Qa performance

The Process Engineering Specialist brings operations-expertise to help the organization in order to optimize production processes and realize substantial efficiency and cost saving. Act as a strategic partner, providing value-added solutions, developing and implementing hands-on measures in order to realize the required process improvements and ultimately improve margins; Drive changes and efficiencies by recommending new ways to operate, contributing actively to their actual implementation and providing feedbacks; Build realistic and comprehensive action plans to reduce cost, increase quality and improve service level; Participate at meetings with Automation department in order to define the technical requirement specifications for new equipments considering R&D, QA and Operations requests; Define, execute and validate the production process of new product in collaboration with R&D; Define, write and update production manual (MOP) and guarantee the quality for the entire process; Transfer production process; Execute process changes related to: methods, parameters and material changes; Execute Operational Qualification (OQ) and Performance Qualification (PQ); Execute equipment and production validation using statistical tools such us Gage R&R, Capability analysis, DOE, Regression, Hypothesis tests and others. Promote process improvements using Lean Six Sigma Approach.Medical DevicesGreat growth opportunityGood English level (B1 Level) Management of the validation documents necessary for the process control and improvement and deep knowledge of validation strategy (IQ - OQ - PQ); Knowledge and experience with statistical tools: DOE study, Gage R&R, Capability analysis (Cp, Cpk, Pp, Ppk), sampling size definition preferably by means Minitab sw. Green Belt Certification will be a plus Degree in Engineering At least 4-5 years of experience holding position in process engineering dept.Multinational Company leader in medical devicesGreat growth opportunity

Act as a strategic partner, providing value-added solutions, developing and implementing hands-on measures in order to realize the required process improvements and ultimately improve margins; Drive changes and efficiencies by recommending new ways to operate, contributing actively to their actual implementation and providing feedbacks; Build realistic and comprehensive action plans to reduce cost, increase quality and improve service level; Participate at meetings with Automation department in order to define the technical requirement specifications for new equipments considering R&D, QA and Operations requests; Define, execute and validate the production process of new product in collaboration with R&D; Define, write and update production manual (MOP) and guarantee the quality for the entire process; Transfer production process; Execute process changes related to: methods, parameters and material changes; Execute Operational Qualification (OQ) and Performance Qualification (PQ); Execute equipment and production validation using statistical tools such us Gage R&R, Capability analysis, DOE, Regression, Hypothesis tests and others. Promote process improvements using Lean Six Sigma Approach.Multinational Company leader in medical devicesGreat Growth OpportunityGood English level (B1 Level) Management of the validation documents necessary for the process control and improvement and deep knowledge of validation strategy (IQ - OQ - PQ); Knowledge and experience with statistical tools: DOE study, Gage R&R, Capability analysis (Cp, Cpk, Pp, Ppk), sampling size definition preferably by means Minitab sw. Degree in Engineering Green Belt Certification will be a plusAt least 2-3 years of experience holding position in process engineering dept.Multinational Company leader in medical devicesGreath Growth Opportunity

QUALITY SPECIALIST - 1 anno prorogabile: Azienda di verniciatura industriale, tubi e apparecchiature per il settore Oil & Gas, sta ricercando un Quality Specialist 1.         Descrizione della mansione a.         Verificare la conformità del Sistema di gestione Qualità esiste alla norma ISO 9001 e alle specifiche cliente. Assicurarne il mantenimento. b.        Implementare il Sistema di gestione Salute e Sicurezza sul lavoro, e Ambiente, secondo D.lgs 81/08, ISO 14001 e ISO 45001. Assicurarne il mantenimento. (NB: l'azienda ha un consulente per la tematica in oggetto, che svolge anche ruolo di RSPP) c.         Affiancare i referenti interni nell'implementazione e mantenimento del sistema di controllo performance aziendale, mediante indicatori e strumenti di visual management d.        Affiancare, ed essere referente interno per, il team di implementazione dei progetti lean manufacturing (NB: l'azienda si affida a un consulente esterno per questi progetti) e.        Svolgere l'attività operativa di QA/QC quale: preparazione reportistica (report di verniciatura), rispondere a reclami, gestire NC interne, MOC, azioni correttive e preventive, formalizzare il Rapporto della Direzione, sostenere audit di Qualità da parte di clienti, anche stranieri, ecc.... f.          Affiancare il referente interno per l'aggiornamento della comunicazione digitale (sito web e principali canali social media) 2.         Competenze ed esperienza richieste a.       Conoscenza avanzata della norma ISO 9001 b.      Conoscenza buona del D. lgs 81/2008 e delle norme ISO 14001 e 45001 c.       Conoscenza sufficiente dei principi lean production d.      Conoscenza sufficiente dei principi di controllo di gestione aziendale e.      Esperienza di almeno 5 anni in PMI del settore industriale, preferibilmente in aziende applicatrici di vernici o di trattamenti superficiali f.        Inglese buono  Contratto a tempo determinato di un anno, finalizzato all' inserimento in azienda.