Future Tech Jobs
Future Tech Jobs
The Audit Senior Lead role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the EMEA region. Key responsibilities include evaluating compliance, managing stakeholder engagement, and producing clear audit reports to mitigate risks and ensure regulatory adherence.
This role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the GSK Global Supply Chain. You will evaluate compliance with regulatory requirements and provide sterile manufacturing expertise, engaging with senior stakeholders and producing clear audit reports.
This role involves leading an analytical team in early chemical development, ensuring the delivery of high-quality analytical work to support GMP manufacturing and stability. The position requires extensive experience in analytical science, a passion for team development, and the ability to drive organizational effectiveness and innovation.
This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to studies. The position also involves mentoring others and contributing to strategic discussions with key stakeholders.
This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to study teams and investigators.
The Global Medical Affairs Director leads strategic and operational programs for autoimmune diseases, focusing on innovative evidence, launch readiness, and post-market solutions. They develop and execute medical/scientific engagement strategies, provide expert input on clinical trials, and collaborate with internal and external stakeholders to maximize the value of Novartis medicines.
The Vendor Start-Up Manager for eCOA and Translations ensures vendors are aligned and ready to deliver high-quality services from protocol finalization to database go-live. Key responsibilities include reviewing vendor specifications, coordinating kick-off meetings, performing User Acceptance Testing, and optimizing the study start-up process.
This role involves planning and executing real-world evidence studies to support the commercial success of GSK's oncology products. The Director will work closely with medical and commercial teams to ensure that evidence is aligned with regulatory and payer requirements, and will be responsible for managing timelines, budgets, and deliverables.
This role involves planning and executing real-world evidence studies to support the launch and market positioning of GSK's oncology products. The Director will work closely with medical and commercial teams to ensure the generation of high-quality evidence that meets regulatory and payer requirements, driving successful patient access and commercial outcomes.
This role involves planning and executing real-world evidence studies to support the launch and commercial success of GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and market requirements.
This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include leading technology transfers, process verification, and product qualifications, while collaborating with R&D, manufacturing sites, and regulatory teams to ensure safe and compliant supply.
This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include technology transfers, process verification, regulatory submissions, and cross-functional investigations to ensure safe and compliant supply. The role emphasizes practical problem-solving and collaboration across functions.
This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include leading New Product Introduction (NPI), technology transfers, process verification, and regulatory compliance. The position requires strong technical expertise, collaboration with R&D and manufacturing sites, and a focus on robust and compliant supply.
The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget are met. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and collaborating with the Central Study Team to achieve study deliverables. The role emphasizes innovation, risk management, and stakeholder communication.
The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget adherence. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and ensuring compliance with ICH/GCP guidelines. The role emphasizes innovation, risk management, and stakeholder communication.
