144 jobs
Johnson & Johnson MedTech Leiden, Netherlands €68,600 – €119,600 pa
Leads preparation and finalisation of clinical and regulatory documents for the Immunology therapeutic area within the Regulatory Medical Writing team. Acts as lead writer or point of contact for programmes, guides cross-functional teams, and manages, mentors and develops direct reports including hiring and performance discussions.
Johnson & Johnson MedTech Spring House, United States US$117,000 – US$201,250 pa
Leads regulatory medical writing for the Immunology therapeutic area, preparing and finalizing clinical documents and serving as lead writer or point of contact for assigned programs. Manages direct reports, sets objectives, mentors junior writers and oversees external contractors, while driving process improvements and cross-functional coordination.
TRS Consulting Birmingham £45,000 – £55,000 pa
Account management role selling multi-vendor service contracts across biomedical, ultrasound and endoscopy product ranges. You manage key customer accounts, identify new business, attend exhibitions and local events, analyse competitor activity and produce proposals and sales agreements to exceed area sales targets.
TRS Consulting London £45,000 – £55,000 pa
Account management role selling multi-vendor service contracts across biomedical, ultrasound and endoscopy product ranges. You manage key customer accounts, identify new business, attend exhibitions and local events, analyse competitor activity and produce proposals and sales agreements to exceed area sales targets. Home-based with a territory focus.
Automated Industrial Robotics Wakefield
Designs special purpose machinery from concept through to production-ready drawings, working with AutoCAD 2D/3D and pneumatic and electrical components. Manages schedules, budgets and scope changes while liaising with the Technical Director and section leads, and conducts machinery risk assessments and detail checks on colleagues' work.
Oxford Nanopore Technologies Oxford
Join the Biologics Tech Transfer team to support the onboarding and scale-up of production for analyte and other components used in sequencing kits. The role centres on transferring and scaling biological production processes within a biotech manufacturing environment.
Oxford Nanopore Technologies Oxford
Runs sequencing experiments across the full range of Oxford Nanopore platforms to assess new developments and set performance expectations. Sits within the Product Validation team, working hands-on with sequencing technology to characterise platform capabilities.
Russell Taylor Group Swadlincote £30,000 – £34,000 pa
Supports site validation activities across cleaning, computerised systems, equipment/utilities qualification and process validation, authoring protocols and reports and interpreting data against acceptance criteria. Works cross-functionally to maintain validated status of systems and processes, investigates non-conformances and supports regulatory inspections and internal audits.
QIAGEN Remote United Kingdom
Field-based role owning a strategic territory across the North of the UK and Ireland, driving sales growth for QuantiFERON tuberculosis diagnostics while exploring transplantation market opportunities. Involves building relationships with clinicians, laboratories and KOLs, delivering clinical presentations, and managing activity through Salesforce CRM, with up to 80% travel.
HCRG Care Group Runcorn £30,000 pa
Supports and maintains clinical systems, acting as subject matter expert for TPP SystmOne, handling complex incidents, configuration queries, record management and workflow issues. Also trained to become the organisational expert for Hybrid Mail, providing second-line support. Based at a local office with remote support and occasional travel.
SRG Lancashire
Maintains and improves a medical device Quality Management System in line with ISO 13485 and FDA QSR, leading non-conformance, deviation, complaint and CAPA investigations with root cause analysis. Supports internal, supplier and regulatory audits, risk management under ISO 14971, validation and design transfer, working with Manufacturing, R&D, Regulatory Affairs and Supply Chain.
SPD Development Company Ltd Bedford
Provides statistical expertise across R&D, Clinical, Product Support and Marketing, designing and analysing studies and supporting product algorithms and evidence generation. Sits in a three-person Statistical & Data Services Team, acting as statistical representative on assigned projects and communicating findings to technical and non-technical audiences.
SoCode Cambridge £40,000 – £60,000 pa
Develops high-quality C and C++ software across the full development lifecycle, from concept and design through testing and release, for an engineering consultancy building medical devices. Works in a multidisciplinary team alongside software, electronics and mechanical engineers, writing well-tested code and technical documentation. Embedded systems, RTOS, Linux, Qt and IEC 62304 experience are advantageous.
SRG Stirling
Reviewing quality and batch documentation in a GMP-regulated life science environment, maintaining document control, trackers and status reports, and coordinating SOP review cycles. The role also covers archiving and data accuracy, supporting GMP compliance and continuous QA improvement while reporting to the QA Manager.
Stryker Belfast £12 – £21 ph
Performs visual, dimensional and electrical inspection of sub-assemblies and final medical device assemblies, interpreting prints, drawings and wire lists to approve or reject in-process and final product. Also handles document review and archiving of DHRs, non-conformance quarantine documentation, ERP release transactions and First Article Inspection verification. Night shift role within a GMP-regulated quality team supporting KPI and throughput goals.
