Future Tech Jobs
Future Tech Jobs
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 is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...
The Supplier Quality Engineer will manage and develop the supplier base for a rapidly growing medical devices company, ensuring compliance with ISO 13485 standards. Responsibilities include evaluating suppliers, managing CAPAs, and applying quality expertise to design-for-manufacture considerations.
Technical Project Manager | NPI | Oxford | £60k - £68k plus benefits:MARS Recruitment is proud to have partnered a world leading specialist manufacturer in the search for a Technical Project Manager to lead technical innovation and NPI based projects...
The Scientist role involves reviewing clinical data, writing technical reports, and ensuring regulatory compliance for medical devices. You will work closely with a scientific and clinical team to produce high-quality documentation for product approvals, focusing on safety, efficacy, and meeting strict regulatory standards.
This role involves leading the scientific design and execution of interventional clinical studies in oncology or hematology, ensuring high standards of quality and ethics. You will collaborate with cross-functional teams, provide scientific oversight, and engage with healthcare professionals to deliver impactful results.
This role involves leading the scientific design and execution of interventional clinical studies in oncology or hematology, ensuring high standards of quality and ethics. You will collaborate with cross-functional teams, provide scientific oversight, and engage with healthcare professionals to deliver impactful results.
This role involves leading the technical aspects of medical device design and development projects, from concept to low-volume production. Responsibilities include creating 3D CAD models, supporting product testing, and working closely with manufacturing teams in a regulated environment.
This role involves assembling and testing medical devices, supporting product development, and maintaining quality documentation in a regulated environment. It offers hands-on experience and clear progression into a Development Engineer role.
Your work will change lives. Including your own.The Impact You’ll MakeWe are seeking an innovative Research Scientist to join our Experimental Immunology team at our new state of the art laboratories in Oxford. In this primarily lab-based role, you will...
Field Service Engineer (Cleanroom / Containment)South Central England (West London, Slough, Reading, Oxford, Guildford, Basingstoke, Thatcham, Swindon, Salisbury, Winchester, Andover, Didcot, Wantage, Abingdon)£45,000 - £48,000 + Van & Fuelcard + Overtime & Door to Door Pay (OTE = £60k+) +...
This role involves hands-on manufacturing of pharmaceutical products like tablets, liquids, and gels in a regulated cleanroom environment. Responsibilities include operating production equipment, maintaining GMP standards, and ensuring accurate documentation and traceability.
This role involves working as a technical expert in the Clinical Flow Cytometry group at Moderna's Harwell facility, generating high-quality clinical trial data through advanced flow cytometry assays. Responsibilities include executing clinical sample testing, conducting immune profiling, and ensuring data integrity and compliance with GCLP standards.
This role involves working as a technical expert in the Clinical Flow Cytometry group at Moderna's Harwell facility, focusing on generating high-quality clinical trial data through advanced flow cytometry assays. Responsibilities include executing clinical sample testing, conducting immune profiling, and ensuring data integrity and compliance with GCLP standards.
This role involves building and maintaining a scalable, secure AWS platform to support scientific discovery and clinical delivery. You will work closely with bioinformaticians and scientists to design and implement CI/CD pipelines, workflow automation, and data governance practices.
This role involves leading the development and implementation of CMC regulatory strategies for small molecule drugs in global clinical trials. Responsibilities include managing CMC submissions, providing regulatory guidance, and supporting cross-functional teams in navigating international regulations.
This role involves analysing and interpreting complex biological and high-throughput screening datasets, developing and optimising automated data analysis tools, and supporting laboratory-based screening activities. The position requires strong computational skills and some hands-on lab work, contributing to the identification and optimisation of novel therapeutic molecules.
