Latest Quality Engineer Jobs

Staff Platform Engineer, AI/ML Infrastructure

The Staff Platform Engineer, AI/ML Infrastructure will lead the technical strategy for cloud platforms and AI/ML infrastructure, focusing on reliability, scalability, and security. They will architect and operate scalable cloud platforms using AWS services, define CI/CD pipelines, and mentor engineers to improve operational maturity across multiple teams.

Pfizer

On-site Permanent

Staff Platform Engineer, AI/ML Infrastructure

The Staff Platform Engineer, AI/ML Infrastructure will lead the technical strategy for cloud platforms and AI/ML infrastructure, focusing on reliability, scalability, and security. Key responsibilities include architecting and operating scalable cloud platforms using AWS services, defining reusable infrastructure patterns, and mentoring engineers to improve operational maturity across multiple teams.

Pfizer

On-site Permanent

Engineering Technician

The Engineering Technician role involves providing comprehensive engineering support for the Steriles Business Unit, focusing on equipment maintenance, GMP compliance, and continuous improvement initiatives. Responsibilities include breakdown repairs, calibration, quality documentation, and project support, all while maintaining high safety and regulatory standards.

GSK Barnard Castle, United Kingdom

On-site Permanent Shift-work

Operational Quality Director

The Operational Quality Director at GSK will lead the end-to-end quality oversight of manufacturing activities, ensuring compliance with GMP standards and regulatory requirements. Key responsibilities include managing batch documentation, overseeing real-time quality control, and leading the QP team to maintain high-quality standards and inspection readiness.

GSK East Hertfordshire, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Science, International

This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and contribute to the development of regulatory processes and procedures.

Moderna

On-site Permanent

Associate Director, CMC Regulatory Affairs, International

This role involves developing and implementing CMC regulatory strategies for international submissions, providing guidance on regulatory CMC aspects, and leading regulatory discussions with health authorities. The candidate will also support the creation of CMC submission templates and offer interpretations of regulatory guidance documents, ensuring compliance and efficient delivery of high-quality regulatory documentation.

Moderna

On-site Permanent

Vulnerability Analyst

This role involves assessing known software vulnerabilities in Windows-based applications used in regulated medical devices. Responsibilities include performing exploitability and risk analysis, evaluating third-party component risks, and producing clear security documentation. The position requires 2+ years of commercial experience in application security and a strong understanding of CVEs and secure software concepts.

Real Limerick, Limerick County, Ireland £47 ph

Hybrid Contract

Production Scheduler

This role involves planning, coordinating, and monitoring production activities across multiple projects in a regulated medical device manufacturing environment. You will work closely with manufacturing, engineering, quality, and supply chain teams to ensure delivery targets are met and continuously improve planning processes.

Euro Projects Recruitment Abingdon, Oxfordshire, OX14 5BH, United Kingdom £40,000 – £45,000 pa

On-site Permanent

Regulatory Affairs Specialist

This role involves maintaining technical documentation and ensuring compliance with UK and EU MDR regulations for Class I and IIa medical devices. The specialist will support regulatory submissions, post-market surveillance, and quality management system development within a regulated environment. Collaboration with the QA Manager and ongoing product lifecycle support are key aspects of the position.

Cure Talent Upper Marlbrook, Worcestershire, B61 0RT, United Kingdom £45,000 – £50,000 pa

On-site Permanent

EC&I Technician - Pharmaceutical

Position: EC&I TechnicianLocation: LiverpoolSalary: Circa £35k-£40k+Role OverviewThe EC&I Technician is responsible for managing projects from the control handover stage through to successful completion of Installation Qualification (IQ), Operational Qualification (OQ), and operator training at customer facilities.The role includes connecting safe...

Bennett & Game Recruitment Halewood, Merseyside, United Kingdom £35,000 – £43,000 pa

Senior Specialist I, QA Clinical

The Senior Specialist I, QA Clinical is responsible for quality oversight in clinical development, supporting cross-functional relationships and ensuring compliance with GCP/GVP regulations. Key responsibilities include developing and implementing risk-based audit plans, conducting audits, and managing quality events. The role involves working closely with clinical project teams and external stakeholders, and maintaining the quality management system.

Autolus Stevenage, United Kingdom

Hybrid Permanent Flexible

Director, Statistical Programming

This role involves leading and developing a team of programmers, providing strategic direction for statistical programming in clinical development, and ensuring quality, compliance, and continuous improvement. The Director will partner cross-functionally to drive business impact and maintain industry and regulatory knowledge.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Supply Planner

The Supply Planner ensures uninterrupted production by managing raw material procurement and inventory across clinical and commercial manufacturing operations. This role involves running MRP processes, maintaining inventory policies, coordinating with suppliers and 3PLs, and leading supply continuity efforts. The position works cross-functionally with finance, quality, and manufacturing teams to align supply plans with demand forecasts and resolve supply chain disruptions.

Autolus Stevenage, United Kingdom

Hybrid Permanent

Senior Scientist - Protein and Cell Sciences

In this laboratory-based role, you will design, express, purify, and characterize recombinant proteins to support biologics discovery and development. Your work will directly impact the evaluation of novel therapeutic modalities and inform clinical decisions, using modern computational tools and rigorous experimental methods.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Scientist, Separation Sciences

Your work will change lives. Including your own.The Impact You’ll MakeWe are seeking a Senior Separation Scientist to join our Chemistry Automation team at our labs in Milton Park. In this primarily lab-based role, you will be responsible for maintaining...

Recursion Crathes, Alba / Scotland, United Kingdom