Latest Quality Engineer Jobs

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

This role involves designing, building, and deploying production-grade AI systems to transform clinical development and operations at scale. The director will lead the implementation of LLMs and agentic AI, develop reusable workflows, and partner with stakeholders to drive adoption. Emphasis is placed on MLOps, cloud deployment, and translating complex data into actionable insights within a regulated environment.

Pfizer US$176,600 – US$294,300 pa

On-site Permanent

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

This role involves designing and deploying production-grade AI systems to transform clinical development and operations at scale. The Director will lead the implementation of LLMs and agentic AI in regulated workflows, building reusable, automated solutions for complex clinical processes. They will bridge technical and scientific domains, driving MLOps adoption while ensuring solutions are secure, reproducible, and aligned with enterprise data governance.

Pfizer US$176,600 – US$294,300 pa

On-site 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 New Product Introduction (NPI), technology transfers, process verification, and regulatory compliance. The position requires strong technical expertise, collaboration with R&D and manufacturing sites, and a focus on robust and compliant supply.

GSK

On-site Permanent

Senior Technician

As a Senior Engineering Technician, you will lead the design, installation, and commissioning of new aseptic manufacturing equipment and facilities. You will work closely with project engineering, quality, and external vendors to ensure systems meet business, regulatory, and GMP requirements, and are ready for operational handover.

GSK Barnard Castle, United Kingdom

On-site Permanent

Statistician (Scientist)

The role involves providing statistical support for manufacturing and analytical processes, using advanced data analytics and visualisation techniques. You will work across multiple teams to improve process understanding and drive data-driven decision-making, contributing to AstraZeneca's digital transformation.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Senior Specialist, Data Science

Job Title: Senior Specialist, Data Science — Operational Data Strategy (ODS), BioPharma R&DLocation: United KingdomCompetitive Salary & Excellent Company Benefits!Introduction to the Role:The Operational Data Strategy (ODS) function provides strategic oversight for how clinical operations data is collected, organized, validated,...

AstraZeneca Cambridge, 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, leading quality issue resolution, and ensuring inspection readiness across global clinical programs. The manager will translate regulatory requirements into actionable insights, conduct self-assessments, and drive continuous improvement in compliance. Embedded within cross-functional teams, the role emphasizes proactive risk mitigation, data integrity, and collaboration with Quality Assurance and Development functions.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Hybrid Permanent

Talent Partner (Tech), London

As a Talent Partner at Isomorphic Labs, you will play a critical role in building world-class teams by developing and executing talent acquisition strategies. You will partner with senior leaders to attract top-tier talent, shape the company's future, foster an inclusive culture, and enhance the employer brand in the competitive AI and biotech landscape.

Isomorphic Labs London, United Kingdom

On-site Permanent

Validation/ Quality Assurance Specialist, Pharmaceutical

The Validation/Quality Assurance 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.

NMS Recruit Ltd t/a Russell Taylor Group Swadlincote, Derbyshire, DE11 0AG, United Kingdom £30,000 – £34,000 pa

On-site Permanent

Clinical Quality Assurance - Program Lead (Associate Director)

The Associate Director, Clinical Quality Assurance (QA) will lead quality oversight for clinical trials, ensuring compliance with health authority requirements and patient safety. Responsibilities include implementing quality strategies, monitoring risk management, and supporting governance for quality incidents. The role involves collaboration with key stakeholders and active participation in continuous improvement initiatives.

Novartis London, United Kingdom

Hybrid Permanent

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve data discrepancies and maintain inspection readiness.

Moderna Oxford, United Kingdom

On-site Temporary

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve discrepancies and maintain inspection readiness.

Moderna

On-site Temporary

Head of Quality Assurance and Regulatory Affairs

Evolve are partnering with a fast-growing organisation to appoint a Head of Quality Assurance & Regulatory Affairs. This is a strategic leadership role where you will drive quality and regulatory excellence, support global expansion, and work cross-functionally to ensure consistently...

Evolve Selection London, United Kingdom

Head, PV and Regulatory QA

TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...

CSL

Head, PV and Regulatory QA

TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...

CSL