Mitarbeiter für das Qualitätsmanagement (m/w/d) in Teilzeit
Core
Managing quality management systems, documentation, audits, and regulatory compliance for pharmaceutical and medical device manufacturing.
Role type
Quality Management Specialist
Builds
Quality management processes and documentation for pharmaceutical and medical device clients
Domain
Pharmaceutical manufacturing / Regulatory compliance
Deliverable
dashboards & analysis
Required skills
Document management, SOP administration, CAPA management, Change control, Audit preparation, Data logging analysis, Regulatory certification handling
Preferred skills
GMP environment experience, PC software proficiency
Responsibilities
Maintaining the document management system, tracking SOPs and deviations, communicating with customers on change controls, obtaining manufacturer licenses and GMP certificates, organizing notary visits, preparing for audits, supporting management reviews, archiving QM documents
