Future Tech Jobs
Future Tech Jobs
This role involves leading the clinical development and strategic oversight of a medicine for cardiovascular and renal conditions. Responsibilities include managing the Clinical Development Team, ensuring high clinical and scientific standards, and authoring key study documents and regulatory submissions.
This role involves supporting the delivery of clinical studies from protocol development to final reporting. Responsibilities include maintaining the Trial Master File, coordinating cross-functional teams, and ensuring regulatory compliance. The position is ideal for someone early in their clinical research career who enjoys organization and collaboration.
This is high-end optical medical equipment used by some of the biggest names on the UK high street. Precision kit. Customer-facing. And increasingly software-driven.This isn't just spanners and screwdrivers; it's installing software, configuring, troubleshooting, and explaining tech to end users...
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 cloud infrastructure, CI/CD pipelines, and workflow automation, ensuring data pipelines run reliably and reproducibly at scale.
Territory: South UK with a focus on London, M25 & M4 Corridors. Flexibility is needed to travel to customers further afield in Cardiff, Bristol, Norwich & Portsmouth areasRemote based and ideally living in London or within an hourDo you want...
Position: Compliance ManagerLocation: StevenageSalary: £50,000-£60,000 (dependent on experience)Compliance Manager required for our client based in Stevenage, they are a rapidly growing UK-based health tech start-up that's building wearable technology with the power to support people living with neurological conditions.They are...
Business Development Executive – Remote (UK) – Up to £35,000 pa + Benefits – REF 058Up to £35,000 pa + BenefitsRemote WorkingAn exciting opportunity has arisen for a driven and commercially focused Business Development Executive to join a highly innovative...
This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regional and global regulatory leads, partnering on innovative regulatory strategies, and representing the Global Regulatory Affairs function in senior-level interactions and health authority meetings.
Internal Auditor - Public Sector Services - Cannock - HomebasedDue to recent expansion, a growing Internal Auditing Organisation is currently looking for a few Internal Auditors to help with their growing workload. The offices are based in Cannock, but the...
This role involves analyzing the impact of environmental aerosol exposures on immune cells using advanced sequencing techniques and metabolomics. The successful candidate will work on a project led by Prof Nnenna Kanu, focusing on how these exposures affect immune and epithelial cells in mouse models and comparing the findings to human data.
Benefits Package:£30,000 - £36,000On the job training and developmentGenuine progression opportunities availableExtremely stable companyFurther benefits plus training and development on the job.A world class medical device supplier with a very lucrative product range are rapidly expanding the organisation and as...
As the Staff Product Manager for Agentic Systems, you will define the technical and scientific capabilities for autonomous science, bridging the gap between in silico models and physical automated labs. You will lead hypothesis-driven product development, prioritize high-impact capabilities, and collaborate with cross-functional teams to optimize the drug discovery pipeline.
This role involves leading the clinical safety strategy for drug projects and products, evaluating safety data, and managing risk to patients. You will work closely with regulatory agencies, contribute to global submissions, and ensure the safety and efficacy of AstraZeneca's products throughout their lifecycle.
The Supply Director manages a portfolio of contract manufacturing organizations (CMOs), ensuring alignment with GSK's commercial and manufacturing strategies. Key responsibilities include overseeing CMO performance, establishing strategic goals, managing relationships, and leading a team to achieve business and quality objectives.
The Supply Director manages a portfolio of suppliers and contract manufacturing organizations (CMOs), ensuring oversight and alignment with GSK's commercial and manufacturing strategies. Key responsibilities include establishing strategic goals, managing business and quality relationships, and leading a team to achieve operational and quality objectives.
Balance technical, regulatory and commercial challenges in this fulfilling roleThis highly regraded Cambridge-based medical technologies company is seeking a proven engineering leader to help guide high-value development programmes from concept through to transfer to manufacture. Your leadership will accelerate development...
