GMP Laboratory Analyst Qualification
Quality Assurance
Audits
Starts at: 09:30
Duration: 2 Days
Language: Hebrew
GMP Laboratory Analyst Certification is a practical two-day training course designed to qualify analysts for proper, compliant work in QC laboratories in the pharmaceutical and medical device industries.
The course focuses on the practical implementation of the ״USP-NF״ and ״EP״ pharmacopoeias in the laboratory, understanding the principles behind analytical methods, and performing tests correctly and consistently.
Target audience: Analysts and QC/QA professionals in the pharmaceutical and medical device industries who wish to strengthen their practical understanding of analytical methods.
Two-day course | 09:30-16:00 | Online
What you will learn:
Identification tests and limit tests, titrations including Karl Fischer, laboratory water testing including pH, conductivity and TOC, IR/FTIR/NIR and UV-Vis spectroscopy, AA/AES/ICP techniques, and separation methods including TLC, HPLC, UPLC and GC.
Who should attend:
Analysts and QC/QA professionals seeking practical and precise qualification for performing analytical test methods in a GMP environment.
Immediate value:
A consistent professional language when working with pharmacopoeias, correct and repeatable execution of analytical test methods, and improved readiness for audits and inspections.
The course is led by Dr. Rivka Goldik, an expert in analytical chemistry with nearly two decades of experience in training quality control laboratory personnel in the pharmaceutical industry. Dr. Goldik combines deep scientific knowledge with hands-on experience in implementing GMP principles, validating analytical methods, and leading quality audits, providing participants with high-level, practical professional training.
The course is available as an in-house training program for company teams, on dates to be coordinated in advance.
Alternatively, participants may register for the waiting list for an open course.
Opening of the course is subject to a minimum registration of 6 participants. Once a suitable group is formed, we will contact the registered participants to confirm the course date and complete the registration process.
Registration to the waiting list does not constitute final confirmation that the course will open. The course date will be determined and communicated to registered participants once the minimum number of participants has been reached.
About Rivka Goldik, D.Sc.
A DSc graduate of the Faculty of Chemistry at the Technion and B.Sc. in education of chemistry at the Faculty of Education in Science and Technology at the Technion – Israel Institute of Technology, Haifa, Israel.During her studies she was also involved in laboratory training and teaching analytical chemistry.Dr. Goldik began in the pharmaceutical industry in 1996 and has served...
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The course is available as an in-house training program for company teams, on dates to be coordinated in advance.
Alternatively, participants may register for the waiting list for an open course.
Opening of the course is subject to a minimum registration of 6 participants. Once a suitable group is formed, we will contact the registered participants to confirm the course date and complete the registration process.
Registration to the waiting list does not constitute final confirmation that the course will open. The course date will be determined and communicated to registered participants once the minimum number of participants has been reached.