Development of purification processes for manufacturing biopharmaceuticals, using protein purification methodologies: Robotic, lab scale and scaled up pilot processes.
Design and execution of experiments, using preparative chromatography methodologies within time constraints, while following adequate documentation practices.
Writing of scientific documents: protocols, reports and SOPs, according to industry practices
Being up to date in relevant novel technologies and scientific literature and development
Communication and collaboration with other functions and individuals, at the development team, and with other TEVA units
Summarizing and presenting activities, progress and achievements in various forums
To provide scientific and technical solutions to a wide range of challenges in the field of interest
Supporting tech transfer and registration of products
Your experience and qualifications
B.Sc in biomedical / biotechnology / chemical / biochemical engineering, M.Sc. in life science and experience in the relevant field
Experience and knowledge in purification process of proteins
Basic knowledge of GLP/GMP guidelines
Hebrew - fluent, English - good reading and writing
Excellent teamwork capabilities
Reports To
Imry Yaron, Assoc Dir R&D Unit
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