Future Tech Jobs
Future Tech Jobs
This role involves developing and delivering robust regulatory strategies for oncology products, collaborating with cross-functional teams, and ensuring compliance with global regulatory requirements. The position also focuses on process improvement and innovation in regulatory affairs.
This role involves leading the setup, stabilization, and scaling of end-to-end translational data pathways, ensuring biomarker datasets are reusable and accessible. Key responsibilities include resolving systemic barriers, aligning data delivery with decision timelines, and developing repeatable processes for data re-use across multiple functions.
The Staff Platform Engineer, AI/ML Infrastructure will lead the technical strategy for cloud platforms and AI/ML infrastructure, focusing on reliability, scalability, and security. Key responsibilities include architecting and operating scalable cloud platforms using AWS services, defining reusable infrastructure patterns, and mentoring engineers to improve deployment reliability and operational maturity.
The Staff Platform Engineer, AI/ML Infrastructure will lead the technical strategy for cloud platforms and AI/ML infrastructure, focusing on reliability, scalability, and security. Key responsibilities include architecting and operating scalable cloud platforms using AWS services, defining reusable infrastructure patterns, and improving CI/CD and observability practices.
The Regulatory Affairs Assistant will provide administrative, operational, and compliance support to the Regulatory Affairs team, ensuring accurate data and documentation, supporting team processes, and maintaining compliance with regulatory standards. The role involves a broad range of activities, including regulatory file compilation, database management, project coordination, and administrative support to the Head of Regulatory and the team.
This role involves leading the execution of OT strategy across AstraZeneca's global manufacturing network, ensuring alignment with business priorities and improving reliability, safety, and compliance. Key responsibilities include lifecycle management, risk mitigation, capability building, and regulatory readiness.
Lead and manage pharmaceutical manufacturing operations, ensuring compliance with GMP and regulatory standards while driving safety, quality, and continuous improvement. Oversee production scheduling, KPIs, and cross-functional collaboration with engineering, quality, and supply chain teams. Implement Lean Manufacturing principles and operational efficiencies within a growing, regulated environment.
Operations Manager - PharmaceuticalsI am currently recruiting for an Operations Manager to work within the pharmaceutical industry, for a niche, yet established product, this is a great opportunity for a Production Manager to work standard hours and develop their skillset...
Leads pharmaceutical production operations, ensuring safety, quality, and regulatory compliance while driving continuous improvement through Lean Manufacturing. Oversees large manufacturing teams and collaborates with cross-functional departments to enhance site-wide performance. Focuses on operational excellence and strategic development within a regulated GMP environment.
This role involves leading cross-functional teams in reviewing safety data, mentoring junior staff, and ensuring compliance with GxP guidelines and international regulations. The position also focuses on managing pharmacovigilance procedures, conducting impact assessments of new legislation, and supporting regulatory inspections and audits.
This role involves project managing and tracking the ClinTech roadmap, working closely with Clinical Development Operations and Decision Science to translate priorities into actionable plans. You will also support the communication of ClinTech’s progress to senior leadership and external audiences, contributing to vendor assessments and build-vs-buy evaluations. The role is at the heart of a high-visibility team building a platform to accelerate drug development.
Senior Product ManagerUK Remote FirstSalary up to £105,000This is a high impact Senior Product Manager role where you will shape and elevate a growing product function at the heart of life sciences innovation. You will own the product direction end...
The Global Asset Study Manager (GASM) at Roche/Genentech is responsible for the efficient execution of global clinical trials, ensuring consistency and compliance with IHC-GCP and Roche processes. Key responsibilities include coordinating study management, developing essential documents, driving innovation, and maintaining inspection readiness.
This role involves managing and nurturing strategic scientific and business partnerships in a cutting-edge AI-driven drug discovery environment. The Senior Alliance Manager will oversee alliance governance, align internal and external teams, and ensure successful delivery of collaborative research and development programs. The position plays a key role in scaling operational frameworks and fostering a collaborative culture across high-impact partnerships.
This role involves managing the non-clinical aspects of IND submissions, including CMC, DMPK, pharmacology, and tox reporting. You will create and maintain detailed project plans, manage data and document workflows, and coordinate cross-functional teams to ensure regulatory compliance and successful submission.
