126 Posti di lavoro per Master Black Belt in Italia

Overview

Leads internal and external audits, annual reviews, and quality scheduling. Partners with global QMS teams to share best practices and support training. Drives continuous improvement and supports capital and quality initiatives. Ensures audit readiness and QMS enhancements in collaboration with the QMS Engineer.

• Responsible for managing the site’s Quality Management System (QMS), including maintaining a year-long calendar, coordinating internal audits, facilitating document reviews in CompliantPro, and leading QMS planning and Management Review meetings.
• Delivers quality training for new and current associates, oversees the Quality Quiz process, and supports internal auditor development.
• Drives continuous improvement by aligning business processes with standards, tracking and reporting quality metrics, and supporting site-wide initiatives.
• Manages capital spending activities by tracking financial data, supporting project teams with forecasting and documentation, and ensuring timely reporting and approvals.
• Provides regular QMS updates to leadership through monthly council meetings and fosters collaboration across teams to maintain compliance and quality excellence.

• Associate’s degree required.
• 3+ years of experience supporting corporate functions.

• Experience following standards and procedures.
• Quality auditing experience preferred.
• Attention to detail and effective time management and organization skills.
• Strong computer proficiency, particularly with Microsoft Excel, Powerpoint, Word, and Outlook.
• Strong communication and interpersonal skills when working with auditors, engineers, etc.
• Comfortable facilitating meetings with groups up to 10 people.
• Knowledge of ISO standards preferred.

Goodyear is one of the world’s largest tire companies. It employs about 71,000 people and manufactures its products in 55 facilities in 22 countries around the world. Its two Innovation Centers in Akron, Ohio, and Colmar-Berg, Luxembourg, strive to develop state-of-the-art products and services that set the technology and performance standard for the industry. For more information about Goodyear and its products, go to Goodyear.com.

If you need reasonable accommodation to complete the online application, or any other part of the employment process, please contact the Goodyear Candidate Care Line at .

Goodyear is an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to any characteristic protected by law.

Job Description

We are looking for a Quality Management System Specialist to join our quality department in Piombino Dese (PD).

Stevanato Group is an Italian multinational manufacturing company that develops and produces drug containment solutions in glass and plastics .

The main production process involves the processing of glass tubes through forming, followed by cleaning and sterilization using highly automated machinery .

The ideal candidate will carry out activities to ensure the management system complies with applicable standards, guidelines, and regulations ; maintain the relevant quality management system, processes, procedures, directives, and tools, ensuring continuous compliance.

KEY ACCOUNTABILITIES

• Implement and maintain an up-to-date management system, ensuring compliance with regulations, directives, standards, and requirements.
• Conduct continuous analysis to monitor national and international standards and regulatory changes, collaborating with involved functions.
• Assess efficiency, propose improvements, and keep the management system updated accordingly, working alongside internal audit teams.
• Participate in standardizing procedures across international plants and functions to promote best quality practices and a unified SG quality approach.
• Support audit and inspection preparations to ensure compliance of the quality management system.
• Identify compliance issues, evaluate risks, and implement corrective and preventive actions in collaboration with leadership to reduce non-conformities.
• Participate in training processes on relevant topics, ensuring compliance with standards and procedures, working with HR and other relevant functions.

Qualifications

• Master's degree in a scientific field
• 3-4 years of experience in a similar role
• Full professional proficiency in Italian and English
• Knowledge of applicable regulatory requirements, including local regulations, cGMP, FDA, and ISO standards
• Knowledge of CAPA, Change Control, Deviations processes, and techniques

Adherence to Stevanato Group’s values: Trust and respect everyone; Be accountable; Be ethical always; Listen and communicate with transparency and honesty; Deliver results

Job Description

Siamo la divisione International Surgical di Enovis, un'azienda globale orientata all'innovazione nel settore delle tecnologie mediche. Ci impegniamo quotidianamente per migliorare la qualità della vita dei pazienti, sviluppando soluzioni innovative e clinicamente differenziate. Ricerchiamo i migliori talenti, la costante innovazione e siamo spinti dal desiderio di migliorarci ogni giorno di più.

Per il nostro Headquarter, stiamo cercando un Quality Management System Engineer da inserire all'interno della nostra area Quality Assurance. Il ruolo, riportando al Quality Management System Manager, sarà focalizzato sul definire, attuare, mantenere e distribuire le procedure del Sistema di Gestione Qualità aziendale, garantendo il coinvolgimento appropriato del personale della Società e la conformità agli Standard e Regolamenti applicabili. Monitorerà, altresì, l'avanzamento dei rapporti di non conformità (NC) e delle azioni correttive/preventive (CAPA).

Responsabilità

• Definire e condividere modalità operative e processi
• Implementare e verificare la documentazione del Sistema Qualità
• Gestire rapporti di non conformità (NC) e le azioni correttive/preventive (CAPA)
• Verificare la corretta applicazione di requisiti (es.: audit)
• Raccogliere, analizzare e presentare dati statistici (es. analisi NC e CAPA)
• Gestire feedback dal mercato
• Gestire documentazione di produzione e rilascio

Requisiti

• Laurea in ingegneria, preferibilmente Gestionale o Biomedica
• Pregressa esperienza (due o più anni) maturata in ambito quality assurance, regulatory o engineering, in contesti aziendali riguardanti la progettazione, produzione e/o vendita di dispositivi medici
• Conoscenza delle principali norme di riferimento: ISO 13485, IEC 62304, ISO 14971, ISO 9001
• Buona gestione del tempo e delle priorità
• Precisione e metodo
• Ottima conoscenza della lingua inglese, scritta e parlata (almeno B2)

La posizione sarà basata a Villanova di San Daniele del Friuli (UD), con possibilità di smart working.

Le candidature prive di cv allegato, non verranno prese in considerazione.

About Enovis

Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, global talent and innovation, the Company’s extensive range of products, services and integrated technologies fuels active lifestyles in orthopedics and beyond. For more information about Enovis, please visit

EOE AA M/F/VET/Disability Statement

All qualified applicants will receive consideration for employment and will not be discriminated against on the basis of race, religion, color, national origin, sex, protected veteran status, disability, or any other basis protected by federal, state or local laws.

Overview

Vertiv is looking for a Supplier Quality Engineer to develop, evaluate, and improve the Vertiv product supplier base through quality management system and product process audits. The Supplier Quality Engineer is responsible for maintaining working relationships with suppliers to ensure the highest quality possible of purchased components/materials with a focus on continuous improvement. The role includes pursuing quality objectives, ensuring timely delivery of project PPAPs, and driving the development and continuous improvement of our supplier base.

• Initiate and lead supplier performance improvement by partnering with suppliers to identify, understand, and abate issues for New Product Development Introduction (NPDI), Production Part Approval Process (PPAP) as well as Mass Production.
• Monitor and address supplier nonconformance issues by developing robust quality control plans and implementing effective, sustainable corrective actions.
• Drive permanent resolution of supplier issues reported by Vertiv facilities and by customers.
• Lead and own PPAP requirements associated with a change.
• Lead problem definition and preventative problem solving through containment, identification of root cause and corrective action with Supplier Corrective Action Report (SCAR).
• Develop root cause analysis and supplier reports on reported issues. Communicate internally and externally on outcomes of investigations. Work with internal teams including Engineering, Service, Manufacturing/Operations, Sales, Offering Management, and Plants Quality to resolve quality issues impacting Vertiv facilities and customers.
• Simplify complex information and prepare concise verbal and written executive summaries for the Leadership Team.
• Perform supplier on-site audits to monitor Supplier Quality Management System (QMS) compliance and effectiveness.
• Identify areas for quality improvements. Visit suppliers to proactively see installations and document improvement needs, and initiate definite corrective action within the organization.
• Evaluate potential new suppliers by conducting on-site audits and scoring of Quality Management System.
• Provide monthly reporting and status updates to management on supplier performance and various quality initiatives.
• Support the execution and maintenance of an ISO 9001 certified Quality Management System.
• Other responsibilities may be assigned as needed based on the evolution of the company and department requirements.

• 1-3 years of experience in a Supplier Quality Engineer role or related field.
• Experience with problem solving tools and techniques (e.g., 8-D, 5 Whys, SCAR, Fishbone, Pareto, Six Sigma, PPAP).
• Ability to manage multiple tasks by priority, difficulty, and severity.
• Background in applying statistical tools for process and product development and control (e.g., Gage R&R, Process Capability, Control Plans, SPC, PFMEA).

• 3-5 years of experience in a Supplier Quality Engineer role or related field.
• Knowledge of metal fabrication/machining, electrical components, wiring, or thermal systems.
• Proficiency in quality tools and methodologies (root cause analysis, control plans, capability studies).
• Strong verbal and written communication skills.
• Ability to work independently and as a team member.

• Bachelor’s Degree with 1-3 years of experience
• ASQ certifications (e.g., Certified Quality Engineer – CQE) are a plus

• Frequent standing.
• Working in a manufacturing environment around machinery and equipment.
• Protective equipment required (safety shoes, eyewear, earplugs, gloves, etc. where required).

• 35% +

Work Authorization: No calls or agencies please. Vertiv will only employ those who are legally authorized to work in the United States. This is not a position for which sponsorship will be provided. Individuals with temporary visas such as E, F-1, H-1, H-2, L, B, J, or TN or who need sponsorship for work authorization now or in the future, are not eligible for hire.

Equal Opportunity Employer: We promote equal opportunities for all with respect to hiring, terms of employment, mobility, training, compensation, and occupational health, without discrimination as to age, race, color, religion, creed, sex, pregnancy status (including childbirth, breastfeeding, or related medical conditions), marital status, sexual orientation, gender identity/expression (including transgender status or sexual stereotypes), genetic information, citizenship status, national origin, protected veteran status, political affiliation, or disability.

• Mid-Senior level

• Full-time

• Business Development and Sales

• Appliances, Electrical, and Electronics Manufacturing

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Adecco Rivalta di Torino, Piedmont, Italy

Il Diversity & Inclusion Hub di Adecco ricerca, per azienda leader nel settore aerospace con stabilimenti in varie sedi in Italia, un/a Ingegnere/a appartenente alle categorie protette (Legge 68/99).

La risorsa, come Manufacturing Engineer, si occuperà di supportare le operazioni quotidiane degli impianti, con l’obiettivo di garantire l'affidabilità e l’efficienza dei processi produttivi. In particolare, si occuperà di:

1. Analizzare e ottimizzare i processi produttivi in linea con gli standard aziendali
2. Collaborare con il team di progettazione per supportare le attività di ingegneria concorrente
3. Definire e implementare soluzioni per la risoluzione di problematiche operative
4. Monitorare e garantire che la produzione venga eseguita secondo le procedure e le linee guida stabilite
5. Sviluppare e applicare strategie per il miglioramento continuo e l'innovazione dei processi
6. Supportare l'analisi dei dati e la gestione della documentazione tecnica

Requisiti:

1. Laurea in Ingegneria Meccanica, Aerospaziale, Materiali o affini
2. Esperienza pregressa in un ruolo analogo in contesti industriali complessi (preferibilmente nel settore aerospaziale)
3. Conoscenza di Microsoft Office e software di analisi (es. SAP, ERP, CAD)
4. Ottima conoscenza della lingua italiana e buona conoscenza della lingua inglese
5. Iscrizione alle categorie protette (Legge 68/99)
6. Capacità di lavorare in team e di comunicare efficacemente con diverse funzioni aziendali
7. Attitudine al problem solving e alla gestione delle priorità

Dettagli del lavoro:

1. Orario: Full time, prevista mensa aziendale.
2. RAL: commisurata all’esperienza del candidato
3. Sedi: Rivalta di Torino, Pomigliano D'arco, Brindisi

Se sei interessato/a a questa posizione e possiedi le competenze richieste, ti invitiamo a inviare il tuo curriculum vitae e a candidarti all'annuncio. La ricerca è rivolta a persone tutelate dalla Legge 68 del 12 marzo 1999, per il collocamento mirato delle persone con disabilità e categorie protette.

Adecco Rivalta di Torino, Piedmont, Italy

Il Diversity & Inclusion Hub di Adecco ricerca, per azienda leader nel settore aerospace con stabilimenti in varie sedi in Italia, un/a Ingegnere/a appartenente alle categorie protette (Legge 68/99).

La risorsa, come Manufacturing Engineer, si occuperà di supportare le operazioni quotidiane degli impianti, con l’obiettivo di garantire l'affidabilità e l’efficienza dei processi produttivi. In particolare, si occuperà di:

1. Analizzare e ottimizzare i processi produttivi in linea con gli standard aziendali
2. Collaborare con il team di progettazione per supportare le attività di ingegneria concorrente
3. Definire e implementare soluzioni per la risoluzione di problematiche operative
4. Monitorare e garantire che la produzione venga eseguita secondo le procedure e le linee guida stabilite
5. Sviluppare e applicare strategie per il miglioramento continuo e l'innovazione dei processi
6. Supportare l'analisi dei dati e la gestione della documentazione tecnica

Requisiti:

1. Laurea in Ingegneria Meccanica, Aerospaziale, Materiali o affini
2. Esperienza pregressa in un ruolo analogo in contesti industriali complessi (preferibilmente nel settore aerospaziale)
3. Conoscenza di Microsoft Office e software di analisi (es. SAP, ERP, CAD)
4. Ottima conoscenza della lingua italiana e buona conoscenza della lingua inglese
5. Iscrizione alle categorie protette (Legge 68/99)
6. Capacità di lavorare in team e di comunicare efficacemente con diverse funzioni aziendali
7. Attitudine al problem solving e alla gestione delle priorità

Dettagli del lavoro:

1. Orario: Full time, prevista mensa aziendale.
2. RAL: commisurata all’esperienza del candidato
3. Sedi: Rivalta di Torino, Pomigliano D'arco, Brindisi

Se sei interessato/a a questa posizione e possiedi le competenze richieste, ti invitiamo a inviare il tuo curriculum vitae e a candidarti all'annuncio. La ricerca è rivolta a persone tutelate dalla Legge 68 del 12 marzo 1999, per il collocamento mirato delle persone con disabilità e categorie protette.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Eli Lilly Italia is looking for a Process Improvement Lead to join our Manufacturing Operations team at the Sesto Fiorentino (FI) plant, within one of the production departments dedicated to injectable pharmaceuticals (Formulation, Filling, Visual Inspection).

In this role, the Process Improvement Lead reports directly to the Line Manager and is responsible for coordinating manufacturing activities, optimizing process phases and sequences to ensure efficiency and full compliance with regulations. The role supports production processes by adapting the production plan to evolving needs and driving continuous improvement initiatives alongside Production Supervisors, maximizing output while keeping personnel safety as the top priority and ensuring product quality and data integrity.

As a member of the Process Team, the role engages with all functions to foster a responsible, proactive, and cross-functional culture. Open communication with team members and shift personnel ensures alignment and supports the achievement of departmental targets. The role collaborates also with Shift Supervisors and crews, driving the implementation of process changes and monitoring consistency between practices and procedures.

Key Responsibilities:

• Actively participates in the shop floor organization

• Drive continuous improvement of production processes, facilitating a strong cross-functional collaboration together with Shop Floor personnel, Process Team and Technical Team

• Collaborates with Planning to the definition of the production plan

• Create and encourage a tight collaboration with Production Supervisors to achieve the best possible execution of the production plan, reacting promptly to unforeseen situations while ensuring Safety and Quality

• Collects, organizes and shares production metrics

• Performs investigations of deviations and write reports

• Handles small Capital and Operating Expenses projects

• Sustains technical excellence and the training of the department

• Sustain and enforce an interdependent HSE culture

• Sustain and enhance, in tight collaboration with QA Associate, a Quality culture in the department ensuring that activities are performed and documented according to procedures

Basic Requirements:

• Master’s degree in scientific disciplines (Engineering, Biology, Chemistry, Biotecnology

• 2–5 years of experience in high-complexity manufacturing environments (preferably pharmaceutical).

• Good knowledge of English

• Good knowledge of Good Manufacturing Practices and HSE regulations

• Excellent knowledge of production processes

Additional Skills/Preferences:

• Relevant organizational skills

• Strong Leadership

• Strong Communication skills

• Highly results oriented

• Negotiation skills

What We Offer
Step into a role where your expertise is recognized, appreciated, and rewarded. As a member of our team, you can expect:

• Competitive Salary: We offer a competitive base salary supplemented by an annual variable component based on achieving objectives.

• Relocation Package: You will be eligible for a relocation package based on your location.

• Comprehensive Benefits: Enjoy a well-rounded welfare package, including an extensive insurance plan.

• Annual Salary Review: We recognize and reward your continued effort with an annual salary review, providing opportunities for advancement based on your performance. As part of our commitment to your future, you may also be eligible to receive a stock option package, aligning your success with the company's growth.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form () for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lillydoes not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

#WeAreLilly

• Location: Italy, Sesto Fiorentino
• Type: Full time

HR Management & Development | Talent acquisition | Head Hunter - gruppo FTH spa (Tomasi Auto srl & Noleggiare srl)

Tomasi auto è un'organizzazione dinamica e in crescita, operante nel settore automotive multimarca con sedi a Mantova, Verona, Roma e Milano. Siamo alla ricerca di una figura professionale con focus sulla revisione dei processi interni (back office e logistici) al fine di ottimizzare le nostre operazioni interne e contribuire al miglioramento continuo dell’efficienza aziendale.

Responsabilità

• Analizzare i processi interni per individuare inefficienze e aree di miglioramento.
• Progettare e proporre soluzioni innovative per l’ottimizzazione dei flussi operativi.
• Implementare nuovi processi, monitorandone l’applicazione e misurandone i risultati.
• Gestire il cambiamento e supportare i team interni durante la transizione verso nuove modalità operative.
• Coordinare progetti di miglioramento continuo, nel rispetto dei tempi e dei budget definiti.
• Utilizzare strumenti e software gestionali (ERP, WMS) per l’analisi e l’ottimizzazione dei processi.
• Esperienza comprovata nella revisione di processi aziendali, preferibilmente in contesti strutturati.
• Ottime competenze analitiche, organizzative e di problem solving.
• Esperienza nella gestione di progetti.
• Capacità di comunicare efficacemente con interlocutori interni ed esterni.
• Conoscenza operativa di software ERP (es. SAP, Oracle, Microsoft Dynamics) e WMS.
• Un ambiente di lavoro dinamico e orientato all’innovazione.
• Progetti sfidanti e ad alto impatto sull'organizzazione.
• Percorsi di formazione e sviluppo professionale.
• Opportunità di crescita in una realtà strutturata e in espansione.

Overview

Per un a0interessante societ e0 commerciale dinamica e in forte crescita, riconosciuta a livello nazionale e con sede in provincia di Mantova, siamo alla ricerca di una figura di Process Improvement Specialist.

• Analisi e ottimizzazione dei processi interni;
• Progettazione e proposta di soluzioni atte al miglioramento dei flussi operativi;
• Implementare nuovi processi, monitorandone lcapplicazione e misurandone i risultati;
• Sviluppo di progetti di miglioramento continuo;
• Gestire il cambiamento e supportare i team interni durante la transizione verso nuove modalit e0 operative.

• Laurea in Ingegneria Gestionale e/o materie equipollenti;
• Esperienza di almeno tre anni nel ruolo, all7interno di contesti organizzati;
• Ottima conoscenza e padronanza del pacchetto Office e strumenti di programmazione di flussi (ERP, WMS);
• Gradita conoscenza Principi Lean e sistemi MES.

Proattivit e0, organizzazione, doti di problem solving, precisione e ottime capacit e0 di team working completano il profilo ricercato.

provincia di Mantova (MN)