340 Posti di lavoro per Lean Management in Italia

Summary
The Quality Control Head leads Saluggia Quality Control (QC) team by developing and executing strategic plans, providing direction for organizational structure, GMP and safety strategy, lean and continuous improvement initiatives and people training and development.

The QC Head is responsible for ensuring that the lab unit meets all agreed-upon objectives and Key Performance Indicators (KPI), specifically related to Compliance and Quality-related topics.

About The Role
Key responsibilities:

• Certify that each batch of manufactured drugs agrees with the current applicable laws and with drug marketing authorizations or investigational medicinal product dossier.
• Ensure compliance with the rules of hygiene and safety and protection according to Legislative Decree 81/2008
• Full end-to-end responsibility, ownership and accountability for the whole process from sample receipt to result release (including ownership of the equipment).
• Together with the Site Quality Head and the Leadership Team, QC Head formulates strategies and makes decisions which ensure the efficient and compliant operations of Saluggia Site.
• Writes and/or approves laboratory relevant SOPs and reviews guidelines, Quality Modules, and all analytical work-related documentation.
• Ensures that lab operations are following a compliant processes including a high degree of Data Integrity assurance.
• Partners with the Site Quality Head to establish budgets and manages operating expense budget in laboratory area.
• Ensures that all activities are performed according to the local Quality system and SOPs.
• Ensures that appropriate corrective / preventative actions are defined and implemented in due time.
• Supports internal audits and external inspections, according to the Novartis Corporate Quality Manual and supports / participates in NEM cases as required.
• Drives lab objectives by providing leadership, direction and support to the team members and ensuring that they are adequately qualified and trained to achieve a high level of competence and are motivated to excel.
• Actively works at retaining and developing talents, identifying and responding to their technical and interpersonal development needs.

Essential Requirements

• Scientific Degree (CTF, Pharmacy or Chemistry preferred).
• Previous experience in a leadership role within a laboratory of a pharmaceutical company.
• Knowledge of Quality System and GMP requirements, analytical technology and equipment, incl. qualification and calibration.
• Fluent in Italian and English.

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.

Summary

The Quality Control Head leads Saluggia Quality Control (QC) team by developing and executing strategic plans, providing direction for organizational structure, GMP and safety strategy, lean and continuous improvement initiatives and people training and development.

The QC Head is responsible for ensuring that the lab unit meets all agreed-upon objectives and Key Performance Indicators (KPI), specifically related to Compliance and Quality-related topics.

• Certify that each batch of manufactured drugs agrees with the current applicable laws and with drug marketing authorizations or investigational medicinal product dossier.
• Ensure compliance with the rules of hygiene and safety and protection according to Legislative Decree 81/2008
• Full end-to-end responsibility, ownership and accountability for the whole process from sample receipt to result release (including ownership of the equipment).
• Together with the Site Quality Head and the Leadership Team, QC Head formulates strategies and makes decisions which ensure the efficient and compliant operations of Saluggia Site.
• Writes and/or approves laboratory relevant SOPs and reviews guidelines, Quality Modules, and all analytical work-related documentation.
• Ensures that lab operations are following a compliant processes including a high degree of Data Integrity assurance.
• Partners with the Site Quality Head to establish budgets and manages operating expense budget in laboratory area.
• Ensures that all activities are performed according to the local Quality system and SOPs.
• Ensures that appropriate corrective / preventative actions are defined and implemented in due time.
• Supports internal audits and external inspections, according to the Novartis Corporate Quality Manual and supports / participates in NEM cases as required.
• Drives lab objectives by providing leadership, direction and support to the team members and ensuring that they are adequately qualified and trained to achieve a high level of competence and are motivated to excel.
• Actively works at retaining and developing talents, identifying and responding to their technical and interpersonal development needs.

• Scientific Degree (CTF, Pharmacy or Chemistry preferred).
• Previous experience in a leadership role within a laboratory of a pharmaceutical company.
• Knowledge of Quality System and GMP requirements, analytical technology and equipment, incl. qualification and calibration.
• Fluent in Italian and English.

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.

Summary

The Quality Control Head leads Saluggia Quality Control (QC) team by developing and executing strategic plans, providing direction for organizational structure, GMP and safety strategy, lean and continuous improvement initiatives and people training and development.

The QC Head is responsible for ensuring that the lab unit meets all agreed-upon objectives and Key Performance Indicators (KPI), specifically related to Compliance and Quality-related topics.

About The Role

Key responsibilities:

• Certify that each batch of manufactured drugs agrees with the current applicable laws and with drug marketing authorizations or investigational medicinal product dossier.
• Ensure compliance with the rules of hygiene and safety and protection according to Legislative Decree 81/2008
• Full end-to-end responsibility, ownership and accountability for the whole process from sample receipt to result release (including ownership of the equipment).
• Together with the Site Quality Head and the Leadership Team, QC Head formulates strategies and makes decisions which ensure the efficient and compliant operations of Saluggia Site.
• Writes and/or approves laboratory relevant SOPs and reviews guidelines, Quality Modules, and all analytical work-related documentation.
• Ensures that lab operations are following a compliant processes including a high degree of Data Integrity assurance.
• Partners with the Site Quality Head to establish budgets and manages operating expense budget in laboratory area.
• Ensures that all activities are performed according to the local Quality system and SOPs.
• Ensures that appropriate corrective / preventative actions are defined and implemented in due time.
• Supports internal audits and external inspections, according to the Novartis Corporate Quality Manual and supports / participates in NEM cases as required.
• Drives lab objectives by providing leadership, direction and support to the team members and ensuring that they are adequately qualified and trained to achieve a high level of competence and are motivated to excel.
• Actively works at retaining and developing talents, identifying and responding to their technical and interpersonal development needs.

Essential Requirements

• Scientific Degree (CTF, Pharmacy or Chemistry preferred).
• Previous experience in a leadership role within a laboratory of a pharmaceutical company.
• Knowledge of Quality System and GMP requirements, analytical technology and equipment, incl. qualification and calibration.
• Fluent in Italian and English.

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.

Overview

Quality Control Analyst position at Philogen S.p.A. reports to the Quality Control Laboratory Supervisor.

• Management of chromatography sistems related to biological products (HPLC, SEC analysis, etc.).
• Carry out chemical and biological analytical determinations by managing multiple products and using a large number of diversified equipment, in compliance with the regulations cGMP / GLP and department procedures.
• Preparation of reports and SOPs
• Compiling Data forms, Registers, and Certificates.
• Management and maintenance of laboratory instruments.

• A good scientific background.
• Experience in chromatography sistems.
• Experience in analytical validation.
• Comprehensive knowledge of GMP.
• A high level of attention to detail and the ability to prioritize working tasks.
• The ability to work independently, as well as coordinate membersof his/her team.
• Excellent interpersonal skills and ability to work in teams.

A contract and salary proportional to the experience (seniority) of the successful candidate.

Siena -Italy

• Associate

• Full-time

• Quality Assurance

• Pharmaceutical Manufacturing

Overview

The QC Supervisor supports the QC Head to ensure that Quality Control processes for materials acceptance, batches quality control and QC equipment validation/qualification are executed and fully compliant to cGMPs regulation, corporate and national guidelines.

• Be the Deputy of QC Head in managing, coordinating and approving the execution of the analytical activities for the batch release and in raw materials and packaging materials acceptance according to specifications.
• Ensure that the stock of materials, reagents, standards is properly available and ordered; ensure that all QC materials are properly and safely stored, identified, labelled, recorded and monitored according to SOPs and specifications.
• Ensure the correct storage of Reference and Retention Samples of the raw materials and products.
• In case of analytical results out of specification (OOS), out of trend (OOT), out of expectation (OOE) or System Suitability Test failures, and in case of deviations, in collaboration with QC Head, perform the investigation and verify the implementation of the related CAPAs.
• Ensure that all methods used in QC analysis are validated according to SOPs, MA and cGMPs; support the QC Head to assure the adequacy of the SOPs of Quality Control department; redaction and review of SOPs, Protocols and Reports.
• Collaborate with QC Head for the redaction of the stability programs and the annual product review; ensure that the stability analyses are performed on time.
• Collaborate with QC Head to ensure the initial and periodic training of QC analysts; manage the presence, shifts and performances of the QC Technicians when the QC Head is not on site.
• Maintain, review and approve the records of the QC activities (i.e. logbook, forms, analytical batch records).
• Collaborate with QC Head for the periodical self-inspections and external audits (Health Authorities, Certified Bodies, Suppliers); contribute in maintaining the local quality system as per GMPs and corporate guidelines and in assuring the respect of GMPs and Health Authorities requirements at local level.
• Guarantee the cleanliness and tidiness and application of Good Laboratory Practice.
• Ensure high level of attention for handling of radioactive materials within the area of responsibility.
• Run operations in full compliance with HSE guidelines (internal/external).
• Support the development and implementation of projects related to new or existing products.

• Scientific Degree (CTF, Pharmacy or Chemistry preferred).
• Previous experience in a similar role within a GMP lab environment.
• Available to work in shifts, including night shifts and weekends.
• Fluent in Italian. Good knowledge of English.
• This is a site-based role and it requires to work in shifts, including night shifts and weekends.

• Mid-Senior level

• Full-time

• Quality Assurance

• Pharmaceutical Manufacturing

Brave Kid è un’azienda leader nella ricerca & sviluppo prodotto, produzione e distribuzione di collezioni di abbigliamento e accessori per bambini.
Attualmente, il suo portfolio licenze comprende Diesel, MM6 Maison Margiela, Marni, Dsquared2, N°21, MYAR e Max&Co.
Grazie al suo know-how unico, che fa leva su un'esperienza trentennale nel settore, Brave Kid interpreta perfettamente le visioni di designers e marchi traducendole in collezioni originali e di qualità per ragazzi e ragazze internazionali.
Brave Kid è anche un player globale di e-commerce, con uno store online multi-brand dedicato al mondo del kidswear.

Per la nostra sede di Marostica (VI) ricerchiamo un/una Tecnico/a Controllo Qualità Abbigliamento, da inserire nell’area Produzione.

La risorsa si occuperà delle seguenti attività:

• Analisi dei capi di campionario ed industrializzazione degli stessi prima della loro messa in produzione; inserimento nella scheda tecnica dei commenti e invio delle schede tecniche ai vari fornitori
• Confronto con l’area R&D per prevenire e risolvere eventuali problematiche di produzione migliorando l’aspetto qualitativo del capo
• Gestire il processo di approvazione dei capi pre-produzione dal punto di vista estetico, tecnico e qualitativo
• Effettuare visite periodiche principalmente c/o i fornitori dell’area del bacino mediterraneo per controllo in linea della produzione e per verificare che vengano rispettati gli standard qualitativi aziendali
• Controllo del prodotto finito nel nostro magazzino. Seguire c/o le strutture esterne eventuali riparazioni sui capi non conformi
• Richiesta e monitoraggio dei test chimici per assicurare la conformità dei capi prima della spedizione al nostro magazzino; inserimento dei report nel database

Il/La candidato/a ideale possiede:

• Percorso di studi presso Istituti tecnici del settore abbigliamento
• Conoscenza sia della parte Woven che Knitwear
• Pregressa esperienza di 2-3 anni maturata in ruolo analogo all’interno di aziende strutturate del settore Moda
• Disponibilità a saltuarie trasferte per periodi limitati
• Buona conoscenza della lingua inglese sia scritta che parlata;
• Conoscenza del PLM Link
• Conoscenza del pacchetto Office

Sede: Marostica (VI)

Overview

Job Title: Quality Control Manager

Location: NAS Sigonella

Scope: Dedicated to enforcing the QMS at the operational level; reports directly to the QM.

Description: The responsibilities and qualifications describe the general nature and level of work performed by those in this position. The company reserves the right to modify duties or assign additional duties as needed.

• Performs daily inspections of services and deliverables against contract standards.
• Verifies technical compliance of maintenance, custodial, pest control, transportation, and utility services.
• Conducts sampling, testing, and checklists in accordance with the QCP.
• Documents deficiencies and verifies corrective action completion.
• Coordinates with shop supervisors and WCC to ensure quality integration into workflow.
• Provides immediate feedback to crews on observed deficiencies.
• Monitors subcontractor work for adherence to quality standards.
• Compiles inspection reports and submits findings to the QM.

• Must meet/exceed technical qualifications of personnel they inspect.
• Minimum three years of experience enforcing QMS on similar size, scope, and complexity contracts.

• ISO 9001:2015 Internal Auditor certification.
• Lean Six Sigma Yellow/Green Belt.

Must be able to successfully pass, as required, a federal, state, or local government background investigation.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities: We maintain a drug-free workplace and perform pre-employment substance abuse testing. The contractor will not discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c)

We are an Equal Opportunity Employer and provide reasonable accommodations for applicants with disabilities as required by law.

Job Information : Job Description last Updated: 09/25/2025

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Quality Assurance
• Industries: Facilities Services

Location notes: Busto Garolfo, Lombardy, Italy; Pregnana Milanese, Lombardy, Italy; other nearby locations may be considered.