Future Tech Jobs
Future Tech Jobs
This role involves leading pharmacovigilance and risk management for GSK's global assets, ensuring scientifically sound review and interpretation of safety data. The director will develop and execute safety strategies, manage safety governance, and lead cross-functional teams to address product safety issues and ensure patient safety globally.
This role involves applying advanced statistical and computational methods to large-scale genetic, genomic, and clinical datasets to drive insights in drug discovery and development. The scientist will work across therapeutic areas to interpret causal disease mechanisms, support target and biomarker identification, and enable precision medicine strategies within a collaborative, multidisciplinary R&D environment.
The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for GSK's oncology portfolio, focusing on hematological malignancies. Key responsibilities include collaborating with multidisciplinary teams, ensuring patient safety, and contributing to regulatory submissions and publications.
The Quality Validation and CSV Manager will lead a team responsible for ensuring all validation activities, including process, cleaning, facility, and computer systems validation, comply with regulatory requirements and GSK quality standards. The role involves managing validation protocols, collaborating with cross-functional teams, and providing technical expertise and training.
This role leads the development and execution of precision diagnostics strategies for oncology programs, integrating biomarker and assay development across clinical trials. The position involves cross-functional leadership to align diagnostic solutions with therapeutic assets, manage regulatory requirements, and partner with external diagnostic companies and labs. It focuses on advancing patient-centric innovation by ensuring the right therapies reach the right patients through robust diagnostic frameworks.
Develops and executes internal communications strategies to support organizational change and strategic priorities at a global biopharma company. Works closely with senior leaders to craft messaging, drive employee engagement, and manage change through compelling content and data-driven insights. Focuses on building confidence during transformation using storytelling, AI, and cross-functional collaboration.
GSK Oncology is committed to discovering and developing new therapies with the potential to change the lives of patients with cancer. The Oncology Clinical Development Statistics group is seeking exceptionally talented Statisticians to provide end-to-end statistical leadership across oncology evidence...
The Engineering Technician role involves providing comprehensive engineering support for the Steriles Business Unit, focusing on equipment maintenance, GMP compliance, and continuous improvement initiatives. Responsibilities include breakdown repairs, calibration, quality documentation, and project support, all while maintaining high safety and regulatory standards.
This role involves leading the RTSM function, partnering with clinical development, operations, quality, and external vendors to design and deliver patient-focused randomization and clinical supply solutions. Responsibilities include managing cross-functional teams, ensuring on-time randomization and supply availability, and improving RTSM processes and governance.
This senior role involves leading business development and transactions in biomarker and diagnostics for GSK's Oncology R&D. Responsibilities include negotiating deals, aligning with R&D strategy, and collaborating with internal and external stakeholders to drive strategic alliances and complex collaborations.
This role involves leading Extractables and Leachables (E&L) assessments for biopharmaceutical manufacturing processes, container closure systems, and dosing devices. The Specialist will work with internal and external labs to ensure E&L testing is completed scientifically, compliantly, and cost-effectively, while also managing risk identification and escalation.
The RTSM Project Manager is responsible for the design, development, testing, and maintenance of clinical studies using the RAMOS IRT system. Key responsibilities include ensuring data integrity, configuring complex study designs, and driving continuous improvements in clinical supplies systems. The role involves technical oversight, problem-solving, and collaboration with cross-functional teams to enhance IRT processes and support clinical development.
The Laboratory Lead Analyst role involves supporting the Ware manufacturing site’s laboratories by providing expert analytical services, troubleshooting, and ensuring compliance with GMP and EHS regulations. Responsibilities include overseeing batch testing, verifying data accuracy, and collaborating with cross-functional teams to drive continuous improvement initiatives.
This role involves ensuring regulatory compliance for pharmaceutical manufacturing by interpreting cGMP, QMS, and pharmacopoeial standards. The specialist supports product lifecycle changes, leads NPI submissions, maintains quality specifications, and acts as the site's regulatory liaison, handling audits and compliance deviations across a high-volume production environment.
The Senior Scientist will work within the ETCT Biology Unit, contributing to pre-clinical and early clinical biologics programs. Responsibilities include designing and executing experiments, providing input on pharmacokinetics and non-clinical safety, and mentoring junior scientists.
