
