Specjalista/-ka ds. Jakości
Core
Supporting quality systems, managing quality documentation, and participating in continuous improvement initiatives within a regulated environment.
Role type
Quality Specialist (GMP)
Builds
Quality management systems and compliant pharmaceutical/medical device products
Domain
Pharmaceutical/Medical Devices / Quality Assurance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GMP environment experience, Quality Assurance experience, ISO 9001/13485 knowledge, audit support, quality documentation management, CAPA management, change management, deviation management, batch review support
Preferred skills
Pharmaceutical industry experience, Medical devices industry experience, Regulated environment experience
Technologies
Microsoft Office (Word, Excel, Outlook, PowerPoint)
Responsibilities
Supporting teams in quality system operations, creating and maintaining quality documentation, leading and maintaining quality records, participating in GMP/ISO audits, supporting batch review and product release decisions, collaborating with cross-functional teams for compliance
Seniority
Mid-level, hands-on IC