Validation Engineers Pharmaceutical Industry: Qualification Course for Systems and Equipment
Nov 25, 2024
By Elias Morany, M.Sc. & Jose (Yossi) Chvaicer, M.Sc.
מחזור 6
Engineering & Validation
Starts at: 09:30
Duration: 3 Meetings
Language: Hebrew
Join our specialized training course designed for Validation Engineers in the Pharmaceutical Industry, focusing on the validation life cycle for systems and equipment according to cGMP requirements.
This hands-on program provides a deep understanding of:
- The validation life cycle: DQ, FAT, SAT, Commissioning, IQ, OQ, PQ
- Key regulatory aspects and real-world case studies
- Practical skills to qualify pharmaceutical equipment and systems effectively
By completing this course, you will strengthen your expertise as a Validation Engineer and enhance your career in the pharmaceutical industry.
📅 Course Dates:
- 25/11/2024
- 02/12/2024
- 08/12/2024
🕘 Hours: 09:00–16:00
📍 Location: Building 22, Matam Park, Haifa
🎯 Registration Information:
- Early Registration Discount: 3,800 + VAT until 15.11.24
- Standard Price: 4,500 + VAT starting 16.11.24
Don't miss the opportunity to advance your career as a leading Validation Engineer in the Pharmaceutical Industry
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...
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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.