Latest Quality Engineer Jobs

Director, AI Engineering--Clinical Development and Operations (CD&O)

This role involves designing and deploying production-grade AI systems to enhance clinical development and operations at Pfizer. The director will lead the implementation of LLMs and agentic AI, building scalable, reproducible workflows that improve clinical trial processes such as protocol feasibility, site selection, and supply forecasting. They will collaborate closely with scientific and operational teams to translate complex needs into trusted, enterprise-scale AI solutions while championing MLOps and data governance best practices.

Pfizer United States US$176,600 – US$294,300 pa

On-site Permanent

Director, AI Engineering--Clinical Development and Operations (CD&O)

This role involves leading the design and deployment of production-grade AI systems within Pfizer's Clinical Development & Operations organization. The Director will focus on applying LLMs and agentic AI to real-world clinical workflows, building scalable MLOps pipelines, and translating complex data into decision-support tools. They will collaborate closely with scientists and digital teams to drive trusted, enterprise-wide AI adoption in a regulated environment.

Pfizer London, SW7 2AP, United Kingdom US$176,600 – US$294,300 pa

Hybrid Permanent

MSAT Drug Product Lead (Parenteral Products)

This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include leading technology transfers, process verification, and product qualifications, while collaborating with R&D, manufacturing sites, and regulatory teams to ensure safe and compliant supply.

GSK Worthing, United Kingdom

Hybrid Permanent

MSAT Drug Product Lead (Parenteral Products)

This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include technology transfers, process verification, regulatory submissions, and cross-functional investigations to ensure safe and compliant supply. The role emphasizes practical problem-solving and collaboration across functions.

GSK

On-site Permanent

VP & Global Head, Discovery Chemistry and DMPK, Oncology Targeted Delivery

This role involves leading the global Discovery Chemistry and DMPK function within AstraZeneca's Oncology Targeted Delivery (OTD) organization. Responsibilities include setting strategic direction, driving innovation in small molecules, ADCs, and RCs, and fostering a high-performing, collaborative culture across R&D sites in Cambridge (UK), Cambridge (MA), and Gaithersburg (US).

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Process Leader (First Line Manager) – Sterile Production

This role involves leading a team of operators in a fast-paced, highly regulated sterile manufacturing environment. Responsibilities include managing daily operations, ensuring compliance with cGMP standards, and driving continuous improvement through Lean principles and digital technologies.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent Shift-work

Research Associate, Compound Management

The Research Associate will manage inventory, prepare reagents, and run automated systems for high-throughput screening. They will collaborate with cross-functional teams to optimize workflows and adopt new technologies, contributing to the company's drug discovery platform.

Recursion United Kingdom

On-site Permanent

Support technician

This role involves building, installing, and maintaining advanced electromechanical instruments across the UK, with significant time spent on customer sites. The technician will troubleshoot and repair equipment, support manufacturing processes, and contribute to product improvements through direct feedback to R&D. It combines field service, hands-on technical work, and collaboration across teams in a regulated environment.

Matchtech Whiteley, Hampshire, PO15 7LW, United Kingdom £30,000 – £35,000 pa

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing compliance oversight for clinical programs and trials, ensuring adherence to Good Clinical Practice standards. You will act as a primary compliance partner to Clinical Trial Teams, enabling decision-making on complex regulatory scenarios and leading cross-functional discussions to resolve quality issues.

Novartis Ireland

Hybrid Permanent

Head of Research and Development

We’re partnering with a market-leader in the Ophthalmology sector, who are looking to recruit an experienced Head of R&D (Research & Development)!The successful candidate will lead R&D strategy, manage a multidisciplinary team, and work closely with key internal functions to...

Evolve Selection Cambridge, Cambridgeshire, United Kingdom

Remote Permanent

PKPD Modelling Lead, London

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A...

Isomorphic Labs London, United Kingdom

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing expert Good Clinical Practice (GCP) compliance guidance to clinical trial teams, supporting decision-making on complex regulatory issues, and ensuring adherence to quality standards across global clinical programs. The manager will lead investigations into quality issues, drive inspection readiness, and translate regulatory requirements into practical actions. Collaboration with cross-functional stakeholders is central to strengthening compliance and fostering a culture of data integrity and accountability.

Novartis London, United Kingdom

Hybrid Permanent

Senior Research Investigator, (Biologics Pharmacology), London

As a Senior Research Investigator, you will contribute to the pharmacology and translational biology strategy of novel large molecule therapeutics, leveraging Isomorphic Labs' cutting-edge AI drug design engine. You will design and execute pharmacology plans, lead in vivo and in vitro evaluations, and collaborate with interdisciplinary teams to advance drug discovery projects from early stages to clinical candidates.

Isomorphic Labs London, United Kingdom

On-site Permanent

Technical Documentation and Development Engineer

This role involves creating, managing, and improving technical documentation and CAD models for medical devices, ensuring compliance with MDR regulations. The engineer will own technical files, support product development and legacy improvements, and collaborate with R&D, regulatory, and manufacturing teams. Emphasis is placed on accuracy, regulatory adherence, and structured design control processes.

Michael Page Sheffield, South Yorkshire, United Kingdom £42,000 pa

On-site Permanent

Quality & Regulatory Associate

This role involves supporting the development and maintenance of a Quality Management System aligned with ISO13485 and FDA requirements in a growing med-tech company. The candidate will manage regulatory documentation, design controls, and quality processes, contributing to audit readiness and continuous improvement. It's a hands-on position with direct impact on product compliance and regulatory submissions.

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

Hybrid Permanent