Stellvertretende Leitung Herstellung GMP (m/w/d)

Fürthonsite

via Personio

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About this role

Deine Aufgaben Produktionsfreigabe: Du prüfst und genehmigst Produktionsaufträge für die Herstellung patientenindividueller Zubereitungen in unserem Manufacturing Execution System (MES) SteriBase. Batch Record Review: Du führst die Reviews der Herstellprotokolle durch und verantwortest deren Prüfung und Genehmigung. GMP-Qualitätsmanagement: Du steuerst das Abweichungs-, Change- und CAPA-Management konsequent und trägst zur kontinuierlichen Weiterentwicklung unseres Qualitätsmanagementsystems bei. QM-Dokumentation: Du erstellst, prüfst und genehmigst Herstellanweisungen, Standardarbeitsanweisungen (SOPs) und weitere qualitätsrelevante Dokumente.…

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What we'd score you on

reqspace match rubric

Five dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.

Skills match

For this role: r

Level fit

We check your title trajectory against the seniority signal of the role.

Domain experience

Your work in the role's domain matters more than your years total. We weight recent and direct experience.

Recency

A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.

Location fit

This role is based in Fürth. We weight your proximity and willingness to relocate.

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Skills in this role

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