Associate Expert Drug Supply

Salary Range: €30,200.00 - €56,000.00   Job Description Summary Carry out the production of radiopharmaceuticals according to GMP rules and approved SOPs.  The role foresees working in shifts including morning and afternoon work according to an internal rotation plan. #LI-Onsite Location: Ivrea, Italy Relocation Support: This role is based in Ivera, Italy. Novartis is unable to offer relocation support: please only apply if accessible.   Job Description Major accountabilities: • Work in shifts, is responsible to perform the necessary activities for the preparation, production and packaging for shipping of sterile radioactive drugs  • Execute all assigned activities in compliance with internal procedures (HSE, EU GMP Annex 1 / Annex 3, others) and in compliance with applicable laws and regulations  • Perform routine setup and cleaning, microbiological verification of pharmaceutical areas and equipment and all areas of the Plant with a need for periodic cleaning activities based on GMP   • Perform the preparation of all raw materials needed for the production (batch related kit preparation)  • According with the Production Supervisor, perform the management of material stocks and waste materials   • Follow the GDP in printing, filling and signing all documents (ALCOA+)  • Promptly report to the Production Supervisor and the Qualified Person and/or the HSE Manager any deviation and/ or out of specification detected during the production process   • Perform logistics activities (transportation and documentation related) about the incoming of materials, refilling of the stock areas and packaging materials for shipping.  • Perform activities related to waste management (transportation and documentation related) for radioactive waste   • Support external specialized personnel in carrying out ordinary and extraordinary maintenance/qualification activities  • Collaborate with the Production Supervisor to the training of new personnel   • Support the site quality system by providing input from the production area and sustaining the continuous improvement of the facility  • Observe all safety requirements (D.Lgs. 81/08; D.lgs 101/95, Global and local HSE SOPs), GMP regulations (AIFA, FDA), and housekeeping practices while performing duties.  • Provides continuous feedback and is the point of contact for generating improvements and changes aimed at optimizing the quality and efficiency of production processes. • Responsible for performing technical tests and supporting the qualification and validation phases of processes and products. • undefined Education & Qualifications    Technical/Scientific background/education (High School) is mandatory   University degree in Science is desirable, Pharmacy or Chemical Engineering, Pharmaceutical  Technology or equivalent job experience.    Languages     • English: desirable  • Italian (Local Language): proficient     Experiences    • Minimum 2 years experience in GMP manufacturing support / technical role  • Previous experience in sterile injectable pharmaceutical companies (radiopharmaceutical experience is desirable)      Competencies    • Good scientific and technical understanding  • Team player with strong team spirit  • Change management, adaptability, ability to work under pressure  • Good understanding or capacity to quickly understand production processes  • Quality and compliance skills  • Good understanding of regulatory requirements across multiple health authorities    Technical / Functional Skills & Knowledge    • Good working knowledge/understanding of typical manufacturing IT system (SCADA, HMI etc)  • Good office software applications      Benefits & Rewards     At Novartis, we’re committed to reimagining medicine together - and rewarding the people w