The Quality Manager role involves maintaining and improving CSL's quality management systems across Europe and global affiliates. Responsibilities include inspection readiness, process harmonization, and supporting quality initiatives. The role requires collaboration with multiple functions and stakeholders, with a focus on compliance and continuous improvement.
The Quality Manager role involves maintaining and improving CSL's quality management systems across Europe and global affiliates. Responsibilities include coordinating inspection readiness, supporting compliance activities, and implementing global quality initiatives. The role requires strong knowledge of pharmaceutical regulations and quality systems, with a focus on collaboration and process improvement.
This role involves developing, validating, and executing ligand-binding and cell-based assays to support mRNA medicine development. The candidate will generate pharmacodynamic and immunogenicity data in a regulated GcLP environment, manage critical reagent characterization, and contribute to clinical sample testing using Watson LIMS. The position emphasizes scientific rigor, regulatory compliance, and collaboration within a high-performance team advancing novel bioanalytical assays.
This role involves leading and executing phase-appropriate bioanalytical strategies for immunogenicity and ligand binding assays (LBA) within Moderna’s mRNA-LNP therapeutic pipeline. The Principal Scientist will oversee assay development, validation, and sample analysis, ensuring regulatory compliance and scientific rigor across clinical programs. The position emphasizes collaboration with cross-functional teams, integration of emerging technologies including AI-enabled tools, and contribution to regulatory submissions and data interpretation in a GcLP-compliant environment.
This two-year graduate programme at GSK focuses on engineering and manufacturing in the pharmaceutical industry. Participants will work on real manufacturing challenges, manage equipment, implement smart manufacturing technologies, and contribute to sustainability initiatives. The role involves cross-functional projects, rotations, and tailored training to develop technical and leadership skills.
This two-year Supply Chain Graduate Programme at GSK in Barnard Castle focuses on manufacturing and supplying medicines and vaccines. Participants will work on cross-functional projects, gain exposure to external manufacturing, and develop skills in digital data and analytics, sustainability, and project management.
This role involves providing medical and scientific leadership in translational medicine for dermatology programs, spanning early to late-stage drug development. The expert will design and implement strategies for clinical pharmacology, biomarker development, and regulatory submissions, while leading cross-functional teams and supporting in-licensing opportunities. Work includes oversight of clinical studies, publication strategy, and engagement with regulatory and external stakeholders.
This role involves designing and delivering global regulatory strategies for precision diagnostics, including companion diagnostics and in vitro devices, within drug development programs. The individual will lead regulatory submissions across the lifecycle, engage with health authorities, and ensure compliance with global regulations. Collaboration with cross-functional teams and external partners is central to advancing regulatory plans for innovative diagnostics in a hybrid working environment.
This role involves hands-on laboratory work in materials characterisation, supporting the development and manufacture of medicines. You will plan and execute experiments, analyse data, and contribute to live projects, gaining valuable experience in a professional scientific environment.
Product ManagerCambridgeUp to £70,000 + benefitsRole Overview: Product Manager:The company is looking for a technically competent Product Manager to lead global commercial and strategic activities for their range of scientific products used in the food & beverage markets. The role...
Provide on-site service and repair for advanced medical diagnostic systems used in NHS and private laboratories. Troubleshoot complex technical issues and deliver customer-focused solutions in clinical environments. Receive full product training and work with cutting-edge laboratory equipment across a diverse customer base.
Provide on-site service and repair for advanced medical diagnostic systems used in NHS and private laboratories. Perform troubleshooting, maintenance, and technical support across high-value scientific equipment. Receive full product training and work in a customer-facing role engaging with lab managers and technicians.
This role involves pioneering research in synthetic biology, focusing on genome synthesis and genetic isolation to enable safe, scalable biotechnological applications. The postdoctoral fellow will develop novel methods for genome recoding, engineer synthetic genetic codes, and contribute to foundational work in making biology programmable. Work integrates experimental and computational approaches within a multidisciplinary, mission-driven research environment.
This role involves hands-on experience in clinical trial execution, regulatory documentation, and site operations. The candidate will work closely with experienced managers and teams, gaining insights into multiple therapeutic areas and contributing to process improvements.
The Principal Scientist MSAT role involves providing technical leadership in RNA manufacturing, nucleic acid production, and GMP translation. Responsibilities include guiding technology choices, resolving complex challenges, and collaborating with multidisciplinary teams to deliver scalable, commercially relevant solutions.
