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.
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 deliver customer support for complex laboratory analysers. Full product training is provided, with a focus on pathology and clinical chemistry equipment.
This role involves installing, maintaining, and repairing advanced medical diagnostic systems used in NHS and private pathology laboratories. The engineer will provide on-site technical support, troubleshoot complex issues, and ensure equipment operates reliably. Full product training is provided, and the role offers extensive customer interaction across healthcare and scientific environments.
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 scientific literature, and generate insights from real-world data to inform medical strategy and regulatory submissions. They will collaborate across functions, develop external partnerships, and contribute to scientific communications and departmental initiatives.
Leads the strategic direction and AI-driven innovation of Pfizer’s Targets and Mechanisms platforms, overseeing global teams to deliver scalable, data-centric solutions that accelerate drug discovery. Integrates advanced technologies like AI, predictive analytics, and omics data to support target identification and translational research across therapeutic areas. Focuses on building interoperable digital ecosystems and embedding AI into core R&D workflows.
Lead and shape trade compliance strategy across EMEA, ensuring seamless cross-border movement of medicines through robust customs and regulatory frameworks. Drive digital transformation in trade operations using tools like SAP GTS and AI-enabled solutions, while collaborating with cross-functional teams to optimize compliance, reduce costs, and enhance operational agility. Serve as a key liaison with customs authorities and internal stakeholders to maintain regulatory readiness and operational excellence.
Lead the development and execution of CMC regulatory strategies for small molecule drugs in global clinical trials and marketing applications. Author and manage high-quality submissions including INDs, NDAs, and IMPDs across US, EU, and ROW regions. Provide strategic guidance on regulatory requirements, support clinical trial materials, and ensure compliance with evolving GMP standards.
Provide high-level executive support to the CEO of a clinical-stage TechBio company, managing a complex calendar, international travel, and communications while serving as a key liaison across global teams and stakeholders. Enable strategic priorities through proactive coordination of board meetings, investor events, and cross-functional initiatives in a fast-paced biotechnology environment. Operate with discretion and precision in a mission-driven organization focused on accelerating drug discovery through AI and industrialized biology.
This role involves ensuring pharmaceutical products are manufactured and released in compliance with GMP standards, managing quality systems such as deviations, CAPAs, and change controls, and supporting audits and supplier qualification. The Quality Assurance Officer will work closely with Production, QC, and other departments to maintain and improve the Quality Management System. It offers broad exposure to QA processes within a growing specialist manufacturer of CBD APIs and hemp derivatives.
This role involves leading a small QA team, ensuring compliance with regulatory standards, and overseeing quality systems and validation activities. Responsibilities include report writing, internal and external audits, and driving continuous improvement initiatives.
Operate and assemble single-use pharmaceutical products in a regulated cleanroom environment, following strict SOPs and quality procedures. Perform in-process inspections, documentation, and product testing while adhering to cGMP standards. Support continuous improvement and collaborate with quality and engineering teams to resolve issues.
Production Operative (Pharmaceutical Manufacturing)KentPermanent and Full-time roleIntroductionOur client is a growing pharmaceutical manufacturer supplying Active Pharmaceutical Ingredients (APIs) and specialist products to the pharmaceutical and nutraceutical sectors. Due to continued expansion, they are seeking aProduction Operative to join their manufacturing...
This role involves operating manufacturing equipment and handling raw materials in a GMP-regulated pharmaceutical environment. The candidate will prepare and document batch production processes while ensuring compliance with strict quality, safety, and regulatory standards. It is a hands-on position within a close-knit team focused on producing high-quality APIs and specialist products.
Your new companyA global pharmaceutical and life sciences organisation is seeking an experienced Legal Counsel to join its UK & Ireland legal team on a 12-month contract. Operating at the forefront of healthcare innovation, the business develops and delivers medicines,...
