Biotechnology Jobs

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategy for GSK's global assets, with a focus on safety evaluation in immunology and other therapeutic areas. The Scientific Director will lead safety governance, contribute to regulatory submissions, and manage cross-functional teams to address product safety issues. They will also represent GSK in interactions with regulatory authorities and ensure compliance with global pharmacovigilance standards.

GSK £169,950 – £283,250 pa

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK's global assets, with a focus on safety evaluation in immunology and other therapeutic areas. The Scientific Director will oversee safety governance, lead cross-functional teams, and ensure compliance with global regulations. They will analyze clinical data, manage safety issues, and contribute to regulatory submissions and long-term clinical strategy.

GSK US$169,950 – US$283,250 pa

On-site Permanent

Case Management Intake Manager

Oversees the vendor responsible for logging and triaging global adverse event reports in CSL's pharmacovigilance system, ensuring accurate, timely, and compliant case intake. Develops guidance, provides training, and maintains audit readiness for regulatory compliance. Acts as subject matter expert on intake processes across cross-functional projects and procedural documentation.

CSL United Kingdom

Director, Search & Evaluation Early TA Lead (CVR)

Leads strategic sourcing and evaluation of early-stage (preclinical to Phase 1) external innovation opportunities in the Cardiovascular/Renal therapeutic area. Drives due diligence, shapes partnering strategies, and collaborates with Business Development to execute transactions. Embedded in the Therapeutic Area Leadership Team to align external innovation with portfolio planning.

CSL

Associate Principal Scientist, AI and Computational Tools, Oncology R&D (1-year

This role involves designing and deploying AI-powered tools and computational workflows to accelerate oncology drug discovery, with a focus on immuno-oncology. The scientist will build scalable data infrastructure, develop agentic AI and LLM-integrated solutions, and act as a technical leader across dry-lab and wet-lab teams. The position emphasizes translating complex biological data—such as single-cell and spatial transcriptomics—into reproducible, insight-generating systems while mentoring others in AI adoption and best practices.

AstraZeneca Cambridge, United Kingdom

On-site Contract

Senior Scientist (In vivo Pharmacology & Translational Sciences), Cambridge, MA

Lead translational strategies for oncology and immunology programs by designing in vivo pharmacology and PK/PD studies to validate AI-designed drug candidates. Bridge computational predictions with experimental validation through CRO partnerships and biomarker-driven approaches. Drive preclinical data generation to inform clinical trial design and regulatory filings.

Isomorphic Labs England

Hybrid Permanent

12 Month University Industrial Placement Student (UIPS): Analytical Chemistry

This 12-month industrial placement involves supporting the development of pharmaceutical drugs through analytical chemistry techniques such as HPLC, GC-MS, NMR, and XRPD. You'll work within a collaborative team to deliver analytical data that supports drug development timelines, adhering to GMP and GLP standards while gaining hands-on experience in a regulated environment.

AstraZeneca Cambridge, United Kingdom £28,000 pa

Research Leader (DMPK), Cambridge, MA

Lead DMPK strategy for drug discovery projects using an AI-first approach, integrating quantitative pharmacology and ADME data to guide candidate selection. Collaborate with chemistry, pharmacology, and machine learning teams to optimise molecule design and advance predictive models. Contribute to regulatory documentation and drive innovation in human PK prediction and biotransformation understanding.

Isomorphic Labs Cambridge, United Kingdom

QC Analytical Scientist

The role involves performing analytical testing in a GMP-compliant laboratory environment, including in-process and release testing of drug products using techniques such as ddPCR, flow cytometry, sterility testing, and endotoxin assays. The scientist ensures data integrity, supports method validation and tech transfer, investigates quality events, and maintains laboratory compliance. This is a shift-based position requiring hands-on work with cell-based therapies in a regulated, cleanroom setting.

Autolus Stevenage, United Kingdom

On-site Permanent Shift-work

Senior Engineer, CSV Validation

This role involves end-to-end ownership of computerised system validation (CSV) for GxP-regulated systems used in the manufacturing and testing of advanced CAR-T cell therapies. The engineer will author and execute validation documentation, ensure compliance with international regulations (e.g. FDA 21 CFR Part 11, EU GMP Annex 11), manage change controls and CAPAs, and support regulatory inspections. The position requires strong technical writing, cross-functional collaboration, and expertise in GAMP 5 and data integrity within a biopharmaceutical context.

Autolus Stevenage, United Kingdom

(Fixed Term) Scientist, Immunogenicity, Bioanalytical and Molecular Assays

This role involves designing and executing bioanalytical and immunogenicity strategies to support mRNA-based therapeutic development. The scientist will lead assay development for clinical programmes using platforms like ELISA, MSD, and cell-based methods, ensuring regulatory compliance and robust data generation. The position emphasizes collaboration across multidisciplinary teams and integration of digital tools and AI to advance Moderna's pipeline.

Moderna Oxford, United Kingdom

On-site Contract

Analyst, Quality Control, Microbiology

This role involves performing routine environmental monitoring, water sampling, and microbiological testing (including sterility, bioburden, and endotoxin) for mRNA products in a GMP-regulated manufacturing environment. The analyst will support method transfers, data review, investigations, and compliance activities while working closely with internal teams and contract laboratories. Emphasis is placed on digital workflows, data integrity, and adherence to cGMP standards.

Moderna Oxford, United Kingdom

Director, Regulatory Affairs

Lead global regulatory strategy and execution for drug development programs, ensuring compliance across jurisdictions including the US, EU, and UK. Collaborate with cross-functional teams to prepare and manage regulatory submissions such as INDs, NDAs, and orphan drug designations. Provide strategic guidance on regulatory risks and lifecycle management, while engaging with health authorities and shaping regulatory science in the context of AI-driven drug discovery.

Recursion North Tyneside, NE29 8EP, United Kingdom £207,500 – £280,720 pa

Remote Permanent

Machine Learning Scientist - Quantum Chemistry

This role involves developing machine learning models grounded in quantum chemistry to accelerate small-molecule drug discovery. The scientist will create synthetic datasets using quantum mechanical methods, build scalable and reproducible ML pipelines, and collaborate with computational and experimental teams to model molecular energetics and protein–ligand interactions. Work contributes directly to drug design tools at Roche, with opportunities for scientific publication and open-source contributions.

Roche Welwyn Hatfield, United Kingdom

Hybrid Permanent

Software Engineer

Design and build scalable cloud infrastructure for AI and agentic systems, focusing on model serving, reliability, and efficient deployment across the full software lifecycle. Work closely with ML engineers and scientists to deliver robust, high-performance systems on GCP. Implement CI/CD, monitoring, and cloud-native architectures to support production AI workloads.

Experis London, United Kingdom £750 – £830 pd