CareerPlan

Qualification & Documentation Specialist (m/w/d) - Pharma & Food

Viersen, NORDRHEIN_WESTFALENFull-time2026-11-09 → 2026-11-10

Core

Creating, reviewing, and managing quality-relevant documentation (DQ, TRM, IQ, OQ) and certificates for the pharmaceutical and food industries to ensure compliance with GMP and regulatory standards.

Role type

Quality & Documentation Specialist

Builds

Audit-ready documentation and compliance certificates for production equipment and food contact materials

Domain

Pharmaceutical and Food Manufacturing

Deliverable

dashboards & analysis

Required skills

GMP documentation, Qualification processes (DQ/IQ/OQ), Food Contact Materials (FCM) regulations, Document versioning, Regulatory compliance (EU-GMP), Data integrity

Preferred skills

Food industry experience, Technical or pharmaceutical training (PTA/CTA), MS Office formatting

Technologies

Microsoft Word

Responsibilities

Create and edit qualification documents (DQ, TRM, IQ, OQ) according to GMP standards; Review and coordinate corrections for design documents; Issue factory certificates and verify Food Contact Materials (FCM) compliance; Manage document storage, versioning, and audit trails; Ensure Good Documentation Practice (GDocP) adherence

Seniority

Mid-level, hands-on IC