Medical Technology Jobs

• Great Yarmouth
• £30,000 – £37,700 pa

Working within a QA team at a GMP manufacturing site producing pharmaceuticals, medical devices and personal care products, you will monitor and assure the quality of processes and products. Duties include preparing and approving quality documentation, investigating GMP breaches and OOS incidents, managing CAPAs, supporting site audits and QP batch release, and delivering GMP training.

• Weymouth
• On-site
• £37,500 – £40,000 pa
• Junior
• Permanent

Supports customer requirements, drives continuous improvement projects and investigates shop floor issues to find root causes. Manages customer documentation and conducts internal audits, working closely with compliance and operations teams on precision components for defence, aerospace and medtech clients.

• Stirling
• On-site
• £26,436 pa
• Entry level

A varied Quality Assurance and Regulatory Affairs role in a regulated warehouse environment, maintaining compliance documentation, supporting product licence applications, and reviewing labels and packaging. You'll carry out quality checks, assist with investigations, CAPAs, deviations and change controls, and maintain training records and controlled documents alongside warehouse, production and commercial teams.

Microsoft Word · Microsoft Excel

• 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

• 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.

• 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.

• Gloucester
• On-site
• £45,000 – £50,000 pa
• Mid-level
• Permanent

Support and maintain the effectiveness of a medical device manufacturer's QMS in line with ISO 13485, MDR and FDA requirements. Day-to-day work covers CAPA effectiveness, quality data and trend analysis, non-conformances, change control and complaint investigation, plus writing and updating procedures and work instructions.

ISO 13485 · FDA Quality System

• Derby
• On-site
• £35,000 – £45,000 pa

Supports the Quality Management System for a medical device and healthcare services provider, coordinating change requests, customer investigations, root cause analysis and audit documentation. Maintains Post Market Surveillance records and works closely with the Director of Quality Assurance & Regulatory Affairs at the Castle Donington head office.

• 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.

• Lancashire
• On-site
• Mid-level
• Contract

Maintains and improves a medical device Quality Management System in line with ISO 13485 and FDA QSR, leading non-conformance, deviation, complaint and CAPA investigations with root cause analysis. Supports internal, supplier and regulatory audits, risk management under ISO 14971, validation and design transfer, working with Manufacturing, R&D, Regulatory Affairs and Supply Chain.

• Fareham
• Hybrid
• Mid-level
• Permanent

Maintains and improves a medical device Quality Management System, planning and reporting internal audits and leading external audit readiness with evidence packs and follow-up actions. Supports ISO 13485 compliance, ISO 14971 risk activities, CAPA and document control, and leads quality improvement projects in a regulated scale-up environment.

• Luton
• On-site
• £65,000 pa
• Senior · manages people

Hands-on operational leadership across manufacturing, quality assurance, supply chain, purchasing and facilities at a medical equipment manufacturer. Sits on the Senior Leadership Team, owning site health and safety, ISO compliance and continuous improvement, while partnering with executive leadership on business planning and representing the site at group forums.

ISO · 5S

• Bolton
• £35,116 – £48,149 pa
• Permanent

Deliver and develop undergraduate and postgraduate mechanical engineering programmes, covering teaching, assessment, curriculum design and student supervision. Engage in research, scholarly activity and professional practice, with subject knowledge in areas such as signal processing, finite element methods, additive manufacturing or sustainability.

• Henley-on-Thames
• £32,000 – £38,000 pa
• Mid-level
• Permanent

Support regulatory affairs and compliance across healthcare, digital health and medical-device activity. Maintain the Quality Management System, medical-device technical documentation, risk registers and audit actions, while coordinating evidence for tenders, CQC inspections and information governance. Acts as a link between clinical, technical and commercial teams.

ISO 13485 · ISO 14971 · IEC 62304 +7

• 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