Medical Technology Jobs

• Prague, Czech Republic
• Hybrid
• CZK 704,000 – CZK 1,135,050 pa
• Mid-level

Supports end-to-end medical coding of clinical trial data, ensuring consistent, accurate and reproducible coding aligned with regulatory and industry standards. Maintains global thesauri and dictionary encoding systems (MedDRA, WHO Drug), handles coding specifications, quality reviews and sign-off, and advises cross-functional partners on coding issues.

MedDRA · WHODrug

• Beerse, Belgium
• €79,800 – €137,770 pa
• Mid-level · manages people

Leads preparation and finalisation of clinical and regulatory documents for the Immunology therapeutic area within the Regulatory Medical Writing team. Acts as lead writer or point of contact for programmes, guides cross-functional teams, and manages, mentors and develops direct reports in medical writing.

• Glasgow
• £55,040 – £82,560 pa
• Senior

Drive sales and clinical education for the Perioperative Complications portfolio (BIS, INVOS, NOL) across Scotland, growing targets in line with the ACM strategy. Provide in-theatre clinical support, product training and best-practice education while building relationships with clinicians, KOLs and advisory boards. Also leads product evaluations, trials and conversion projects, partnering with Sales Specialists and Marketing to expand adoption.

BIS · INVOS · NOL

• Watford
• £60,560 – £90,840 pa
• Lead

Senior individual contributor leading customer experience improvement across EMEA for a Service & Repair customer care organisation. Uses NPS, Voice of the Customer, journey data and operational metrics to drive cross-functional initiatives, executive reporting and digital self-service adoption.

CRM · AI · Automation

• Cambridge
• Mid-level

Design and develop mechanical components for genomics instrumentation, working within a multidisciplinary team of physicists, electronics engineers, software developers and life sciences specialists. The role spans the full product lifecycle from concept and prototyping through to design for manufacture and launch, ideally within medical devices, diagnostics or scientific instrumentation and regulated environments such as ISO 13485 and FDA QSR.

• London
• On-site
• £36,000 – £42,000 pa
• Mid-level
• Permanent

Multi-skilled engineer maintaining and repairing mechanical and electrical systems on a manufacturing site, driving continuous improvement and supporting NPI. Involves fault-finding, designing fixtures and jigs, and helping develop new equipment across robotics, medical and aerospace production.

• Uttoxeter
• On-site
• £31,000 – £34,000 pa

Manufacture high-accuracy calibration gases and reference materials using gravimetric methods, producing oxygen and flammable gas mixtures to strict ISO 6142 and ISO 17034 standards. Duties include preparing cylinders, valve fitting, stock control and site logistics, working within a specialist production team for a global industrial and medical gases leader.

Microsoft Office

• 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.

• 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.

• Manchester
• £48,000 – £57,000 pa
• Mid-level

Designs analogue and digital electronics for scientific instrumentation, owning specifications, schematics, PCB layouts and PLD/FPGA configurations across the full product life cycle. Works closely with suppliers, fitters and test engineers, building and evaluating prototypes to ISO61010, ISO13485 and 21CFR820 standards, with Cadstar, HV design and Xilinx MicroBlaze firmware as advantageous skills.

Cadstar · Xilinx MicroBlaze · PLD +2

• Birmingham
• £45,000 – £50,000 pa

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

X-Ray Systems · Laboratory Systems · Scientific Equipment +3

• Stockton-on-Tees
• £40,000 – £46,000 pa
• Mid-level

Deliver NPI and engineering projects in a regulated medical manufacturing environment, focusing on process validation, PPAP documentation and quality compliance. Support projects from RFQ and feasibility through validation, customer approval and handover to production, working closely with Engineering, Quality, Operations and customers.

• Pilning
• On-site
• £32,000 – £36,000 pa
• Mid-level
• Permanent

Assemble and wire high-tech semiconductor production equipment, working from electrical drawings to solder, crimp and loom complex panel configurations. The role sits in a production team building cutting-edge systems and also involves fault finding and implementing corrective action. Double day shifts with an early Friday finish.

• Southampton
• £40,000 – £50,000 pa

Servicing, calibrating and repairing advanced aesthetic laser and medical electro-mechanical systems across London and the Home Counties, combining planned maintenance with on-site fault-finding and remote customer support. Works within a small engineering team, with manufacturer-led training and mostly M25-region travel.

Aesthetic Laser Systems · Medical Devices · Laser Systems +3

• Bridgwater
• On-site
• £55,000 pa
• Mid-level

Owns quality operations across a precision manufacturing site, maintaining QMS, certifications and audit readiness while leading continuous improvement. Acts as main contact for customers, auditors and suppliers, managing non-conformances, root cause investigations and corrective actions using SPC, PFMEA, PPAP and 8D. Also supports day-to-day Health & Safety activities alongside Production and Engineering teams.