3 484 Posti di lavoro Barazzetto

Il nostro Studio è in crescita e desideriamo ampliare il nostro team con un/una odontoiatra pedodonzista che possa prendersi cura dei nostri pazienti più piccoli.

Cerchiamo una persona che sappia:

• instaurare un rapporto di fiducia con bambini e famiglie,
• lavorare con delicatezza, empatia e professionalità,
• collaborare in un ambiente giovane, dinamico e attento alla formazione continua.

Cosa offriamo:

• un team multidisciplinare e affiatato,
• uno studio moderno, accogliente e in costante aggiornamento,
• possibilità di crescita professionale e confronto con colleghi specializzati,
• contratto di collaborazione.

Sede di lavoro: Ivrea (TO)

Per candidarsi: inviare CV a

o contattaci al

Introduzione

Siamo alla ricerca di apprendisti Assistant Store Manager da inserire nel percorso di formazione e lavoro “Lidl 2 your career” , che abbiamo progettato in collaborazione con AHK Italien , la Camera di Commercio Italo-Germanica e l’Istituto Tecnico di Firenze .

I candidati saranno assunti da ottobre e novembre 2025 in diversi Punti Vendita dislocati nelle Città e Provincia di Torino

Vuoi lavorare e studiare allo stesso tempo, preparandoti al meglio per il tuo futuro professionale? Allora Lidl2your career è il percorso che fa per te!

La posizione

Svolgerai un percorso di 2 anni di formazione e lavoro , al termine del quale avrai acquisito tutte le competenze necessarie per ricoprire il ruolo di Assistant Store Manager nei Punti Vendita di Lidl.

• Sarai assunto/a da ottobre o novembre 2025 in uno degli Store Lidl dislocati nelle Città e Provincia di Torino
• Durante i due anni, per ca. 1 settimana al mese sarai in formazione teorica con l’intero gruppo classe presso l’Istituto Tecnico Superiore di Firenze.
• Per 3 settimane al mese sarai impiegato/a presso il punto vendita Lidl per ore di lavoro e formazione on-the-job
• In ITS avrai la possibilità di focalizzarti su materie in ambito economia e marketing, con approfondimenti su management, logistica e retail
• In azienda ti confronterai con l’operatività quotidiana degli store Lidl e potrai scoprire tutte le dinamiche del core business aziendale. Collaborerai con lo Store Manager per una ottimale gestione commerciale ed economica del Punto Vendita e sarai il punto di riferimento per colleghi e clienti
• Al termine dei due anni, al superamento degli esami, otterrai un doppio titolo: il Diploma ITS di Assistant Store Manager (livello 5 del Quadro Europeo delle Qualifiche) e il Certificato della Camera di Commercio Italo-Germanica per il profilo tedesco di riferimento, che attesta le competenze professionali pratiche acquisite on-the-job e ha un valore internazionale sul mercato del lavoro
  
  

• Hai un’età compresa tra i 18 e i 29 anni
• Sei in possesso di un diploma di maturità o di diploma professionale (conseguito con percorsi quadriennali di IeFP integrati a un quinto anno di percorso IFTS)
• Sei disponibile a svolgere la formazione teorica presso un ITS (ca. 1 settimana al mese)
• Sei motivato/a ad acquisire competenze professionali ed esperienza lavorativa in un’azienda solida e strutturata, con un ambiente di lavoro giovane, dinamico e stimolante
• Hai raggiunto un livello di inglese A2/B1
• Ti ritieni una persona flessibile, proattiva e intraprendente
• Ti piace il lavoro di squadra
• Ti entusiasma assumerti responsabilità e risolvi i problemi con prontezza e pragmaticità
  
  

• Percorso di studio interamente finanziato, incluso eventuale alloggio nei pressi dell’ITS di riferimento durante i due anni
• Regolare retribuzione mensile e accesso ai benefit previsti per i collaboratori di Lidl
• Impiego full-time da ottobre o novembre 2024 con contratto di Alto Apprendistato di Formazione e Ricerca, che prevede fasi di formazione presso un ITS e attività pratica lavorativa presso i punti vendita di Lidl
• Sarai seguito/a da un tutor didattico in ITS e da un tutor aziendale in Lidl, quali figure di supporto e riferimento per tutta la durata del percorso
• Al termine dei due anni, la tua carriera sarà pronta per decollare: potrai proseguire la tua esperienza lavorativa in Lidl Italia, e nel medio-lungo termine ti saranno offerte opportunità di avanzamento carriera
• Al superamento degli esami finali otterrai due titoli: il Diploma ITS (titolo di studio ministeriale di livello terziario) e la Certificazione delle competenze professionali della Camera di Commercio Italo-Germanica
  
  

• Support discipline/service provision individually or within a team; provide functional expertise to QA/Line Units as needed.
• Review, approve, and release GMP-relevant deliverables and tools to ensure cGMP compliance.
• Manage project-related activities (e.g., process/quality initiatives, facility upgrades, IT validation) as per responsibility.
• Ensure compliance with internal/external quality and safety guidelines (e.g., GMP, SOPs, Quality Manual).
• Drive continuous quality improvements for manufacturing, collaborating with production, engineering, and supply chain.
• Oversee qualification/validation of processes, equipment, facilities, and software for GMP use.
• Review and approve GMP documents, including URS, IQ/OQ/PQ, Change Controls, CAPAs, and SOPs.
• Support inspection preparations and maintain oversight of external maintenance and qualification activities.
  
  
• Degree in Pharmacy, Biology, Chemistry, Engineering, or equivalent.
• Fluency in English (verbal and written).
• Strong awareness of quality issues and urgency in task completion.
• Open and clear collaboration and communication skills.
• Scientific, technical, and regulatory knowledge in the specific area, with basic understanding of drug development.
• Detailed knowledge of cGMP and familiarity with safety/environmental regulations.
• Minimum 5 years of experience in pharmaceutical companies in equivalent roles.
• Strong organizational skills.
  
  

• Support discipline/service provision individually or within a team; provide functional expertise to QA/Line Units as needed.
• Review, approve, and release GMP-relevant deliverables and tools to ensure cGMP compliance.
• Manage project-related activities (e.g., process/quality initiatives, facility upgrades, IT validation) as per responsibility.
• Ensure compliance with internal/external quality and safety guidelines (e.g., GMP, SOPs, Quality Manual).
• Drive continuous quality improvements for manufacturing, collaborating with production, engineering, and supply chain.
• Oversee qualification/validation of processes, equipment, facilities, and software for GMP use.
• Review and approve GMP documents, including URS, IQ/OQ/PQ, Change Controls, CAPAs, and SOPs.
• Support inspection preparations and maintain oversight of external maintenance and qualification activities.
  
  

• Degree in Pharmacy, Biology, Chemistry, Engineering, or equivalent.
• Fluency in English (verbal and written).
• Strong awareness of quality issues and urgency in task completion.
• Open and clear collaboration and communication skills.
• Scientific, technical, and regulatory knowledge in the specific area, with basic understanding of drug development.
• Detailed knowledge of cGMP and familiarity with safety/environmental regulations.
• Minimum 5 years of experience in pharmaceutical companies in equivalent roles.
• Strong organizational skills.
  
  

Join to apply for the RLT Drug Product Project Leader role at Novartis Italia

Join to apply for the RLT Drug Product Project Leader role at Novartis Italia

Role Purpose

Leads and manages all Drug Product (DP) project activities linked to the development of radiopharmaceutical parenteral, both ready to use and freeze-dried products. Supports & coaches team members, participates in scientific teams and contributes to the overall Technical Research and Development (TRD) strategies and goals. Designs, plans, performs, interprets, and reports the results of scientific experiments for the preparation and timely delivery of drug product.

Summary

Role Purpose

Leads and manages all Drug Product (DP) project activities linked to the development of radiopharmaceutical parenteral, both ready to use and freeze-dried products. Supports & coaches team members, participates in scientific teams and contributes to the overall Technical Research and Development (TRD) strategies and goals. Designs, plans, performs, interprets, and reports the results of scientific experiments for the preparation and timely delivery of drug product.

About The Role

Role Responsibilities :

• Leads and manages all formulation and process development activities for assigned projects.
• Support the development and the qualification of analytical methods together with the AS&T team leader in accordance with ICHs guidelines and internal SOPs.
• Represents DP project teams in TRD sub-team, with strong sense of accountability and responsibility.
• Develops sound DP project strategy including contingency planning and risk assessments in line with the overall TRD project plan, development guidelines (as applicable), SOPs and TRD / RLT strategy.
• Monitors project plans and ensures timely availability of agreed deliverables. Proactively communicates overall project strategy, key issues, and any other critical topics in a timely manner to the appropriate management level, to the TRD project leader and / or to any other relevant project team member(s).
• Ensures adherence to the EP / LP project review process through relevant governance boards. No delays or missed reviews due to poor planning. Full compliance to other governance board processes, e.g. DMC. Ensure high quality documentation and pre-reads are provided per guidelines to facilitate these reviews.
• Ensures support to due diligence as applicable. Ensures availability of pre-requisites for transfer of projects to other sites as applicable (e.g. licenses, equipment, resource plan).
• Ensures application of IP process for all projects assigned and that all IP is accurately captured.
• Ensures contribution to respective Network deliverables and cross-functional workstreams / initiatives and ensure sharing of actions and learnings across global teams.
• Minimum : PhD in Pharmaceutics or related sciences with a minimum of 6 years of proven experience within the pharmaceutical / biotech industry or a Master’s degree with a minimum of 8 years experience.
• Fluent knowledge of English (oral and written). Desirable knowledge of site language.
• Broad and profound understanding of development activities and processes in pharmaceutical sciences. (early phase and late phase development)
• Excellent knowledge of laboratory and / or technical tools (e.g. Quality by Design, statistical software, Process Analytical Technology).
• Strong experience with outsourcing and supervising work done by CRO / CMOs including technical overview of agreement set up.
• Strong experience in writing CMC documents for regulatory submissions and responding to health authority questions.
• Solid understanding of relevant GLP, GMP regulations and policies.
• Strong presentation skills and scientific / technical writing skills.

Commitment to Diversity and Inclusion : Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Why Novartis : Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? our Novartis Network : Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up : and Rewards : Read our handbook to learn about all the ways we’ll help you thrive personally and professionally :

Seniority level

Seniority level

Mid-Senior level

Employment type

Employment type

Full-time

Job function

Job function

Product Management and Marketing

Pharmaceutical Manufacturing

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RLT Analytical Product Project Leader (m / f / d)

Castagneto Po, Piedmont, Italy 2 weeks ago

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• Define and develop an overall science and quality driven analytical project strategy including contingency plans and risk evaluations for RLT DS and RLT DP.
• Ensure transparent communication to the appropriate management level and / or to any other relevant project team members(s).
• Be a core member of the TRD sub-team representing RLT Analytical Science; co-own the technical development together with the DSPL and RLT DPPL, actively contribute to the definition of the overall technical development plan.
• Lead & coordinate, together with RLT analytical experts and subject matter experts, analytical activities (such as method development and validation, DS/DP stability, DS/DP release, reference nomination and transfer activities) across all analytical sites and partnering functions.
• Accountable for driving the testing strategy of RLT DS/DP and specifications setting. Be the RLT Analytical Science project representative in peer review and governance boards as well as in internal and external audits.
• Support the assessment, forecast & monitoring of monthly resource needs and reflect in TRD planning tools (internal/external costs and FTE requirements) ensuring budget adherence.
• Ensure the creation of an overall high-quality control strategy with partnering functions (CHAD, PHAD) and the documentation of the analytical/testing control strategy (e.g. SSS, risk assessments).
• Accountable for handover of analytical documents to internal and external partners (for e.g., including Health authority questions /CMC modules / Manufacturing & supply operations etc.) Understand & actively lead the interactions of project related RLT analytical activities across sites and line functions. Support EPM colleagues in outsourcing projects and provide input to QA agreements.
  
  

• Minimum: PhD in chemistry, pharmaceutical technology, or equivalent scientific degree with minimum 5 years of successful industry experience in the field of analytical chemistry and/or radiochemistry development and/or quality control with project management experience.
• Fluent knowledge of English (oral and written). Desirable knowledge of site language.
• Proficiency in quality principles driving drug development such as GMP; clear understanding of current and anticipated regulatory and quality expectations preferably in the radiopharmaceutical industry.
• Strong experience in writing CMC documents for regulatory submissions and responding to health authority questions.
• Strong experience with outsourcing and coordinating work done by CRO/CMOs including technical overview of agreement set up.
• Awareness for safe handling of chemicals, potentially dangerous materials, and equipment.
  
  

• Provide quality assurance expertise, guidance and support to operational activities in development and research organizations to ensure compliance with applicable regulatory requirements and Novartis procedures and quality standards. Manage projects, including Quality Plan initiatives, and processes that support quality objectives to assure their compliance with GxP regulations.
  
  

• Support discipline/service provision individually or within a team; provide functional expertise to QA/Line Units as needed.
• Review, approve, and release GMP-relevant deliverables and tools to ensure cGMP compliance.
• Manage project-related activities (e.g., process/quality initiatives, facility upgrades, IT validation) as per responsibility.
• Ensure compliance with internal/external quality and safety guidelines (e.g., GMP, SOPs, Quality Manual).
• Drive continuous quality improvements for manufacturing, collaborating with production, engineering, and supply chain.
• Oversee qualification/validation of processes, equipment, facilities, and software for GMP use.
• Review and approve GMP documents, including URS, IQ/OQ/PQ, Change Controls, CAPAs, and SOPs.
• Support inspection preparations and maintain oversight of external maintenance and qualification activities.
  
  

• Degree in Pharmacy, Biology, Chemistry, Engineering, or equivalent.
• Fluency in English (verbal and written).
• Strong awareness of quality issues and urgency in task completion.
• Open and clear collaboration and communication skills.
• Scientific, technical, and regulatory knowledge in the specific area, with basic understanding of drug development.
• Detailed knowledge of cGMP and familiarity with safety/environmental regulations.
• Minimum 5 years of experience in pharmaceutical companies in equivalent roles.
• Strong organizational skills.
  
  

• Support a discipline and/or provide a service individually or within a team of associates. May provide functional expertise to Line Unit and other QA Units in area of responsibility
• Write review, decide on approval and/or release of GMP-relevant deliverables, as applicable, and/or related tools as per area of responsibility in order to ensure compliance with cGMP and project quality deliverables.
• Manage project related activities (e.g. TRD product portfolio, development of new tools, processes, Quality initiatives, Quality Manual implementation, Quality Plans, Quality Risk Assessments, training activities, qualification and facility upgrade activities, IT validation projects) as per area of responsibility.
• Support Project management functions as a project team member.
• Provide support to TRD line functions in GMP related topics as per area of responsibility.
• Comply with internal and external guidelines regarding quality and safety (Quality Manual, regulatory cGMP guidelines, Health Authority guidance, SOPs etc.).
  
  

• Support the TRD QA function within a team, providing expertise to Line Units and other QA units in areas of responsibility.
• Write, review, and ensure compliance of GMP-relevant deliverables and tools with cGMP standards and project quality requirements.
• Oversee quality assurance for technical activities during development stages, including technical transfers and release requirements.
• Support project-related activities such as process development, quality initiatives, risk assessments, facility upgrades, and IT validation.
• Ensure alignment and consistency of regulatory submissions (IMPD/IND, NDA/MAA) and address health authority queries.
• Assist clinical trial teams with QA activity timelines and supply chain oversight.
• Perform QMS-related activities, including training, KPI oversight, SOP maintenance, and audit/inspection support.
• Act as QA point-of-contact for assigned CMO, including audits, CAPAs, documentation reviews, and compliance monitoring.
  
  

• Degree in Pharmacy, Biology, Chemistry, Engineering, or equivalent.
• Fluency in English (verbal and written).
• Strong awareness of quality issues and urgency in task completion.
• Open and clear collaboration and communication skills.
• Scientific, technical, and regulatory knowledge in the specific area, with basic understanding of drug development.
• Detailed knowledge of cGMP and familiarity with safety/environmental regulations.
• Minimum 5 years of experience in pharmaceutical companies in equivalent roles.
• Strong organizational skills.
  
  

• Support a discipline and/or provide a service individually or within a team of associates. May provide functional expertise to Line Unit and other QA Units in area of responsibility
• Write review, decide on approval and/or release of GMP-relevant deliverables, as applicable, and/or related tools as per area of responsibility in order to ensure compliance with cGMP and project quality deliverables.
• Manage project related activities (e.g. TRD product portfolio, development of new tools, processes, Quality initiatives, Quality Manual implementation, Quality Plans, Quality Risk Assessments, training activities, qualification and facility upgrade activities, IT validation projects) as per area of responsibility.
• Support Project management functions as a project team member.
• Provide support to TRD line functions in GMP related topics as per area of responsibility.
• Comply with internal and external guidelines regarding quality and safety (Quality Manual, regulatory cGMP guidelines, Health Authority guidance, SOPs etc.).
  
  

• Support the TRD QA function within a team, providing expertise to Line Units and other QA units in areas of responsibility.
• Write, review, and ensure compliance of GMP-relevant deliverables and tools with cGMP standards and project quality requirements.
• Oversee quality assurance for technical activities during development stages, including technical transfers and release requirements.
• Support project-related activities such as process development, quality initiatives, risk assessments, facility upgrades, and IT validation.
• Ensure alignment and consistency of regulatory submissions (IMPD/IND, NDA/MAA) and address health authority queries.
• Assist clinical trial teams with QA activity timelines and supply chain oversight.
• Perform QMS-related activities, including training, KPI oversight, SOP maintenance, and audit/inspection support.
• Act as QA point-of-contact for assigned CMO, including audits, CAPAs, documentation reviews, and compliance monitoring.
  
  

• Degree in Pharmacy, Biology, Chemistry, Engineering, or equivalent.
• Fluency in English (verbal and written).
• Strong awareness of quality issues and urgency in task completion.
• Open and clear collaboration and communication skills.
• Scientific, technical, and regulatory knowledge in the specific area, with basic understanding of drug development.
• Detailed knowledge of cGMP and familiarity with safety/environmental regulations.
• Minimum 5 years of experience in pharmaceutical companies in equivalent roles.
• Strong organizational skills.
  
  

• Provide quality assurance expertise, guidance and support to operational activities in development and research organizations to ensure compliance with applicable regulatory requirements and Novartis procedures and quality standards. Manage projects, including Quality Plan initiatives, and processes that support quality objectives to assure their compliance with GxP regulations.
  
  

• Support discipline/service provision individually or within a team; provide functional expertise to QA/Line Units as needed.
• Review, approve, and release GMP-relevant deliverables and tools to ensure cGMP compliance.
• Manage project-related activities (e.g., process/quality initiatives, facility upgrades, IT validation) as per responsibility.
• Ensure compliance with internal/external quality and safety guidelines (e.g., GMP, SOPs, Quality Manual).
• Drive continuous quality improvements for manufacturing, collaborating with production, engineering, and supply chain.
• Oversee qualification/validation of processes, equipment, facilities, and software for GMP use.
• Review and approve GMP documents, including URS, IQ/OQ/PQ, Change Controls, CAPAs, and SOPs.
• Support inspection preparations and maintain oversight of external maintenance and qualification activities.
  
  

• Degree in Pharmacy, Biology, Chemistry, Engineering, or equivalent.
• Fluency in English (verbal and written).
• Strong awareness of quality issues and urgency in task completion.
• Open and clear collaboration and communication skills.
• Scientific, technical, and regulatory knowledge in the specific area, with basic understanding of drug development.
• Detailed knowledge of cGMP and familiarity with safety/environmental regulations.
• Minimum 5 years of experience in pharmaceutical companies in equivalent roles.
• Strong organizational skills.