Latest Quality Engineer Jobs

Product Director, Evidence Preparation

The role involves leading the development and strategy of AI-enabled digital products for structured authoring and regulatory content across clinical, non-clinical, CMC, safety, and publications domains. The Product Director will drive innovation in automated content generation, modular reuse, and compliance within a GxP environment, working closely with cross-functional stakeholders and technical teams to scale enterprise-grade solutions.

GSK United Kingdom

Hybrid Permanent

Head of RII or Oncology Programming

This senior leadership role involves overseeing the transformation of clinical data into regulatory-ready evidence for GSK's Respiratory, Immunology & Inflammation (RII) or Oncology Research Unit. The Head of RII or Oncology Programming will lead a global team, drive strategic initiatives, and champion innovation in clinical programming, ensuring high standards of quality, compliance, and timely delivery of medicines and vaccines.

GSK Stevenage, United Kingdom

On-site Permanent

Global Development Lead, Early Clinical Development, Internal Medicine

The Global Development Lead will drive clinical research for cardiometabolic diseases, creating early clinical development strategies and leading the translation of pre-clinical observations into Phase 1/2 studies. They will work closely with cross-functional teams to ensure medical and scientific excellence, manage clinical trial execution, and engage with regulatory authorities and external collaborators.

Pfizer Sandwich, United Kingdom

On-site Permanent

Senior Manager, HTA, Value and Evidence (HV&E), Rare Disease

This role involves developing and executing high-quality HTA, Value & Evidence strategies to support patient access and reimbursement for Rare Disease treatments. The Senior Manager will manage health economics and outcomes research, collaborate with cross-functional teams, and ensure a consistent evidence generation strategy across markets.

Pfizer United States

On-site Permanent

Trial Vendor Associate Director

This role involves managing all clinical vendor-related aspects of global clinical trials, including vendor service delivery, cost control, contract negotiations, and user-acceptance testing for eCOA and IRT systems. You will collaborate closely with the study team and ensure quality and service standards are maintained throughout the study lifecycle.

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

Permanent

Precision Medicine Director

Job Description Summary#LI-HybridWork Arrangement: Hybrid WorkingNovartis is unable to offer relocation support: please only apply if accessible.The Precision Medicine Director is responsible for developing and executing precision medicine strategies aligned to disease area and clinical program objectives. This role leads...

Novartis

Scientist, Analytical Operations - Small Molecule Stability Data Management

This role involves managing and improving stability data for small molecule studies, creating and maintaining study protocols, and producing clear data visualizations for regulatory submissions. You will work closely with cross-functional teams and external partners to drive process improvements and ensure data integrity.

GSK Stevenage, United Kingdom

Hybrid Permanent

Scientist, Analytical Operations - Small Molecule Stability Data Management

In this role, you will manage and improve stability data for small molecule studies, create and maintain study protocols, collect and analyse datasets, and produce clear summaries and visualisations for regulatory submissions. You will also support audits, collaborate with cross-functional teams, and drive process improvements through digital tool adoption.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role leads operational excellence for Supported Studies at GSK, focusing on data governance, system ownership, and digital integration. The individual will ensure data integrity, drive compliance with regulatory requirements like Transfer of Value, and translate operational needs into scalable digital solutions. Working across cross-functional teams, they will enhance efficiency, quality, and transparency in clinical operations through robust dashboards, automation, and process improvements.

GSK Stevenage, United Kingdom US$154,275 – US$257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role focuses on strengthening the operational and digital foundations of GSK's Supported Studies, ensuring data integrity, system performance, and compliance. The individual will lead data governance, dashboard development, and system integration—particularly for platforms like Veeva and IdeaPoint—while acting as a bridge between business and technology teams to drive efficiency and compliance in clinical study delivery.

GSK London, United Kingdom US$154,275 – US$257,125 pa

Hybrid Permanent

Principal Medical Writer

This role involves authoring and delivering high-quality clinical regulatory documents, leading cross-functional teams, and managing complex writing projects. The Principal Medical Writer will interpret clinical and statistical data, ensure compliance with regulatory requirements, and contribute to global regulatory submissions.

GSK Stevenage, United Kingdom

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for hematological malignancies, collaborating with a multidisciplinary team to ensure patient safety, scientific integrity, and regulatory compliance. This role involves medical monitoring, data review, and strategic partnerships with thought leaders in the oncology field.

GSK United States

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the end-to-end development of oncology drugs.

GSK

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the strategic development of GSK's oncology portfolio.

GSK

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for GSK's oncology portfolio, focusing on hematological malignancies. Key responsibilities include collaborating with multidisciplinary teams, ensuring patient safety, and contributing to regulatory submissions and publications.

GSK

Hybrid Permanent