
5001 - 10000 funcionários
🏥 Saúde
🏭 Manufatura
🤝 B2B
💰 Private equity em 2017-01
Healthcare • Manufacturing • B2B
A Viant Medical é uma fabricante contratada e parceira de design de produtos focada em dispositivos médicos. A Viant oferece serviços completos, incluindo design e desenvolvimento de dispositivos, fabricação clínica-comercial e produção escalável com capacidade de sala limpa e presença global para ajudar OEMs a acelerar o tempo de lançamento no mercado. A empresa se posiciona como um parceiro de fonte única para engenheiros e fabricantes de dispositivos médicos que buscam um desenvolvimento mais rápido, pronto para regulamentação e opções de produção responsiva onshore/regional.
🕒 6 dias atrás
🗣️🇺🇸🇬🇧 Inglês obrigatório
🗣️🇪🇸 Espanhol obrigatório
Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

5001 - 10000 funcionários
🏥 Saúde
🏭 Manufatura
🤝 B2B
💰 Private equity em 2017-01
Healthcare • Manufacturing • B2B
A Viant Medical é uma fabricante contratada e parceira de design de produtos focada em dispositivos médicos. A Viant oferece serviços completos, incluindo design e desenvolvimento de dispositivos, fabricação clínica-comercial e produção escalável com capacidade de sala limpa e presença global para ajudar OEMs a acelerar o tempo de lançamento no mercado. A empresa se posiciona como um parceiro de fonte única para engenheiros e fabricantes de dispositivos médicos que buscam um desenvolvimento mais rápido, pronto para regulamentação e opções de produção responsiva onshore/regional.
• Lead the process development cycle across molding and manufacturing programs • Evaluate processes for robustness, accuracy, and optimization • Initiate improvement projects • Provide quality and metrology support for KPIs/KPOs impacting part quality and process control • Partner with GTS/site tooling engineers and tool engineers on design and development requirements • Support business development by selling tooling solutions and resolving processing issues • Support corrective actions, re-validations, and tool/process optimization • Oversee process development through IQ and OQ runs and report results • Apply scientific molding using Decoupled 2 and Decoupled 3 principles • Manage cavity pressure monitoring and control using RJG principles • Participate in technical reviews with customers and mold shops • Support DFM and tool design reviews • Support molding cell development and execution • Support EOAT design and fabrication • Manage mold shop deliverables and expectations, including SIM reports • Confirm receiving-site requirements and conduct machine capability studies • Develop processes and review Moldflow data for startup and debugging • Travel to customer sites, tool shops, and Viant facilities; submit trip reports • Prepare, track, and communicate process DOEs, results, and recommendations • Manage a minimum of 20 concurrent projects • Serve as a technical interface between Viant, customers, tool shops, and internal teams • Support NPI, sustaining engineering, and business development initiatives • Ensure regulatory compliance and best-in-class production outcomes
• Bachelor of Science Degree in Engineering or related plastics discipline, 4-year engineering degree, or equivalent completion of a 4,000 hour or 2-year process engineering apprenticeship • Certification from a school in advanced molding or RJG Master Molder 2 (or equivalent) • Fully bilingual in English and Spanish • 10+ years of experience in processing and in a molding environment, process development, qualification, and validation of molds • Extensive knowledge of processing and process development techniques in scientific molding principles (MM2 skill level) • Knowledge of plastics injection molding; LSR preferred • Proficiency with Excel, PowerPoint, Word, and general computer skills • SolidWorks drawing experience • Knowledge of 3D printing/3D software preferred • Some knowledge of FDA, QSR, and ISO 13485 medical device regulations and standards • Understanding of statistics and Cp & Cpk studies for process • Understanding of I.Q., O.Q., and P.Q. requirements • Strong understanding of DOE methods and implementation • Expert knowledge of cavity pressure technologies and advanced control principles • Familiarity with engineering-grade thermoplastic resins and Mold Flow analysis • Authorized to work in the U.S. • Ability to travel up to 75% to Viant sites in the U.S., Costa Rica, Tijuana, and Vega Baja, Puerto Rico
• Remote work model • Travel opportunities to Viant locations, customer sites, and tool shops
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