Latest IT Recruitment Jobs

MSAT Drug Product Lead (Parenteral Products)

This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include leading New Product Introduction (NPI), technology transfers, process verification, and regulatory compliance. The position requires strong technical expertise, collaboration across functions, and a focus on quality and patient safety.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

CMC Leader (Director)

Leads end-to-end CMC strategy and execution for a pharmaceutical product from early development through commercialisation, including process development, regulatory filings, and lifecycle planning. Coordinates cross-functional global teams across R&D, supply chain, and regulatory to deliver clinical and commercial supply, ensuring technical transfer, quality compliance, and launch readiness. Focuses on complex modalities such as small molecules and oligonucleotides, with strong emphasis on regulatory strategy, risk management, and transition to commercial operations.

GSK Stevenage, United Kingdom

Hybrid Permanent

Director, AI for Cell Therapy Clinical Development

This role involves bridging clinical cell therapy expertise with AI innovation, translating unmet medical needs into high-impact AI solutions for clinical development. The Director will shape scientific questions, guide AI solution design and validation, and drive adoption across AstraZeneca’s cell therapy portfolio. Working at the intersection of clinical science and machine learning, the role emphasizes evidence generation, stakeholder engagement, and strategic roadmap development in a fast-evolving field.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Senior Research Scientist - Biologics Engineering - Protein Engineering and Novel Modalities - Novel Modalities R&I

This role involves designing and characterising innovative biologics, particularly multivalent and multi-specific formats and inhaled delivery. You will lead in silico design, integrate wet-lab data, and collaborate with ML scientists and experimentalists to translate digital concepts into validated molecules, accelerating the discovery pipeline.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development will lead clinical research activities, develop and execute oncology clinical trials, and engage with key external experts. Responsibilities include protocol development, medical monitoring, safety data review, and collaborating with various stakeholders to advance GSK’s clinical portfolio.

GSK

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities to advance GSK’s oncology portfolio. Key responsibilities include developing and executing phase 1-3 clinical trials, collaborating with cross-functional teams, and engaging with key external experts to ensure the successful development and regulatory approval of innovative oncology treatments.

GSK United States

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology portfolio, focusing on advancing the development of antibody drug conjugates (ADCs) for solid tumors. Key responsibilities include collaborating with multidisciplinary teams to design and execute clinical trials, ensuring high-quality protocol development, and engaging with key external experts to drive data generation and regulatory approvals.

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

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