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.

• London
• £100,000 – £150,000 pa
• Lead

Leads cross-functional teams to design, implement and commercialise digital and electro-mechanical medical devices, managing multiple complex projects from initiation through delivery. Involves risk management, requirements planning and acting as liaison between functional and business management within a regulated R&D environment.

PMP · PRINCE2 · SAFe

• Watford
• Remote
• £58,320 – £87,480 pa
• Senior

Supports sourcing for IHS-managed Catheterization Labs and Operating Theatres in the UK, developing sourcing strategies and managing strategic supplier relationships. Negotiates pricing, commercial terms and supply agreements, analyses procurement data for cost savings, and partners with hospitals and internal stakeholders. Remote-based with occasional office meetings and up to 25% travel, mainly around London.

Microsoft Excel · Microsoft PowerPoint

• Telford
• £43,000 pa

Servicing, installing, repairing and calibrating sophisticated laboratory and scientific X-ray systems on customer sites across pharmaceutical and research environments. Requires a field service background with high-value capital equipment and an electronics qualification, with full product training provided.

X-Ray Systems

• Cambridge
• Senior

Design, build and test the hardware of a novel life-saving biotech manufacturing device, accelerating proof of concept through to testing. Work with physicists, scientists, electronics and design engineers, using 3D CAD (ideally SOLIDWORKS) on mechatronics, automation, robotics or precision electro-mechanical technology. Involves third-party meetings and attending biotech and medical device conferences.

SOLIDWORKS

• Gloucestershire
• £58,000 – £63,000 pa
• Senior

Owns packaging and labelling validation for a global medical device portfolio, leading transportation testing, shelf-life studies and equipment validation projects. Reviews technical documentation, BOMs and labelling content, leads CAPAs and non-conformance investigations, and acts as key contact during regulatory audits. Works cross-functionally with Quality, Regulatory, R&D and Manufacturing, mentoring junior staff.

ASTM

• Basildon
• £29,389 pa

Deliver and install medical devices to hospitals and healthcare facilities across the Essex area from a Basildon depot, driving a 3.5 tonne Luton van. You'll communicate with healthcare professionals, demonstrate products on site, and carry out basic installation, maintenance and repair with full training provided.

Luton Van

• Houghton le Spring
• On-site
• Mid-level
• Temporary

Support the design, manufacture, testing and regulatory compliance of medical devices, maintaining quality control systems, production protocols and documentation. Investigate non-conformances and complaints, run CAPA, testing and validation, and assist with EU MDR, ISO 13485 and audit readiness, including clean room operations.

• Houghton le Spring
• On-site
• Temporary

Support quality assurance, product compliance and regulatory activities in a medical device manufacturing environment. Maintain quality control systems, prepare technical documentation, conduct testing and inspections, investigate non-conformances using CAPA, analyse quality data and support internal and external audits, working closely with the QA Manager and production teams.

ISO 13485 · EU MDR

• Witney
• On-site
• £17 ph
• Temporary · Shift work

Investigates returned medical devices to identify root causes of complaints, using internal systems and Excel to track trends and ensure regulatory compliance. Collaborates with international colleagues on quality improvements and pre-launch readiness for new products. Night shift role (4 on, 4 off, 7pm-7am) with full training provided, distinct from customer service.

Excel · Word

• Edinburgh
• Mid-level

Design and develop compact, low-power wearable medical devices from concept to production, covering system architecture, schematic and multi-layer PCB design, analog and mixed-signal circuits, and sensor/optical signal conditioning. Work on ultra-low-power battery systems and wireless interfaces (Wi-Fi, BLE, LTE-M/NB-IoT, GNSS) within a small health-tech startup, with scope to lead a hardware team.

Wi-Fi · BLE · LTE +7

• United Kingdom, YY9 9YY
• Remote
• Entry level
• Internship

A two-year fixed-term trainee programme maintaining and repairing medical equipment at hospitals across an assigned UK region. Working under experienced engineers, you build fault-finding, calibration, installation and customer-service skills, with formal training and possible support towards a BTEC in Electronics. The role is mobile and field-based, involving regular independent travel and occasional overnight stays.

BTEC · HNC · HND +2

• Guildford
• £48,337 – £70,878 pa
• Senior
• Permanent

Develop an independent, externally funded research programme as a Principal Investigator, applying AI and data science to human, animal and environmental health data within a One Health framework. Collaborate across medicine, veterinary science, computer science and engineering, secure UK and international funding, publish high-quality work, and teach AI and data science at undergraduate and postgraduate level.

• Belgrade, Serbia
• Mid-level · manages people

Oversees local literature surveillance across 80+ territories, leading outsourced vendor operations and governance for global pharmacovigilance. Acts as business owner for controlled documents, policies and standards, driving standardisation and process improvement while partnering with cross-functional stakeholders across EMEA, Asia Pacific and other regions.

• UK - Field
• Hybrid
• Senior

Leads complex, S+N-sponsored clinical studies from start-up to close-out, acting as project leader within cross-functional teams spanning biostatistics, data management, regulatory affairs and vendors. Develops protocols, monitoring plans and consents, oversees vendors and site management, manages study budgets, and ensures GCP and ISO 14155 compliance. Also trains junior clinical study management staff.

ISO 14155 · ISO 9001 · ICH-GCP