Associate Director, GMP Analytical Operations — Hybrid Ivrea

IT58 (FCRS = IT058) Advanced Accelerator Applications Italy Srl

Ivrea

In loco

EUR 62.000 - 115.000

Tempo pieno

4 giorni fa
Candidati tra i primi
Generatore di candidature

Trasforma questa candidatura in un colloquio — un curriculum e una lettera di presentazione creati in base a ciò questo datore di lavoro sta cercando.

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Vantaggi offerti da questo lavoro

Insurance plans
Retirement plans
Wellbeing resources
Global recognition programs
Flexible and hybrid working options
Minimum 14 weeks paid parental leave

Descrizione del lavoro

Novartis in Ivrea, Italy seeks an Associate Director, Analytical Operations to lead GMP Analytical Operations at the TRD RLT Pilot Plant. The role focuses on analytical operations, quality compliance, lab performance, and team development.

Responsibilities include end-to-end oversight from sample receipt through result release, GMP/data integrity, CAPAs, budgeting, audits, and building a high‑performing, safety‑driven team.

Competenze

  • Degree in a scientific discipline (pharmacy/biology/chemistry/engineering) is required.
  • Minimum 7 years in Quality Control and/or Analytical Science within pharma.
  • Strong GMP, data integrity, and laboratory qualification knowledge.

Mansioni

  • Lead GMP Analytical Operations team and KPIs.
  • Oversee sample receipt through analytical result release.
  • Ensure GMP compliance, data integrity, and quality systems.
  • Lead deviations investigations and implement CAPAs.
  • Develop lab strategies, SOPs, and budget plans.

Conoscenze

Leadership
Communication
Organizational skills
Bilingual Italian/English

Formazione

Bachelor's degree in Pharmacy, Biology, Chemistry, Engineering, or related scientific discipline

Strumenti

LIMS
Chromeleon
QEM
Microsoft Office

Descrizione del lavoro

Novartis in Ivrea, Italy seeks an Associate Director, Analytical Operations to lead GMP Analytical Operations at the TRD RLT Pilot Plant. The role focuses on analytical operations, quality compliance, lab performance, and team development.

Responsibilities include end-to-end oversight from sample receipt through result release, GMP/data integrity, CAPAs, budgeting, audits, and building a high‑performing, safety‑driven team.

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