Medical Technology Jobs

• Ringaskiddy, Ireland
• Hybrid
• €64,300 – €102,925 pa
• Senior

Operational leader driving regulatory program management for the Immunology portfolio, translating global regulatory strategy into executable plans and coordinating cross-functional teams. Facilitates health authority meetings, worldwide submissions and marketing applications, while leading change management and process improvements within the RPM department.

Veeva · Microsoft Project · Planisware

• Maidenhead
• Hybrid
• Senior

Operational leader driving process improvement and change management within a Regulatory Program Management team, supporting global regulatory strategy for the Immunology portfolio. Facilitates cross-functional teams, translates regulatory strategy into executable plans, and leads operational execution of marketing applications and health authority meetings. Hybrid role with up to 10% international travel.

Planisware · Veeva · Microsoft Project

• 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

• Hengoed
• On-site
• Contract

Responsible for ensuring the IT Quality Management System, validation documentation, processes and systems meet applicable GxP and regulatory requirements. Supports the continued development and improvement of the Global IT validation strategy and approach within a pharmaceutical environment.

• 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.

• 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.

• London
• Remote
• £50 – £65 ph
• Senior
• Temporary

Analyses post-market complaints and quality data for a global medical device portfolio, leading monthly product quality monitoring and statistical trending to surface emerging risks. Builds and maintains Power BI dashboards and reporting tools, conducts complaint investigations and ad hoc reviews, and supports EU MDR trending, audits and CAPA activities alongside Quality, Regulatory, Clinical, R&D and Operations teams.

Power BI · Excel · Minitab

• 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

• Burgess Hill
• On-site
• £32,000 – £40,000 pa

Coordinating quality processes, managing non-conformances, supporting investigations and corrective actions, and maintaining ISO 9001 and ISO 13485 compliance. Reporting to the Head of Quality, the role covers document control, CAPA, supplier quality and audit support within a regulated packaging business, with scope to broaden experience across auditing and regulatory compliance.

Microsoft Office

• Gloucester
• On-site
• £45,000 – £50,000 pa
• Mid-level
• Permanent

Support and maintain the effectiveness of a medical device manufacturer's QMS in line with ISO 13485, MDR and FDA requirements. Day-to-day work covers CAPA effectiveness, quality data and trend analysis, non-conformances, change control and complaint investigation, plus writing and updating procedures and work instructions.

ISO 13485 · FDA Quality System

• Welwyn Garden City
• £339 – £500 pd
• Lead

Role: Clinical Study Start Up LeadLocation: Welwyn Garden City, Hertfordshire (Hybrid)Hours: Full-timeContract: 6 months, Inside IR35Pay: £339.27 - £376.97 per day PAYE basic excluding holiday pay or £450 - £500 per day UmbrellaAn excellent opportunity has arisen for an experienced…

• London
• Hybrid
• £75,000 – £85,000 pa
• Mid-level

Drive software safety activities across the product lifecycle for software-based medical devices, including hazard analysis, risk assessments and safety documentation. Work with Software, Quality, Regulatory and Product Development teams to ensure compliance with standards such as ISO 14971 and IEC 62304, and support verification, validation and software risk management.

ISO 14971 · IEC 62304

• Cambridge
• £80,000 – £100,000 pa
• Senior

Job Title: Senior QA Validation EngineerLocation - Cambridge: On Site (some flex on occasionSalary - £80k - £100k (depending on experience) + up to 10% bonus (company performance dependent) + equityOverviewWe are seeking an experienced Senior QA Validation Engineer to…

• Abingdon
• On-site
• £28,000 – £35,000 pa
• Permanent

Create, maintain and publish technical documentation including Instructions for Use, service manuals, production procedures and product artwork for medical devices. Work with engineering, quality and production teams to verify technical information, manage change control and prepare files for printing. Involves desktop publishing, technical illustrations and coordinating external translations.

Microsoft Word · Microsoft Excel · Adobe InDesign +3