Global Leader, Supplier & External Manufacturing Quality

Alfasigma

Turbigo

Ibrido

EUR 100.000 - 130.000

Tempo pieno

14 giorni+
Generatore di candidature

Una candidatura mirata per questo annuncio — un curriculum e una lettera di presentazione pensati per rispondere alle esigenze dell'annuncio.

Supera i filtri ATS

Descrizione del lavoro

A leading pharmaceutical company in Italy is seeking an experienced Senior Leader in Quality Management. This role is critical for defining and executing the global quality strategy concerning suppliers and contract manufacturers. The ideal candidate will have over 12 years of experience in quality roles within the pharmaceutical sector and must possess strong leadership and stakeholder management skills. This position requires a deep understanding of GMP and regulatory compliance, as well as fluency in English.

Competenze

  • 12+ years in pharmaceutical quality roles, with at least 2 years in global leadership.
  • Proven experience in external manufacturing and supplier quality management.
  • Fluent in English; any additional languages a plus.

Mansioni

  • Develop and implement a global quality strategy for suppliers.
  • Ensure compliance with regulatory requirements and quality standards.
  • Drive investigations, CAPAs, and root cause analysis for quality issues.

Conoscenze

Leadership
Stakeholder management
Negotiation
GMP knowledge
Regulatory compliance understanding

Formazione

Degree in Life Sciences, Pharmacy, Chemistry, or Engineering
Advanced degree (MBA or comparable)

Strumenti

eQMS systems
Digital quality tools

Descrizione del lavoro

A leading pharmaceutical company in Italy is seeking an experienced Senior Leader in Quality Management. This role is critical for defining and executing the global quality strategy concerning suppliers and contract manufacturers. The ideal candidate will have over 12 years of experience in quality roles within the pharmaceutical sector and must possess strong leadership and stakeholder management skills. This position requires a deep understanding of GMP and regulatory compliance, as well as fluency in English.
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