Qc Analyst

**Summary**:
The QC Analyst is responsible for the execution and documentation of biologic and microbiological testing in conformity to GMP standards and SOPs in force efficiently, competently and in the planned terms and the compliance with the existing regulation on ecology and security.

**About the Role**:
**Major Accountabilities**:

- Perform 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
- 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
- Collaborate in the maintenance of good conditions of laboratories, instruments and work environment
- Collaborate in keeping quality control SOPs updated

**Obligatory requirements**:

- Education: Master degree in Biology (or equivalent) or biology technical high school education.
- Languages: Basic knowledge of English, verbally and in writing
- Experiences: Previous experience in pharmaceutical companies is desirable

**Commitment to Diversity and Inclusion**: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Division

Operations

Business Unit

Innovative Medicines

Location

Italy

Site

Saluggia

Company / Legal Entity

IT58 (FCRS = IT058) Advanced Accelerator Applications Italy Srl

Alternative Location 1

Ivrea, Italy

Functional Area

Quality

Job Type

Full time

Employment Type

Temporaneo (tempo determinato)

Shift Work

No