CareerPlan

Compliance Expert GMP Quality Systems (m/w/d)

Wasserburg am InnFull-time2026-11-04 → 2026-11-11

Core

Manage central elements of the pharmaceutical Quality Management System including document management, training management, and supplier qualification to ensure data integrity and audit readiness.

Role type

Compliance Expert GMP Quality Systems

Builds

Pharmaceutical Quality Management System (QMS) documentation, training curricula, and approved supplier lists

Domain

Pharmaceutical industry + GMP Quality Assurance

Deliverable

dashboards & analysis

Required skills

GMP regulatory knowledge, electronic QMS management, supplier qualification, audit coordination, change control, risk assessment, CAPA management

Preferred skills

Veeva Vault experience, audit experience, natural science degree

Technologies

Veeva Vault QualityDocs

Responsibilities

Administer GMP document lifecycle and review processes, manage electronic training curricula and compliance, coordinate supplier qualification and audits, support regulatory inspections and CAPA handling

Seniority

Mid-level, hands-on IC