Quality Control Lab Supervisor — GMP & Analytics Leader

PHIBRO ANIMAL HEALTH CORP

Medolla

In loco

EUR 45.000 - 60.000

Tempo pieno

8 giorni fa
Generatore di candidature

Ottieni una risposta da questo datore di lavoro — un curriculum e una lettera di presentazione personalizzati, che corrispondono esattamente a ciò che sta cercando.

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Vantaggi offerti da questo lavoro

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Descrizione del lavoro

Phibro Animal Health Corporation in Medolla, Italy is seeking a QC Supervisor to lead the laboratory and QC team, plan workload, and ensure testing meets quality specifications. The role requires GMP/GLP compliance, review of analytical results, and coordination with QA and production.

The position involves writing stability protocols, managing investigations, and ensuring equipment and methods are up to date. A 2+ year QC background is expected.

Competenze

  • Bachelor's degree in chemistry/biology/chemistry and Pharmaceutical Technologies required.
  • At least 2 years of experience in QC testing including HPLC and GC.
  • Good knowledge of GMP regulations and quality systems

Mansioni

  • Oversee laboratory operations and QC team in Medolla, ensuring on-time work completion.
  • Review analytical results and ensure compliance with specifications.
  • Prepare stability protocols and manage documentation for release of materials.
  • Conduct lab investigations and manage deviations using DMAIC methodology.
  • Collaborate with production, engineering and QA to meet site goals.

Conoscenze

GMP regulations
Communication
Multitasking
Planning & Organizing
Problem solving
Written and spoken English

Formazione

Bachelor’s degree in chemistry/biology/chemistry and Pharmaceutical Technologies

Strumenti

HPLC
GC

Descrizione del lavoro

Phibro Animal Health Corporation in Medolla, Italy is seeking a QC Supervisor to lead the laboratory and QC team, plan workload, and ensure testing meets quality specifications. The role requires GMP/GLP compliance, review of analytical results, and coordination with QA and production.

The position involves writing stability protocols, managing investigations, and ensuring equipment and methods are up to date. A 2+ year QC background is expected.

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