Dokumentationsassistent Qualitätskontrolle – Pharma (m/w/d)
Core
Creating, maintaining, and reviewing GMP-compliant documentation for quality control in a radiopharmaceutical manufacturing environment.
Role type
Documentation Assistant, Quality Control
Builds
GMP-compliant documentation for radiopharmaceuticals
Domain
Pharmaceutical industry, Quality Control, Radiopharmaceuticals
Required skills
GMP requirements knowledge, pharmaceutical documentation practice, MS Office, laboratory report management, audit preparation, structured work, quality awareness
Preferred skills
Experience in pharmaceutical industry, quality control, laboratory, or regulated environments
Technologies
MS Office, GMP systems
Responsibilities
Create, maintain, and update GMP-compliant documents for quality control; Administer and archive laboratory reports and quality data; Support deviation, CAPA, and change-control processes; Assist in laboratory work including proper GMP documentation; Prepare and accompany audits and inspections; Ensure complete, traceable, and quality-compliant documentation
