Global Clinical Artwork Lead - Labeling & Compliance

Roche

Kaiseraugst

Vor Ort

CHF 120.000 - 180.000

Vollzeit

Vor 6 Tagen
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

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Zusammenfassung

Roche is seeking a Global Clinical Artwork Manager to lead the design and delivery of compliant clinical labeling artwork for a worldwide portfolio of investigational medicinal products. You will coordinate cross‑functional teams, external partners and regulatory networks to ensure timely labeling that supports clinical trials globally.

You will manage the full label lifecycle, collaborate with study planning and manufacturing, and drive continuous improvement in labeling processes while

Qualifikationen

  • 3+ years in pharmaceutical/biopharmaceutical or clinical supply chain environment.
  • Knowledge of pharma supply chain operations, clinical packaging processes, and regulatory/cGMP standards.
  • Excellent communicator fluent in English with negotiation and cross‑cultural collaboration skills.

Aufgaben

  • Design and manage clinical labeling artwork for a global portfolio of IMPs across internal sites and CMOs.
  • Lead end-to-end clinical label lifecycle from initiation through approval and delivery (booklet, single panel, shelf-life).
  • Collaborate cross-functionally with Clinical Study Planning, global manufacturing, external suppliers, and regulatory label representatives.
  • Drive issue resolution in label creation, monitor labeling regulations, maintain master data and documentation.
  • Lead supplier relationship management and performance reviews with external booklet vendors.

Kenntnisse

English fluency
Cross-cultural collaboration
Communication
Problem solving

Ausbildung

University degree in Pharmaceutical Sciences or related field

Tools

SAP ERP
Label creation software

Jobbeschreibung

Roche is seeking a Global Clinical Artwork Manager to lead the design and delivery of compliant clinical labeling artwork for a worldwide portfolio of investigational medicinal products. You will coordinate cross‑functional teams, external partners and regulatory networks to ensure timely labeling that supports clinical trials globally.

You will manage the full label lifecycle, collaborate with study planning and manufacturing, and drive continuous improvement in labeling processes while

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