Design, develop & oversee validation components & comply with 21 CFR Part 11 & Part 8, & GAMP5. Author & review Validation plan & Summary reports. Track & manage defects & change controls using HP QC & ALM. Write & execute IQ/OQ/PQ scripts for functional, system, & regression testing. Perform Periodic & Audit Trail reviews.
Requirements:
Master's degree in Science, Technology, or Engineering (any discipline) required.
Application Instructions:
Mail CV to: Pharma Tek Solutions, Inc, 6101 Bollinger Canyon Rd, Ste 336, San Ramon, CA 94583
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