Medical Technology Jobs

• London

This role involves selling point-of-care diagnostic solutions to healthcare providers, including care homes, pharmacies, and GP practices. The Field Sales Agent will leverage existing relationships and market knowledge to introduce Adexa Labz's comprehensive supported solution, which includes devices, training, and ongoing support. The position is commission-only, offering 10% on initial sales and 5% on recurring monthly consumables.

• 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…

• South Yorkshire
• Entry level

Operates and performs basic setups on CNC 2 and 3 axis lathes, EDM wire and plunge machines, running multiple machines simultaneously to produce medical device components. Also uses manual machine tools to cut, drill, shape and finish parts, completing shop work orders, inspection documentation and daily maintenance sheets while following QMS procedures and safety standards.

CNC 2 Axis Machines · CNC 3 Axis Machines · Lathes +3

• Oxford
• On-site
• Mid-level
• Permanent

Accountable for end-to-end delivery of strategic New Product Development programmes, leading multidisciplinary teams across R&D, regulatory, quality, operations and commercial functions. Drives integrated programme plans, stage-gate governance, risk management, resource planning and budget forecasting for complex medical device development in a regulated environment, supporting the metra® organ perfusion platform.

FDA Quality System · Design History Files

• Cambridge
• Senior
• Permanent

Medical Devices Consultant - Senior Mechanical Engineer - CambridgeDue to the growth of a leading Medical Devices organisation, we are currently seeking a Senior Mechanical Engineer, Project Manager, Medical Devices Inventor, or Mechanical Design Consultant for a newly approved role.…

• 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

• Blackpool
• On-site
• Lead · manages people

Frontline leadership role on a manufacturing shop floor, supervising daily production output, allocating headcount and resources, and resolving problems to root cause. Drives continuous improvement through Lean and Process Excellence, enforces GMP, and manages performance, absence and disciplinary matters within a regulated orthopaedics environment.

Resource Scheduler

• Leeds
• Lead

Responsible for scenario planning, capacity planning, inventory management, and product deployment across multiple suppliers and brands. Drives continuous improvement through value stream mapping and builds complex statistical models to support master scheduling and S&OP integration. Works with MRP and ERP systems (SAP/JDE/APO/OMP) in a matrix environment.

SAP · JDE · APO +3

• Oxford
• On-site
• Mid-level
• Permanent

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.

IEC 62304 · ISO 14971 · ISO 13485 +5

• Andover
• On-site
• £40,000 – £45,000 pa
• Mid-level
• Permanent

Maintains and develops the Quality Management System in a high-end cleanroom, supported by a team of six. Ensures compliance with ISO 9001, ISO 13485 and AS9100, applying CAPA, 8D and 5 Whys methods, with training provided where needed. Distinct for its medical devices focus within a growing specialist manufacturer serving aerospace, automotive and medical clients.

• Banbury
• Mid-level

Lead Quality, Risk and Assurance across a pharmaceutical transport operation, maintaining EU GDP/GMDP compliance, managing audits, deviations, CAPA and client Quality Technical Agreements. Acts as primary regulatory escalation point, monitors quality KPIs and drives continuous improvement, with regular travel to other sites.

Quality Management System

• United Kingdom
• On-site
• £30,000 – £32,000 pa
• Senior
• Permanent

Coordinates technical documentation reviews for the UK Medical Devices team, monitoring KPI reports and driving resulting actions. Manages complaints, supports key client calls and meetings, and raises purchase orders for client invoicing. Requires practical experience of Medical Device or Auditing Regulations and strong documentation control.

MS Office · Outlook · Word +3

• United Kingdom
• On-site
• £30,000 – £32,000 pa
• Senior
• Permanent

Coordinate and support technical documentation reviews for the UK Medical Devices team, managing review processes, monitoring KPI reports and driving resultant actions. Handle complaints, raise purchase orders for client invoicing, and strengthen key client relationships through calls and meetings. Requires practical experience of Medical Device Regulations or auditing regulations and strong documentation control.

MS Office · Outlook · Word +3

• Cambridge
• Mid-level

Provide regulatory support across a Cambridge product development business, guiding multidisciplinary engineering and science teams on compliance with ISO 9001, ISO 13485 and FDA 21 CFR 820. Monitor international regulatory changes, support external audits and contribute to quality management system improvements across medical and non-medical projects.

• Melton, UK
• Hybrid
• Senior · manages people
• Permanent · Shift work

Leads a large packaging operations team including Line Leaders, Operators and Process Technicians, owning People, Safety, Quality, Cost and Delivery. Drives value-stream mapping, Kaizen projects and operational excellence, with accountability for Tier 2 actions and the operation's P&L, OEE, MUV and labour efficiency. Requires a manufacturing supervision background and shift flexibility.