Sterile Manufacturing Supervisor — Lead GMP Operations

Thermo Fisher Scientific Inc.

Italia

In loco

EUR 55.000 - 75.000

Tempo pieno

5 giorni fa
Candidati tra i primi
Generatore di candidature

Distinguiti per questo ruolo — genera un curriculum e una lettera di presentazione personalizzati in circa un minuto.

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Descrizione del lavoro

Thermo Fisher Scientific Inc. is seeking a PDS Sterile Manufacturing Supervisor to lead our sterile manufacturing operations. You will coordinate production activities, ensure regulatory compliance, and drive continuous improvement while maintaining a strong safety and quality culture.

The role requires 3+ years in pharma/biotech manufacturing with 2+ years in supervision within GMP environments, and a Bachelor's degree in a STEM field. This is a full-time on-site position in Italy.

Competenze

  • Bachelor’s degree in a STEM field is required.
  • 3+ years in pharmaceutical or biotechnology manufacturing.
  • 2+ years of supervisory/leadership experience in a GMP-regulated environment.

Mansioni

  • Supervise and coordinate daily sterile manufacturing operations
  • Ensure compliance with cGMP, FDA, and company quality standards
  • Monitor production performance and maintain adherence to schedules
  • Review batch records and ensure accurate documentation
  • Lead, coach, and develop manufacturing team members
  • Support investigations, deviations, and corrective actions
  • Promote a strong culture of safety, quality, and continuous improvement
  • Collaborate cross-functionally with Quality, Engineering, and other departments
  • Identify and implement process and operational improvements

Conoscenze

Leadership
cGMP knowledge
FDA compliance
Aseptic processing
Quality documentation
Continuous improvement
Cross-functional collaboration

Formazione

Bachelor's degree in Science/Engineering/Chemistry/Economics/Business or related STEM field

Descrizione del lavoro

Thermo Fisher Scientific Inc. is seeking a PDS Sterile Manufacturing Supervisor to lead our sterile manufacturing operations. You will coordinate production activities, ensure regulatory compliance, and drive continuous improvement while maintaining a strong safety and quality culture.

The role requires 3+ years in pharma/biotech manufacturing with 2+ years in supervision within GMP environments, and a Bachelor's degree in a STEM field. This is a full-time on-site position in Italy.

Ottieni la revisione del curriculum gratis e riservata.

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