עדיין מחפשים עבודה במנועי חיפוש? הגיע הזמן להשתדרג!
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
חן ולעבודה
- אשדוד
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חן ולעבודה
- אשדוד
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מלאה
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BTG, a global pharmaceutical company located in the Beer-Tuvia Industrial Zone, is looking for a Head of Downstream Process Development.
The group specializes in developing downstream processes, to provide protein of the appropriate quality with high yield, in a process that is manufacturing friendly. The Group works in full cooperation with other groups in the development of protein production and analytics, other departments in the local organization: manufacturing, QC / QA maintenance, engineering, and cooperation with other sites around the world.
Job description
Responsible for development of protein purification processes in various systems - Chromatography, UF/DF, filtration, precipitation
The group specializes in developing downstream processes, to provide protein of the appropriate quality with high yield, in a process that is manufacturing friendly. The Group works in full cooperation with other groups in the development of protein production and analytics, other departments in the local organization: manufacturing, QC / QA maintenance, engineering, and cooperation with other sites around the world.
Job description
Responsible for development of protein purification processes in various systems - Chromatography, UF/DF, filtration, precipitation
Requirements:
PhD in Biotechnology Engineering / Biochemistry / Life Sciences
5 years of experience in the pharmaceutical industry, and at least 3 years in management (scientists and technicians). Experience in GMP manufacturing-advantage
Experience and proficient in process validation, process upscaling and technological transfer, support for clinical batch manufacturing.
Experience in executing and submitting CMC development, DSP Development in accordance with regulatory requirements. continuous process and PAT development - an advantage
Writing development reports and submission chapters CTD)
responsible for planning, Gantt, budget management an
PhD in Biotechnology Engineering / Biochemistry / Life Sciences
5 years of experience in the pharmaceutical industry, and at least 3 years in management (scientists and technicians). Experience in GMP manufacturing-advantage
Experience and proficient in process validation, process upscaling and technological transfer, support for clinical batch manufacturing.
Experience in executing and submitting CMC development, DSP Development in accordance with regulatory requirements. continuous process and PAT development - an advantage
Writing development reports and submission chapters CTD)
responsible for planning, Gantt, budget management an
This position is open to all candidates.
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
