About this role
Validation Engineer II at Kindeva. Location: Bridgeton, Missouri, United States. Role: executing qualification, authoring documentation, ensuring compliance Requirements: Bachelor's in life science/engineering or 5+ years GMP lab experience; 3+ years qualifying lab equipment; knowledge of GMP, 21 CFR Part 11, data integrity, AIQ; strong technical writing and cross-functional collaboration skills. Category: Engineering Seniority: Senior Level Commitment: Full Time Workplace: Onsite Languages: English