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Manufacturing engineer

Como
JR Italy
Pubblicato il Pubblicato 18h fa
Descrizione

PSocial network you want to login/join with: /ppCreanova - Create Innovate Healthcare solutions for a better quality of life /ph3Location: /h3h3Job Category: /h3pOther /pp- /ph3EU work permit required: /h3pYes /ph3Job Reference: /h3p642526511769636044833710 /ph3Job Views: /h3p2 /ph3Posted: /h3p26.04.2025 /ph3Expiry Date: /h3p10.06.2025 /ph3Job Description: /h3pbCreate Innovate Healthcare Solutions /b for a bbetter quality of life /b? /ppbCreanova /b is a leading B2B partner in bMedical Device Development Contract Manufacturing /b, specializing in innovative b(electro-)medical devices /b with plastic binjection molded /b enclosures. /ppFor our facility in Como, we are seeking a highly skilled bManufacturing Process Engineer /b to join our dynamic growing team. /ppYou will be bresponsible /b for managing the bdesign transfer to production /b and bseries-production /b assembly lines for several bmedical devices /b. /ppKey Responsibilities: /pulliLead and manage the bdesign transfer /b to production and bvalidation /b of new bmanufacturing and assembly line processes /b for the setup of new series-production assembly lines of medical devices, including plastic injection molding and electronics (PCB); /lilibManage /b the entire series-production process of (recurring) binternal orders /b of the production lines under your responsibility; /lilibDefine /b and bimplement /b necessary bcorrective /b and bpreventative actions /b in response to internal, regulatory, and customer audit requirements; /liliFoster a culture of bcontinuous process improvement /b with a focus on bquality, efficiency, /b and bcost-effectiveness /b; /lilibCreate, review /b and bensure compliance /b with Master Batch Records, internal operational procedures, Qualification/Validation plans, protocols and reports, and other essential GMP documents; /liliPlan and conduct btraining /b and development for employees regarding new processes; /liliCollaborate and ensure effective communication with internal departments (e.g. quality assurance, quality control and warehouse) as well as externally with suppliers and customers, to ensure seamless operations and timely release of goods. /li /ulpPreferred Qualifications: /pullibBachelor's or Master's Degree /b in a scientific, (bio-)engineering, technology or related discipline. /liliMinimum of b5 years of experience /b in bmedical device manufacturing /b or a similar field. /liliKnowledge of bplastic injection molding /b processes and belectronics manufacturing /b (PCB) is a plus; /lilibKnowledge of ISO13485 /b is desirable; /liliAdvanced computer skills and proficiency in bMS Office Suite /b; /liliValid bdriver's license /b (B category); /liliExcellent organizational, communication, and analytical skills; /liliProven ability to lead and manage teams, ensuring efficient and successful manufacturing operations. /li /ulpIf you are ready to contribute to our passionate team dedicated to making a positive impact in the healthcare industry, we would love to hear from you! Join us at Creanova and be part of our mission to create innovative healthcare devices. /p #J-18808-Ljbffr

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