Overview
As a Purification Development Scientist in Cambridge, UK, you'll play a pivotal role in channelling our scientific capabilities to make a positive impact on changing patients' lives. We're constantly pushing the boundaries of science to deliver life-changing medicines to patients, with a passion for discovery and a pipeline to show for it. We're pioneering innovative research and exploring novel pathways across key therapeutic areas including Oncology, Respiratory and Immunology, Cardiovascular and Renal Metabolism, and Vaccines and Immune Therapies. And we're industry-leading in immunology, protein engineering and translational science. As part of the Purification Process Sciences (PPS) group within the Biopharmaceutical Development (BPD) organization at AstraZeneca, this position will support the development of scalable processes for the purification of a wide range of biologics modalities to support our growing portfolio of recombinant proteins as well as new molecular formats.
Responsibilities
* Design, planning, execution and reporting of biomolecule purification experiments at different scales, including antibody, Fc fusion, multispecific formats as well as a wide range of novel biologic formats.
* Product Quality analysis - using standard methods including HPLC, Capillary Electrophoresis, Spectrophotometer.
* Maintaining a current and accurate laboratory record (electronic lab notebook) of all activities through data management system.
* Authorship of reports and internal documentation.
* General laboratory activities including preparation of buffer and routine maintenance of equipment.
* Advise on developability requirements for early stage portfolio assets.
* Scale up of processes to GMP relevant scales.
* Technology Transfer and support of ongoing GMP manufacturing activities.
Qualifications
* At least a BSc in a related biochemistry/bioprocessing/biochemical engineering field, ideally with further post graduate qualification and/or extensive post graduate experience in a related field.
* Understand the principles of Biologics purification and a good understanding of chromatography techniques, e.g. Affinity/IEX/HIC.
* Experience with chromatography systems (AKTAs) at various scales.
* Experience with tangential flow filtration (TFF).
* Experience with biologics downstream process development.
* Familiar with data management system such as LIMS.
Desirable
* Application of Multifactorial Statistical Design software to the development of Bioprocesses.
* Experience using high throughput methodologies for the development of novel Bioprocesses.
Behavioural competencies
* Demonstrate significant autonomy in terms of experimental design and execution.
* Able to work with multiple projects concurrently.
* Hard working, organised, balanced and meticulous with an ability to work well under pressure.
* Adaptable and a team player with a conscientious attitude and enthusiasm.
* Participate in group discussions and provide novel solutions to a variety of problems of diverse scope involving basic scientific principles.
* Desire to learn and build on the role.
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