Sachbearbeiter QA Systems (m/w/d) Pharma
Core
Administration of an electronic document management system (SmartSolve) for GMP-relevant documents, SOPs, and training materials within a pharmaceutical company.
Role type
QA Systems Administrator (Document Management)
Builds
GMP-compliant documentation and training materials
Domain
Pharmaceutical / Quality Management
Required skills
GMP documentation handling, electronic document management systems (EDMS), quality key indicator (KPI) analysis, audit support, MS Office proficiency
Preferred skills
Experience in pharmaceutical or GMP-regulated environments, Quality Management System (QMS) knowledge, English language skills
Responsibilities
Managing and administering the electronic document management system (SmartSolve), verifying and maintaining GMP-relevant documents and SOPs, conducting GMP and training sessions, collecting and evaluating quality KPIs, supporting internal and external audits
Seniority
Entry-level to Mid-level
