Future Tech Jobs
Future Tech Jobs
The Head of DMPK will lead the strategic direction of drug metabolism and pharmacokinetics, ensuring robust scientific excellence and predictive modeling. Key responsibilities include defining DMPK strategies, collaborating with data science teams, and leading a high-performing team.
This role involves leading the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs. Responsibilities include designing clinical studies, authoring regulatory documents, and collaborating with cross-functional teams to expedite drug development.
This role involves developing and executing a translational data strategy that bridges the gap between disease biology and clinical outcomes. The Senior Director will lead a team in integrating multi-omics data with AI-driven analytics, collaborate with R&D and clinical development, and establish high-value partnerships with external organizations.
This role involves performing and managing GMP and compliance audits of Biopharm, Vaccines, and Pharmaceutical facilities. You will evaluate compliance with GMP, policies, and regulatory requirements, and provide subject matter expertise on sterile manufacturing. The role requires strong communication and influencing skills, and involves travel to various sites across the network.
This role involves providing on-site and remote technical support for state-of-the-art robotics solutions in the pharmaceutical and biotechnology sectors. You will become the service subject matter expert, manage customer escalations, perform diagnostics, and ensure preventative maintenance. The position requires extensive travel within the Manchester area and occasional travel outside this region.
As a Field Service Engineer, you will be the primary point of contact for customers in the Manchester area, providing technical support and maintenance for state-of-the-art robotics and automation solutions in the pharmaceutical and biotechnology sectors. You will perform remote diagnostics, manage escalations, and ensure preventative maintenance, while working closely with R&D, customer service, and other teams to deliver exceptional service.
The Manufacturing Associate I will operate production equipment for mRNA vaccines, ensuring compliance with cGMP and safety regulations. They will work in a highly technological environment, collaborating with QA teams, troubleshooting issues, and participating in continuous improvement projects.
The Director of Biostatistics leads the statistical aspects of clinical development programs, ensuring robust study design, data analysis, and regulatory submissions. They collaborate closely with cross-functional teams and regulatory authorities to drive the success of clinical trials and ensure high-quality statistical insights.
This role involves maintaining and improving CSL's global pharmacovigilance (PV) system, ensuring compliance with GVP and regulatory requirements. Responsibilities include leading investigations, managing deviations, coordinating inspections, and providing PV training across various functions and affiliates.
As a Lead Automation Engineer, you will take technical ownership of laboratory automation systems, focusing on optimizing and maintaining liquid handling platforms and automated workflows. You will collaborate with scientists, software engineers, and data teams to improve workflow efficiency and drive continuous improvements in throughput and operational efficiency.
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.
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.
This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and work closely with manufacturing and quality teams.
As a Data Curator at Isomorphic Labs, you will work closely with AI experts and drug discovery scientists to curate high-quality, ML-ready datasets. Your role involves integrating large-scale biomedical and biochemical data, enhancing data quality, and collaborating across teams to build and improve data assets that fuel the company's mission to accelerate drug discovery using AI.
As a Lead Automation Engineer, you will take technical ownership of laboratory automation systems, focusing on optimizing and maintaining liquid handling platforms and automated workflows. You will collaborate with scientists, software engineers, and data teams to improve workflow efficiency and support the company's R&D operations.
