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.
Role 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
Please note, this is a lab based role and expectation to be onsite 4-5 days per week.
Experience:
Essential:
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.
Experience with Liquid Handlers for the execution of downstream unit operations and general liquid handling tasks
Experience with the authoring and development of high throughput methodologies for the development and evaluation of novel bioprocesses
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:
Experience with integration of liquid handlers into wider automated workflows
Experience with the integration of Automated systems into a wider Data environment
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.
Location:
Cambridge UK
Salary:
Competitive + Excellent Benefits
Next Steps?
Are you ready to step up and take ownership of your work, solutions for the business and your personal career development? Apply now and join us in our mission to bring life-changing medicines to people!
Where can I find out more?
Our Social Media,
Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/
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