Quality Assurance Specialist | Spezialist Qualitätssicherung (m/w/d)

Job Summary

This role is for an engaged Quality Assurance Specialist focused on GMP-compliant documentation review within the pharmaceutical industry, specifically in Parenteral manufacturing in Mannheim. The specialist will be crucial in ensuring quality and compliance, actively driving process optimizations, and managing critical quality systems. Day-to-day tasks include performing operational review of electronic batch records, monitoring GMP documentation, and managing deviations, root cause analyses, and CAPA implementation using systems like Veeva. They will also coordinate change control processes, update SOPs, and identify error trends for continuous improvement. The ideal candidate holds a degree in Biotechnology, Pharmacy, or a comparable natural science field, possesses deep knowledge of GMP regulations, and is proficient in both German (fluent) and English (good). This position offers the chance to be part of a dynamic team, shape the future of quality assurance, and ensure long-term job security within a major corporate structure.