About this role
Process Validation Associate III at Simtra BioPharma Solutions. Location: Bloomington, Indiana, United States. Role: developing protocols, executing validation, analyzing data Requirements: Bachelor’s degree in science/engineering,5+ years technical experience (validation preferred) in parenteral manufacturing,proficiency with Microsoft Word/Excel/Outlook and enterprise systems,strong communication and independent working ability. Category: Skilled Trades - Manufacturing and Industrial Seniority: Senior Level Tools: Microsoft Word, Microsoft Excel, Microsoft Outlook, JDE, BPLM, Pilgrim, Trackwise Commitment: Full Time Workplace: Onsite Languages: English