Future Tech Jobs
Future Tech Jobs
This role involves leading the global medical strategy for a lung cancer asset, working with cross-functional teams to translate scientific insights into practical patient impact. Responsibilities include chairing a global medical team, managing partnerships with academic centers, and ensuring scientific quality and compliance.
This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, managing product lifecycle activities, and ensuring compliance with GMP standards. The position also involves supporting CMOs in audits, technical transfers, and continuous improvement initiatives.
The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally.
The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally.
The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The AD provides for statistical excellence in clinical development plans, trial planning, data analysis, interpretation and reporting, and regulatory interactions and...
CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an...
This role involves leading the onboarding and continuous improvement of IRT standards and studies for AstraZeneca's clinical trials. Responsibilities include technical documentation, risk assessment, test script development, training, and process optimization. The position requires deep knowledge of R&D supply chain, clinical development processes, and IRT systems, with a focus on delivering high-quality, efficient clinical trial supplies.
This role involves leading a team of operators in a fast-paced, highly regulated sterile manufacturing environment. Responsibilities include managing daily operations, ensuring compliance with cGMP standards, and driving continuous improvement through Lean principles and digital technologies.
Your work will change lives. Including your own.The Impact You’ll MakeAt Recursion, our mission is to industrialize and transform the development of medicines by integrating data-driven insights and advanced analytics throughout the entire development lifecycle. As Executive Director, Asset Project...
Your work will change lives. Including your own.The Impact You’ll MakeAs a key member of Recursion's partnership-facing data science team, you will be at the forefront of reimagining drug discovery from first principles using Recursion’s massive data and compute capabilities....
This role involves leading a small QA team, ensuring compliance with regulatory standards, and overseeing quality systems and validation activities. Responsibilities include report writing, managing QA documentation, participating in audits, and driving continuous improvement initiatives.
The Product Development Scientist will work on the development and improvement of diagnostic products, from feasibility to launch, ensuring compliance with quality standards. Responsibilities include participating in product development phases, troubleshooting issues, and collaborating on technical analysis and material testing.
The Chief Technology Officer will lead the technology and product development strategy for a rapidly growing MedTech company. Key responsibilities include guiding multidisciplinary teams, translating customer and commercial requirements into product priorities, and ensuring regulatory compliance. The role involves close collaboration with executive leadership and external stakeholders.
This role involves architecting and implementing a lean, scalable Quality Management System (QMS) for a fast-paced, advanced manufacturing company. The QMS Architect will create compliance frameworks that accelerate delivery, coordinate with external regulatory specialists, and embed quality into the product lifecycle across multiple regulated industries.
This role involves supporting quality, regulatory, and information security processes in a growing laboratory setting. Responsibilities include maintaining the Integrated Management System, ensuring compliance with various standards, managing controlled documentation, and assisting with audits and risk management.
