About this role
Quality Systems Engineer – CAPA and Process Improvement at DEKA Research & Development. Location: Manchester, New Hampshire, United States. Role: managing CAPA, conducting audits, revising SOPs Requirements: BS/MS in engineering, life sciences, or related field; 3+ years in quality systems in a regulated industry (medical device preferred); working knowledge of FDA QSR (21 CFR Part 820) and ISO 13485; strong technical writing and communication; proficiency with Microsoft Excel, Word, and Visio. Category: Engineering Seniority: Mid Level Tools: Microsoft Excel, Microsoft Word, Microsoft Visio Commitment: Full Time Workplace: Onsite Languages: English