Specjalista/-ka ds. Jakości
Core
Supporting quality systems, documentation management, and continuous improvement initiatives in a regulated pharmaceutical/medical device environment.
Role type
Quality Specialist (GMP)
Builds
Quality management systems and compliant product releases
Domain
Pharmaceutical/Medical Device Manufacturing
Required skills
GMP environment experience, Quality Assurance experience, ISO 9001/13485 knowledge, CAPA management, Change control, Deviation management, Batch review support, Audit support, Documentation management
Preferred skills
Pharmaceutical industry experience, Medical device industry experience, Microsoft Office proficiency
Responsibilities
Supporting teams on 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 cross-functionally for compliance
Seniority
Mid-level, hands-on IC
