Salary Range: €30,****** - €56,****** 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.
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 areasand equipmentand 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/qualificationactivities
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. *****; D.lgs ******, 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.
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 who make it happen.
insurance plans
retirement plans
wellbeing resources
global recognition programs
flexible and hybrid working options, where possible
minimum 14 weeks paid parental leave
Expected Annual Base Salary Range for role: €30,200 to €56,000
Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.
Read our brochure to learn more about our global total rewards offering:
Commitment to Diversity and Inclusion / EEO paragraph Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
Skills Desired Environment Health and Safety, Environment Management, Laboratory Instrumentation, Manufacturing Processes, Materials Science, Process Simulation, Standard Operating Procedure (SOP)
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