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Pharmaceutical
Validation expert will be responsible to all validation testing deliverables in a GxP environment
Defining validation and tests plan for the systems according to system developments life cycle (SDLC)
Responsible for writing & reviewing validation documents, including test scripts (IQ/OQ/PQ), test plan and summary reports
Execution and Management of the test plan, test execution, system versions and defects at the gALM system
Management of the system changes by using ServiceNow system and the validation related activities
Works closely with project managers and gives support on validation issues
. Information systems/Software engineer
. 2 to 4 years of experience in software testing in a pharma/biotech/healthcare company
. Experience working in a GxP environment
. Experience with writing & reviewing of validation documents such as, test scripts (IQ/OQ/PQ), test plan, test summary report
. Experience in execution and management of the test plan, system versions and defects
. Experience working with testing tools, such as HP ALM or Jira
. Excellent English- speaking & writing
. Team player & good communication skills
. Fast learner
Senior Manager Application Support
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Date Posted: 12/11/2024
Job ID: 100055877
Teva Pharmaceutical Industries Ltd. is an Israeli multinational pharmaceutical company with headquarters in Petah Tikva, Israel. It specializes primarily in generic drugs, but other business interests include active pharmaceutical ingredients and, to a lesser extent, proprietary pharmaceuticals.