Tasks
Perform lentiviral vector production processes according to the instructions of the manufacturing guidelines under GMP regulations.
Writing manufacturing protocols, standard operating procedures (SOPs) and other relevant documents related to manufacturing.
Complying with and ensuring compliance with internal production standards.
Being part of a multidisciplinary team to carry out process optimisations and investigations.
Carry out maintenance of production areas to ensure their condition and compliance with GMP regulations.
Key skills
BASIC ACADEMIC EDUCATION
Degree in Biology, Biochemistry, Pharmacy or Chemistry
SPECIFIC TRAINING
PhD or Master's degree in Biotechnology.
WORK EXPERIENCE
Experience in biochemical techniques
Experience in instrumental analytical techniques
Experience in validation of analytical methods, preferably in the biotechnology / biopharmaceutical industry.
USP: Knowledge of microbiology is essential.
Experience working with bioreactors and filtration systems is desirable.
Experience in upstream processes with yeast, bacterial and mammalian cells is also a plus.
DSP: Experience in purification of recombinant proteins and monoclonal antibodies, from lysis to molecule dosing.
Extensive practical experience in the use of ÄKTA Pilot and ÄKTA Ready chromatographic equipment on small, medium and large scale.
Experience in performing chromatographic methods using Unicorn 5 software, or higher version.
LANGUAGES
English
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