MedImmune Analytical Development scientist (AS I/II) in Liverpool, United Kingdom
Title: Analytical Development (AS I/II)
Location: Liverpool, UK
MedImmune is the global biologics research and development arm of AstraZeneca. We work as partners in bringing life changing medicines to patients, sharing and benefiting from each other's strengths. Our science lives beyond our labs – our global perspective means we use talent and expertise from all over the world to make our medicines a success.
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The Flu Manufacturing Science and Technology group is a multi-disciplinary scientific function providing expertise in Virology, Process Development and Analytical Development responsible for influenza strain development for manufacture of the seasonal live attenuated influenza vaccine.
The Analytical Development Group is a is a dynamic function with a strong focus on science and technology, accountable for analytical development providing expertise in analytical biochemistry, microbiology, immunology, cell culture, validation, laboratory automation, validation, and technology transfer. Core capabilities are tightly aligned with our pipeline, business strategy and enable important medicines to be manufactured, tested and delivered to patients.
The team have now a requirement for an experienced analytical development scientist to join them to support the seasonal vaccine strain development activities and the commercial manufacture of seasonal vaccine strains. In addition, the successful applicant will contribute and function effectively in one or more development projects, generating high quality, accurate data to support the project.
To be considered, you will have considerable experience in analytical development, method validation and technology transfer of a range of Virology/Immunological, Biosafety/Tissue culture, Microbiological and Analytical Chemistry methods, with experience in technology, method and operational improvements.
This is a rewarding and challenging development role within a commercial setting. You must be prepared to deliver against tight deadlines.
Other responsibilities include:
May mentor and provide bench supervision of junior scientists or associates to support the development of analytical techniques to support strain development activities, in a time sensitive environment
Be able to handle challenging tasks to develop new analytical methodologies and optimise/improve existing methodologies
May represent the company at regulatory inspections (including FDA & MHRA) and respond to questions
May prepare, provide information or review regulatory documentation to support company responses to any requests from regulatory agencies
You will have a life science degree, preferable in Biochemistry, Microbiology, Molecular Biology, Virology or other science related field, as a minimum
Considerable experience and knowledge of analytical testing requirements of biological manufacturing processes, as well as analytical development of methodologies used to test biological products
Considerable knowledge of ICH guidelines and experience in analytical validation
Considerable knowledge of laboratory equipment, facilities, engineering and instrumentation
Knowledge and experience with analytical testing requirements of biological manufacturing processes
Knowledge of good experimental design and statistical analysis
Knowledge of GMP, in particular manufacturing and/or laboratory practices and quality systems
Opening date: 14th September 2017
Closing date: 15th October 2017
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.