This role involves developing and executing the analytical network strategy for GSK's supply chain, ensuring alignment with quality objectives. Responsibilities include defining QC testing principles, driving innovation in QC testing, and collaborating with cross-functional teams to integrate analytical testing into the end-to-end supply chain process.
This role involves developing and executing the analytical network strategy for GSK's supply chain, ensuring alignment with quality objectives. Responsibilities include defining QC testing principles, driving innovation in QC testing, and collaborating with cross-functional teams to integrate analytical testing into the end-to-end supply chain process.
The Trial Vendor Senior Manager is a key member of the Clinical Trial Team, responsible for managing and overseeing clinical trial vendors to ensure study outcomes are met. This role involves direct operational oversight, vendor financial management, and collaboration with cross-functional teams to deliver high-quality clinical trials.
This role involves leading early clinical pharmacology studies from protocol development to finalisation, ensuring high-quality data and informed program decisions. The Senior Clinical Pharmacology Trial Leader will work closely with internal teams, investigators, and CROs, overseeing study execution and risk management.
This role involves servicing, installing, repairing, and calibrating sophisticated medical laboratory automation systems across Europe. You will work with scientific products in various settings, including pathology departments, university research labs, and pharmaceutical environments, requiring extensive travel and overnight stays.
This role involves servicing, installing, repairing, and calibrating sophisticated medical laboratory automation systems across Europe. You will support scientific products in various settings, including pathology departments, university research labs, and pharmaceutical environments, with extensive travel and frequent overnight stays.
Lead clinical pharmacology strategy for small molecule programs in oncology and non-oncology areas, designing and executing studies from Phase 1 through late development. Utilize AI-driven models for PK/PD prediction, dose optimization, and regulatory submissions, while managing CROs and translating preclinical data into human dosing strategies.
Lead the development and execution of nonclinical safety strategies for small molecule drug candidates in oncology and non-oncology programs, integrating AI-driven predictive models with traditional toxicology. Build and scale the nonclinical safety function within an AI-first drug discovery environment, ensuring high-quality data feedback to refine computational models. Collaborate across preclinical, clinical, and regulatory teams to advance compounds through IND and NDA/MAA-enabling studies.
Lead and conduct high-impact research in tumour immunology within a research-intensive academic environment. Contribute to teaching and academic leadership in the School of Medicine, advancing the University's strategic focus on regenerative medicine and advanced therapies. Play a key role in mentoring researchers and shaping future directions in immunological research.
The role involves conducting research on the biological mechanisms of fatigue and post-exertional symptom exacerbation in Long COVID. Responsibilities include participant recruitment, physiological assessments, biological sample collection, and project coordination, working closely with multidisciplinary teams.
This role involves leading all quality and regulatory functions in a growing pharmaceutical company, ensuring GMP compliance, patient safety, and continuous improvement. Responsibilities include managing quality systems, regulatory inspections, and supplier audits, as well as driving a culture of quality and compliance.
This role involves operating and maintaining manufacturing equipment in a clean room environment, following cGMP and quality procedures, and ensuring precise batch documentation. The position requires night shift work and a background in biotechnology or a related field.
This role involves full lifecycle software development and project management for Nuclera's new product platform and support tools. You will also provide technical support for the current generation of the Instrument, manage risks, and ensure quality through planning and execution.
This role involves working on customer-facing cloud and instrument software, as well as internal tools for protein screening. Responsibilities include collaborating with biologists to define requirements, designing technical solutions, and implementing and testing code. The role requires a full-stack software engineer with a product mindset and strong ownership of code.
The Senior R&D Scientist will execute complex experimental workstreams, analyse data, and present findings to stakeholders. They will apply Design for Manufacture (DFM) principles to optimise product formulations and ensure compliance with GLP, GMP, and GDP standards in a laboratory setting.
