Experience

Medimor

• Israel
• Medical Equipment Manufacturing
• 1 - 100 Employee

• Head of GMP Compliance

  • Mar 2023 - Present



Minovia Therapeutics

• Israel
• Biotechnology Research
• 1 - 100 Employee

• Head Of Manufacturing Israel

  • Jul 2020 - Sep 2022



Floris Hadas

• Acre Area, Israel

• Pharma Technologist

  • Jul 2017 - Jul 2020

  Process & Cleaning Validation Management. Pharma Department Projects Managment. New products technology transfer from R&D to production scale. Deviations handling and Investigations. Process & Cleaning Validation Management. Pharma Department Projects Managment. New products technology transfer from R&D to production scale. Deviations handling and Investigations.



MSD

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Clinical Trial Coordinator Intern, MSD, Hod Hasharon, Israel

  • Aug 2016 - May 2017

  Submissions for Ethics Committees and Ministry of Health. Preparation of Investigator files, consent forms and all documents relating to clinical trial management. Submissions for Ethics Committees and Ministry of Health. Preparation of Investigator files, consent forms and all documents relating to clinical trial management.



Protalix Biotherapeutics

• Israel
• Biotechnology Research
• 100 - 200 Employee

• Senior Team leader, Protalix therapeutics, Carmiel, Israel

  • Jun 2006 - Aug 2016

  Senior Team leader, Protalix therapeutics, Carmiel, Israel Extensive experience in Clean room working ISO-8, ISO-7 and Hoods. Specialization in chromatography, filtration processes and systems, Columns, Operating systems (AKTA) and UNICORN software Experience in cell cultures (bioreactors) Freeze drying processes (Lyophilization) Extensive experience in investigations, Deviations handling, Change control and tasks (writing and by computerized software- Trackwise) Experience in inspections authorities (Ministry of Health, EU, EMEA and FDA) Management of staff, training and qualification of employees Audits performing in the department Promotion and optimization of manufacturing processes Documents writing and Data process statistical analysis Recruiting patients for clinical trials Control in GMP and GCP regulations R&D small projects management Show less