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- ...and optimize manufacturing processes for new or existing medical devices Document and validate equipment/process changes under ISO and FDA standards Use tools like DOE (Design of Experiments) or Six Sigma for process improvement Product Transfers...SugeridoPrácticaPasantías remuneradas
- ...RESPONSIBILITIES ~ Support training and certification activities with guidance of the Quality Systems team. ~ Support compliance with ISO 13485 and 21CFR 820 quality systems regulations ~ Support, promote, and enforce site-wide safety and general EHS initiatives and...SugeridoPrácticaTiempo completo
- ...years of manufacturing experience, with at least 2 years in a regulated industry (preferably medical). • Intermediate knowledge of ISO 13485 and FDA regulations. • Ability to interpret technical drawings and instructions in English (minimum B2 level). • Experience...Sugerido
- Sobre el Puesto Buscamos un Profesional en Salud Ocupacional con experiencia en Sistemas de Gestión Integrado ISO, específicamente en normas ISO 9001:2015, 14001:2015 y 45001:2018. Comprometido con la seguridad, la calidad y el medio ambiente, que pueda garantizar...SugeridoTiempo completo
- ...cumplimiento de normativas de seguridad industrial, medioambientales y de calidad. Aplicar y promover buenas prácticas alineadas con la norma ISO 90012015. Requisitos Técnico o Ingeniero en Electromecánica, Mantenimiento Industrial o carrera afín. Experiencia...SugeridoPrácticaTiempo completo
- ...process validation protocols and reports. Support other functional areas during the validation activities. Knowledgeable on QSR and ISO/MDD standards, constantly promoting awareness of best industry practices, supporting decision making on a daily basis utilizing the...SugeridoPráctica