GMP Radiopharmaceutical Production Specialist

Novartis Italia; Ivrea; On-site; EUR 30,000 - 56,000; Full time

Benefits offered by this job

Insurance plans

Retirement plans

Wellbeing resources

Global recognition programs

Hybrid working options

14 weeks parental leave

Job summary

Novartis Italia in Ivrea, Italy, is seeking a capable Radiation Pharma Production Operator to manufacture radiopharmaceuticals in compliance with GMP and approved SOPs. The role covers shift work (morning/afternoon) per a rotation plan and involves packaging for shipping, material handling and strict ALCOA+ documentation.

You will support qualification activities, assist maintenance, and help train new personnel while ensuring safety, regulatory compliance across EU health authorities, and

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.
• English: desirable; Italian: proficient.

Responsibilities

• Work in shifts, perform production and packaging for shipping of sterile radiopharmaceuticals.
• Ensure compliance with internal procedures (HSE, EU GMP Annex 1 / Annex 3) and applicable laws.
• Perform routine setup/cleaning and microbiological verification of areas and equipment.
• Prepare raw materials for production (batch-related kit preparation).
• Manage material stocks and waste under supervision; follow ALCOA+ documentation.

Skills

Scientific understanding

Team work

Change management

Regulatory knowledge

Education

Technical/Scientific background

University degree in Science/Pharmacy/Chemical Eng

Tools

SCADA

HMI

Office software

Job description

Novartis Italia in Ivrea, Italy, is seeking a capable Radiation Pharma Production Operator to manufacture radiopharmaceuticals in compliance with GMP and approved SOPs. The role covers shift work (morning/afternoon) per a rotation plan and involves packaging for shipping, material handling and strict ALCOA+ documentation.

You will support qualification activities, assist maintenance, and help train new personnel while ensuring safety, regulatory compliance across EU health authorities, and