Medical Technology Jobs

• Spring House, United States
• US$117,000 – US$201,250 pa
• Mid-level · manages people

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.

• Marousi, Greece
• €43,700 – €75,325 pa
• Lead · manages people

Leads commercial expansion of intracardiac echocardiography (ICE) across West EMEA, building country growth plans with local electrophysiology teams to drive revenue, procedure adoption and market share. Manages a team of six EP clinical specialists, develops strategic accounts and coordinates with Marketing, Professional Education and Health Economics. Combines regional strategy translation with hands-on account planning, forecasting and pricing discipline.

CARTOSOUND

• United Kingdom
• On-site
• £55,000 – £70,000 pa
• Senior

Lead and execute in-vitro regulatory and genetic toxicology studies, developing and applying Neutral Red, Ames and micronucleus assays within a quality-assured laboratory. Provide technical direction across pre-clinical research, product development and regulatory programmes, collaborating with multidisciplinary teams and external CROs and academic partners.

OECD Guidelines · ECVAM · ICCVAM +3

• Hertfordshire

Own product regulatory compliance end to end, acting as the company's official representative and evidencing compliance to external parties. Advise on sourcing, development, composition, packaging, labelling and marketing, horizon-scan regulatory changes, and support domestic and European product registrations plus safety data sheet software. Requires REACH/CLP knowledge and a chemical or QA background.

MS Office · Word · Outlook +2

• Bacup
• Manages people

Maintains and improves a Quality Management System to ISO 13485, ISO/IEC 17025 and FDA 21 CFR Part 820 standards within medical device manufacturing. Conducts internal audits, supports external inspections and supplier audits, manages document control and CAPA investigations, and may supervise quality team members.

• Nottingham
• On-site
• £16 ph
• Lead · manages people
• Temporary

Lead and coordinate technical aspects of clinical trial activities across QMC and City Hospital, supervising dispensing, accountability records for IMPs/NIMPs, and stock control. Manage clinical trials technical and support staff, liaise with sponsors and research teams, and prepare for sponsor audits and MHRA inspections.

ChemoCare

• Welwyn Garden City
• Hybrid · 3 days in office
• £450 – £500 ph
• Lead
• Contract

Coordinate clinical study start-up, site activation and UK regulatory submissions, managing trial amendments, essential documentation, site contracts, budgets and payment processes. Work with R&D, clinical sites, global study teams and CROs to ensure ICH-GCP compliance, using UK systems such as IRAS, CPMS, iCT and ARSAC. Practical UK study set-up experience is essential.

IRAS · CPMS · iCT +1

• Warwick
• Lead

Lead multidisciplinary medical device development programmes from early concept through to commercial launch, bringing structure and momentum to complex engineering challenges. Requires expertise in high-volume manufacture and injection-moulded plastic components, plus mentoring of junior engineers. Based in Warwick within a fast-moving team focused on improving patient outcomes.

• Cambridge
• Senior · manages people

Lead multiple programmes advancing next-generation drug delivery platforms, mentoring junior engineers while owning core mechanical design work. Requires hands-on experience with autoinjectors, inhalers, infusion systems or wearable devices, translating clinical and regulatory requirements into robust mechanical solutions. Involves close collaboration with internal teams, external partners, clients and suppliers, with electro-mechanical device experience advantageous.

Autoinjectors · Inhalers · Infusion Systems +3

• Swindon
• Remote
• £45,000 – £55,000 pa
• Mid-level

Owns quality and regulatory affairs for a growing orthopaedic device maker, maintaining ISO 13485, CE and EU MDR approvals and running internal and external audits. Leads the CAPA process and supports new product development, including manufacturing process control and additive manufacturing, drafting procedures and work instructions. Fully remote with flexible hours and real ownership from development through market release.

QMS Software

• Darlington
• £65,000 – £85,000 pa
• Director · manages people
• Permanent

Senior leadership role overseeing operations across biologics, RNA and medicines manufacturing facilities at two sites. Leads multidisciplinary teams covering operations, engineering, facilities and site services, ensuring GMP, health & safety and quality compliance while driving continuous improvement, capital projects and operational strategy.

NEBOSH

• Cambridge
• Lead · manages people
• Permanent

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.

• Cambridge
• Hybrid
• £50,000 – £65,000 pa
• Senior · manages people

Hands-on role turning system and sub-system requirements into verification strategies, including test protocols, bespoke rigs and automated Python scripts, through to formal sign-off. Results feed back to design teams and regulatory submissions, and you'll lead and mentor a small group of verification engineers on a complex electromechanical medical device.

• Houghton le Spring
• £37,000 – £40,000 pa
• Contract

Support quality and regulatory requirements across design, manufacture and testing of medical devices. Maintain quality procedures, analyse performance data, manage CAPA activities, and assist with inspections, audits and clean-room production standards. A 12-14 month maternity cover contract within a specialist manufacturing environment.

• Welwyn Garden City
• Hybrid · 2–3 days in office
• £339 – £500 pd
• Lead
• Contract

Coordinate UK clinical study start-up activities and site activation, managing regulatory submissions, approvals and amendments. Liaise with NHS R&D departments, clinical sites and CROs, prepare site contracts, budgets and costing templates, and track timelines and regulatory milestones. Requires hands-on UK start-up experience with HRA, Ethics, MHRA, IRAS, CPMS and ICH-GCP knowledge.

IRAS · CPMS · iCT +4