Latest IT Recruitment Jobs

Specialist - Extractables and Leachable - MSAT EM

This role involves working with internal and external labs to ensure E&L testing is completed scientifically and compliantly. Responsibilities include conducting risk assessments, delivering technical information, and managing risk escalation for biopharmaceutical manufacturing processes and packaging systems.

GSK £70,650 – £117,750 pa

On-site Permanent

Therapy Supply Chain Manager

Leads end-to-end supply planning and execution for a designated therapy area, ensuring uninterrupted patient access to medicines. Works cross-functionally across planning, manufacturing, quality, and commercial teams to resolve supply disruptions, drive inventory optimisation, and implement continuous improvement initiatives using data analysis and planning systems. Focuses on risk mitigation, regulatory compliance, and performance monitoring within a global pharmaceutical supply chain.

GSK United Kingdom

Hybrid Temporary

Executive Director, Oncology Global Programme Management (TDR / DDR / Epigenetics)

This role involves leading and influencing strategic decisions in AstraZeneca's Oncology Global Programme Management, focusing on TDR, DDR, and Epigenetics. You will guide comprehensive programme strategies, connect various stages of drug development, and ensure optimal portfolio delivery.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Associate Director Integrated Bioanalysis – Biopharma Bioanalytical Program Lead

This role involves leading the bioanalytical strategy for diverse therapeutic modalities, collaborating with global project teams to develop robust assays, and translating complex data into clear program decisions. The position is highly visible, requiring cross-functional influence and external representation of scientific findings.

AstraZeneca Cambridge, United Kingdom

On-site 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

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

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

SLDC Coordinator (Site Launch and Data Control) - 12-month / Secondment

This role involves managing the creation and changes of packaging for new and existing products within GSK’s supply chain, using systems like SAP, GLAMS, and CHAMPS. The coordinator ensures compliance with GMP and EHS standards while working across functions such as Quality, Regulatory, Procurement, and Logistics to maintain supply security. The position supports new product launches and pack amendments, drives process improvements, and maintains data integrity across site master records.

GSK Barnard Castle, United Kingdom

On-site Contract

Senior Engineering Technician /Secondment

This role involves providing hands-on engineering leadership to support the introduction and scale-up of new pharmaceutical products within a regulated manufacturing environment. The technician will ensure equipment and processes meet safety, compliance, and reliability standards, lead technical issue resolution, and coordinate engineering activities across teams during product launches and validation. Emphasis is placed on operational readiness, change control, and continuous improvement in a GMP-compliant setting.

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

Associate Director, Diagnostic Planning Lead - Oncology

Leads diagnostic planning activities within oncology translational medicine, coordinating cross-functional teams and external partners to advance diagnostic development programs. Oversees project timelines, regulatory documentation, budget management, and strategic alignment, with a focus on biomarker technologies and IVD development in support of oncology assets.

GSK Stevenage, United Kingdom US$151,500 – US$252,500 pa

Hybrid Permanent

Associate Director, Diagnostic Planning Lead - Oncology

This role involves leading diagnostic planning for oncology projects within GSK’s Translational Medicine team, coordinating cross-functional activities across clinical development, regulatory, and external partners. The Associate Director will manage timelines, budgets, and deliverables for diagnostic development programs, ensuring alignment with biomarker strategies and regulatory requirements. The position plays a key strategic role in advancing oncology assets through integrated project management and collaboration with diagnostics manufacturers and internal stakeholders.

GSK London, United Kingdom US$151,500 – US$252,500 pa

Hybrid Permanent

Quality Manager (on Shift)

The Quality Manager on Shift ensures compliance with GMP and regulatory requirements during manufacturing and non-manufacturing activities. Key responsibilities include monitoring quality systems, investigating deviations, and supporting product release. The role involves working in a 24/5 shift pattern, including weekends, and promoting team collaboration and continuous improvement.

GSK East Hertfordshire, United Kingdom

On-site Permanent Shift-work

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

Protein Engineering and Innovation Scientist

This role involves leading the development and deployment of advanced in-silico protein engineering and design principles to generate complex reagents for drug discovery. You will collaborate with computational experts, protein expression teams, and external partners to design, generate, and test engineered proteins, contributing to scientific innovation and project delivery.

GSK Stevenage, United Kingdom

Hybrid Permanent