261 Posti di lavoro Rieti

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.

Since 1972, Takeda has had two sites in Italy for producing plasma-derived drugs in Rieti and Pisa, supporting patients with rare and complex diseases. These sites focus on the production of therapies derived from immunoglobulins, albumin, and coagulation factors. As a partner of the National Health System, we transform plasma into life-saving drugs under the “National Self-Sufficiency of Blood and its Products” program. We provide high-quality drugs worldwide, with a strong presence in Europe, America, and Asia.

Across Italy and the world, Takeda is recognized as a Top Employer by the Top Employers Institute based on our commitment to career development, inclusion, learning, sustainability, wellness, and, most importantly, our values.

Join us to make a difference.

OBJECTIVES/PURPOSE:

• Manage the activities related to Process Improvement & Stewardship Team 

• Lead process improvement initiatives, monitoring, and stewardship

• Provide technical support about manufacturing processes, investigations, optimization, yield improvement projects, cycle time reduction 

ACCOUNTABILITIES:

• Manage and coordinate the Process Improvement team, ensuring that all team members are aligned with business objectives and operate efficiently

• Lead process improvement initiatives, monitoring, and stewardship

• Provide technical support about manufacturing processes, investigations, optimization, yield improvement projects, cycle time reduction, process robustness, Technology Transfer

• Oversee product and process investigations, product impact assessment, risk assessment

• Collaborate with all other departments to ensure an integrated and cohesive approach

• Ensure compliance with regulations and quality standards, keeping Quality by Design documents up to date

• Manage process validation strategy

• Support the preparation of regulatory submission / meetings

• Support regulatory inspections and defending technical decisions to regulatory agencies

CORE ELEMENTS RELATED TO THIS ROLE:

• Excellent leadership and team management skills

• Strong strategic orientation and analytical thinking ability

• Excellent communication, collaboration and influencing skills

• Experience in managing complex projects and implementing innovative technologies

• Ability to anticipate changes and solve complex problems

• Project management skills and results orientation

• Development of the team, providing strategic direction and support in complex scenarios

• Development of strategic plans for departmental growth and operational efficiency

DIMENSIONS AND ASPECTS - REQUIREMENTS:

Technical/Functional (Line) Expertise

• Master or PhD degree in technical/scientific education, preferably pharmaceutical sciences, chemistry, biotechnology, bioinformatics or pharma - process engineering

• 5/7 previous experience in Leadership Role

• Previous experience in plasma fractionation processes (Ideal - Preferred) or in biotechnology field > knowledge of proteins > Knowledge of GMP/GDP (mandatory)

• Experience in Process Validation (Preferred)

• Experienced in process optimization, capable of implementing strategies to enhance productivity

• Proficient in continuous improvement processes

• Proven experience in statistics, data analysis or equivalent academic experience/course record

• Proven knowledge of six-sigma and DMAIC methodology 

• Excellent knowledge of Italian and English, both written and spoken - Fluent level

Leadership

• Focuses on the few priorities and delivers superior results 

• Elevates the capabilities of the organization for now and the future 

• Strategic enterprise thinking, finding innovative ways to serve patients build reputation and trust

• Good understanding of industry, scientific trends and market conditions to develop solutions enhancing compliance and quality of life for patients

• Organizational skills

• Good communication and presentation skills as well as influencing skills

Decision-making and Autonomy

• Creating the environment that inspires and enables people

• Creates clarity, fostering alignment and accountability

• Is courageous in making decisions based on sound business judgment or appropriately escalate topics with high criticality

ADDITIONAL INFORMATION:

• Willingness to travel to various internal/external Takeda meetings and events

We want our employees to succeed in everything they do - at work, at home, and in the community. This is why we offer world-class benefits and access to resources that can support people.

Health and Finance

• Health Care Assistance Insurance

• Employee Stock Purchase Plan

• Employee discount programs on commercial establishments, shops, medical services

Training and Development

• Technical skill training and professional development

• Job Rotation programs for working in other departments

• Spontaneous employee groups for awareness on Diversity, Equity, and Inclusion issues and community engagement activities

• Value-based culture

Individual Support

• Wellness programs

• On-site cafeteria and bar

• Resources for mental, physical, financial, and spiritual health

• Parental Leave

NOTE:

• Belonging to protected categories (Law No. 68/99) will be considered a preferential qualification.

At Takeda, our patients rely on us to create quality products, and we aim to create a safe environment for our team members. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product or putting anyone at the site in harm's way. In this role, you may:

• Work in a controlled environment requiring special gowning and wearing protective clothing.

• Need to remove all make-up, jewelry, contact lenses, nail polish, and/or artificial fingernails while in the manufacturing environment.

At Takeda, we are transforming patient care through the development of innovative specialty medicines and first-class patient support programs. Takeda is a patient-oriented company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and aims for excellence in everything we do. We promote an inclusive and collaborative work environment where our teams are united by an unwavering commitment to delivering Better Health and a Brighter Future to people worldwide.

Takeda is proud of its commitment to creating a diverse workforce and offering equal employment opportunities to all employees and applicants without distinction of race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information, marital status, or any other characteristic protected by law.

#GMSGQ

#LI-LA1

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.

Since 1972, Takeda has had two sites in Italy for producing plasma-derived drugs in Rieti and Pisa, supporting patients with rare and complex diseases. These sites focus on the production of therapies derived from immunoglobulins, albumin, and coagulation factors. As a partner of the National Health System, we transform plasma into life-saving drugs under the “National Self-Sufficiency of Blood and its Products” program. We provide high-quality drugs worldwide, with a strong presence in Europe, America, and Asia.

Across Italy and the world, Takeda is recognized as a Top Employer by the Top Employers Institute based on our commitment to career development, inclusion, learning, sustainability, wellness, and, most importantly, our values.

Join us to make a difference.

We are looking for a candidate with expertise in Process Analytical Technology (PAT) applied to continuous monitoring in biotechnology production processes. You will be responsible for searching, testing, and implementing innovative solutions aimed at improving monitoring and optimization across our production processes.

You will ensure real-time monitoring of production processes through the implementation and management of in-line, on-line and at-line analytical technologies. The role also requires integrating data analysis skills to optimize process performance and support evidence-based decision-making.

• Lead the development and research of PAT solutions by studying and implementing in-line, on-line and at-line probes (such as NIR, Raman, FTIR spectroscopy, pH sensors, conductivity, turbidity, flow rate, flow imaging, DLS, particle counting) to monitor and inspect production processes in real-time.

• Conduct feasibility studies for analytical methods using in-line, online, and at-line instruments.

• Ensure accurate data collection and analysis to optimize production processes.

• Collaborate with cross-functional teams, to develop monitoring solutions aligning with industry standards and regulations.

• Support in-line PAT instruments qualification (IQ/OQ/PQ) and related documentation writing

• Support and execute controlled research experiments and trials

• Manage and perform scientific research, development, and testing of new Process Analytical technologies for continuous process monitoring.

• Stay updated on emerging technologies in sensoristics and biotech.

• Execute manufacturing runs and scale-down experiments participating in their design and execution

• Prepare and present comprehensive technical and/or project reports and formal presentations to a full range of internal / external audiences.

• PhD or Master Degree in Pharmaceutical Sciences, Chemistry, Biotechnology, Bio-Chemical Engineering )

• At least 2-3 years of relevant University/Industry experience (pharmaceutical, chemical, biotech) in Process Analytical Technology for development of probes to characterize protein material.

• Profound knowledge in in-line process analytical technology and proteins.

• Mandatory: proficiency in protein characterization techniques, including but not limited to optical methods

• Preferrable: Knowledge in biochemistry, protein purification and engineering principles

• Preferrable: expertise in analytical chemistry methodologies to support the analysis and characterization of protein-based therapeutics

• Basic understanding of relevant manufacturing processes

• Knowledge of statistics and main statistical analysis tools (Minitab, etc.)

• Fluent English and Italian and good redaction skills

We want our employees to succeed in everything they do - at work, at home, and in the community. This is why we offer world-class benefits and access to resources that can support people.

Health and Finance

• Health Care Assistance Insurance

• Employee Stock Purchase Plan

• Employee discount programs on commercial establishments, shops, medical services

Training and Development

• Technical skill training and professional development

• Job Rotation programs for working in other departments

• Spontaneous employee groups for awareness on Diversity, Equity, and Inclusion issues and community engagement activities

• Value-based culture

Individual Support

• Wellness programs

• On-site cafeteria and bar

• Resources for mental, physical, financial, and spiritual health

• Parental Leave

NOTE:

• Belonging to protected categories (Law No. 68/99) will be considered a preferential qualification.

At Takeda, our patients rely on us to create quality products, and we aim to create a safe environment for our team members. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product or putting anyone at the site in harm's way. In this role, you may:

• Work in a controlled environment requiring special gowning and wearing protective clothing.

• N eed to remove all make-up, jewelry, contact lenses, nail polish, and/or artificial fingernails while in the manufacturing environment.

• Willingness to travel to various internal/external Takeda meetings and events

• Flexibility to work in shifts

At Takeda, we are transforming patient care through the development of innovative specialty medicines and first-class patient support programs. Takeda is a patient-oriented company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and aims for excellence in everything we do. We promote an inclusive and collaborative work environment where our teams are united by an unwavering commitment to delivering Better Health and a Brighter Future to people worldwide.

Takeda is proud of its commitment to creating a diverse workforce and offering equal employment opportunities to all employees and applicants without distinction of race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information, marital status, or any other characteristic protected by law.

#GMSGQ

#LI-LA1

Posizione

• Hotel del Lago Active & Spa
• Piediluco
• vicino alle Cascate della Marmore ricerca
• Hotel Manager
• che si occupi di :

Gestione dei servizi e dei reparti; Organizzazione del personale, cura dell’ospite, supervisione delle offerte; Gestione delle recensioni; Monitoraggio dei costi e ricavi; Gestione delle attività vendita e redazione di un piano operativo commerciale.

Si richiede : esperienza pluriennale, conoscenza della lingua inglese; conoscenza dei sistemi di prenotazione, competenze amministrative, doti relazionali, leadership, flessibilità ed empatia; Ottime capacità di analisi, autonomia decisionale, entusiasmo e resistenza allo stress.

Si offre : contratto full-time, alloggio, salario commisurato alle esperienze pregresse.

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description:

Since 1972, Takeda has had two sites in Italy for producing plasma-derived drugs in Rieti and Pisa, supporting patients with rare and complex diseases. These sites focus on the production of therapies derived from immunoglobulins, albumin, and coagulation factors. As a partner of the National Health System, we transform plasma into life-saving drugs under the “National Self-Sufficiency of Blood and its Products” program. We provide high-quality drugs worldwide, with a strong presence in Europe, America, and Asia.

Across Italy and the world, Takeda is recognized as a Top Employer by the Top Employers Institute based on our commitment to career development, inclusion, learning, sustainability, wellness, and, most importantly, our values.

Join us to make a difference.

About The Role

As a Senior Data Scientist, you will manage and execute local data science initiatives to improve productivity not limited to data availability enhancement, process modeling using ML tools, digital twins. Identifies local data science possibilities/initiatives/requests in collaboration with local team, DD&T, Engineering, Quality and global Data Science.

How you will contribute

• Provide technical support to manufacturing processes, investigation, yield optimization, process monitoring and support internal and/or external functional/ multifunctional teams in trouble shooting and problem solving
• Identify patterns, trends and anomalies in batch data providing valuable insights into process variability, process performance and product quality
• Support and drive the Manufacturing Science department activities (i.e. yield improvement projects, process robustness initiatives, process monitoring and CPV) and the site initiatives (i.e. cycle time reduction projects) with advanced data analysis (Machine Learning) and promote use off the shelf data analysis software (Minitab, SIMCA, Qlik, …)
• Drive and support local digital data science initiatives according to prioritization (e.g. Yield Improvement, real-time monitoring, predictive process performance etc.).
• Expand and unlock new knowledge for effective process monitoring and process improvement optimizations (e.g. descriptive statistics and visualization, statistical process control, out-of-the-box-tools).
• Provide technical support to manufacturing processes, investigation, yield optimization and process monitoring with advanced data analysis.
• Own and maintain Manufacturing Science/ Manufacturing related dataset
• Manage investigations and support internal and/or external functional/ multifunctional teams in trouble shooting and problem solving
• Translate business problems into opportunities and effectively communicate findings with stakeholders.
• Gathers and identify local data science possibilities/initiatives/requests in collaboration with local team, DD&T, Engineering, Quality and global GMS data science.
• Supports and participates in global/functional/local GMS data science community
• Support in maintaining the GMP archive for the group, including responsibility of document withdrawal and destroy
• Responsible for day-to-day operation of local data science function, covering all data science levels and related technologies.
  
  

• Master or PhD degree in technical/scientific education, preferably pharmaceutical sciences, chemistry, biotechnology, bioinformatics or pharma - process engineering
• Previous experience in Data Analysis (3 years)
• Proven experience in statistics, data analysis or equivalent academic experience/course record. Proven knowledge of six-sigma and DMAIC methodology
• Good written and spoken Italian and English mandatory
• Mathematical and Statistical Knowledge
• Experience in coding skills es in Python/R (preferred)
• Proficiency in database languages (SQL), understanding of data models and databases
• Expertise and experience in Machine Learning, Artificial Intelligence/Deep Learning, Big Data and Digital (preferred)
• Proven experience in statistics, data analysis or equivalent academic experience/course record. Proven knowledge of six-sigma and DMAIC methodology
• Good written and spoken Italian and English mandatory
• Mathematical and Statistical Knowledge
• Experience in coding skills es in Python/R (preferred)
• Proficiency in database languages (SQL), understanding of data models and databases
• Expertise and experience in Machine Learning, Artificial Intelligence/Deep Learning, Big Data and Digital (preferred)
• Knowledge of plasma fractionation process (preferred)
• Capabilities to translate business needs into data analytics concepts and the other way
• Strategic enterprise thinking, finding innovative ways to serve patients build reputation and trust.
• Good understanding of industry, scientific and data science trends and market conditions to develop solutions enhancing compliance and quality of life for patients.
• Good communication and presentation skills as well as influencing skills.
  
  

• Health Care Assistance Insurance
• Employee Stock Purchase Plan
• Employee discount programs on commercial establishments, shops, medical services
  
  

• Technical skill training and professional development
• Job Rotation programs for working in other departments
• Spontaneous employee groups for awareness on Diversity, Equity, and Inclusion issues and community engagement activities
• Value-based culture
  
  

• Wellness programs
• On-site cafeteria and bar
• Resources for mental, physical, financial, and spiritual health
• Parental Leave
  
  

• Belonging to protected categories (Law No. 68/99) will be considered a preferential qualification.
  
  

• Willingness to travel to various internal/external Takeda meetings and events
  
  

Mission

Inserito/a nel Team dedicato ad un importante Cliente del Gruppo, il/la candidato/a ha la responsabilità del processo di ricerca e selezione del personale in somministrazione da inserire presso le sedi del Cliente sul territorio di competenza. Per la seguente opportunità si offre un contratto a tempo determinato con la finalità di coprire un picco di lavoro stagionale.

Sarà responsabile del processo di recruiting dedicato alle necessità del Cliente.

• Ricerca dei candidati nel DB aziendale e altri database online.
• Gestione dell’attività di social recruiting ai fini dell’ottimizzazione del reclutamento.
• Screening delle candidature e phone interview di prima valutazione.
• Gestione colloqui di gruppo.
• Cura del processo di comunicazione verso i singoli candidati.
• Gestione aspetti amministrativi del rapporto di lavoro.
• Gestione del servizio complessivo al Cliente.

Laurea, anche breve, preferibilmente in materie umanistiche, economiche e/o giuridiche.

Almeno 6 mesi in posizioni analoghe, preferibilmente in Agenzie per il Lavoro.

• Predisposizione al lavoro in team e per obiettivi.
• Spiccate capacità relazionali e di problem solving.
• Customer orientation.
• Buona conoscenza del pacchetto Office e Outlook.
• Buona conoscenza della lingua inglese.

Con oltre 34.000 colleghi in tutto il mondo, The Adecco Group è presente in Italia con oltre 2.800 professionisti ed è la più importante piattaforma multibrand di HR Solutions per il mondo del lavoro. Ha sede a Zurigo, è presente in oltre 60 Paesi con più di 5.100 uffici e impiega quotidianamente lavoratori presso aziende clienti.

The Adecco Group Italia dispone di tre business unit: Adecco, Akkodis, LHH. L’azienda si impegna a garantire opportunità e sviluppo, promuovendo diversità e inclusione.

Questo annuncio di lavoro è pubblicato da The Adecco Group - Direzione Risorse Umane - Via Tolmezzo, 15, 20132 Milano, Italia – I candidati sono invitati a leggere l’informativa sulla privacy sul sito Adecco è un datore di lavoro di pari opportunità che sostiene la diversity.

Overview

Adecco - Administrative Specialist CCBU Passo Corese (RI)

Ha la responsabilità di sviluppare il processo di gestione amministrativa del personale somministrato della Business Unit, di supportare le attività amministrative relative allo sviluppo dei servizi e di contribuire alla redazione di report e analisi dei dati funzionali alle previsioni, alla consuntivazione e alla presa di decisioni.

Disponibilità ad applicare la prestazione lavorativa anche nei fine settimana, su rotazione rispetto agli altri colleghi del team, nel rispetto dei tempi di riposo previsti dalla normativa e in riferimento all’orario di lavoro settimanale. La sede di lavoro sarà a Passo Corese, Rieti. Per questa opportunità si offre Contratto a Tempo Determinato per copertura sostituzione maternità.

• Gestione dell’area dedicata alla redazione e al controllo di documenti amministrativi (Firma Elettronica Avanzata, Firma Elettronica Semplice, Controllo Visa etc.);
• Monitoraggio della sottoscrizione di contratti e proroghe;
• Comunicazione delle scadenze ai diversi soggetti coinvolti nel processo;
• Gestione del processo di dimissioni dei lavoratori somministrati;
• Overview sul processo di Payroll;
• Comunicazione e verifica delle espansioni connesse alla somministrazione con Monte Ore Garantito;
• Gestione delle variazioni percentuali orarie, ovvero delle trasformazioni;
• Esecuzione e monitoraggio della procedura relativa alla gestione degli infortuni.

• Supporto nella gestione della turnistica;
• Contributo alla redazione di documenti utili alla gestione amministrativa della Business Unit;
• Facilitazione di passaggi di informazioni amministrative fra Filiali e fra Filiali e Team Onsite.

• Gestione di reportistica finalizzata alle attività di previsione e consuntivazione;
• Redazione di report e presentazioni di dati e informazioni funzionali alla presa di decisioni.

• Conoscenza di MS Office
• Conoscenza avanzata di Excel
• Consapevolezza dei processi amministrativi
• Conoscenza della struttura del payroll dei lavoratori somministrati
• Utilizzo degli strumenti aziendali dedicati alla gestione della somministrazione
• Abilità nella gestione della reportistica

• Capacità di analisi
• Attenzione al dettaglio
• Comunicazione efficace
• Teamworking
• Problem solving

Laurea preferibilmente in Economia, Scienze bancarie e finanziarie, Giurisprudenza.

Minimo sei mesi di esperienza su attività amministrative del personale.

Con oltre 34.000 colleghi in tutto il mondo, The Adecco Group, presente in Italia con oltre 2.800 professionisti, è la più importante piattaforma multibrand di HR Solutions per il mondo del lavoro, leader a livello globale nei servizi dedicati alla gestione delle Risorse Umane. La sua sede principale è a Zurigo, è presente in oltre 60 Paesi con più di 5.100 uffici e ogni giorno impiega oltre 800.000 lavoratori presso 100,000 aziende clienti. The Adecco Group Italia dispone di tre business unit: Adecco, Akkodis, LHH. Let’s make the world a better place to work: il nostro impegno è garantire che le persone siano ispirate, motivate e formate per affermarsi in un contesto lavorativo in continua evoluzione, e che le aziende, le istituzioni e la scuola siano supportate e sostenute nella loro strategia di miglioramento e sviluppo. Adecco è la società di The Adecco Group che si occupa di mettere in contatto le persone con le giuste opportunità di lavoro e le imprese con i migliori candidati. Siamo presenti in oltre 60 Paesi nel mondo, in Italia con un team di oltre 2.000 professionisti e con più di 300 filiali sul territorio nazionale.

Questo annuncio di lavoro è pubblicato da The Adecco Group - Direzione Risorse Umane - Via Tolmezzo, 15, 20132 Milano, Italia – I candidati, nel rispetto delle normative vigenti, sono invitati a leggere l’informativa sulla privacy sul sito Adecco è un datore di lavoro di pari opportunità che sostiene la diversity e l’inclusione. Il presente annuncio è rivolto ad entrambi i sessi e a persone di tutte le età, nazionalità, etnia, orientamento o espressione di genere, orientamento sessuale e credo religioso.

Posting date:

Overview

Cerchiamo Farmacista Collaboratore da inserire all’interno delle nostra Farmacia , contratto a tempo determinato, full-time, retribuzione commisurata all'esperienza e professionalità.

Il Farmacista Boots, in diretto riporto al Direttore di Farmacia, ha la responsabilità della cura e soddisfazione dei nostri pazienti-clienti.

Grazie alla stretta collaborazione con il direttore e i colleghi avrai la possibilità di sviluppare a 360° le tue competenze in ambito consulenziale, gestionale e legislativo. Inoltre, avrai una formazione costante che si articola nei due grandi ambiti della farmacia: scientifica e prodotto.

• Sistema incentivante
• Ambiente dinamico e stimolante

• Laurea in Farmacia o CTF
• Iscrizione all'albo

Overview

Since 1972, Takeda has had two sites in Italy for producing plasma-derived drugs in Rieti and Pisa, supporting patients with rare and complex diseases. These sites focus on the production of therapies derived from immunoglobulins, albumin, and coagulation factors. As a partner of the National Health System, we transform plasma into life-saving drugs under the “National Self-Sufficiency of Blood and its Products” program. We provide high-quality drugs worldwide, with a strong presence in Europe, America, and Asia.

Across Italy and the world, Takeda is recognized as a Top Employer by the Top Employers Institute based on our commitment to career development, inclusion, learning, sustainability, wellness, and, most importantly, our values.

Join us to make a difference.

• Manage the activities related to Process Improvement & Stewardship Team
• Lead process improvement initiatives, monitoring, and stewardship
• Provide technical support about manufacturing processes, investigations, optimization, yield improvement projects, cycle time reduction

• Manage and coordinate the Process Improvement team, ensuring that all team members are aligned with business objectives and operate efficiently
• Lead process improvement initiatives, monitoring, and stewardship
• Provide technical support about manufacturing processes, investigations, optimization, yield improvement projects, cycle time reduction, process robustness, Technology Transfer
• Oversee product and process investigations, product impact assessment, risk assessment
• Collaborate with all other departments to ensure an integrated and cohesive approach
• Ensure compliance with regulations and quality standards, keeping Quality by Design documents up to date
• Manage process validation strategy
• Support the preparation of regulatory submission / meetings
• Support regulatory inspections and defending technical decisions to regulatory agencies

• Excellent leadership and team management skills
• Strong strategic orientation and analytical thinking ability
• Excellent communication, collaboration and influencing skills
• Experience in managing complex projects and implementing innovative technologies
• Ability to anticipate changes and solve complex problems
• Project management skills and results orientation
• Development of the team, providing strategic direction and support in complex scenarios
• Development of strategic plans for departmental growth and operational efficiency

• Technical / Functional (Line) Expertise
• Master or PhD degree in technical / scientific education, preferably pharmaceutical sciences, chemistry, biotechnology, bioinformatics or pharma - process engineering
• 5 / 7 previous experience in Leadership Role
• Previous experience in plasma fractionation processes (Ideal - Preferred) or in biotechnology field >
• knowledge of proteins >
• Knowledge of GMP / GDP (mandatory)
• Experience in Process Validation (Preferred)
• Experienced in process optimization, capable of implementing strategies to enhance productivity
• Proficient in continuous improvement processes
• Proven experience in statistics, data analysis or equivalent academic experience / course record
• Proven knowledge of six-sigma and DMAIC methodology
• Excellent knowledge of Italian and English, both written and spoken - Fluent level
• Leadership
• Focuses on the few priorities and delivers superior results
• Elevates the capabilities of the organization for now and the future
• Strategic enterprise thinking, finding innovative ways to serve patients build reputation and trust
• Good understanding of industry, scientific trends and market conditions to develop solutions enhancing compliance and quality of life for patients
• Organizational skills
• Good communication and presentation skills as well as influencing skills
• Decision-making and Autonomy
• Creating the environment that inspires and enables people
• Creates clarity, fostering alignment and accountability
• Is courageous in making decisions based on sound business judgment or appropriately escalate topics with high criticality

• Willingness to travel to various internal / external Takeda meetings and events

• We want our employees to succeed in everything they do - at work, at home, and in the community. This is why we offer world-class benefits and access to resources that can support people.
• Health and Finance
• Health Care Assistance Insurance
• Employee Stock Purchase Plan
• Employee discount programs on commercial establishments, shops, medical services
• Training and Development
• Technical skill training and professional development
• Job Rotation programs for working in other departments
• Spontaneous employee groups for awareness on Diversity, Equity, and Inclusion issues and community engagement activities
• Value-based culture
• Individual Support
• Wellness programs
• On-site cafeteria and bar
• Resources for mental, physical, financial, and spiritual health
• Parental Leave

• Note : Belonging to protected categories (Law No. 68 / 99) will be considered a preferential qualification.
• Important Considerations : At Takeda, our patients rely on us to create quality products, and we aim to create a safe environment for our team members. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product or putting anyone at the site in harm's way. In this role, you may:
  • Work in a controlled environment requiring special gowning and wearing protective clothing.
  • Need to remove all make-up, jewelry, contact lenses, nail polish, and / or artificial fingernails while in the manufacturing environment.

At Takeda, we are transforming patient care through the development of innovative specialty medicines and first-class patient support programs. Takeda is a patient-oriented company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and aims for excellence in everything we do. We promote an inclusive and collaborative work environment where our teams are united by an unwavering commitment to delivering Better Health and a Brighter Future to people worldwide.

Takeda is proud of its commitment to creating a diverse workforce and offering equal employment opportunities to all employees and applicants without distinction of race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information, marital status, or any other characteristic protected by law.

GMSGQ

LI-LA1

Locations

ITA - Rieti

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Ottieni i suggerimenti dell’IA su questa offerta di lavoro e altre funzionalità esclusive.

Geopavia da oltre 35 anni offre servizi di ingegneria multidisciplinare e consulenza per infrastrutture altamente tecnologiche al servizio delle collettività. Il nostro focus principale è l’energia, ma ci occupiamo anche di mobilità, telecomunicazioni, risorse idriche e ambiente.

La nostra missione è quella di fornire ai nostri partner solide competenze tecniche e scientifiche, soluzioni e tecnologie innovative che possano accelerare la transizione verso un futuro migliore: più sostenibile, più resiliente e più inclusivo.

Siamo oltre 130 tra ingegneri, progettisti, architetti e specialisti di varie discipline, talentuosi ed appassionati, impegnati a seguire un modello di business etico e socialmente responsabile, con un’attenzione particolare alla sicurezza e all’ambiente.

La nostra aderenza a principi di correttezza e integrità è riconosciuta e certificata attraverso la norma SA8000, standard globale che attesta l'adozione di politiche e pratiche di lavoro rispettose dei diritti umani.

Posizione:

La posizione è dedicata al coinvolgimento nel team di supervisione lavori sugli impianti di trasporto e distribuzione gas nell'area est del Lazio, con centro geografico delle attività presso Rieti, in qualità di Supervisore Lavori e Coordinatore della Sicurezza (CSE).

Le attività riguarderanno: interventi di sostituzione, estensione rete, upgrade degli impianti di linea, ecc.

Le principali attività previste sono le seguenti:

• Attività di Supervisione Lavori delle imprese coinvolte;
• Assistenza in campo per la risoluzione di problematiche, interferenze o criticità;
• Compilazione, verifica e validazione documentale;
• Assistenza alle riunioni del Committente con le imprese appaltatrici dei lavori e redazione dei relativi verbali;
• Aggiornamento periodico dei programmi lavori redatti dalle imprese appaltatrici e verifica dell’avanzamento dei lavori;
• Amministrazione dei contratti d'appalto e contabilità.
  
  

• Ingegnere Civile, Ambientale, Edile, Energetico, Meccanico o Architetto con Laurea triennale o magistrale, Geometra, Perito Meccanico o equivalente;
• Iscritto all'albo professionale di riferimento;
• Abilitato ai sensi della 81/08 al ruolo di coordinatore della sicurezza con attestazione di aggiornamento quinquennale;
• Conoscenza base aspetti HSEQ;
• Buona conoscenza del pacchetto Microsoft Office;
• Buona conoscenza di AutoCAD;
• Automunito o con accesso a mezzi di trasporto affidabile per raggiungere le aree di intervento;
• Conoscenza della lingua Italiana (C1).
  
  

• Esperienza pregressa nella Supervisione Lavori su cantieri di condotte, reti e impianti di trasporto e distribuzione fluidi o su cantieri di opere pubbliche;
• Incarichi nel ruolo di CSE;
• Buone capacità comunicative e propensione a lavorare in team.
  
  

• Collaborazione Professionale (Partita Iva) compatibile con altre attività.
  
  

• Se il curriculum sarà valutato positivamente si riceverà una call conoscitiva, cui seguirà eventualmente un incontro con i Coordinatori e/o la Direzione, in presenza o da remoto a seconda delle disponibilità;
• La ricerca ha carattere di urgenza.
  
  

• Livello di anzianità Livello medio-alto

• Settori Petrolio e gas

Le referenze raddoppiano le tue probabilità di ottenere un colloquio presso Geopavia

Ricevi avvisi per le nuove offerte di lavoro per Petroleum Engineering Manager in Rieti .

Stiamo creando un modo nuovo per condividere le conoscenze della community. Gli esperti aggiungono informazioni direttamente a ogni articolo, che all’inizio viene generato con l’aiuto dell’intelligenza artificiale.