Future Tech Jobs
Future Tech Jobs
Bespak are looking for a Senior Development Engineer (Nasal - SMI) for the Kings Lynn site, PE30 2JJ. The salary range for this permanent, role is between £55k to £62k plus a discretionary annual bonus. Our generous benefits package includes...
Bespak are looking for a Senior Development Engineer (pMDI - Inhaler) for the Kings Lynn site, PE30 2JJ. The salary range for this permanent, role is between £55k to £62k plus a discretionary annual bonus. Our generous benefits package includes...
This role involves servicing, installing, repairing, and calibrating sophisticated medical diagnostic systems in pathology departments and NHS laboratories. You will support flow cytometry, cell separation, and diagnostics products, working one weekend in four with alternative days off.
This role involves servicing, installing, repairing, and calibrating sophisticated medical diagnostic systems in pathology departments and NHS laboratories. You will support flow cytometry, cell separation, and diagnostics products, working one weekend in four with alternative days off.
The Audit Lead role involves designing and maintaining audit strategies for key technology areas like sterile biologics, medical devices, and digital health. Responsibilities include leading audits, ensuring regulatory compliance, coaching auditors, and collaborating with cross-functional teams to identify and mitigate risks. The role also focuses on continuous improvement of Pfizer's Quality Management System and fostering a culture of innovation and excellence.
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 position also involves supporting CMOs in audits, technical transfers, 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, managing product lifecycle activities, and ensuring compliance with GMP standards. The role also involves supporting CMOs in audits, technical transfers, and continuous improvement initiatives.
The Head of Translational and Precision Medicine (TPM) will lead the TPM division, designing and implementing strategies to enhance clinical program success. Key responsibilities include collaborating with R&D leadership, developing biomarker strategies, and advising on TPM-related aspects of science, medicine, and regulatory strategy. The role involves managing TPM personnel, budgets, and resources, and fostering a collaborative environment within and across R&D teams.
This role involves leading the clinical safety strategy for drug projects and products, evaluating safety data, and managing risk to patients. You will work closely with regulatory agencies, contribute to global submissions, and ensure the safety and efficacy of AstraZeneca's products throughout their lifecycle.
ROLE SUMMARYThe Medical Affairs AI Lead is the strategic architect and technical product owner for AI transformation across HQ Medical Affairs and Field Medical. This role defines the AI vision and roadmap, identifies and prioritizes high-impact use cases, builds rapid...
This role involves leading the clinical safety strategy for drug projects and products, ensuring the safety and risk management of AstraZeneca's pharmaceuticals. You will work on evaluating adverse events, communicating safety data, and contributing to regulatory submissions, all while collaborating with a global team of experts.
The Senior Medical Affairs Manager is a key scientific leader responsible for external engagement with key opinion leaders, healthcare organizations, and policy stakeholders. The role involves developing and executing the UK Medical Affairs strategy, leading scientific exchanges, and representing Seqirus at national scientific forums. The position also focuses on internal collaboration, evidence generation, and ensuring compliance with regulatory standards.
Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...
As a Commercial Partnerships Manager, you will drive impactful collaborations and partnerships to accelerate the transition to human-specific research methods. You will secure sponsorships, grow supplier relationships, and manage the antibodies database to ensure it is a core commercial platform. Your role involves representing the Centre for Human Specific Research, building relationships with stakeholders, and aligning scientific innovation with real-world impact.
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...
