Future Tech Jobs
Future Tech Jobs
The SERM Scientific Director role involves leading pharmacovigilance and risk management planning, developing safety strategies, and ensuring the scientific soundness of data reviews. The position requires expertise in evaluating safety risks, managing cross-functional teams, and communicating safety issues to senior management.
This role involves leading pharmacovigilance and risk management strategies for GSK's global assets, with a focus on safety evaluation in clinical development and post-marketing settings. The Scientific Director provides expert scientific input into safety governance, drives cross-functional teams, and ensures compliance with global regulatory standards. They play a key role in signal detection, safety surveillance, and shaping long-term clinical strategies to protect patient safety.
As a Senior Engineering Technician, you will provide comprehensive engineering support for the Sterile Value Stream, ensuring all production processes meet business and regulatory requirements. You will lead and supervise the Engineering Technician team, manage equipment breakdowns, and drive continuous improvement initiatives in a shift-based environment.
This role involves performing and managing GMP and compliance audits of Biopharm, Vaccines, and Pharmaceutical facilities. You will evaluate compliance with GMP, policies, and regulatory requirements, and provide subject matter expertise on sterile manufacturing. The role requires strong communication and influencing skills, and involves travel to various sites across the network.
This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across the EMEA region. You will evaluate compliance with GMP, regulatory requirements, and quality management systems, and provide subject matter expertise in sterile manufacturing. The role requires strong communication and influencing skills to engage with senior stakeholders and produce clear audit reports.
The Audit Senior Lead role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities. Responsibilities include evaluating compliance, conducting various types of audits, and producing clear audit reports to inform senior management of risks and corrective actions.
The role involves applying expertise in -omics and imaging, using state-of-the-art computational methods to support drug discovery and development, particularly in Hepatology. Responsibilities include generating and evaluating genomic and histopathology imaging evidence, collaborating with multi-disciplinary teams, and communicating results to peers and leaders.
The Principal Scientist role involves leading target discovery and early biologics programs, specifically focusing on antibody drug conjugates (ADCs) and T cell engaging bispecific antibodies (TCEs). You will collaborate with internal and external teams to accelerate the development of next-generation biologics for cancer therapy, contributing to the preclinical development of novel biologics.
This role involves leveraging cutting-edge computational approaches to understand and treat cancer. You will analyze and integrate multi-omics and clinical data to characterize disease heterogeneity, model disease evolution, and investigate treatment response. Collaboration with experimental and clinical teams is key to translating complex data into actionable insights for drug discovery.
The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.
The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects from internal and external donor sites to external Contract Manufacturing Organizations (CMOs). Key responsibilities include managing project schedules, mitigating risks, and ensuring timely delivery within budget, while acting as the main point of contact between GSK and suppliers.
The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.
The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.
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.
Leads clinical operations strategy and delivery across Hepatology, Renal, and Cardiovascular disease portfolios within GSK’s R&D engine. Oversees end-to-end development from early phase through life-cycle management, driving operational excellence, team development, and cross-functional alignment. Champions data-driven decision-making, risk management, and innovation adoption to accelerate high-impact assets.
