Medical Technology Jobs

• Glasgow
• Remote
• £45,000 – £50,000 pa

Consultative territory sales role selling surgical oncology implants to Consultant Surgeons and NHS clinicians across Scotland and Northern England. Split roughly 80% new business generation and 20% account development, working in operating room environments, preparing quotations and demonstrating equipment, plus attending fairs and congresses. Full training, mentoring and a personalised development plan are provided.

Surgical Implants · Medical Devices · Medical Consumables

• Southampton
• Remote
• £45,000 – £50,000 pa

Consultative territory sales role selling surgical oncology implants, spending time in operating rooms and driving 80% new business alongside 20% account development. Covers the South-West, South Wales and parts of the West Midlands, with quotations, equipment demonstrations and attendance at fairs and congresses. Full training and mentoring provided.

• Limerick, Ireland
• Hybrid
• Entry level
• Temporary

Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance, and safety-native architecture. You will design reproducible experiments, prototype layered safeguards, publish results, and work with platform engineers to move validated methods into a GenAI platform.

OPA/Rego · Cedar

• Leiden, Netherlands
• Hybrid
• Entry level
• Temporary

Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance, and safety-native architecture. Build and validate prototypes on real GenAI platform workflows, publish results, and work with engineering partners to move validated methods into production.

OPA · Rego · Cedar

• Hull
• On-site
• Director · manages people

Leads a major multi-year transformation across Hull and Melton manufacturing sites, embedding lean management systems, tiered accountability and structured problem solving. Acts as trusted advisor to senior leaders, coaching capability and shaping the future operating model as a new facility is introduced alongside a legacy site.

• Warsaw, Poland
• Hybrid
• PLN 88,000 – PLN 132,000 pa
• Entry level

Primary point of contact for customers through the service and repair journey, managing requests, quotations, orders and escalations while coordinating with service engineers, repair centres and logistics teams. Supports quality and compliance in a regulated MedTech setting and contributes to process improvements, system enhancements and UAT activities.

Microsoft Office · Outlook · Excel +3

• Heerlen, Netherlands
• Hybrid
• €40,000 – €60,000 pa
• Entry level

Serve as the primary point of contact for customers throughout the service and repair journey, managing requests, quotations, orders and escalations while coordinating with service engineers, repair centers and logistics teams. Support quality and compliance in a regulated MedTech setting and contribute to process improvements, system enhancements and UAT activities.

Microsoft Office · Outlook · Excel +3

• Ireland
• On-site
• Senior · manages people
• Permanent

Lead the end-to-end performance of a regional clinical laboratory in Sandyford, Dublin, managing turnaround times, QC, repeat rates, stock control and cost efficiency. Oversee Team Leads, write SOPs and work instructions, and keep the lab audit-ready against ISO 17025, ISO 15189, GCP and MHRA standards. The lab runs 24/7, so some evenings, mornings and weekend work is required.

Microsoft Excel · Microsoft Outlook · Microsoft Word +1

• Great Yarmouth
• £30,000 – £37,700 pa
• Mid-level

Day-to-day you will control, prepare, review and approve quality documentation, investigate GMP breaches and OOO incidents, and recommend and review CAPAs. You will also help deliver GMP training, support site audits and QP batch release, and contribute to continuous improvement projects within a busy manufacturing QA team.

• 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

• Newcastle-under-Lyme
• £50,000 – £60,000 pa
• Mid-level

Own and continually improve the Quality Management System in line with ISO 9001 and/or ISO 13485, maintaining documentation, procedures and records. Investigate complaints, supplier issues and non-conformances, lead root cause analysis and CAPA, and conduct internal audits supporting external certification. The role also involves hands-on support for purchasing, goods-in, stock control and warehouse operations.

ERP

• Burgess Hill
• £50,000 pa
• Senior
• Part time

Part-time role maintaining quality and regulatory compliance for a Class I(s) medical device manufactured by an approved contract manufacturer. You will oversee supplier quality, review batch documentation, validation and change control, maintain technical files, and support audits, vigilance and post-market surveillance, working closely with the Head of Quality and sharing PRRC responsibilities.

• Cambridge
• Hybrid · 2 days in office
• £65,000 – £80,000 pa
• Senior
• Permanent

Lead regulatory strategy for a cardiology device company expanding into the US, UK, EU and Middle East, owning FDA, CE and UKCA submissions from Class I to Class II/III. Drive an audit-ready QMS (ISO 13485, 21 CFR Part 820, ISO 14971) and advise senior leadership on regulation, quality and clinical governance, working directly with the FDA, MHRA and notified bodies.

FDA · MHRA · UKCA +2

• 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

• 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