Cure Talent Ltd

Cure Talent are delighted to be partnered with an emerging wearable medical technology company at a defining stage of its growth. Developing next-generation physiological monitoring solutions, the business is transitioning from advanced product development towards regulatory approval and commercial launch. We are looking for an experienced Principal Software Engineer to provide technical leadership across the company's software function, working closely with the Head of Engineering and multidisciplinary teams spanning Software, Signal Processing and Firmware. This is a hands-on technical leadership role, combining software architecture and technical decision-making with day-to-day engineering, development and problem-solving. Key Responsibilities Provide technical leadership across software development, architecture and engineering best practice Own and evolve the software architecture across the medical device platform Lead technical decision-making across Software, Signal Processing and Firmware interfaces Ensure software development aligns with IEC 62304 and wider medical device requirements Support regulatory submissions and the progression of products towards commercial release Provide technical guidance to internal engineers, contractors and external development partners Remain hands-on with software development, code reviews, testing, documentation and troubleshooting Experience & Skills Required Extensive software engineering experience within regulated medical devices Principal, Lead, Architect or equivalent senior technical experience Strong knowledge of IEC 62304 and the medical device software development lifecycle Strong software architecture and systems-level engineering experience Broad technical understanding across software, embedded/firmware and signal processing or algorithm development Experience supporting medical devices through regulatory approval and commercial release Hands-on technical background with the ability to contribute directly to development and complex problem-solving This is an excellent opportunity for an experienced software engineer to take a leading technical role in bringing innovative wearable medical technology to market, while helping shape the architecture and engineering foundations for future products.

Cure Talent are delighted to be partnered with a global manufacturer of medical technology, part of a wider FTSE 100 group, supporting healthcare professionals worldwide with innovative instrumentation. We are looking for a Quality professional to join the team in a documentation and administration-focused role, supporting the day-to-day operation of the Quality Management System. This is not a traditional QA role requiring deep prior experience in medical devices. Instead, the focus is on process ownership, coordination, and ensuring quality records and activities are accurately managed and audit-ready. The position would suit either someone already working in QA within a regulated environment, or someone in the medical device sector looking to transition into Quality from an adjacent function. The role centres on administering and coordinating quality activities across complaints, deviations, CAPAs, and change control within an electronic QMS. You will act as a central point of control, ensuring quality events are logged, progressed, and closed in line with internal processes and regulatory requirements. Key responsibilities Own the administration of customer complaints within the eQMS, ensuring accurate logging, categorisation, triage, and progression through to closure Coordinate investigations by gathering data, supporting root cause analysis, and documenting outcomes in line with internal procedures Support the management of deviations and nonconformances, ensuring correct classification, tracking, and timely closure Maintain and control QMS documentation, ensuring records are accurate, complete, and audit-ready at all times Administer CAPAs and quality events within the eQMS, ensuring workflows, approvals, and traceability are maintained Support design and engineering change control processes, ensuring documentation is complete and aligned with quality and regulatory expectations Assist with audit preparation and support audit activities by providing relevant documentation and evidence What we are looking for Experience working within a regulated environment, either in a QA role or within a medical device organisation Strong administrative and organisational capability, with a high level of attention to detail Comfortable working with documentation, systems, and structured processes Exposure to quality systems, compliance processes, or regulated documentation Ability to coordinate activities across multiple stakeholders and maintain accurate records Clear communication skills and the ability to manage information in a structured and compliant way

Cure Talent are delighted to be partnered with a medical device manufacturer operating across international markets, with a well-established UK operation supporting the distribution of a broad product portfolio. As the business continues to evolve, they are now looking to appoint a Supply Chain Manager to take ownership of supply chain operations on site in Hereford. As the new Supply Chain Manager, you will take responsibility for purchasing, inventory, warehousing and distribution activities, working closely with cross-functional teams to support operational delivery. This role requires someone who can operate in a fast-paced, reactive environment, embedding themselves within the business, contributing to day-to-day operations and building credibility before driving longer-term improvements. To be successful as the new Supply Chain Manager, you will have proven experience operating within supply chain and purchasing functions, with the depth to assess existing processes, challenge where needed, and gradually implement improvements across supplier performance, cost, delivery and inventory management within a regulated environment. Key Responsibilities Oversee day-to-day supply chain operations including purchasing, inventory, warehousing and distribution Manage supplier relationships, including performance monitoring, service levels and cost control Support supply chain planning and logistics activities, ensuring continuity of supply and efficient product flow Manage inventory levels and stock control through ERP systems Work cross-functionally with Quality, Finance and Operations to ensure alignment and compliance Support integration of supply chain considerations into new product development activities Monitor and report on supply chain performance, identifying areas for improvement Ensure compliance with applicable regulatory and quality requirements within the supply chain Experience and Skills Required Proven experience within supply chain, purchasing or logistics roles Experience managing suppliers and supply chain performance Strong understanding of material planning, lead times and inventory management Experience working within a regulated environment Ability to operate effectively in a fast-paced or changing environment Strong communication skills with the ability to influence cross-functional stakeholders Experience contributing to process improvement or continuous improvement activities If you have the necessary skills and experience, please get in touch with Kris Holmes today or click apply now

Cure Talent are delighted to be partnered with a growing medical device manufacturer with a broad and diverse product portfolio across areas including IV therapy, diabetes care, surgical, anaesthesia and consumer health. Following continued expansion, they are now looking to add another Regulatory Affairs Specialist to their Quality & Regulatory team. As the new Regulatory Affairs Specialist, you will support the ongoing development, maintenance and execution of regulatory activities across the business. This is a hands-on role with exposure across the full product lifecycle, working closely with internal teams to ensure products remain compliant across multiple global markets while helping to define regulatory strategy. To be successful as the new Regulatory Affairs Specialist, you will have proven experience operating within Regulatory Affairs in the medical device sector, with detailed exposure to technical documentation, global regulatory frameworks including MDR and FDA, and supporting regulatory strategy across a range of products. Key Responsibilities Support and maintain the Quality Management System in line with ISO 13485 requirements Prepare, review and maintain technical documentation across MDD, MDR, IVDR, UKCA, FDA and procedure packs Ensure ongoing compliance with applicable regulatory requirements and standards Support document control activities including procedures, labelling and product documentation Contribute to UDI implementation and product lifecycle activities Coordinate and support internal and external audits Monitor regulatory changes and support implementation across the business Experience and Skills Required Proven Regulatory Affairs experience within the medical device industry Experience supporting regulatory strategy and submissions activities Working knowledge of MDR and FDA regulatory frameworks Strong understanding of ISO 13485 Experience working with technical documentation and regulatory files Strong organisational skills with attention to detail Ability to work cross-functionally within a regulated environment If you have the necessary skills and experience, please get in touch with Kris Holmes today or click apply now

Cure Talent are delighted to be partnered with a global manufacturer of medical technology, part of a wider FTSE 100 group, supporting healthcare professionals worldwide with innovative instrumentation. We are looking for a Quality professional to join the team in a documentation and administration-focused role, supporting the day-to-day operation of the Quality Management System. This is not a traditional QA role requiring deep prior experience in medical devices. Instead, the focus is on process ownership, coordination, and ensuring quality records and activities are accurately managed and audit-ready. The position would suit either someone already working in QA within a regulated environment, or someone in the medical device sector looking to transition into Quality from an adjacent function. The role centres on administering and coordinating quality activities across complaints, deviations, CAPAs, and change control within an electronic QMS. You will act as a central point of control, ensuring quality events are logged, progressed, and closed in line with internal processes and regulatory requirements. Key responsibilities Own the administration of customer complaints within the eQMS, ensuring accurate logging, categorisation, triage, and progression through to closure Coordinate investigations by gathering data, supporting root cause analysis, and documenting outcomes in line with internal procedures Support the management of deviations and nonconformances, ensuring correct classification, tracking, and timely closure Maintain and control QMS documentation, ensuring records are accurate, complete, and audit-ready at all times Administer CAPAs and quality events within the eQMS, ensuring workflows, approvals, and traceability are maintained Support design and engineering change control processes, ensuring documentation is complete and aligned with quality and regulatory expectations Assist with audit preparation and support audit activities by providing relevant documentation and evidence What we are looking for Experience working within a regulated environment, either in a QA role or within a medical device organisation Strong administrative and organisational capability, with a high level of attention to detail Comfortable working with documentation, systems, and structured processes Exposure to quality systems, compliance processes, or regulated documentation Ability to coordinate activities across multiple stakeholders and maintain accurate records Clear communication skills and the ability to manage information in a structured and compliant way

Cure Talent are delighted to be partnered with an emerging wearable medical technology company at an exciting stage of its growth. Developing next generation wearable medical devices designed to deliver clinically meaningful physiological insights beyond the hospital environment, the business is progressing from research and development into clinical validation and regulated market entry. We have an opportunity for a Mechanical Design Engineer to join the organization and support the development of innovative wearable medical devices. Reporting into the engineering team, this role will focus on the design, development and validation of mechanical systems for wearable medical devices. You will work across the full product lifecycle, contributing to the transition of early-stage concepts into robust, manufacturable and regulatory-compliant products. Working closely with multidisciplinary teams across electronics, software and quality, you will play a key role in delivering high-quality, clinically relevant wearable solutions. Key Responsibilities: Design and develop mechanical components and assemblies for wearable medical devices from concept through to production Create detailed 3D CAD models, engineering drawings and technical specifications Support prototyping, testing and iterative design activities across the product lifecycle Apply structured medical device development processes, including design control, risk management and verification & validation Collaborate with cross-functional teams and external suppliers to ensure designs meet manufacturing and quality requirements Experience and Skills Required: Minimum 2 years experience in mechanical design within MedTech or a regulated product development environment Proficiency in CAD preferably SolidWorks, with experience producing detailed engineering drawings Knowledge of materials and manufacturing processes relevant to wearable devices, including plastics, elastomers and precision assembly Understanding of structured product development processes, including exposure to design control and risk management methodologies (e.g. FMEA) This is a great opportunity to join a growing wearable MedTech business developing next generation physiological monitoring solutions, suited to a Mechanical Design Engineer who enjoys working across the full product lifecycle within a regulated environment.

Cure Talent are delighted to be partnered with an emerging wearable medical technology company at a defining stage of its growth. Developing next-generation physiological monitoring solutions, this organisation is advancing its data science and sensing capabilities to deliver medical-grade insights beyond the hospital environment. We have an opportunity for a Senior Data Scientist (Signal Processing) to join the team and play a key role in developing algorithms and modelling techniques used to interpret complex physiological data from non-invasive wearable sensors. This is a hands-on, technically focused role working at the intersection of signal processing, machine learning, and physiology, translating real-world sensor data into clinically meaningful insights. Key responsibilities Design and implement signal processing pipelines to analyse non-invasive physiological data Develop algorithms and models to extract clinically relevant cardiorespiratory and haemodynamic metrics Analyse complex time-series data from wearable sensors, including noisy real-world signals Support experimental design and analyse data from internal testing and controlled clinical studies Collaborate with engineering, data science, and clinical teams to integrate algorithms into products Experience and skills required Strong experience in signal processing and analysis of time-series or physiological data Experience developing algorithms or models using MATLAB, Python, or similar high-level tools Understanding of techniques such as filtering, noise reduction, and feature extraction Experience working with non-invasive physiological signals (e.g. ECG, PPG, respiratory data) Ability to design experiments and work with real-world and clinical datasets Nice to have Experience working with wearable sensors or digital health technologies Exposure to machine learning techniques applied to signal or physiological data Understanding of cardiorespiratory physiology or haemodynamics Experience translating algorithms into production or embedded environments Familiarity with C/C++ or similar for deployment If you re a Data Scientist with strong signal processing experience and an interest in applying your work to real-world physiological challenges, we d love to hear from you.

Cure Talent are delighted to be partnered with an established medical device manufacturer as they appoint a Product Development Scientist to join their R&D function on an initial 12 month fixed term contract. This is offered on an initial 12 month fixed term contract, with a strong likelihood of transitioning into a permanent position thereafter. The position has arisen due to maternity leave within the team and is positioned as a genuine opportunity to embed yourself within a growing development function. As the new Product Development Scientist, you will play a hands on role within new product development, line extensions and design changes across a portfolio of sterile, single use medical devices. This is a practical, laboratory focused role, with clear responsibility for physical testing, design control documentation and validation support. You will work closely with Regulatory, Quality, Operations and Commercial teams to ensure projects are delivered in line with medical device regulatory and quality requirements. Key responsibilities Conduct laboratory based testing, primarily focused on physical and performance testing to support development and product improvement activities. Contribute to the creation and maintenance of design history file documentation and associated design control records. Support new product development projects from concept through to verification and validation. Assist with process validation activities and provide technical input where required. Act as an R&D representative within cross functional project teams. Maintain accurate, organised and audit ready documentation throughout the product development lifecycle. Manage multiple project priorities, escalating risks or timeline challenges where appropriate. Experience and skills required A degree in a science based discipline. Proven experience within the medical device sector, ideally within a product development or R&D environment. Hands on laboratory experience, particularly physical testing rather than purely research or analytical work. Experience contributing to design history files and operating within a regulated quality management environment. Exposure to new product development and process validation activities. A background in microbiology would be advantageous but is not essential.