Biotechnology Jobs

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

Engineering Technician (6-month Secondment / Fixed-Term

The Engineering Technician role involves providing technical support for the Dermatologicals Filling and Packaging function, including equipment maintenance, GMP compliance, and continuous improvement initiatives. The position operates on a 16/5 shift rota and is a 6-month fixed-term contract.

GSK Barnard Castle, United Kingdom

On-site Contract Shift-work

Senior Director, Global Clinical Program Lead, Immunoglobulin

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...

CSL

Head, PV and Regulatory QA

TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...

CSL

Process Engineer - Drug Substance Manufacture (DSM)

This role involves optimizing chemical manufacturing processes for drug substances in a regulated pharmaceutical environment. The engineer will lead process improvements, scale-up projects, and technology transfers while ensuring compliance with safety, quality, and environmental standards. Work includes root-cause analysis, change control management, and cross-functional collaboration to enhance capacity, robustness, and efficiency in API production.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Senior Scientist (Synthetic Chemistry)

This role involves designing and synthesizing complex small molecules for Antibody-Drug Conjugates (ADCs) within a multidisciplinary oncology research team. The scientist will develop novel payloads and linker-payload architectures using advanced organic synthesis techniques, supporting early drug discovery. Emphasis is on lab-based innovation, data sharing, and contributing to high-impact therapeutic development in cancer.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading scientific strategy and execution for immunogenicity and ligand binding assay (LBA) bioanalysis within Moderna’s mRNA-LNP therapeutic development programs. The Principal Scientist will oversee regulated assay development, validation, and sample testing, ensuring compliance with GcLP, GLP, and regulatory standards. The position emphasizes cross-functional collaboration, data interpretation, and integration of emerging technologies, including AI-enabled analytics, to support clinical decision-making across the drug development lifecycle.

Moderna

Hybrid Permanent

Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves generating and analyzing high-parameter flow cytometry data from clinical trial samples to support immunology research in a GCLP-compliant environment. The scientist will operate advanced spectral flow platforms like the Cytek Aurora, perform ex vivo immune functional assays, and ensure data integrity through rigorous documentation and compliance. Emphasis is placed on innovation through AI-enabled tools, assay development, and mentoring within a collaborative, regulated laboratory setting.

Moderna

Hybrid Permanent

Disease Level Partner - South Central UK

The Disease Level Partner (DLP) is responsible for implementing Roche's strategy and objectives within therapy areas, focusing on patient outcomes. Key responsibilities include deep customer engagement, gathering actionable insights, and driving positive customer experiences. The role involves leveraging resources to secure access for key customers and contributing to the development of local and national brand advocates.

Roche United Kingdom

On-site Permanent

Field Service Engineer - Stoke-on-Trent to Wrexham

As a Field Service Engineer, you will provide essential electro-mechanical support for Roche’s diagnostic systems, ensuring maximum uptime and operational efficiency. You will perform troubleshooting, preventive maintenance, and customer training, working across Stoke-on-Trent, Wrexham, and surrounding areas.

Roche

On-site Permanent

Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development for oncology, specifically genitourinary (GU) cancers, within GSK’s global portfolio. The Senior Medical Director will design and execute Phase 1–3 trials, provide medical oversight, interpret clinical data, and collaborate with internal teams and external experts to support regulatory submissions and product lifecycle management. The position requires deep expertise in GU oncology and strong leadership in a matrixed, science-driven environment.

GSK US$284,250 – US$473,750 pa

On-site Permanent

Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development for genitourinary (GU) oncology programs within GSK’s pipeline, with responsibility for designing and executing phase 1–3 trials, ensuring scientific integrity, and supporting regulatory submissions. The Senior Medical Director will collaborate across functions and represent GSK externally with key experts and at medical meetings, driving data generation and strategic input for innovative oncology therapies.

GSK £284,250 – £473,750 pa

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology antibody drug conjugate (ADC) portfolio, focusing on advancing the development of clinical trials from early to late stages. Key responsibilities include protocol development, medical monitoring, safety data review, and collaboration with a multi-disciplinary team of experts to ensure the scientific integrity and timely delivery of clinical trials.

GSK

Hybrid Permanent

Translational Science Lead

Job Title: Translational Science LeadLocation CambridgeSalary: competitiveIntroduction to role:Are you ready to turn human biology into decisive clinical evidence that advances medicines for people living with respiratory disease? Based in Cambridge, you will lead end-to-end translational strategies that move confident...

AstraZeneca Cambridge, United Kingdom