Latest Recruitment Jobs

Associate Director, Safety Epidemiology – Global Patient Safety

Lead the design and execution of post-authorisation safety studies using real-world data to assess and communicate the safety profiles of AstraZeneca’s medicines. Provide strategic epidemiological input to regulatory submissions, safety signal evaluations, and diversity initiatives, collaborating with internal teams and external partners. Drive methodological excellence in pharmacoepidemiology and contribute to global patient safety decision-making across a broad product portfolio.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Associate Process Leader (Trainee Manager) – Sterile Production

This role involves supporting sterile manufacturing operations within a cGMP environment, focusing on production planning, compliance, and continuous improvement. The candidate will gain experience in deviation management, root-cause analysis, and cross-functional collaboration with Quality, Engineering, and Operations teams. Emphasis is placed on developing leadership skills and contributing to a culture of safety, efficiency, and manufacturing excellence.

AstraZeneca Macclesfield, United Kingdom

QA Associate

The role involves supporting the quality assurance of autologous CAR T-cell therapies in a GMP-compliant environment, with responsibilities including batch record review, documentation control, label verification, and compliance risk identification. The position operates within a multi-product cell and gene therapy facility, contributing to batch release activities and inspection readiness across international markets. Work includes collaboration with internal teams and adherence to strict regulatory and safety standards.

Autolus Stevenage, United Kingdom

On-site Permanent

Associate Director of Clinical Sciences

Lead clinical sciences strategy and execution for global oncology studies, with responsibility for end-to-end protocol development, clinical data review, and cross-functional collaboration. Focus on immuno-oncology with strong emphasis on regulatory compliance, patient safety, and scientific leadership across clinical development phases. Work within a matrix environment to guide study design, interpretation, and regulatory submissions.

GSK Stevenage, United Kingdom

Platform Equipment Lead (Metrology)

This role involves leading metrology and calibration systems at GSK’s Ware site, ensuring compliance with GMP and engineering standards. You’ll oversee calibration services, lead technical investigations, improve measurement systems, and support capital projects using data-driven insights. The position offers technical leadership, cross-functional collaboration, and strategic impact within a regulated pharmaceutical manufacturing environment.

GSK East Hertfordshire, United Kingdom

Executive Director, Asset Strategy Leadership

Leads strategic positioning of clinical assets in oncology and immunology, leveraging AI-driven insights from the Recursion OS to inform go/no-go decisions, competitive differentiation, and portfolio prioritization. Works cross-functionally with clinical, platform, and business development teams to align resource allocation and advance transformative medicines. Focuses on integrating mechanistic, biomarker, and market data to build compelling narratives for internal and external stakeholders.

Recursion North Tyneside, NE29 8EP, United Kingdom £297,000 – £356,400 pa

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

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

Software Engineer

Build and maintain scalable AI systems that integrate large language models with biomedical research tools, focusing on agent development, data workflows, and deployment within a multidisciplinary environment. Work on real-time, interactive systems that empower researchers through robust backend engineering and AI integration.

Owkin Paris, France

Remote Permanent

Manager, Oncology Regulatory Strategy

This role involves leading and implementing regional regulatory strategies for oncology products in the Rest of World (ROW) region, ensuring alignment with global objectives and commercial goals. The individual will represent the region on the Global Regulatory Strategic Team, manage submissions and approvals, and shape interactions with health authorities. A key focus is ensuring compliance while influencing the regulatory environment to accelerate patient access to medicines.

Pfizer Marlow, United Kingdom

Manager, Oncology Regulatory Strategy

Leads regional regulatory strategy for oncology products across the Rest of World (ROW), ensuring alignment with global objectives and timely submissions to health authorities. Works closely with cross-functional teams and external agencies to shape regulatory pathways, influence policy, and secure commercially viable labeling. Focuses on compliance, risk mitigation, and strategic engagement in a dynamic regulatory environment.

Pfizer Sandwich, United Kingdom

Medical Safety Lead - CRM

The role involves monitoring clinical safety data, conducting medical assessments of adverse events, and identifying safety signals using both individual and aggregate data. The Medical Safety Lead will apply AI-enabled tools to enhance pharmacovigilance processes and provide critical medical input into regulatory submissions and safety documentation. Collaboration with global cross-functional teams is central to integrating safety insights across drug development programs.

Novartis London, United Kingdom £67,900 – £126,100 pa

Director, Biopharma Data Science

Lead the development of an AI scientist platform for drug discovery, combining multimodal biological data and agentic AI to automate target identification and hypothesis generation. Guide a team of data and research scientists in building systems that reason over omics, clinical, and literature data to accelerate pharmaceutical R&D. Work at the intersection of machine learning, computational biology, and pharmaceutical strategy.

Owkin France

Remote Permanent

Technical Service Engineer

This role involves providing on-site and remote technical support for advanced robotics systems used in pharmaceutical and biotech environments. The engineer will perform preventative maintenance, diagnose and resolve technical issues, manage spare parts forecasting, and act as a subject matter expert for customers. With extensive training provided, the role emphasizes customer collaboration, problem-solving, and use of D365 and KPI reporting tools across a rotating 24/7 on-call schedule.

Wallace Hind Selection Marston, Cheshire West And Chester, Cheshire, United Kingdom £52,000 – £56,000 pa

Technical Service Engineer

This role involves providing on-site and remote technical support for advanced robotics systems used in pharmaceutical and biotech environments. The engineer will perform preventative maintenance, diagnose and resolve technical issues, manage spare parts forecasting, and act as a customer-facing subject matter expert. The position includes 24/7 on-call responsibilities and extensive training on proprietary systems, with a strong focus on customer satisfaction and cross-functional collaboration.

Wallace Hind Selection Oldham, Manchester, United Kingdom £52,000 – £56,000 pa