QC Specialist (m/w/d)
Core
Coordinate QC projects and manage quality documentation, risk assessments, and deviations within a BSL3 pharmaceutical laboratory.
Role type
Senior QC Specialist (Coordination & Documentation)
Builds
Quality systems, validated processes, and compliant documentation for vaccine active pharmaceutical ingredients.
Domain
Biopharmaceuticals / Vaccine Manufacturing
Required skills
GMP-regulated lab experience, QC process knowledge, deviation/Change control, Quality Risk Assessment, GMP documentation, project coordination, digital transformation, AI tool usage, Microsoft 365
Preferred skills
Biopharmaceutical industry background, experience with electronic quality systems, familiarity with Microsoft Copilot, German (fluent), English (good)
Responsibilities
Lead and coordinate QC projects across cross-functional teams; Create and manage deviations, event reports, and change requests; Plan and document investigations and risk-based solutions; Support internal and external audits; Drive digital transformation and automation of QC processes; Ensure complete and timely GMP documentation.