Pilot Plant Manufacturing Technician

Ivrea - Italy

Monthly Salary: Not Disclosed

Posted on: 31-10-2025

Vacancies: 1 Vacancy

Job Summary

Job Description Summary

The Pilot Plant Manufacturing Technician performs end-to-end production of radiopharmaceuticals in strict adherence to current Good Manufacturing Practices and approved Standard Operating Procedures ensuring quality sterility and regulatory compliance at every stage. It prepares handles operates and documents materials and equipment according to validated procedures maintaining accurate traceable records and promptly escalating any deviations. The position follows an internal rotation plan with morning and afternoon shifts requiring flexibility and consistent coordination to meet operational timelines and batch release objectives.

Job Description

Key responsibilities:

Shift work for preparation production and packaging/shipping of sterile radioactive drugs in compliance with HSE EU GMP Annex 1/3 and applicable regulations
Perform setup cleaning and environmental microbiological monitoring (viable and non-viable) of areas and equipment with GMP-based periodic cleaning
Prepare raw materials and batch kits; manage stock and waste per Production Supervisor instructions and HSE SOPs
Complete GMP documentation per ALCOA and promptly report deviations/OOS to Production Supervisor Qualified Person and HSE Manager
Handle inbound logistics restock areas prepare shipping packaging; check for radioactive contamination and perform decontamination
Manage proper radioactive waste disposal with related records and transport
Support maintenance/qualification train new personnel contribute to the site quality system and continuous improvement in line with safety and GMP
Perform technical tests and support process/product qualification and validation; drive feedback and improvements tracking KPIs (successful batches delays OOS/deviations audit findings qualifications)

Essential requirements:

Technical or scientific high school education required; university degree in Science (Pharmacy Chemical Engineering Pharmaceutical Technology) or equivalent experience desirable
Minimum 2 years in GMP manufacturing support or technical roles preferably in sterile injectables; radiopharmaceutical experience is a plus
Strong scientific/technical understanding and quick grasp of production processes
Quality and compliance mindset with knowledge of regulatory requirements across multiple health authorities
Proficiency with manufacturing IT systems (e.g. SCADA HMI) and good office software skills
Team player with strong team spirit adaptability and change management
Ability to work under pressure and maintain standards
Language skills: Italian proficient; English desirable

Why Novartis Our purpose is to reimagine medicine to improve and extend peoples lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: will receive: You can find everything you need to know about our benefits and rewards in the Novartis Life

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Environment Health And Safety (Ehs) Laboratory Equipment Manufacturing Process Materials Science Process Simulation Sop (Standard Operating Procedure)

Required Experience:

Job Description SummaryThe Pilot Plant Manufacturing Technician performs end-to-end production of radiopharmaceuticals in strict adherence to current Good Manufacturing Practices and approved Standard Operating Procedures ensuring quality sterility and regulatory compliance at every stage. It prepar...