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.Per il seguente ruolo potrebbero essere richieste diverse soft skill ed esperienze. La preghiamo di consultare attentamente la panoramica riportata di seguito.#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 accountabilitiesWork in shifts, is responsible to perform the necessary activities for the preparation, production and packaging for shipping of sterile radioactive drugsExecute all assigned activities in compliance with internal procedures (HSE, EU GMP Annex 1 / Annex 3, others) and in compliance with applicable laws and regulationsPerform routine setup and cleaning, microbiological verification of pharmaceutical areasand equipmentand all areas of the Plant with a need for periodic cleaning activities based on GMPPerform 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 materialsFollow 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 processPerform 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 wasteSupport external specialized personnel in carrying out ordinary and extraordinary maintenance/qualificationactivitiesCollaborate with the Production Supervisor to the training of new personnelSupport the site quality system by providing input from the production area and sustaining the continuous improvement of the facilityObserve 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.Education & QualificationsTechnical/Scientific background/education (High School) is mandatoryUniversity degree in Science is desirable, Pharmacy or Chemical Engineering, Pharmaceutical Technology or equivalent job experience.LanguagesEnglish: desirableItalian (Local Language):
proficientExperiencesMinimum 2 years experience in GMP manufacturing support / technical rolePrevious experience in sterile injectable pharmaceutical companies (radiopharmaceutical experience is desirable)CompetenciesGood scientific and technical understandingTeam player with strong team spiritChange management, adaptability, ability to work under pressureGood understanding or capacity to quickly understand production processesQuality and compliance skillsGood understanding of regulatory requirements across multiple health authoritiesTechnical / Functional Skills & KnowledgeGood working knowledge/understanding of typical manufacturing IT system (SCADA, HMI etc)Good office software applicationsBenefits & RewardsAt Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.insurance plansretirement planswellbeing resourcesglobal recognition programsflexible and hybrid working options, where possibleminimum 14 weeks paid parental leaveExpected Annual Base Salary Range for role: €30,200 to €56,000Pay 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. xysqume Read our brochure to learn more about our global total rewards offering: 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)#J-18808-Ljbffr
refilling of the stock areas and packaging materials for shipping.Perform activities related to waste management (transportation and documentation related) for radioactive wasteSupport external specialized personnel in carrying out ordinary and extraordinary maintenance/qualificationactivitiesCollaborate with the Production Supervisor to the training of new personnelSupport the site quality system by providing input from the production area and sustaining the continuous improvement of the facilityObserve 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.Education & QualificationsTechnical/Scientific background/education (High School) is mandatoryUniversity degree in Science is desirable, Pharmacy or Chemical Engineering, Pharmaceutical Technology or equivalent job experience.LanguagesEnglish: desirableItalian (Local Language):
proficientExperiencesMinimum 2 years experience in GMP manufacturing support / technical rolePrevious experience in sterile injectable pharmaceutical companies (radiopharmaceutical experience is desirable)CompetenciesGood scientific and technical understandingTeam player with strong team spiritChange management, adaptability, ability to work under pressureGood understanding or capacity to quickly understand production processesQuality and compliance skillsGood understanding of regulatory requirements across multiple health authoritiesTechnical / Functional Skills & KnowledgeGood working knowledge/understanding of typical manufacturing IT system (SCADA, HMI etc)Good office software applicationsBenefits & RewardsAt Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.insurance plansretirement planswellbeing resourcesglobal recognition programsflexible and hybrid working options, where possibleminimum 14 weeks paid parental leaveExpected Annual Base Salary Range for role: €30,200 to €56,000Pay 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. xysqume Read our brochure to learn more about our global total rewards offering: 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)#J-18808-Ljbffr