Future Tech Jobs
Future Tech Jobs
CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...
The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The AD provides for statistical excellence in clinical development plans, trial planning, data analysis, interpretation and reporting, and regulatory interactions and...
As a Field Service Engineer, you will be the primary point of contact for customers in the Manchester area, providing on-site and remote support for state-of-the-art robotics and automation solutions in the pharmaceutical and biotechnology sectors. Your responsibilities will include performing diagnostics, managing escalations, and ensuring preventative maintenance, while working closely with R&D, customer service, and other teams to maintain high customer satisfaction.
Biomedical Scientist | Pathology | Full Time | Perm | ManchesterWe're looking for a motivated Biomedical Scientist to join our Pathology team at Manchester Hospital. This full‑time, role offers the chance to work in a supportive, well‑equipped laboratory while playing...
This role involves driving the adoption of advanced clinical applications in microsurgery and tumour workflows, working closely with surgeons, clinical teams, and hospital decision-makers. The Specialist will support technology integration, engage key stakeholders, and contribute to strategic business development and revenue growth.
The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves strategic planning, innovative thinking, and engagement with external stakeholders to drive the clinical development program.
The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves strategic planning, regulatory submissions, and engagement with external stakeholders to drive the clinical development program.
This role involves leading a small QA team, ensuring compliance with regulatory standards, and overseeing quality systems and validation activities. Responsibilities include report writing, managing QA documentation, participating in audits, and driving continuous improvement initiatives.
The Principal Scientific Programme Manager will lead and support the delivery of specialist External Quality Assessment (EQA) schemes in clinical genomics. This role involves managing timelines, quality, and programme performance, as well as supporting the design and development of new EQA schemes. The position requires strong scientific knowledge, experience in genomics and quality assurance, and the ability to communicate effectively with senior stakeholders.
The Scientific Programme Manager will play a crucial role in international genomics quality assurance, ensuring diagnostic laboratories worldwide produce accurate and reliable genetic test results. Responsibilities include managing EQA schemes, interpreting complex genomic data, and collaborating with senior scientific leaders and stakeholders to maintain high standards and improve diagnostic genomics practices.
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 Systems Engineer, you will manage development lifecycle involvement to provide Automated Robotic sample storage systems to deliver cutting edge scientific applications and integrated platforms for biological sample and clinical intelligence.Systems Engineer provide the cohesion and co-ordination between engineering and...
As Senior Systems Engineer / Senior Product Development Engineer you will manage development lifecycle involvement to provide Automated Robotic sample storage systems to deliver cutting edge scientific applications and integrated platforms for biological sample and clinical intelligence.Systems Engineer provide the...
This role involves leading the execution of Moderna's strategic partnership with the UK government, focusing on mRNA-based vaccines and biomanufacturing. You will manage day-to-day interactions with key government stakeholders, represent Moderna on the UKHSA operations board, and drive cross-functional collaboration to deliver public health impact.
QA Officer, Pharmaceutical/BiotechLocation: Cheshire (onsite)Type: PermanentSalary: £28,000-£33000 (dependant on experience)Hours: Days (Monday - Friday), parking onsiteAdditional: 25 days holiday + BH, private medical, share options scheme, company pensionOur Client a Biotech company is looking to strengthen their QA team and...
The Senior Process Engineer role at AstraZeneca involves developing and scaling up sustainable drug substance manufacturing processes. Responsibilities include introducing new equipment, optimizing processes, and collaborating with cross-functional teams to ensure robust and efficient production for clinical and preclinical trials.
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.
