Manufacturing engineer medical devices

Azienda leader settore elettromedicali ricerca coordinatore ufficio tecnico riporta direttamente al responsabile operation e collabora con i reparti r&d, assistenza tecnica, marketing, produzione e qualità.Dovra' rendere chiari, efficienti ed efficaci i flussi di lavoro dell’area tecnica, ottimizzare i carichi di lavoro, implementare un approccio culturale al miglioramento continuo, essere il riferimento aziendale per le tematiche di competenza, acquisire know how e trasferire conoscenze per far crescere collaboratori e colleghi Attività e responsabilità: industrializza e finalizza i prodotti sviluppati dal team r&d al fine di ottimizzarne qualità, affidabilità, costi e tempi di realizzazione, implementa e gestisce i dati tecnici dei prodotti nel sistema gestionale aziendale (codici, anagrafiche, distinte base, cicli di lavorazione, tempi etc.), redige e aggiorna la documentazione tecnica dei prodotti (fascicolo, manuali, disegni e schemi elettrici, idraulici, pneumatici), si interfaccia con gli enti terzi per le certificazioni dei prodotti e loro mantenimento (e.g. test emc, elettrici, di sicurezza macchine, certificazione ce - ivd – ul), analizza, propone, sviluppa e implementa azioni di miglioramento continuo sul prodotto e sul processo in collaborazione con gli enti aziendali coinvolti, si interfaccia con il servizio di assistenza tecnica per l’analisi e miglioramento continuo dei prodotti inclusa redazione ed emissione dei bollettini tecnici di aggiornamento, si interfaccia con i reparti acquisti, produzione e logistica per la gestione degli impatti relativi alle modifiche ai prodotti e retrofitting, si interfaccia con gli enti tecnici delle aziende fornitrici di prodotti oem e/o commercializzati per la risoluzione di problemi e il miglioramento, gestisce la manutenzione delle attrezzature e degli impianti produttivi presenti in azienda e/o presso i fornitori, custodendone ed aggiornandone la documentazione tecnica, i ricambi e la giacenza al fine di evitare interruzioni delle attività produttive aziendali. si richiede: consolidata esperienza acquisita nella progettazione – industrializzazione di macchinari con componentistica hw elettromeccanica, idraulica, pneumatica, elettronica, sw e fw, conoscenza modellazione pezzi meccanici e parti tramite cad 3d solid edge e gestione assiemi complessi, conoscenza delle principali lavorazioni meccaniche su acciai e leghe, di stampaggio poliuretani e di stampaggio ad iniezione, conoscenza della direttiva macchine, marcatura ce, certificazioni di prodotto ul e gestione brevetti, esperienze acquisite nel miglioramento continuo (lean manufacturing, tps), esperienza lavorativa maturata in aziende strutturate e certificate iso9001 e preferibilmente iso13485, conoscenza del gestionale sap. laurea in ingegneria meccanica / diploma di perito meccanico, inglese fluente retribuzione a partire da 40.000 euro.

MUST - ONE YEAR AS PROJECT MANAGER EXCELLENT opportunity to be mentored by Expert for a year - someone with a strong desire to go into a Project Manager role - plastics as it relates to medical products, global firm. Knowledge of Injection Molded micro components is helpful. is responsible for planning and driving each project to its successful conclusion by ensuring that its scope is well defined, and resource estimates and project schedules are specified and appropriate to the project. The Program Manager organizes and leads activities to ensure completion of the projects on schedule, within budget constraints, and quality that exceeds customers expectations. Requirements: Education, Experience 4 year Engineering Degree or equivalent experience. Experience in the areas of project management, preferably in the medical device field working with minimally invasive, single use medical devices in the endoscopy, cardiovascular, neurovascular, and urology markets. Ideally project management experience in the product or process development of plastic components. Ability to apply engineering principles to an idea or set of user requirements -- and then convert this into design requirements, considering manufacturability, cost of goods, and the regulatory requirements for a device or combination product. Good understanding of Design for Manufacturability principals. Knowledge of product development process according to FDA regulations Proficient with Microsoft Project and very proficient in Microsoft Office products. Experience in building complex schedules utilizing sub-schedule integration structure and logic Experienced with and efficient at capturing and recording technical details and commitments Experienced with and effective in communicating program challenges to appropriate team members Experienced with communicating resource conflicts and effective conflict resolutions Experienced utilizing resource management tools Experienced with complex multi-tasking in leading projects and programs Ability to communicate vertically and horizontally through multiple channels, leverage customer contact network to motivate diverse teams, and enable cross-functional collaboration. Preferably have completed a professional program management training program. Experienced with process verification and validation Authoritative command of complexity and ambiguity, ability to see the big picture, ability to collect, digest and assemble information to enable relevant business analyses and influence decision-making. Continuous improvement methodologies (e.g. Six Sigma, lean manufacturing, etc.) and change management methodologies. Experienced with managing programs with annual budgets of $10K - $5M. Responsibilities: Roles, Tasks Perform Project and program management at a high level of professionalism. This role will be responsible to lead high-profile projects and programs that utilize internal and external personnel, contract firms, and partners. Negotiate and resolve project conflicts and drive consensus among team/functional members to accomplish project and business goals. Manage program resources to meet business objectives. Manages external contractors and suppliers to ensure completion of projects on time and on budget. Manages resource allocations from all areas for project support. Documents labor resources and billing hours. Identifies and manages the resolution of any deviations to contract, Project Master, or project documents. Communicates to clients as required on project updates. Communicates regularly to company management on project schedule, budget and any issues that may affect the completion on projects on schedule and on budget. Negotiates any necessary changes with Customers/Clients. Ensure that Customer/Client issues are resolved and documented to their satisfaction. Support new business activities by evaluating new opportunities, assisting on developing quotes and providing product prototypes if requested.

RINA Group is looking for a JUNIOR FIRMWARE ELECTRONIC ENGINEER for our office based in Bologna. As a Junior Firmware Electronic Engineer you will: -Design, documenting and simulating electronics circuits and sub circuits / simulating software/firmware subroutines according to IPC and 60601standards -Accomplish all Verification and Validation tasks -Design for testing, design testing tools -Support if requested other teams in electronic analysis. -Participate in design reviews for medical devices -Identify and address performance bottlenecks -Perform requirements definition, risk analysis -Work to improve overall system architecture and design components Requirements: -M.Sc. (1st or 2:1) in electronics or biomedical engineering -C, C++ mandatory - Assembler highly recommended -FPGA Codesign highly recommended - Microcontrollers Architecture basis requested. The ideal candidate would also have: Good command of English language spoken and written (B2 level and above) Excellent team working attitude Knowledge of biomedical environment and medical devices Experience in automotive will be considered a plus

Supplier Quality Engineer Important international company of healthcare. The Supplier Quality Engineer (SQE) ensures that the supply chain companies (suppliers) continually develop their process in line with the design intent of the customer and verify their systems to ensure they are compliant with the end customer's needs. This includes on-going supplier verification. The SQE is responsible for delivering all aspects of the Supplier Quality Assurance function.He/ She collects root cause analysis and provide corrective feedback to prevent line stops due to supply issues. Establish incoming inspection plans for components with the supplier & R&D department, assemblies and/or finished devices and quality department Ensure the proper risk controls are implemented at both supplier and the company, the measurement system at supplier & the company are identical, and/or capable, Monitore and analyze supplier data internally and externally gathered to identify trends and prevent potential problems Initiate and manage Supplier Corrective Actions (SCAR, SAR) in partnership with Manufacturing/Process Engineering and Quality Engineering to ensure complete and effective root cause analysis and corrective action implementation is performed promptly Use appropriate methods such as Statistical Process Control (SPC), Advanced Quality Process (AQP) tools and the metrics, proactively to identify and help implement improvement to supplier quality and supplier quality tools and processes Collaborate with other members of the supply team to establish and maintain a meaningful supplier quality scorecard. Permanent position. Inserzionista: Page Personnel

Our client is an International manufacturing company, leader in the mechanical sector, with offices and production units located worldwide. For this company we are looking for a: CONTROL ENGINEER (ALGORITHM EXPERT) The selected candidate will collaborate with the design team on the development of new devices having control algorithms and the adaptation and integration of existing and new systems in automotive applications. He will interact with colleagues, customers, suppliers and with other company units dealing with electronics and sensors. He could also be involved in research projects or in advanced projects related to specific customer needs. Job Requirements:. Fresh graduate or up to...

Provide 1st Level systems support, maintenance and administration within theorganization's computing environment. Performsonsite and remote analysis, diagnosis, and resolution of complex problems for end users. Recommends and implements corrective solutions. Installs, configures tests, maintains, monitors, and troubleshoots end-user related hardware and software (in person, by telephone, or via e-mail) in order to meet or exceed published SLA's; with effective management of the customer relationship during the entire support process Aministers enterprise class tools suche as SCCM to analyze the enterprise computing environment OS Windows, Windows Server, Active Directory VMware Router, Switch, Firewalle PC, mobile devices World's leading manufacturing company Lainate (MI) Good level of conversational and written English Scripting for automated deployments and managements tasks Able to read and understand technical manuals, procedural documentation and OEM guides. Good communicational skillsOne of the world's leading manufactures of medical products, since 1980. Available in over 100 countries. 3 R&D facilities worldwide. About 4.000 employees. Italian offices in Lainate. Permanent ContractRAL and benefit will be discuss with the client Very healty work environmentSalario da 30.000 €/anno a 40.000 €/anno