Latest Quality Engineer Jobs

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating submissions and ensuring compliance with global regulations. Works across cross-functional teams to address complex regulatory challenges and support continuous supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a matrix environment.

GSK Stevenage, United Kingdom €90,000 – €150,000 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for pharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works cross-functionally to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions across complex projects.

GSK London, United Kingdom £90,000 – £150,000 pa

Hybrid 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 lead the generation of health economics and outcomes research, manage global value dossiers, and coordinate with cross-functional teams to ensure a consistent and robust evidence strategy.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

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

The Senior Manager, HTA, Value & Evidence (HV&E) role involves developing and executing strategic efforts to support patient access and reimbursement for rare disease treatments. Responsibilities include managing health economics and outcomes research, generating real-world evidence, and collaborating with cross-functional teams to demonstrate the value of Pfizer's rare disease medicines.

Pfizer

On-site Permanent

Global Program Clinical Head (Neuroscience)

As a Global Program Clinical Head, you will lead the development and execution of clinical programs in Neuroscience, collaborating with global teams to ensure regulatory compliance and patient-centric outcomes. You will define clinical strategies, manage cross-functional teams, and engage with external stakeholders to advance transformative therapies.

Novartis Spain

Hybrid Permanent

Global Program Clinical Head (Neuroscience)

As a Global Program Clinical Head, you will lead end-to-end clinical development programs in Neuroscience, driving strategy, execution, and regulatory compliance. You will collaborate with global teams, define innovative development plans, and ensure high-quality, patient-centric clinical trials.

Novartis Ireland

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the clinical research activities for GSK’s oncology portfolio, including developing and executing phase 1-3 clinical trials. They will collaborate with various stakeholders to ensure high-quality protocol development, medical monitoring, and data interpretation, while also engaging with key external experts and thought leaders.

GSK

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the clinical research and development of GSK’s oncology portfolio, collaborating with various stakeholders to design and execute phase 1-3 clinical trials. Key responsibilities include medical oversight, protocol development, data interpretation, and engagement with key external experts to ensure the successful regulatory filing and market launch of innovative oncology treatments.

GSK

Hybrid Permanent

Regulatory Conformance Officer (12-month / Secondment)

As a Regulatory Conformance Officer, you will ensure that GSK's products meet all licensing and regulatory requirements, maintaining compliance with global market authorisations and supporting regulatory submissions. You will collaborate with multiple functions, including manufacturing, R&D, and global regulatory affairs, to deliver regulatory strategies and inspection readiness.

GSK Barnard Castle, United Kingdom

On-site Contract

Interventional Study Scientist Director

This role involves leading the scientific design and execution of interventional clinical studies in oncology or hematology, ensuring high standards of quality and ethics. You will collaborate with cross-functional teams, provide scientific oversight, and engage with healthcare professionals to deliver impactful results.

GSK United Kingdom

On-site 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 Stevenage, United Kingdom

Hybrid Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategies. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK Stevenage, United Kingdom

Hybrid Permanent

Laboratory Lead Analyst

The Laboratory Lead Analyst role involves supporting the Ware manufacturing site’s laboratories by providing expert analytical services, troubleshooting, and ensuring compliance with GMP and EHS regulations. Responsibilities include overseeing batch testing, verifying data accuracy, and collaborating with cross-functional teams to drive continuous improvement initiatives.

GSK East Hertfordshire, United Kingdom

On-site Permanent

NIS P&D Study Delivery Lead, Associate Director

The NIS P&D Study Delivery Lead, Associate Director, is responsible for leading the full lifecycle of clinical studies and trials within the Non-Interventional Study (NIS) portfolio. This includes designing, executing, and reporting complex regulatory commitment studies, managing team members, and ensuring compliance with regulatory guidelines. The role also involves leading operational decision-making, risk management, and driving innovation in study delivery through new technologies.

GSK Stevenage, United Kingdom £87,000 pa

Hybrid Permanent

NPI Launch Lead

This role leads the logistics and project management for new pharmaceutical and consumer product launches at GSK’s Barnard Castle site, ensuring timely, compliant market rollouts. The NPI Launch Lead coordinates cross-functional teams, manages launch timelines across global markets, and ensures adherence to GMP, quality, and regulatory standards throughout the product introduction lifecycle.

GSK Barnard Castle, United Kingdom

Hybrid Permanent