Future Tech Jobs
Future Tech Jobs
This senior role involves leading business development and transactions in biomarker and diagnostics for GSK's Oncology R&D. Responsibilities include negotiating deals, aligning with R&D strategy, and collaborating with internal and external stakeholders to drive strategic alliances and complex collaborations.
This senior role involves leading business development and transactions in biomarker and diagnostics for GSK's Oncology R&D. Responsibilities include negotiating deals, aligning with R&D strategy, and collaborating with internal and external stakeholders to drive successful collaborations.
This role involves shaping AI and digital health strategies to accelerate clinical development within a collaborative, innovation-driven team. You'll work across project design, protocol development, and digital solution implementation, supporting pharmaceutical partners and AstraZeneca R&D. The position emphasizes strategic consulting, technical evaluation of digital tools, and driving value through scalable, patient-centric innovations in clinical trials.
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 role also includes specialized monitoring, regulatory support, and engaging with external stakeholders to drive strategic insights.
The Global Development Lead (GDL) is responsible for leading the clinical development of internal medicine assets, working with cross-functional teams to design and execute clinical trials. Key responsibilities include creating clinical development plans, ensuring regulatory compliance, and collaborating with external partners to advance Pfizer's clinical programs.
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.
This role involves leading the strategic sourcing and evaluation of external innovation opportunities in Hematology and Cardiovascular/Renal therapeutic areas. Responsibilities include identifying high-potential assets, shaping early partnering strategies, and driving transactions in collaboration with Business Development.
TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...
The Portfolio Innovation Director will lead the integration of cutting-edge technologies, particularly AI-driven solutions, into global clinical operations at Novartis. This role focuses on identifying, evaluating, and scaling innovations to improve clinical trial design, accelerate recruitment, and enhance patient access. The position requires close collaboration with cross-functional teams and external partners to deliver measurable impact across the clinical portfolio.
Designs and leads global regulatory strategies for precision diagnostics, including companion diagnostics and in vitro devices, integrated within drug development programs. Works cross-functionally to manage submissions, health authority interactions, and compliance across lifecycle stages in a collaborative, innovation-driven environment.
This role involves supporting the development and maintenance of a Quality Management System aligned with ISO13485 and FDA requirements in a growing med-tech company. The candidate will manage regulatory documentation, design controls, and quality processes, contributing to audit readiness and continuous improvement. It's a hands-on position with direct impact on product compliance and regulatory submissions.
The Lead Manufacturing Engineer will take ownership of manufacturing development activities, from early concept through to prototype and low-volume production. You will help define manufacturing strategy, assembly processes, tooling, and automation solutions for first-generation products, working closely with design engineers and external suppliers.
This role involves working with bio-reactors and micro-organisms in a lab-based environment, focusing on fermentation, cultivation, and yield optimisation. You'll design experiments, scale processes from lab to production, and apply molecular biology techniques within a growing biotech team. The position offers hands-on impact in a start-up environment with opportunities for development.
Design and develop bioprocesses involving bio-reactors and downstream processing techniques such as membrane filtration, centrifugation, and drying. Scale laboratory methods to pilot and industrial levels while working within a highly skilled technical team. Focus on innovation and process optimisation in a start-up biotechnology environment.
This role involves providing on-site and remote technical support for Genedrive’s molecular diagnostic devices in healthcare settings. You'll troubleshoot, maintain, commission, and repair medical equipment, ensuring compliance with regulatory standards and service agreements. The position requires frequent travel across the UK and internationally, acting as a technical expert and brand ambassador.
