Latest quality assurance Jobs

Quality Assurance & Regulatory Affairs Specialist - MedTech

This role involves ensuring quality assurance and regulatory compliance across the full lifecycle of advanced medical devices, from design through manufacturing, for global markets including Europe, North America, and APAC. The specialist will conduct internal audits, help shape regulatory strategy, and work with complex, innovative technologies in a high-autonomy environment. The role focuses on new product development, requiring strict adherence to ISO 13485, CE Marking, and other international standards.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom £45,000 – £49,000 pa

On-site Permanent

Quality Assurance Specialist

This role involves maintaining and improving a Quality Management System in a regulated medical device environment, with a focus on ISO13485 compliance, technical documentation, internal audits, and managing non-conformities and CAPAs. The specialist will ensure product literature meets regulatory standards and will act as a key contact during external audits, working closely with senior management and consultants.

East Lancashire Services Birch, Manchester, United Kingdom

Hybrid Permanent

Validation/ Quality Assurance Specialist, Pharmaceutical

The Validation Specialist will plan and execute validation activities, author and maintain validation protocols, and collaborate with cross-functional teams to ensure compliance with GMP standards. The role involves maintaining validated status, supporting regulatory inspections, and contributing to the Site Validation Master Plan.

Russell Taylor Group De118Je, DE11 8JE, United Kingdom £30,000 – £34,000 pa

On-site Permanent

Regulatory Affairs and Quality Assurance Assistant - Cambridge

This role involves supporting quality assurance and regulatory affairs activities within a medical devices R&D environment, ensuring compliance with ISO 13485, FDA 510(k), and 21 CFR Part 820 standards. The assistant will collaborate closely with R&D teams, providing guidance on regulatory requirements during product development and improvement. The position plays a key part in maintaining quality management systems and enabling the delivery of innovative, life-improving medical technologies.

Newton Colmore Cambridge, United Kingdom

On-site Permanent

Quality & Regulatory Associate

This role involves supporting the Quality Management System (QMS) and Regulatory processes, including ISO13485 readiness and FDA 510(k) documentation. You will work closely with internal teams to maintain quality documentation, manage change controls, and promote continuous improvement.

Taylorollinson Manchester, United Kingdom £35,000 – £45,000 pa

Hybrid Permanent

QA Officer

Quality Assurance Officer💰 £28,000–£30,000📍 Cheshire | Pharmaceutical Manufacturing🧪 Permanent | Full Time | On‑siteWe are partnering with a fast‑paced pharmaceutical manufacturing organisation that produces a range of regulated medicinal and healthcare products, including licensed and unlicensed medicines. Due to continued...

Nexus Life Sciences Knutsford, Cheshire, United Kingdom £28,000 – £31,000 pa

QA Specialist - NPI

This role involves leading Quality Assurance for new product introductions across a global network of external manufacturers. The specialist ensures compliance with GMP and regulatory standards during technology transfer, supports clinical trial manufacturing, and acts as the QA lead during audits and inspections. Key responsibilities include oversight of CMOs, risk management, and continuous improvement of quality processes.

GE HealthCare Chalfont St Giles, Buckinghamshire, United Kingdom

Hybrid Permanent

CAPA Lead

This role involves leading investigations into quality issues and managing the CAPA (Corrective and Preventive Action) process within a regulated environment, ensuring compliance with quality standards. The candidate will coordinate cross-functional teams, conduct risk assessments, analyse data trends, and support internal and external audits. The position operates in a hybrid model in Folkestone and focuses on continuous improvement in quality systems.

Office Angels Folkestone, United Kingdom

Hybrid Contract

QMS Specialist

As a QMS Specialist, you will ensure the Quality Management System meets global medical device regulations, support key QMS processes, and collaborate with cross-functional teams to maintain audit readiness. Your role involves interpreting regulatory requirements, conducting data analysis, and driving continuous improvement to ensure high-quality, compliant products.

Smith & Nephew Goole, United Kingdom

Hybrid Permanent

Regulatory Affairs Specialist

This role involves maintaining regulatory compliance for medical devices by managing technical documentation, product registrations, and post-market surveillance activities. The specialist will work independently in an SME setting, ensuring adherence to UK and EU regulations including MDR, MDD, and UKCA. Responsibilities include updating clinical evaluations, supporting audits, and managing documentation with a focus on accuracy and efficiency.

ProTech Recruitment Ltd Hertford, Hertfordshire, United Kingdom £35,000 – £40,000 pa

Hybrid Permanent Part-time

QA Manager - New Product Introduction

This role involves providing quality assurance leadership for the development and clinical manufacturing of diagnostic radiopharmaceuticals. The QA Manager will oversee GMP compliance, support technology transfer, manage CMO relationships, and ensure quality systems are integrated across R&D and clinical operations. Key responsibilities include leading investigations, supporting audits and inspections, and driving continuous improvement in quality processes.

GE HealthCare Chalfont St Giles, Buckinghamshire, United Kingdom

Senior I Stat Prog Lead

This role involves leading statistical programming activities for clinical projects, developing programming strategies, and delivering high-quality data analysis and reporting. The Senior Statistical Programming Lead provides technical guidance to teams, ensures compliance with data standards and SOPs, and contributes to submissions and cross-functional initiatives. It emphasizes advanced SAS programming, clinical trial data structures, and collaboration within a regulated environment.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Biomededical Training Engineer

This role involves managing the full return-to-base (RTB) lifecycle of medical devices, including inspection, repair, calibration, and refurbishment to ensure compliance with safety and performance standards. The engineer will also deliver hands-on technical training, mentor junior staff, and support continuous improvement initiatives. Collaboration with hospitals, OEMs, and internal teams is key to reducing equipment downtime and improving service efficiency.

Focus Resourcing Harlow, Essex, United Kingdom

On-site Permanent Clearance Required

Electronics Repair Technician

This role involves diagnosing, repairing, and calibrating high-value medical and electronic equipment such as MRI systems, ultrasound probes, and CT/X-ray devices to component level. Working in a specialist electronics laboratory, the technician will use advanced test equipment and reverse-engineer circuits where documentation is limited. The position emphasizes technical problem-solving, compliance with ISO and regulatory standards, and collaboration within an engineering team to extend the life of critical healthcare technology.

Focus Resourcing Theale, Berkshire, United Kingdom

On-site Permanent Clearance Required

Biomedical Scientist

Biomedical Scientist | Clinical Chemistry Biomedical Scientist | HCPC Registered BMSMilton Keynes | Band 5 & Band 6 | Full-time | Temporary | NHS LaboratoryIntroductionAcorn by Synergie is recruiting HCPC-registered Biomedical Scientists to support a major laboratory transformation project within...

Acorn by Synergie Woolstone, Milton Keynes, Buckinghamshire, United Kingdom