Future Tech Jobs
Future Tech Jobs
This role involves developing and delivering robust regulatory strategies for oncology products, collaborating with cross-functional teams, and ensuring compliance with global regulatory requirements. The position also focuses on process improvement and innovation in regulatory affairs.
The SERM Medical Director role at GSK involves providing in-depth medical and scientific expertise in safety evaluation and risk management for key GSK assets. Responsibilities include leading pharmacovigilance, developing safety strategies, and ensuring compliance with regulatory standards. The role also involves cross-functional team leadership, communication of safety issues, and contributing to the continuous improvement of safety processes.
This role involves managing the post-launch lifecycle of the CFC CRM platform across global markets, ensuring its stability, compliance, and continuous optimization. The Senior Director will work closely with regional teams to prioritize market needs, manage configurations, and ensure successful adoption and value realization.
This role involves managing the post-launch lifecycle of the CFC CRM platform across global markets, ensuring its stability, compliance, and continuous optimization. The Senior Director will work closely with regional teams to prioritize market needs, manage configurations, and ensure successful adoption and value realization from CRM investments.
In this hands-on role, you will ensure seamless warehouse and logistics support within a 24/7 GMP environment at Moderna’s UK manufacturing facility. You will manage inventory, coordinate deliveries, and maintain compliance with safety and operational standards, directly supporting mRNA vaccine production.
This role involves operating in a 24/7 GMP environment at Moderna’s UK manufacturing facility, ensuring seamless warehouse and logistics support. Responsibilities include managing inventory, verifying deliveries, coordinating shipments, and maintaining compliance with safety and operational standards.
The NIS P&D Project Management, Associate Director is responsible for developing and delivering high-quality Non-Interventional Studies (NIS) project plans, managing resources, and collaborating with various functional teams. Key responsibilities include maintaining accurate project schedules, driving cost and resource forecasts, and ensuring alignment with strategic goals.
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 submissions. The position requires strong technical expertise, collaboration across functions, and a focus on quality and compliance.
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 across functions, and a focus on quality and patient safety.
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 Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.
The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects from internal and external donor sites to external Contract Manufacturing Organizations (CMOs). Key responsibilities include managing project schedules, mitigating risks, and ensuring timely delivery within budget, while acting as the main point of contact between GSK and suppliers.
The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.
