About the Role

　　The Production Supervisor ensures the execution of all pertinent production phases in compliance with the requirements of the GMPs supervising the activities carried out by the personnel of the Production Department. The Production Supervisor is responsible for the planning of Production Department (drug production in sterile lines and packaging area).

　　Work location : Saluggia (TO)

　　Your responsibilities include, but are not limited to:

　　• Verify the methods of dressing, behavioral standards, and flow of materials in the areas with controlled contamination (and with regard to the sterile room) in compliance with internal procedures

　　• Execute and supervise the compilation of the Batch Record of the products and logbooks of the equipment in real time and in accordance with GMP requirements

　　• Revise Production Plan on the bases of change requested by Logistic Department, Commercial Director and Operation Director.

　　• Verify the correct compilation of batch product records, logbooks, and worksheets

　　• Report to the function manager of any anomaly / deviation detected during any processing phase of its own relevance

　　• Supervise the activities carried out by the personnel of the Production Department in relation to the various organizational positions

　　• Collaborate with the Production Manager with the aim of ensuring the achievement of production objectives consistent with the GMP (quantity, mix, costs) through the verification of the correct application of the planning of the activities

　　• Detect and report to the Production Manager, STS, the Quality Assurance Service and the Qualified Person QP any deviations from the GMP rules and any defects that could affect the quality of the products and the safety of the operators

　　• Maintain and control the equipment / plants of competence, in accordance with the requirements of the procedures

　　Diversity & Inclusion / EEO

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

　　Role Requirements

　　What you'll bring to the role:

　　• Graduated in life science, chemistry, pharmacy, biology; Bachelor Scientific Level

　　• 2 years of Experience in Production Department within the pharmaceutical industry Lyophilization

　　• Knowledge of Aseptic process and GMP requirements

　　• Excellent Team working and leadership skills

　　• Italian and English fluent, written and spoken

　　Why Advanced Accelerator Applications?

　　Thousands of people die of cancer around the world every day. At Advanced Accelerator Applications, a Novartis company, our mission is to transform lives through radioligand therapy in nuclear medicine to fight several leading types of cancer. How will we continue to be on the cutting edge of medicine? We believe new groundbreaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!

　　Imagine what you could do at Novartis!

　　Join our Novartis Network:

　　If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network

　　Division

　　Oncology

　　Business Unit

　　ADVANCED ACCELERATOR APPLICATIONS

　　Location

　　Italy

　　Site

　　Saluggia

　　Company / Legal Entity

　　AAA Italy Srl.

　　Functional Area

　　Technical Operations

　　Job Type

　　Full Time

　　Employment Type

　　Regular

　　Shift Work

　　No