GMP Validation Specialist - Processes & Packaging

Novartis ACC; Saluggia; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company in Italy is seeking a Validation Expert responsible for executing and managing validation activities in compliance with cGMP requirements. You will support validation planning, author protocols and reports, and ensure all validation activities adhere to regulatory standards. The ideal candidate holds a scientific degree and has previous experience in a sterile GMP environment, with fluency in Italian and English. Join us to make a difference in patients' lives.

Competenze

• Previous experience in a similar role within a sterile GMP environment.

Mansioni

• Support site validation planning by writing and maintaining master plans.
• Author and review validation protocols & reports.
• Ensure that all Site validation activities are compliant with cGMP.

Conoscenze

Fluent in Italian

Fluent in English

Knowledge of Quality and IT tools

Formazione

Scientific Degree (CTF/Pharmacy/Biotechnology/Chemical Engineering or related field)

Descrizione del lavoro

A leading pharmaceutical company in Italy is seeking a Validation Expert responsible for executing and managing validation activities in compliance with cGMP requirements. You will support validation planning, author protocols and reports, and ensure all validation activities adhere to regulatory standards. The ideal candidate holds a scientific degree and has previous experience in a sterile GMP environment, with fluency in Italian and English. Join us to make a difference in patients' lives.