About this role
Technical Documentation Specialist II at CooperSurgical. Location: North Tonawanda, New York, United States. Role: reviewing batches, managing documents, initiating deviations Requirements: 4+ years cGMP manufacturing/document control experience; bachelor’s in health, engineering, or science (or equivalent experience); eQMS administration, document control, batch review, CAPA, deviations, audits; Microsoft 365 proficiency. Category: Quality Assurance Seniority: Mid Level Tools: Microsoft 365, Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft PowerPoint, Microsoft SharePoint, Electronic Quality Management System (eQMS), LIMS, ERP, electronic batch record systems Commitment: Full Time Workplace: Onsite Languages: English