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On-site Permanent

Director, QA Manufacturing

This role involves leading and developing the Front Line QA function at Seqirus Liverpool, ensuring pharmaceutical quality across all products. Responsibilities include providing 24/7 QA coverage, overseeing batch review and IT systems, and ensuring compliance with regulatory requirements. The role holder may also act as a QP, certifying and releasing products to market.

CSL

United Kingdom

Hybrid Permanent

Associate Director, Medical Affairs

This role involves shaping medical strategy for immunology products, supporting post-launch lifecycle management, and driving scientific engagement with key opinion leaders and patient groups. The individual will coordinate investigator-led studies, provide scientific input to commercial teams, and support evidence generation across global markets. Collaboration with cross-functional teams and affiliates is central to advancing clinical understanding and therapeutic impact.

CSL

United Kingdom

On-site Permanent

Associate Director, Safety Epidemiology – Global Patient Safety

This role involves leading the design, execution, and reporting of post-authorisation safety studies using real-world data. The candidate will collaborate with various teams to produce high-quality evidence for regulatory decisions and risk management, ensuring AstraZeneca's medicines are safe and effective.

AstraZeneca

Chatham, ME4 4NP, United Kingdom

On-site Permanent

Associate Engineer, GxP IT Support

This role involves providing hands-on IT support for Moderna’s GMP manufacturing operations at the Harwell site. Key responsibilities include ensuring GMP compliance, triaging IT incidents, managing infrastructure, and collaborating with various teams to maintain robust and compliant systems. The position offers exposure to modern observability and cybersecurity tools, making it a dynamic opportunity for someone who thrives in complex, regulated environments.

Moderna

Oxford, United Kingdom

Hybrid Permanent

Associate Director, R&D Project Management

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...

CSL

£189,750 – £316,250 pa On-site Permanent

Director, Oncology Clinical Biomarkers

This role involves developing and implementing biomarker strategies for late-stage oncology clinical trials, collaborating with cross-functional teams to identify patient populations and optimize drug development. The Director will leverage cutting-edge technologies and methodologies to validate biomarkers and inform clinical decisions.

GSK

Stevenage, United Kingdom