Dokumentationsassistent Qualitätskontrolle – Pharma (m/w/d)
Core
Creating, maintaining, and reviewing GMP-compliant documents for quality control; managing and archiving lab reports and quality data; supporting deviation, CAPA, and change-control processes; assisting in lab work with proper GMP documentation; preparing for and accompanying audits and inspections.
Role type
Documentation Assistant, Quality Control (Pharma)
Builds
GMP-compliant documentation and quality records for a pharmaceutical company
Domain
Pharmaceutical industry, Quality Control, GMP
Required skills
GMP knowledge, pharmaceutical documentation practice, MS Office, archiving, audit preparation, lab work support
Preferred skills
Experience in pharmaceutical industry, quality control, or regulated environments
Technologies
MS Office
Responsibilities
Create and maintain GMP-compliant documents; Archive lab reports and quality data; Support deviation and CAPA processes; Assist in lab work with documentation; Prepare for audits and inspections
Seniority
Entry-level to Mid-level, hands-on IC
