Future Tech Jobs
Future Tech Jobs
This role involves leading pharmacovigilance and risk management for GSK's global assets, ensuring scientifically sound review and interpretation of safety data. The director will develop and execute safety strategies, manage safety governance, and lead cross-functional teams to address product safety issues and ensure patient safety globally.
The SERM Scientific Director role involves leading pharmacovigilance and risk management planning, developing safety strategies, and ensuring the scientific soundness of data reviews. The position requires expertise in evaluating safety risks, managing cross-functional teams, and communicating safety issues to senior management.
This role involves leading a team in the design and optimisation of chemical processes for drug development. Responsibilities include technical direction, project delivery, regulatory submissions, and mentoring scientists. The position leverages innovative technologies and AI to enhance process efficiency and ensure robust commercial processes.
The Senior Counsel provides comprehensive legal support and advice to AstraZeneca's UK marketing company, focusing on AI, data privacy, and commercial matters. They will act as a subject matter expert, draft and review legal documents, and ensure compliance with regulations and internal policies.
This role involves providing compliance oversight for clinical programs and trials, ensuring adherence to Good Clinical Practice standards. You will act as a primary compliance partner to Clinical Trial Teams, enabling decision-making on complex regulatory scenarios and leading cross-functional discussions to resolve quality issues.
This role involves developing and maintaining global labelling strategies and core documents for oncology products, ensuring compliance and consistency across different markets. You will lead cross-functional discussions, present proposals to governance bodies, and mentor colleagues while staying updated on regulatory changes and competitor activities.
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...
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...
This role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, collaborating with global and regional teams to ensure patient-centered, evidence-driven medical impact. The position requires deep oncology expertise and leadership to drive strategic decisions, data interpretation, and communication across international markets.
This senior leadership role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, collaborating with global teams to ensure patient-centered, evidence-driven medical impact. The role requires deep oncology expertise and strong leadership to influence strategic decisions and communicate scientific data effectively across regions.
This role involves ensuring medical device and drug-device combination products meet strict regulatory standards throughout development. The Quality Engineer (Compliance) will lead design controls, risk management, and audit readiness activities, working closely with development teams and external partners. Key focus areas include DHF and RMF maintenance, regulatory compliance, and supporting clinical trial investigations.
This role involves leading quality and regulatory compliance for a multinational manufacturer across Europe and Africa, with a focus on medical devices and consumer products. The candidate will oversee the Quality Management System, drive product launches, conduct audits, and ensure adherence to standards like MDD/MDR, ISO 13485, and MHRA. It requires a technically strong quality professional who can lead cross-functionally and balance strategic oversight with hands-on problem-solving.
The Senior Specialist I, QA Clinical is responsible for quality oversight in clinical development, supporting cross-functional relationships and ensuring compliance with GCP/GVP regulations. Key responsibilities include developing and implementing risk-based audit plans, conducting audits, and managing quality events. The role involves working closely with clinical project teams and external stakeholders, and maintaining the quality management system.
This role leads complex or pivotal clinical trials from conception to closeout, overseeing cross-functional teams and vendor partnerships. The Principal Clinical Project Manager ensures study delivery within quality, timeline, and budget targets, applying risk-based quality management and driving inspection readiness. They also mentor junior staff and contribute to process improvements within clinical operations.
This role involves leading software verification and validation for safety-critical systems within a regulated environment, ensuring compliance with quality standards across the development lifecycle. The engineer will design test strategies, develop automated test frameworks, and maintain traceability between requirements and testing activities. Collaboration with cross-functional teams is essential to support regulatory documentation, risk management, and continuous process improvement.
