About this role
CSV Specialist II at KBI Biopharma. Location: Durham, North Carolina, United States. Role: authoring protocols, executing validation, maintaining archives Requirements: Bachelor's in engineering/IT, 3+ years CSV experience in pharma/biotech, GAMP and 21 CFR Part 11 expertise, validation documentation and testing, and proficiency with Microsoft Excel and electronic document management systems. Category: Research and Development (R&D) Seniority: Mid Level Tools: GAMP, 21 CFR Part 11, Microsoft Office, Microsoft Excel, electronic document management systems Commitment: Full Time Workplace: Onsite Languages: English