Future Tech Jobs
Future Tech Jobs
This role involves leading Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and early lifecycle stages. You will work with cross-functional teams, provide regulatory advice, and manage interactions with regulatory authorities, ensuring compliance and supply continuity.
The Engineering Technician role involves providing technical support for the Dermatologicals Filling and Packaging function, including equipment maintenance, GMP compliance, and continuous improvement initiatives. The position operates on a 16/5 shift rota and is a 6-month fixed-term contract.
Field Service Engineer, Medical Diagnostic SystemsOverall Earnings £60,000+Basic Salary Up To £52,000OvertimeOn Call Allowance10% BonusCompany Car (Electric Or Hybrid)PensionHealthcareLife InsurancePhone, LaptopHolidays** The role will involve working one weekend in four (during this week you will receive two alternative days off...
Field Service Engineer, Medical Diagnostic SystemsOverall Earnings £60,000+Basic Salary Up To £52,000OvertimeOn Call Allowance10% BonusCompany Car (Electric Or Hybrid)PensionHealthcareLife InsurancePhone, LaptopHolidays** The role will involve working one weekend in four (during this week you will receive two alternative days off...
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.
This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, managing product lifecycle activities, and ensuring compliance with GMP standards. The role also involves supporting CMOs in audits, technical transfers, and continuous improvement initiatives.
This role involves leading technical operations and providing strategic support for the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, collaborating with external manufacturing partners, and ensuring compliance with GMP standards and continuous improvement initiatives.
This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, providing technical support, and ensuring compliance with GMP standards. The role also focuses on continuous improvement, change control, and managing critical lifecycle activities.
This role involves providing medical and scientific expertise in safety evaluation and risk management for GSK's clinical and post-marketing assets. Responsibilities include signal detection, data analysis, and communication of safety risks, as well as supporting safety governance and cross-functional teams.
The Medical Director, Oncology Clinical Development will lead clinical research activities for GSK’s oncology portfolio, collaborating with various stakeholders to develop and execute phase 1-3 clinical trials. Key responsibilities include protocol development, medical monitoring, safety data review, and strategic partnerships with key external experts.
The Medical Director, Oncology Clinical Development will lead clinical research activities, develop and execute oncology clinical trials, and engage with key external experts. Responsibilities include protocol development, medical monitoring, safety data review, and collaborating with various stakeholders to advance GSK’s clinical portfolio.
The Medical Director, Oncology Clinical Development, will lead clinical research activities to advance GSK’s oncology portfolio. Key responsibilities include developing and executing phase 1-3 clinical trials, collaborating with cross-functional teams, and engaging with key external experts to ensure the successful development and regulatory approval of innovative oncology treatments.
The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology portfolio, focusing on advancing the development of antibody drug conjugates (ADCs) for solid tumors. Key responsibilities include collaborating with multidisciplinary teams to design and execute clinical trials, ensuring high-quality protocol development, and engaging with key external experts to drive data generation and regulatory approvals.
The Medical Director, Oncology Clinical Development, will lead the clinical research activities for GSK’s oncology portfolio, including developing and executing phase 1-3 clinical trials. They will collaborate with various stakeholders to ensure high-quality protocol development, medical monitoring, and data interpretation, while also engaging with key external experts and thought leaders.
