144 jobs
Johnson & Johnson MedTech Toronto, Canada US$134,000 – US$184,000 pa
Leads preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned programmes, planning and directing writing groups, mentoring junior writers and overseeing external contractors. Also manages direct reports, setting objectives and running performance and development discussions.
Johnson & Johnson MedTech Allschwil, Switzerland
Leads the preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Acts as lead writer or point of contact for assigned programmes, planning and directing writing groups while coaching junior staff and managing direct reports. Involves cross-functional collaboration, regulatory guideline knowledge and departmental process improvement.
Ernest Gordon Recruitment Andover £40,000 – £45,000 pa
Maintains and develops the quality management system in a high-end cleanroom, ensuring compliance with ISO 9001, ISO 13485 and AS9100, with training provided where needed. Uses CAPA, 8D and 5 Whys to drive quality standards, supported by a team of six. Works Monday to Thursday 8:30am-5pm with an early Friday finish.
Ernest Gordon Recruitment Mitcham £40,000 – £45,000 pa
Field-based role servicing a wide range of biomedical devices across a London patch, with occasional UK travel and 2-3 overnight stays per month. The technician receives manufacturer-funded training to become certified on high-complexity medical lasers, with progression into more senior positions. Working Monday to Friday, 40 hours per week, with time off in lieu for excess hours.
Gold Group Falmouth
Hands-on R&D role designing and improving electro-mechanical medical devices for women's health and fertility, covering schematic capture, PCB layout in Altium, verification and validation testing, EMC and IEC 60601 electrical safety compliance, and hardware/software integration. Works within a collaborative international R&D team on both new product development and sustaining engineering, with prototyping, debugging and technical documentation duties.
SoCode Cambridge £40,000 – £50,000 pa
Hands-on electronics design role at a product development consultancy, owning hardware at system and circuit level from concept through prototyping, debug, verification and into production for medical and healthcare clients. Work spans medium and high-volume manufacture in well-equipped labs, with peer review across disciplines and a new technical challenge every few months.
Vertech Group (UK) Ltd London £75,000 – £85,000 pa
Assesses software development processes and technical evidence for AI-enabled medical devices, reviewing lifecycle, V&V, configuration management and risk to determine whether safety-critical products meet certification standards. Uses AI-assisted tools to explore evidence, identify failure modes and flag inconsistencies within a specialist team.
TRS Consulting Reading £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 company car.
TRS Consulting Milton Keynes £45,000 – £55,000 pa
Home-based account management role selling multi-vendor service contracts across biomedical, ultrasound and endoscopy product ranges. Involves managing key customer accounts, identifying new business, attending exhibitions and local events, analysing competitor activity and producing proposals and sales agreements to exceed area sales targets.
Platform Recruitment London
Develops and optimises therapeutic delivery formulations, running lab-based in vitro studies and analytical characterisation to assess stability and performance. Works in a multidisciplinary team progressing early-stage technologies toward manufacturing, with external partner collaboration and scale-up considerations.
Optical Express South East England £40,000 pa
Lead the internal audit programme across a regional network of clinics, conducting on-site compliance audits against HIS, CQC, HIW and RQIA standards and working with local managers on corrective action plans. Deliver regulatory guidance, training and policy support, reporting findings to senior leadership and the Director of Care & Quality. Involves regular travel across the Midlands and South of England.
Optical Express East Midlands £40,000 pa
Lead the internal audit programme across a network of clinics, conducting on-site compliance audits against HIS, CQC, HIW and RQIA standards and working with local managers on corrective action plans. Provide regulatory guidance, deliver training, and report compliance status to the Director of Care & Quality, with regional travel across the Midlands and South of England.
Russell Taylor Group Deeside £29,000 – £34,000 pa
Supports diagnostic testing, assay development and IVD kit manufacture within an established scientific team. Day-to-day work includes processing client samples, operating PCR and capillary sequencing equipment, running quality control checks and managing stability storage. Also involves data analysis, report writing and taking ownership of assigned projects.
Matchtech Fareham
Maintains and improves a medical device Quality Management System, planning and reporting internal audits and leading external audit readiness with evidence packs and follow-up actions. Supports ISO 13485 compliance, ISO 14971 risk activities, CAPA and document control, and leads quality improvement projects in a regulated scale-up environment.
Randstad Construction & Property London
Manages a portfolio of clinical research studies end to end, leading cross-functional teams and client relationships to deliver Patient Cloud projects on time and within budget. Involves risk assessment, study documentation, and meetings, with expertise in eCOA/ePRO, eConsent, virtual trials or wearables. Fully remote, but requires flexibility to work American time.
