Latest Quality Engineer Jobs

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across the EMEA region. You will evaluate compliance with GMP, regulatory requirements, and quality management systems, and provide subject matter expertise in sterile manufacturing. The role requires strong communication and influencing skills to engage with senior stakeholders and produce clear audit reports.

GSK Worthing, United Kingdom

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

The Audit Senior Lead role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities. Responsibilities include evaluating compliance, conducting various types of audits, and producing clear audit reports to inform senior management of risks and corrective actions.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

End-to-End Product Lead, AMP

This role involves leading the development and delivery of an intelligent content operating system called AMP, which connects how marketers plan, create, review, and measure content. The Product Lead will define the product vision, roadmap, and success metrics, manage a team of product owners, and collaborate with stakeholders across content strategy, operations, design, engineering, data, and compliance to ensure alignment and drive measurable outcomes in user productivity, quality, and compliance.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

End-to-End Product Lead, AMP

The AMP Product Lead is responsible for defining and executing the vision, strategy, and roadmap for an intelligent content operating system. This role involves close collaboration with global stakeholders to ensure alignment across marketing and technology, driving measurable outcomes in productivity, quality, and compliance.

Pfizer

Remote Permanent

Director – Process Design and Optimisation in Chemical Development

This role involves leading a team in the design and optimisation of chemical processes for drug development. Responsibilities include technical direction, project delivery, regulatory submissions, and mentoring scientists. The position leverages innovative technologies and AI to enhance process efficiency and ensure robust commercial processes.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Director, Quality Assurance (Diagnostics & Devices)

Director, Quality Assurance (Diagnostics & Devices)Cambridge, UK (3 days on site per week)About AstraZenecaAstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases....

AstraZeneca Cambridge, United Kingdom

(Fixed Term) Analyst, Quality Control, Microbiology

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization,...

Moderna Oxford, United Kingdom

(Fixed Term) Analyst, Quality Control, Microbiology

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization,...

Moderna Gargrave, BD23 3RZ, United Kingdom

GVP Vendor Oversight and QA Lead (EU)

This role involves leading the quality oversight of pharmacovigilance vendors and service providers, ensuring adherence to GVP regulations and continuous improvement. Responsibilities include defining qualification strategies, managing quality agreements, and leading risk assessments and trend analysis.

CSL United Kingdom

On-site Permanent

Senior Principal Statistical Programmer

The Senior Principal Statistical Programmer leads statistical programming activities for multiple clinical studies or large projects, ensuring high-quality and timely deliverables. They collaborate with biostatistics, coordinate programming teams, and maintain compliance with industry standards.

Novartis London, United Kingdom

On-site Permanent

Senior Director Global Clinical Program Lead Cardiovascular & Renal

This role involves leading the clinical development of a medicine for cardiovascular and renal conditions, managing a cross-functional team, and ensuring compliance with regulatory standards. Responsibilities include strategic planning, clinical oversight, and authoring key documents for regulatory submissions and publications.

CSL Switzerland

On-site Permanent

Research Associate, Primary Pharmacology

This role involves developing and optimizing cell-based and biochemical assays to support small molecule drug discovery, with a focus on compound characterization and candidate identification. The scientist will work in a high-throughput, automated lab environment, generating decision-ready data in collaboration with cross-functional teams. The position emphasizes hands-on experimentation, assay innovation, and integration within a multidisciplinary drug discovery pipeline.

Recursion Crathes, Alba / Scotland, United Kingdom £41,000 – £52,000 pa

On-site Permanent

R&D Scientist - Immunology

As an R&D Scientist, you will work in a state-of-the-art lab, generating high-quality immune profiling data using advanced cytometry and single-cell technologies. Your key responsibilities include performing flow cytometry assays, isolating immune cells from human blood, preparing samples for RNA sequencing, and maintaining quality control standards. You will collaborate with multidisciplinary teams and support ongoing research projects, with some weekend work required.

HAYS Specialist Recruitment London, United Kingdom £36,000 – £45,000 pa

On-site Permanent

Director, Neuroscience (In Vitro Cellular Biology)

This role involves leading the development and application of human iPSC-derived cellular models for neurodegenerative disease drug discovery. You will design and oversee cellular and molecular assays, collaborate with cross-functional teams, and mentor scientists to advance therapeutic discovery.

Recursion United Kingdom £198,000 – £237,600 pa

Hybrid Permanent

Regulatory Transparency (Disclosures) Professional

In this role, you will manage the end-to-end execution of clinical trial registration and results posting, ensuring Roche complies with global regulations. You will lead the accurate and timely posting of clinical trial data, manage cross-functional teams, and ensure consistency and quality in all submissions.

Roche Welwyn Hatfield, United Kingdom

On-site Permanent