CareerPlanSign in

Mitarbeiter Qualitätsmanagement (m/w/d)

SchönefeldFull-time2026-09-04 → 2026-10-08

Core

Ensuring compliance with quality and regulatory standards (GMP/GDP) through documentation, validation, and supplier management in the pharmaceutical industry.

Builds

Quality Management Systems, validated processes, and compliant operational workflows

Domain

Pharmaceutical industry / Regulatory Compliance

Required skills

GxP knowledge (GMP/GDP), quality documentation, supplier qualification, validation planning, data analysis, MS Office, English (fluent)

Preferred skills

Quality Auditor certification, Polish language skills, digitalization project experience, Class B driver's license

Technologies

GxP tools, MS Office, computerized systems

Responsibilities

Create and maintain QM documents and SOPs, plan and execute qualification/validations for systems and facilities, evaluate service providers per GDP/GMP, support customer onboarding, coordinate quality tasks, optimize the QMS

Seniority

Mid-level, hands-on IC