QA Officer

The QA Officer will guarantee the quality oversight over the entire working time of the facility for all the GMP activities on going.

**Your key responsibilities**:
Your responsibilities include, but are not limited to:

- Be responsible for the appropriate level of quality oversight during the GMP activities of the facility verifying they are executed according to the applicable standards in manufacturing, quality control, distribution and quality processes, working in shift (including NIGHT SHIFTS) with other QA officers
- Responsible for the provisional release for the shipment of batches manufactured at the facility.
- Involvement in investigation, training, redaction/review of deviation, OOS, complaints, CAPA, change control implementation and redaction/review of site GMP documentation, SOP, protocols, reports, APR.
- Support the QP in the preparation of batches and batches release documents.
- Review of batch records and assure the timely closure of the manufactured batches.

**Commitment to Diversity & Inclusion**:

- We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve._

**Minimum requirements**
- Scientific degree.
- At least 1-year experience in a Quality department of a pharmaceutical company.
- Fluent in Italian. Good knowledge of English.
- Willing to work in shifts, including night shifts.

**Division**

Oncology

**Business Unit**

ADVANCED ACCELERATOR APPLICATIONS

**Country**

Italy

**Work Location**

Colleretto Giacosa

**Company/Legal Entity**

AAA Italy Srl.

**Functional Area**

Quality

**Job Type**

Full Time

**Employment Type**

Regular

**Shift Work**

Yes

**Early Talent**

Yes