About this role
QA Specialist at Acrotech Biopharma Inc. Location: East Windsor, New Jersey, United States. Role: organizing documentation, reviewing documents, supporting audits Requirements: 3+ years GMP experience, strong attention to detail, documentation and SOP authorship, review of deviations/CAPA, proficiency with Microsoft Office and SharePoint/Visio/Oracle, audit support and metrics tracking. Category: Quality Assurance Seniority: Mid Level Tools: Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, SharePoint, Visio, Oracle Commitment: Full Time Workplace: Onsite Languages: English