Future Tech Jobs
Future Tech Jobs
This role involves providing medical leadership within GSK's oncology clinical development team, focusing on genitourinary (GU) cancers. The Medical Director will lead medical monitoring, ensure patient safety, interpret clinical data, and contribute to study design and regulatory submissions. Working closely with cross-functional teams, the role integrates physician-level insight into clinical strategy and drug development execution.
Lead scientific input into oncology clinical trial design, data interpretation, and regulatory documentation within a global pharmaceutical environment. Contribute to study-level execution and strategic insights while collaborating across multidisciplinary teams. Focus on advancing cancer therapies with high unmet need through rigorous clinical science and cross-functional partnership.
Install, maintain, and repair advanced medical diagnostic systems in NHS and private laboratory settings, providing on-site technical support and troubleshooting. Work independently to resolve complex breakdowns and ensure minimal downtime for critical healthcare equipment. Receive full product training and benefit from a structured career path within a global leader in medical technology.
This role involves servicing and repairing advanced medical diagnostic systems used in NHS and private laboratories. The engineer will conduct on-site maintenance, troubleshoot technical issues, and provide expert support to laboratory staff. Full product training is provided, with a strong emphasis on customer service and technical problem-solving in clinical environments.
Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...
This role leads the global quality and compliance function for pharmacovigilance (PV) systems, ensuring adherence to international regulations and internal standards across clinical safety, regulatory affairs, and medical affairs. The position combines strategic oversight with hands-on operational leadership, including audit strategy, inspection readiness, deviation and CAPA management, and cross-functional GxP guidance. It requires deep technical expertise in PV processes and strong leadership to drive quality across global teams and third-party vendors.
This role involves providing Quality Assurance leadership on the night shift for aseptic manufacturing and packaging operations, ensuring compliance with GMP and internal standards. The specialist will oversee cleanroom practices, manage deviations and change controls, support product release, and coach manufacturing staff on cGMP and contamination control. It plays a critical part in maintaining regulatory compliance and patient safety within a lean, science-driven environment.
Operate production equipment for mRNA vaccines in compliance with cGMP and safety standards, perform routine maintenance, troubleshoot technical issues, and contribute to continuous improvement initiatives in a fast-paced, highly regulated manufacturing environment.
This role involves operating and monitoring advanced production equipment for mRNA vaccine manufacturing in compliance with cGMP and safety standards. The Manufacturing Associate will maintain clean, compliant environments, execute production processes, perform equipment maintenance, and contribute to continuous improvement initiatives within a highly regulated, digital-first environment. Collaboration with QA and cross-functional teams is essential to ensure batch quality and operational excellence.
The role involves leading and supporting global real-world evidence and epidemiological studies across Pfizer's Internal Medicine portfolio. The candidate will design and deliver high-quality research, synthesize literature, and generate actionable insights from observational data to inform medical strategy and regulatory submissions. They will collaborate with cross-functional teams, develop external partnerships, and contribute to scientific communications and departmental initiatives.
This role involves leading real-world evidence and epidemiological research to support Pfizer's Internal Medicine portfolio. The individual will design and conduct global studies, synthesize literature, and generate insights from observational data to inform medical strategy and regulatory submissions. Collaboration with cross-functional teams and external partners is central, along with authoring scientific outputs and advancing the use of AI in research.
Lead clinical pharmacology and pharmacometrics strategy across rare disease and oncology programs, designing studies and supporting regulatory submissions. Oversee modeling and simulation to inform dose selection and development decisions, working closely with cross-functional teams in a TechBio environment powered by AI-driven drug discovery. Serve as the primary expert in regulatory interactions related to clinical pharmacology.
Lead clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs, designing studies and guiding regulatory submissions. Oversee modeling and simulation to inform dose selection and accelerate drug development. Collaborate across translational, clinical, and preclinical teams in a tech-driven biopharma environment.
Lead end-to-end manufacturing, logistics, and warehouse operations within a regulated life sciences environment, driving performance in safety, quality, delivery, and cost. Champion lean principles and continuous improvement while developing teams and supporting new product introductions and site expansion initiatives.
Role: Pharmaceutical Legal CounselLocation: Welwyn Garden City / Hybrid (3 days per week in the office)Hours: Full-timePay: £450 - £580 (PAYE) per day or £595.96 - £768.13 (UMB) per dayContract: 12-month contract, inside IR35Start Date: 7th September 2026, subject to...
