Senior Computerized System Validation Csv Specialist
IVY Works Advisors LLP
2d ago

Developing validation documentation for pharmaceutical equipment facilities and computerized systems used in GLP GMP and GCP environments Project Deliverables will encompass validation plans specifications test protocols and standard operation procedures and systems may include Process Automation Laboratory Automation Enterprise IT Applications and Network Infrastructure Experience Bachelors degree in engineering science 4-

6 years of work experience is a must 3 years of experience exposure to Computerized System Validation CSV US FDA 21 CFR Part 11 EU Annex 11 and GAMP 5 Good communication and

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