الرجاء اختيار مسمى وظيفي أو مهارة واحدة على الأقل

الموقع

مسافة

غير محدد
غير محدد

المسمى الوظيفي

المهارات

التعليم

الغاء
بحث

نتائج البحث عن الوظيفة

تصفية نتائج البحث
نتيجة ل: Occupational Health and Safety in Roma, Italia
جنس
العمر
مسافةغير محدد

SITE MANAGER

Role descriptionHe reports functionally to the Project Manager and hierarchically to the Construction Department Manager. He is the Tecnimont official Representative towards Client and Subcontractor at Site and, whenever necessary, local Authorities. He is responsible for the performance of all mobilized personnel and for all site activities, in particular for the final result, in terms of HSE performance, quality, duration and costs of construction. He manages all site activities and ensures the Responsible of the Project for construction and site management, in compliance with HSE, time schedules, costs and quality, managing the allocated resources in agreement with the respective Departments. He is also responsible for the full implementation of all applicable Legal and other Requirements.Main ResponsibilitiesYou will:(at Home Office)— To define the approach to Construction and in particular to develop the detailed construction schedule;— To co-operate in selecting Subcontractors and awarding subcontracts, checking the documents issued for Inquiry, ensuring that management specifications and subcontract schedule are prepared, preparing technical tabulations and indicating the order of preference for bids deemed technically acceptable.(at Site)— As first responsible for HSE, he has to ensure the implementation at site of the Tecnimont HSE policy, HSE management system and related performance objectives and targets.— To activate all organizational and logistic aspects of the Site;— To manage the allocated resources in agreement with the referenced Department;— To ensure the Responsible of the Project, the construction and site management, in compliance with time schedule, cost, quality and HSE;— To manage the contract with Client according to the Project Manager’s guidelines;— Through site management personnel, to manage site subcontracts;— To organize and develop procurement activities for materials to be purchased locally;— To guarantee continuity between the completion of Construction and Precommissioning, so as to optimize Project schedule timing;— To establish and check reporting for Head Office and, according to the Project Manager’s directives, to Client; — To organize any corrective action required to prevent interruptions to erection activities, to reduce delays in work schedule, and bring costs back to budget levels;— To prepare the Site final report.Knowledge & QualificationsYour skills are:o Technical diploma/degree;o Good level of English;o Additional foreign language is a plus;o Knowledge of EPC multidisciplinary activities is a must;o Knowledge of the principle Oil & Gas construction sequences;o Availability to be relocated abroad for the entire duration of the assigned project;o 4-5 or more years of experience in a similar position is a plus;o Organization, analytical approach and abstraction and synthesis skills;o Good communication skills;

WorKorner • Milano, Italia

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Inventory Control Coordinator

Umoja Biopharma is a game-changing biotech start-up with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington, and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting edge drug development. We are committed to the principles of Diversity Equity and Inclusion and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja as a leader in this front.We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.Umoja Biopharma – Your Body. Your Hope. Your Cure.POSITION SUMMARYWe are seeking a passionate and capable Inventory Specialist to join our Supply Chain team. As a member of the Supply Chain group, you will be working with Manufacturing, Quality, and Laboratory Operations groups to ensure that all the material needs of the business are met.The Inventory Specialist will be responsible for managing and maintaining accurate records of company inventory, including supplies, materials, and equipment necessary for day-to-day operations in our GMP-compliant facility. This role will also provide detailed inventory reports and conduct periodic cycle counts, as well as propose and execute projects to improve material and inventory tracking through both SOPs and business processes. The ideal candidate will possess strong analytical skills, advanced proficiency in Microsoft Excel, and the ability to work efficiently in a fast-paced environment.Additional activities include internal communication with multiple Umoja teams and providing feedback for continuous improvement on warehouse processes. Our ideal candidate will have excellent communication skills, be highly organized, and detail oriented. Prior experience with a GMP environment is highly preferred.This role will support supply chain activities, reporting to the Associate Director of Supply Chain. This position will be based in Louisville, CO and is required to be onsite 5-days a week.CORE ACCOUNTABILITIESSpecific responsibilities include:Monitor and maintain stock levels through regular physical and system checks, ensuring accuracy and efficiency in inventory counts.Utilize advanced Excel functions to create and manage detailed spreadsheets; experience with pivot tables and data analysis is crucial.Implement and maintain inventory management systems to accurately track, record, and report inventory status.Coordinate with procurement and warehouse departments to optimize inventory levels and replenish stock as needed.Conduct regular audits to ensure compliance with GMP standards and internal policies.Resolve discrepancies between inventory records and physical stock quickly and accurately.Prepare detailed reports and forecasts related to inventory for upper management, highlighting potential issues and improvements.Assist in developing and implementing improvements to existing inventory management procedures to increase efficiency and accuracy.Operating the warehouse according to Umoja SOPs and Quality SystemsThe successful candidate will have:A GED or equivalent degree with 3 years of experience in inventory management, preferably in a GMP-regulated environment.Advanced proficiency in Microsoft Excel, including expertise in pivot tables, VLOOKUP, and other data management functions.Strong analytical skills and attention to detail.Excellent organizational and problem-solving skills.Ability to work independently and as part of a team.Strong communication skills, both written and verbal.Knowledge of GMP guidelines and their application in inventory management.Preferred Qualifications:Experience with SAP or other Inventory management softwarePhysical Requirements:Ability to work onsite 5 days a week, as this role requires regular on-site presence to complete essential job-related functions.100% compliance with personal protective equipment (PPE) requirements including gloves, protective clothing, and eye safety glasses.Must have the ability to work around laboratories, manufacturing areas and equipment to perform physical tasks required for the role, including standing, walking, bending, kneeling, sitting, working your hands, and lift/push/pull materials up to 50 pounds.Comfortable being on your feet for extended periods of time.Exposure to warehousing and manufacturing areas at +5°C including storage freezer at –20°C and work in the walk in cold room at 2-8°C.Salary Range: $23.00 - $27.90/hour. This is a non-exempt role and is eligible for overtime.Benefits OfferingsUmoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 6% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the Benefits section of our website.

Glassdoor Inc. • Louisville, Stati Uniti

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RESPONSABILE SISTEMA DI GESTIONE INTEGRATO (QUALITA’, AMBIENTE E SICUREZZA)

RESPONSABILE SISTEMA DI GESTIONE INTEGRATO (QUALITA’, AMBIENTE E SICUREZZA)La risorsa riporterà gerarchicamente all’Amministratore Delegato e sarà affiancato dal Responsabile Qualità Prodotto per tutto quanto concerne la gestione delle non conformità, dei reclami clienti e delle azioni correttive/preventive oltre a riportare funzionalmente al Delegato in Materia di Salute, Sicurezza e Ambiente per tutto quanto concerne le attività legate al Sistema Sicurezza ed il Sistema Ambiente. Si occuperà, in stretta collaborazione con la Direzione, di gestione e coordinamento del Sistema Qualità, rispetto delle normative cogenti e promozione dello sviluppo del Sistema di Gestione Integrato. Più in dettaglio:1. Gestione e coordinamento del Sistema Qualità:Assicura il mantenimento degli accreditamenti ISO 9001 ed è responsabile di tutto l’iter burocratico richiesto dagli organismi di vigilanza e controllo del Sistema Qualità per il conseguimento e le verifiche periodiche della certificazione;Organizza le verifiche ispettive esterne (Enti Certificatori, Clienti ed Organi di Vigilanza) e supervisiona gli audit;Svolge verifiche ispettive interne sui processi e sulle aree funzionali per garantire che tutte le attività dell’organizzazione si svolgano nel rispetto delle procedure definite dall’azienda;In collaborazione con i responsabili funzionali:Analizza le problematiche, le non conformità e le opportunità di miglioramento o Individua le soluzioni organizzative e tecnologiche funzionali agli adeguamenti prescritti e supporta nella predisposizione dello studio di fattibilità attraverso un’analisi di costi/benefici;Supporta la pianificazione e la prioritizzazione delle azioni di miglioramento.Monitora l’avanzamento delle azioni di miglioramento e il rispetto del budget e dei tempi;Individua esigenze formative del personale aziendale e le relative modalità di soddisfacimento pianificando le attività formative di concerto con il responsabile del personale;Verifica, aggiorna e gestisce la documentazione di Sistema Qualità (manuali, procedure e relazioni tecniche) e ne garantisce la revisione e l’aggiornamento periodico;Revisiona e predispone le procedure aziendali e redige le istruzioni operative;Partecipa attivamente alla definizione e/o modifica della struttura organizzativa;Definisce gli indicatori di processo e ne monitora l'andamento;Propone azioni di miglioramento;Mantiene aggiornata la Direzione sulle prestazioni e opportunità di miglioramento del Sistema Qualità e organizza le riunioni di Riesame della Direzione.2. Rispetto delle Normative Cogenti: Monitora costantemente gli aggiornamenti relativi alle Normative Cogenti, tra cui:MOCAREACH/SCIPPOLIECOPUNTO VERDESMALTIMENTO RIFIUTI D’IMBALLO Garantisce l’implementazione ed il mantenimento di un sistema di gestione della Normativa Cogente con l’obiettivo di:Identificare problematiche e opportunità di miglioramento nel rispetto delle normative;Individuare soluzioni per garantire rispetto degli adeguamenti prescritti;Monitorare la corretta implementazione e gestione delle procedure per garantire il rispetto delle normative; Gestisce i rapporti con gli enti di controllo esterni (es. Enti Certificatori, Clienti, Organi di Vigilanza).3. Promozione dello sviluppo del Sistema di Gestione Integrato: Promuove processi di miglioramento e di accrescimento delle politiche del Sistema di Gestione Integrato (es. accreditamento nuove prove, implementazione nuovi sistemi di gestione in ambiti di interesse aziendale);Supporta il Delegato in Materia di Salute, Sicurezza e Ambiente nella gestione e coordinamento delle attività legate al Sistema Ambiente e al Sistema Sicurezza:Analizza la normativa del settore di riferimento;Supporta nel controllare attraverso specifici audit, il rispetto delle normative, individua le criticità aziendali, definisce azioni di miglioramento, valuta la relativa fattibilità attraverso un’analisi di costi/benefici, e monitora l’avanzamento e il rispetto di budget e tempi; Mantiene aggiornato il Sistema di Gestione ed eventuali certificazioni.Si richiede:Pregressa esperienza di almeno 5 anni come Responsabile Sistema di Gestione Integrato – Qualità, Ambiente e Sicurezza maturata preferibilmente presso aziende operanti nel settore metalmeccanico;Laurea in Ingegnera Gestionale/Meccanica o formazione equipollente;Conoscenza della normativa vigente e degli standard internazionali dei Sistemi di Gestione della Qualità (ISO 9001);Preferibile conoscenza Normativa MOCA, Normativa REACH/SCIP e Regolamento Gestione Rifiuti d’Imballaggio;Preferibile conoscenza della normativa vigente del Sistema di Gestione Ambientale (ISO 14001) e del Sistema di Salute e Sicurezza nei luoghi di lavoro (ISO 45001);Conoscenza dei principali tools della qualità e dei sistemi di Project Management;Ottima conoscenza del pacchetto office e sistemi informatici di base;Buona conoscenza dell’inglese (livello B2).Si offre:Lavoro full time su giornata + eventuali straordinari;Assunzione diretta da parte dell'azienda cliente con contratto a tempo indeterminato.Luogo di Lavoro: OSPITALETTO (BS)

AXL Spa • Bonate Sotto, Italia

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