Medical Technology Jobs

• 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

• Madrid, Spain
• Hybrid
• €27,200 – €40,800 pa
• Entry level

Acts as the primary point of contact for customers throughout the service and repair journey, managing requests, quotations, orders and escalations. Collaborates with service engineers, repair centres and logistics teams in a regulated MedTech environment, and contributes to process improvements and UAT activities.

Microsoft Office · Outlook · Excel +3

• High Wycombe
• Mid-level

Lead Pharmacovigilance process and training projects, including process development, mapping, and training qualification and delivery, while acting as a quality partner to the Innovative Medicines Office of the Chief Medical Officer. Drive digital transformation toward data-centric content and a qualification management system, managing timelines, risks, and audits within a matrixed life sciences environment.

• Beerse, Belgium
• €81,400 – €140,530 pa
• Mid-level

Leads Pharmacovigilance process and training projects, including process development, mapping, and training qualification and delivery. Acts as a quality partner for the Innovative Medicines Office of the Chief Medical Officer, linking business partners, quality groups, and governance while supporting a digital transformation toward data-centric content and qualification management. Manages timelines, risks, and audits or inspections.

• Cambridge

Hands-on regulatory support across multiple engineering projects, working alongside design engineers and scientists to embed compliance into product development. Applies ISO 9001, ISO 13485 and FDA 21 CFR 820 to interpret requirements, manage design controls and track international regulatory changes. Also supports QMS improvement and external audit preparation.

ISO 9001 · ISO 13485 · FDA 21 CFR 820

• Cambridge
• Senior

Lead multiple electro-mechanical medical device projects, taking on mechanical design work directly while mentoring junior staff. Requires hands-on development experience with EN60601 and ISO 13485 standards, plus regular communication with internal and external stakeholders.

Implantable Medical Devices · Wearable Technology

• Cambridge
• £40,000 – £60,000 pa
• Mid-level

Develops high-quality C and C++ software across the full development lifecycle, from concept and design through testing and release, for an engineering consultancy building medical devices. Works in a multidisciplinary team alongside software, electronics and mechanical engineers, writing well-tested code and technical documentation. Embedded systems, RTOS, Linux, Qt and IEC 62304 experience are advantageous.

Git · Linux · Qt +1

• Cambridge
• Hybrid
• £35,000 – £45,000 pa
• Mid-level

Develops FPGA and embedded firmware for high-performance data acquisition and signal processing systems used in biomedical research products. Writes VHDL for FPGA functionality and C for low-level hardware control, integrating and debugging digital electronics across the full product lifecycle alongside hardware and software engineers.

AMD/Xilinx Vivado · Intel Quartus · USB +1

• Cambridge
• £60,000 – £73,000 pa
• Senior

Hands-on mechanical design role developing precision systems for next-generation drug delivery devices, taking designs from early concept through to high-volume manufacture. Involves 3D CAD, prototype builds and testing, DFM/DFA optimisation and tolerance stack-up analysis within a multidisciplinary team.

• Wolverhampton
• Remote
• £45,000 – £48,000 pa
• Mid-level

Field-based new business role selling a broad medical equipment portfolio into NHS and private hospitals across the West Midlands and North Wales, covering A&E, Renal, Oncology, Day Surgery and Patient Handling. You build your own pipeline, run product demonstrations and negotiate complex multi-stakeholder procurement processes, with existing accounts to develop alongside largely untapped territory.

• Stoke-on-Trent
• Remote
• £45,000 – £48,000 pa
• Mid-level

Field-based new business role selling medical equipment into NHS and private hospitals across the West Midlands and North Wales, covering A&E, Renal, Oncology, Day Surgery and Patient Handling. You build your own pipeline, run product demonstrations and negotiate complex multi-stakeholder procurement processes, with existing accounts to develop alongside largely untapped territory.

• 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.

• Watford
• On-site
• £35,000 – £37,000 pa
• Senior
• Permanent

Hands-on senior role in a single-site MHRA-licensed pharmaceutical QC lab, testing raw materials, stability, in-process and finished products to validated and compendial methods. You'll be the go-to person for chromatography (HPLC, GC, UV, FTIR, Raman), lead OOS/OOT and deviation investigations with root cause analysis and CAPA, own equipment and documentation standards, and train junior analysts while supporting audits and inspections.

HPLC · GC · UV +2

• Waterlooville
• £50,000 – £60,000 pa
• Mid-level
• Permanent

Supports manufacturing process development, prototype builds, testing and process validation for products used in biopharmaceutical and medical device industries. Works with design, product management and production teams on new product introduction, continuous improvement and integration of new manufacturing equipment, using ERP systems and validation to industry standards.

ERP

• 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.