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-OnsiteLocation: Ivrea, ItalyRelocation 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.
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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. 
  
Expected Annual Base Salary Range for role: €30,200  to €56,000
  
The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. 
  
In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. 
  
The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.
 
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:
https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf
 
Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.
 
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)