Qualification of Validation Engineers in Pharmaceutical Industry for Systems and Equipment Course

Gstudy > Courses and seminars > Qualification of Validation Engineers in Pharmaceutical Industry for Systems and Equipment Course

Nov 5, 2024

By Elias Morany, M.Sc. & Jose (Yossi) Chvaicer, M.Sc.

מחזור 6

Engineering & Validation

Location: Frontal

Starts at: 09:30

Duration: 3 Meetings

Language: Hebrew

The training includes a comprehensive overview of the validation life cycle for systems and
equipment in the pharmaceutical industry according to the cGMP requirements. The training provides you with the latest regulatory aspects, validation life cycle review, DQ/ FAT/
SAT/ Commissioning/ IQ/ OQ/ PQ requirements and real-life case studies.

Course dates:
05/11/2024
12/11/2024
19/11/2024
Course Hours - 09:00-16:00
Location - Building 22 Matam Park, Haifa
Price - 4,500 NIS + VAT

  • About Elias Morany, M.Sc.

    Elias Morany has a Bachelor’s degree (B.Sc.) from the Faculty of Biotechnology and Food Engineering at the Technion – Israel Institute of Technology, and of a Master’s degree (MSc) in System Engineering. Elias has wide knowledge of production processes and experience in leading, promoting and conducting cross-organizational engineering projects, validation and technical characterization of systems, equipment and utilities, manufacturing plants...
  • About Jose (Yossi) Chvaicer, M.Sc.

    Mr. Jose Chvaicer graduated in Mechanical Engineering from the State University of Rio de Janeiro, Brazil, and he has a Master’s Degree in Industrial and Management Eng. from the Technion – Israel Institute of Technology, Haifa, Israel. Jose holds a lead auditor certificate from the IIS (ISO9001, ISO13458).He has over 25 years of international experience in the Pharmaceutical Industry. While...

Comments

A full training that includes a comprehensive overview for the validation life cycle for systems and
equipment in the pharmaceutical industry according to the cGMP requirements. The training provides you with the latest regulatory aspects, validation life cycle review, DQ/ FAT/
SAT/ Commissioning/ IQ/ OQ/ PQ requirements and real life case studies.

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