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 in pharmaceutical environment; strong attention to detail, organization, and communication; proficiency with Microsoft Word, Excel, PowerPoint, Outlook; SharePoint/Visio/Oracle a plus. 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