Latest Quality Engineer Jobs

Vials Filling & Inhalations Operations Manager

This role involves leading vials filling and inhalation device production at a GSK manufacturing site, ensuring safety, quality, and compliance. You will manage day-to-day operations, coach team members, and drive continuous improvement projects.

GSK Barnard Castle, United Kingdom

On-site Permanent

Inspection Assembly & Packaging Operations Manager

You will lead inspection, assembly, and packaging operations at a GSK site in the UK, managing day-to-day production, quality, and safety while coaching your team to improve. You will work closely with quality, engineering, and supply chain colleagues to deliver on-time, compliant output and drive continuous improvement projects.

GSK Barnard Castle, United Kingdom

On-site Permanent

Senior Director, CFC CRM Lifecycle & Value Lead

This role involves managing the post-launch lifecycle of the CFC CRM platform across global markets, ensuring its stability, compliance, and continuous optimization. The Senior Director will work closely with regional teams to prioritize market needs, manage configurations, and ensure successful adoption and value realization.

Pfizer

On-site Permanent

Senior Director, CFC CRM Lifecycle & Value Lead

This role involves managing the post-launch lifecycle of the CFC CRM platform across global markets, ensuring its stability, compliance, and continuous optimization. The Senior Director will work closely with regional teams to prioritize market needs, manage configurations, and ensure successful adoption and value realization from CRM investments.

Pfizer

On-site Permanent

Director, Portfolio Development Process & Standards Lead

This role leads the establishment and maintenance of processes and standards across CSL's global Portfolio Development function, ensuring high-quality clinical trial planning, evaluation, and reporting. The Director will drive process improvement, SOP governance, training curriculum development, and cross-functional change initiatives within a dynamic biotech R&D environment. They will work closely with leadership and international teams to reduce complexity, improve quality and speed, and align procedural frameworks across clinical development, biomarkers, and commercial operations.

CSL

Hybrid Permanent

Associate Director, Biostatistics (2)

The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, ensuring appropriate methodologies for study design, data analysis, and regulatory submissions. They collaborate with cross-functional teams, manage outsourcing operations, and represent Biostatistics in regulatory interactions.

CSL United Kingdom

On-site Permanent

Clinical Study Administrator

As a Clinical Study Administrator, you will coordinate and manage the administrative aspects of clinical trials, ensuring that all documentation, regulatory submissions, and stakeholder communications are accurate and timely. You will work closely with various teams to maintain inspection readiness and support the smooth operation of multi-site studies.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Senior Global Clinical Operations Director

This role leads the operational strategy and end-to-end delivery of global clinical programs in oncology, spanning early and late-phase development. The director will drive trial design, cross-functional collaboration, and regulatory readiness while managing complex multinational studies, CRO partnerships, and high-performing teams. Emphasis is placed on innovation, efficiency, and patient impact through advanced trial methodologies and strategic leadership.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Associate Director, CMC Regulatory Affairs

This role involves leading the development and implementation of CMC regulatory strategies for small molecule drugs in global clinical trials. Responsibilities include managing CMC submissions, providing regulatory guidance, and collaborating with cross-functional teams to ensure compliance with US, EU, and ROW regulations.

Recursion United Kingdom £176,400 – £228,250 pa

Hybrid Permanent Flexible

Associate Director/Director of Statistical Programming

This role involves leading statistical programming activities across clinical programs, ensuring the development and quality control of tables, listings, figures, and analysis datasets. You will oversee external vendors, develop standards and innovative technologies, and support data-driven decision-making in drug discovery.

Recursion United Kingdom £200,600 – £260,200 pa

Remote Permanent

(Fixed Term) Senior Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves working as a technical expert in the Clinical Flow Cytometry group at Moderna's Harwell facility, generating high-quality clinical trial data through advanced flow cytometry assays. Responsibilities include executing clinical sample testing, conducting immune profiling, and ensuring data integrity and compliance with GCLP standards.

Moderna Oxford, United Kingdom

On-site Contract

(Fixed Term) Senior Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves working as a technical expert in the Clinical Flow Cytometry group at Moderna's Harwell facility, focusing on generating high-quality clinical trial data through advanced flow cytometry assays. Responsibilities include executing clinical sample testing, conducting immune profiling, and ensuring data integrity and compliance with GCLP standards.

Moderna

On-site Contract

Biomedical Scientist (BMS)

The Biomedical Scientist (BMS) role involves performing analytical testing, operating and maintaining laboratory equipment, and processing patient samples in Blood Sciences disciplines. Responsibilities include result authorisation, quality assurance, and supporting patient care through collaboration with clinical and laboratory teams.

Acorn by Synergie Milton Keynes, Buckinghamshire, United Kingdom £16 – £20 ph

On-site Temporary Shift-work

Buyer - Pharmaceuticals

This role involves managing procurement activities, supplier relationships, and quality management within a regulated pharmaceutical manufacturing environment. You will work closely with the Manufacturing, Quality, and Operations teams to ensure effective sourcing and compliance with GMP standards.

Cranleigh Scientific Ditton, Kent, ME20 6AE, United Kingdom £22,800 – £28,800 pa

Hybrid Flexible

Biomedical Scientist Team Manager - Infectious Sciences

This role involves leading a team of biomedical scientists in the Infectious Sciences laboratory, with responsibilities spanning bacteriology, virology, molecular diagnostics, and mycology. The candidate will drive quality management, support staff development, and ensure compliance with health and safety standards in a 7-day operational environment. They will rotate across lab disciplines, provide technical guidance to clinicians, and participate in out-of-hours rotas while maintaining professional registration and continuous development.

Synlab Taunton, Somerset, TA1 1HP, United Kingdom £49,387 – £56,515 pa

On-site Permanent