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Purification Development Scientist – Early Material

Cambridge, UK

Competitive salary and benefits

Make a more meaningful impact to patients’ lives around the globe!

Here you’ll have the opportunity to make a meaningful difference to patients’ lives. With science at its heart, this is the place where breakthroughs born in the lab become transformative medicines – for the world’s most complex diseases. Answer unmet medical needs by pioneering the next wave of science, focusing on outcomes and shaping the patient ecosystem.

In Cambridge, we have the best tech around. This is a place where the history and future of scientific breakthrough come together. The diversity of our people is essential to bringing new discoveries to life.

Join the team that follows the science unlike anywhere else. This is the place for curious minds. Dig deep into the biology of complex disease and uncover breakthroughs.

Typical Accountabilities

• Supplies to the plans and designs of purification processes and provides general scientific advice on specific topics to the team
• Leads own work to ensure that agreed targets are met in a timely manner and to agreed quality standards, communicating progress appropriately
• Performs relevant experiments and interprets results based on a standard methodology
• May modify or improve processes and systems, depending on purpose of experiments
• Assesses and reports data, with little or no mentorship, in a clear and concise manner, with a clear understanding of its implications within the overall context of drug development
• Discusses and defends the findings of experiments at follow-up meetings, or corresponding forums
• Provides technical instruction to the team and allocates administrative work where possible
• Liaises with colleagues from other subject areas with the purpose of discussing project-related matters, sharing experiences and reporting progress
• Develops own level of proficiency by reading articles, collaborating with peer scientists or through contacts by other internal groups
• Searches for information which may improve research methodology and procedures
• Ensures that work is performed in accordance with appropriate Safety, Health & Environment (SHE), quality and compliance standards, e.g. Good Laboratory Practice (GLP)

Education, Qualifications, Skills and Experience

Essential

• Graduate or experienced non-graduate
• Understanding of the principles and concepts associated with purification methodologies (chromatography/TFF) and an appreciation of the relevant science and literature
• Practical experience in preparative purification techniques e.g. column chromatography, TFF
• Purification of Protein or nucleic acid will be an advantage
• Problem-solving skills related to data analysis
• Understanding of the basic principles and concepts in a broad range of bioprocessing technology, or substantial experience in a narrower field of technology
• Understanding of compliance systems

Desirable

• Understanding of range of subject areas within R&D
• Experience in the pharmaceutical industry

Why AstraZeneca

At AstraZeneca, we 're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.

So, what’s next?

Complete your application before the below closing date.

This role is open from 18AUG2023, we encourage your application no later than 17SEP2023

Where can I find out more?

Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/

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