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.
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.
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.
Lead clinical operations strategy for Hepatology, Renal, and Cardiovascular disease portfolios, driving end-to-end delivery from early phase through life-cycle management. Oversee a matrix team, align operational execution with R&D goals, and champion data-driven decision-making and innovation in clinical development. Shape culture, manage risks, and ensure inspection readiness across global assets.
This role involves leading statistical strategies for key oncology programs, designing robust clinical trials, and mentoring statisticians. The position emphasizes innovation, regulatory interactions, and cross-functional collaboration to advance the development of new cancer therapies.
Leads global CMC regulatory strategy for small molecule medicines, shaping development and approval pathways across international markets. Works at the intersection of R&D, supply, quality, and commercial functions to ensure regulatory compliance and uninterrupted patient access. Focuses on solving complex regulatory challenges, mentoring talent, and improving processes to support long-term product success.
The Laboratory Analyst supports product testing and analysis within GMP-compliant laboratories at GSK’s Ware site, ensuring safe and effective oral and solid dose medicines are produced. The role involves sample preparation, analytical testing using methodologies like HPLC, and maintaining compliance with safety and quality standards. Collaboration with cross-functional teams is key to maintaining supply and driving continuous improvement in a fast-paced manufacturing environment.
This role involves providing hands-on engineering support within a sterile pharmaceutical manufacturing environment, focusing on maintenance, compliance, and continuous improvement of production systems. The technician will work across complex equipment and processes, ensuring GMP standards, managing SAP systems, and supporting projects such as new product introductions. Key responsibilities include breakdown repairs, PPM activities, calibration, and supervision of contractors in a regulated, shift-based operation.
This role involves providing advanced statistical expertise to support oncology clinical development across all phases, from early-stage trials to late-phase studies. The Senior Principal Statistician will lead the design and analysis of clinical trials using innovative methodologies such as Bayesian statistics and simulation techniques, working closely with cross-functional teams. The position emphasizes methodological innovation, risk assessment, and decision-making support within a global biopharma environment.
This role involves providing expert process safety leadership at GSK’s Barnard Castle manufacturing site, ensuring compliance with EHS regulations and delivering process safety improvements. The engineer will lead hazard assessments, support incident investigations, and drive safe working practices across production operations, with a strong focus on regulatory standards like DSEAR and CDM. The position plays a key part in maintaining safety integrity within a high-value, regulated pharmaceutical environment.
Leads oncology business development and external innovation scouting within GSK's R&D organization, driving technical evaluation and due diligence of potential assets. Responsible for building strategic investment cases, engaging with biotech partners, and advising senior leadership on high-impact opportunities. Works cross-functionally to advance oncology portfolio growth through licensing and partnerships.
