GMP QA Analyst – Pharmaceutical Quality (Hybrid)

Johnson & Johnson Innovation

Latina

In loco

EUR 30.000 - 49.000

Tempo pieno

14 giorni+
Generatore di candidature

Trasforma questo ruolo in un colloquio — un curriculum e una lettera di presentazione personalizzati in base a ciò che cerca questo datore di lavoro.

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Descrizione del lavoro

Johnson & Johnson Innovation in Latina, Italy, is seeking a Quality Assurance Associate to join the Borgo San Michele site on a 12-month fixed-term contract. The role sits in the Quality department and ensures product conformity with GMP and regulatory standards.

The ideal candidate holds a master's degree in a relevant science, has at least 6 months in pharma QA, excellent English, and solid Office skills.

Competenze

  • Master's degree in a relevant field (Chemistry, Pharmacy, Biology, Engineering).
  • At least 6 months of pharma QA experience or similar.
  • Excellent English language skills.
  • Good knowledge of the Office package.

Mansioni

  • Review batch data to verify product conformity with regulatory requirements.
  • Handle quality issues on pharmaceutical batches and investigate deviations.
  • Lead investigations and propose corrective/preventive actions with cross-functional teams.
  • Collaborate with multiple departments and international affiliates for investigations.
  • Identify improvement opportunities through daily presence in production and process checks.
  • Define and execute QA controls and related SOPs.

Conoscenze

Accountability
Administrative Support
Compliance Management
Detail-Oriented
Document Management
Execution Focus
Goal Attainment
Quality Control
Quality Management Systems
Quality Standards
Report Writing

Formazione

Master's degree in Chemistry and Pharmaceutical Technologies / Pharmacy / Chemistry / Biology / Engineering

Strumenti

Microsoft Office

Descrizione del lavoro

Johnson & Johnson Innovation in Latina, Italy, is seeking a Quality Assurance Associate to join the Borgo San Michele site on a 12-month fixed-term contract. The role sits in the Quality department and ensures product conformity with GMP and regulatory standards.

The ideal candidate holds a master's degree in a relevant science, has at least 6 months in pharma QA, excellent English, and solid Office skills.

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