Future Tech Jobs
Future Tech Jobs
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...
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...
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 industries. You will handle service calls, perform diagnostics, and ensure customer satisfaction through timely and professional communication.
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 customer satisfaction through timely and professional service.
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.
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...
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.
The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...
The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization,...
