402 jobs for “Medical Services”
Johnson & Johnson MedTech Beerse, Belgium €79,800 – €137,770 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 in medical writing.
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.
Medtronic Manchester £55,040 – £82,560 pa
Field-based territory role supporting the Structural Heart Operating Unit across the Northwest, covering TAVI (Evolut) and TPV (Melody, Harmony) portfolios. Combines territory sales, account and therapy development, clinical and cath lab procedural support, training delivery, and consignment inventory management with clinicians, procurement and referral partners.
Medtronic London £76,800 – £115,200 pa
Designs and builds automated test frameworks for embedded and connected hardware used in operating rooms, covering device software, firmware integrations and hardware-software interaction rather than web or mobile apps. Works with Android AOSP, Linux edge devices and IoT gateways, validating drivers, connectivity, OTA updates and service APIs, and embedding quality gates into CI/CD pipelines alongside hardware, firmware and systems engineers.
OrganOx Oxford
Assures software quality across the full lifecycle for medical devices up to IEC 62304 safety class C, covering design controls, requirements, verification and validation, and release management. A central duty is software risk management, developing and maintaining SFMEAs, hazard analyses and cybersecurity risk assessments aligned with ISO 14971. Works with R&D, Engineering, Post-Market Operations, Regulatory Affairs and Cybersecurity to support EU MDR and FDA compliance.
Smith & Nephew Cambridge
Field-based role owning a strategic orthopaedic revision territory from the M1 corridor to the East of England, acting as clinical and commercial expert. You'll support complex surgical cases in theatre, build surgeon relationships, lead product introductions and tenders, and drive adoption of advanced technologies including robotics.
Smith & Nephew Luton
Owns and grows a strategic orthopaedic revision territory from the M1 corridor to the East of England, supporting complex surgical cases in theatre and building relationships with surgeons and theatre teams. Drives new business, account plans, tenders and adoption of advanced technologies including robotics, working alongside Account Managers and Area Business Managers.
OrganOx Oxford
Technical lead for electronics design across current and next-generation medical device products, combining hands-on design with mentoring junior engineers. Defines electronic architecture, reviews schematics and PCB layouts, and oversees verification and validation including EMC and safety testing to IEC 60601, IEC 62304 and ISO 14971 standards. Works closely with suppliers, manufacturing partners, and cross-functional quality and regulatory teams on-site in Oxford.
TTP Cambridge
Consulting mechanical engineer role focused on drug delivery devices and combination products, taking projects from early feasibility through design, verification and transfer to manufacture. Involves first-principles analysis, modelling, rapid prototyping and hands-on lab work, plus client engagement, proposal creation and project leadership within a collaborative consultancy team.
SPD Development Company Ltd Bedford £30,000 – £35,000 pa
Supports the conduct and monitoring of clinical studies, covering study set-up, sourcing and shipping supplies, volunteer recruitment, tracking study status, administering volunteer payments and maintaining inspection-ready documentation. Works within a clinical programme under GCP, with exposure to IVDR and ISO standards, in a 12-month fixed term contract.
TTP Cambridge
Leads complex medical-device and drug-delivery development programmes from concept through to manufacture, shaping technical strategy amid significant uncertainty. Manages multidisciplinary teams, guides clients through regulatory and commercial decisions, and mentors colleagues while building new business. Based at TTP's Melbourn campus near Cambridge.
Impact Recruitment Aldershot £45,000 – £55,000 pa
Hands-on mechanical design role taking safety-critical respiratory protective equipment from concept through 3D CAD modelling, prototyping, testing and production. Involves detailed drawings, DFMEA, jig and fixture design, NPI and technical support, working closely with manufacturing, quality, customers, suppliers and external test organisations.
Jazz Pharmaceuticals Cambridge
Lead statistician responsible for the statistical design, analysis and reporting of Phase I–IV clinical trials and regulatory filings, including writing and reviewing statistical analysis plans and validating CRO deliverables. Works cross-functionally with clinical development, regulatory affairs and medical writing, using SAS and R, with CDISC standards and Bayesian/adaptive design experience preferred.
Jazz Pharmaceuticals London
Lead statistician responsible for the statistical design, analysis and reporting of Phase I–IV clinical trials and regulatory filings, including writing and reviewing statistical analysis plans and validating CRO deliverables. Works cross-functionally with clinical development, regulatory affairs and medical writing, using SAS and R, with CDISC standards and Bayesian or adaptive designs preferred.
SPD Development Company Ltd Bedford £50,000 – £60,000 pa
Lead mechanical engineering across the full product lifecycle for fertility and pregnancy diagnostics, from concept and prototyping through to manufacture and launch. The role combines hands-on design in SolidWorks, DFM/DFA, FEA and tolerance analysis with process engineering, risk management (FMEA) and design transfer within a multidisciplinary R&D team, including work with suppliers in China.
