BTG is looking for a Head of Downstream Process Development.
מעבר למשרות נוספות ביו-טכנולוגיה כללית (ישראל)
פורסם לפני 1 ימים
- באר טוביה
- משרה מלאה
- לא צוין שכר
פרטי מגייס/ת המשרה:
תיאור המשרה:
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, continuous well as batch process
• Management of about 8-10 scientists and technicians.
• Identification, development and adjustment of advanced relevant technologies
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, continuous well as batch process
• Management of about 8-10 scientists and technicians.
• Identification, development and adjustment of advanced relevant technologies
דרישות המשרה:
Job 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 and updating management.
• Good understanding of pharmaceutical regulation
• Proficiency in statistical tools in experimental design and analysis (use of DOE-advantage tools)
• Willingness to support extended hours as needed.
• Excellent communication ability.
• Corporate Responsible – Safety – GMP compliance.
• 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 and updating management.
• Good understanding of pharmaceutical regulation
• Proficiency in statistical tools in experimental design and analysis (use of DOE-advantage tools)
• Willingness to support extended hours as needed.
• Excellent communication ability.
• Corporate Responsible – Safety – GMP compliance.
מעבר למשרות דומות בתחומים:
משרה מספר 9150238