לצערנו המשרה כבר לא בתוקף
• Dedication, motivation, leadership and strong team working skills
• Performance, Development, Validation, follow-up and documentation of Sterile production and analysis of cell-based products in a clean room environment
• Experienced in high quality performance of cell cultures, FACS, ELISA, PCR, Western blot, microscopy, and in vitro tests.
• Assuring quality of raw materials, intermediate and final products in compliance with GMP regulations.
• Writing SOPs and methods.
• Working in compliance with FDA/EMA guidelines.
• Academic education – MSC, or PhD in cell biology/immunology
• Experienced in working in Biotech under GMP regulations.
• The ability to concentrate and function during lengthy processes and in stressful situations.
• Highly reliable with precision capabilities, ability to prepare precise documentation of the results and write technical documents in English and Hebrew.
• Strong organizational skills with ability to plan ahead
• Streamlining and development capability alongside ability to follow precise instructions
• Flexible to work long hours when needed
Only qualified candidates will be considered for the position