Radiopharma GMP Production Associate - Shifts

IT58 (FCRS = IT058) Advanced Accelerator Applications Italy Srl; Ivrea; Sur place; EUR 30 000 - 56 000; Plein temps

Avantages offerts par ce poste

Insurance plans

Retirement plans

Wellbeing resources

Global recognition programs

Flexible and hybrid working options

Minimum 14 weeks paid parental leave

Résumé du poste

Novartis in Ivrea, Italy, is seeking a production specialist to carry out radiopharmaceutical production in accordance with GMP rules and approved SOPs. The role involves shift work and internal rotation planning, with responsibilities spanning preparation, production, packaging, and shipping of sterile radioactive drugs.

Qualifications include a technical/high school background (university science degree desirable). English is desirable; Italian is the local language.

Qualifications

• High School technical background mandatory
• Science degree desirable (Pharmacy/Chemical Engineering)

Responsabilités

• Perform preparation, production and packaging for shipping of sterile radiopharmaceuticals
• Ensure compliance with GMP, EU regulations and internal SOPs
• Conduct routine setup, cleaning and microbiological verification of production areas and equipment
• Prepare raw materials and manage stock for production
• Follow ALCOA+ in printing, filling and signing documents
• Report deviations to Production Supervisor and Qualified Person/HSE Manager
• Handle logistics for incoming materials and packaging for shipping
• Assist maintenance/qualification activities as needed
• Support training of new personnel and continuous improvement of the facility
• Observe safety requirements and GMP regulations during duties
• Provide input for quality improvements and process validation

Connaissances

GMP manufacturing

Radiopharmaceutical production

SCADA/HMI systems

ALCOA+ documentation

Quality compliance

Formation

High School technical background

Science degree desirable

Outils

SCADA

HMI

Description du poste

Novartis in Ivrea, Italy, is seeking a production specialist to carry out radiopharmaceutical production in accordance with GMP rules and approved SOPs. The role involves shift work and internal rotation planning, with responsibilities spanning preparation, production, packaging, and shipping of sterile radioactive drugs.

Qualifications include a technical/high school background (university science degree desirable). English is desirable; Italian is the local language.