Lead cross-functional project teams in a regulated medical device and pharma environment, managing complex initiatives from planning to execution. Focus on strategic alignment, budget oversight, risk management, and process improvement within a remote-working framework. The role involves high-level coordination with stakeholders and demands strong leadership in a compliance-driven setting.
This role involves maintaining regulatory compliance for medical devices by managing technical documentation, product registrations, and post-market surveillance activities. The specialist will work independently in an SME setting, ensuring adherence to UK and EU regulations including MDR, MDD, and UKCA. Responsibilities include updating clinical evaluations, supporting audits, and managing documentation with a focus on accuracy and efficiency.
Leads a team of technicians while performing hands-on repair and maintenance of GE Healthcare's Patient Care Solutions and Ultrasound systems, diagnosing faults and ensuring quality service delivery. Manages workload, parts ordering, and service records while ensuring compliance with ISO 9001 and EHS standards. Serves as a technical and operational leader within a fast-paced medical technology environment.
This role involves working on cutting-edge defence technologies, including communications, sensors, and detection systems. You will collaborate with multidisciplinary teams and have opportunities for continuous learning and career development.
Perform on-site service and repair of advanced medical diagnostic systems in NHS and private laboratories. Provide technical troubleshooting and support to lab staff, ensuring minimal downtime. Receive full product training and work across a range of high-value diagnostic equipment.
Perform installation, maintenance, and repair of advanced medical diagnostic systems in NHS and private laboratory settings. Provide on-site technical support and troubleshooting for complex diagnostic equipment. Work closely with laboratory staff and benefit from full product training within a globally recognised healthcare technology organisation.
This role involves designing and optimizing manufacturing processes for medical devices, with a focus on instrumentation and electromechanical systems. The engineer will lead process improvements, support verification and validation at contract manufacturing organizations (CMOs), and ensure compliance with quality standards. Key responsibilities include driving design for manufacturability, managing technical projects, and maintaining rigorous documentation within a regulated environment.
This role involves field-based service, repair, calibration, and validation of medical washer disinfectors and associated equipment in hospitals and clinical environments. The engineer will conduct technical fault-finding, produce validation reports, and provide training to end users, operating within a highly regulated healthcare setting. Full technical training and mentoring are provided, with opportunities for long-term career development.
This role involves leading the design and implementation of data collection tools for clinical research studies within the National Haemophilia Database. The individual will coordinate data management activities across NHS haemophilia centres, develop study-specific databases and Case Report Forms, and ensure data quality and compliance with research governance standards. They will also provide training and operational support to clinical sites and collaborate with external research partners.
This role involves providing technical leadership and shaping the software architecture for a wearable medical device platform. The engineer will work across software, signal processing, and firmware teams to ensure compliance with medical standards like IEC 62304 and support regulatory approval. The position is hands-on, requiring active development, code reviews, and troubleshooting while guiding internal and external engineering efforts.
Lead a maintenance team responsible for ensuring the reliability and compliance of laboratory, manufacturing, and facility assets in a regulated environment. Coordinate planned and reactive maintenance, oversee contractor activities, and support continuous improvement initiatives. The role combines technical leadership with hands-on oversight across critical systems including GMP facilities, cleanrooms, and utilities.
This role involves designing and maintaining embedded C/C++ firmware for life-changing medical and mechatronic devices, with full ownership of the software lifecycle. The engineer will lead the transition of code from external contractors, establish internal processes, and collaborate closely with hardware teams using test equipment like oscilloscopes. It's a rare opportunity to build software infrastructure from the ground up within a small, mission-driven engineering team.
This role involves reviewing batch manufacturing and packaging records to ensure compliance with GMP standards prior to product release, supporting batch release activities, and collaborating with external manufacturing partners and internal teams. The candidate will maintain quality documentation and ensure adherence to the Quality Management System within a virtual pharmaceutical model. The position offers hybrid working and is part of a supportive Quality team in a growing organisation with a diverse product portfolio.
Talentmark are recruiting for a Medical Affairs Coordinator to join a company in the pharmaceutical industry on a contract basis for 12 months from mid-September 2026.Company:Our client is one of the largest pharmaceutical companies in the world. They focus on...
This role involves leading product regulatory compliance for a portfolio of chemical and healthcare products, with responsibilities including monitoring regulations, preparing Safety Data Sheets, and supporting product registrations in the UK and Europe. The Compliance Officer will act as the main contact for external regulators, deliver internal training, and ensure compliance across product development and marketing. The position requires a scientific background and experience with chemical regulations such as REACH and CLP.
