About this role
Specialist/Sr. Specialist, Quality – Document Control and Training at Kiniksa Pharmaceuticals. Location: Lexington, Massachusetts, United States. Role: processing documents, supporting training, maintaining archives Requirements: 3+ years regulated life science experience, bachelor's degree required, direct document control/quality systems/training experience, Veeva Vaults preferred, knowledge of US/EU cGMP preferred, Microsoft Office and eDMS/LMS proficiency. Category: Research and Development (R&D) Seniority: Mid Level Tools: Veeva Vaults, eDMS, LMS, Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft Outlook, Microsoft SharePoint Commitment: Full Time Workplace: Onsite Languages: English