descrizione del lavoro

Purpose of the role:
Execution and documentation of biologic and microbiological testing in conformity to GMP standards and SOPs in force efficiently, competently and in the planned terms.
Compliance with the existing regulation on ecology and security.
Organization and control of the laboratory and analytical equipment in the field of expertise.
Your key responsibilities:
Your responsibilities include, but are not limited to:
• Perform microbiological analysis on excipients, drug substances, drug products, water and primary packaging according to internal SOPs
• Execute stability study protocols, process validation protocols, method validation protocols and every study tied to drug products involved in technology transfer for the field of expertise
• Perform the sterility test on the products from AAA sites, including radioactive samples
• Perform instrument performance qualification tests whenever required
• Register the analysis correctly and in compliance with ALCOA+ principles other than the relevant applicable SOPs
• Collaborate with management for reaching the department objectives
• Know and apply the relevant SOPs for the field of expertise
• Collaborate in the maintenance of good conditions of laboratories, instruments and work environment
• Collaborate in keeping quality control SOPs updated

Diversity & Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

What you’ll bring to the role:
• Education: Chemical or biological degree
• Languages: Good knowledge of English language and Italian
• Previous experience in a similar role and/or in pharmaceutical company

Work location: Saluggia