SUPERVISOR LABELING & TECHNICAL DOCUMENTATION
Descrizione dell'offerta di lavoro
The Supervisor Labeling & Technical Documentation is responsible for a broad range of medical device labeling and technical publications (instructions for use, product and packaging labels, etc.) and is responsible for coordinating activities for labeling internally with other stakeholders, and also with external vendors for tech writing and translations.
This position is located within the R&D organization reporting directly to the R&D Director Cardiopulmonary Equipment.
Hybrid role, we will consider candidates close to our office in Milan or our production site in Mirandola (MO) Duties and Responsibilities Be responsible for the overall labelling (instructions for use, product and packaging labels) of medical devices, their components and accessories in accordance with organizational policies, procedures and objectives.
Manage/supervise team members activities Develop standardized methods and tools to efficiently produce high-quality documents.
Plan and direct the creation of IFUs and labels for timely delivery Raise and manage change requests for labelling updates (instructions for use and product/packaging labels) and coordinate with relevant stakeholders and action item owners, driving changes from planning phase to closure in an effective manner.
Coordinate with other departments involved, such as regulatory affairs, production/operations, logistics, customer service, and others.
Coordinate and drive external vendors, such as agencies for translation and technical writing services in order to deliver high-quality technical publications (mostly instructions for use).
Oversee the introduction of a Component Content Management System in collaboration with external partners Order placement (translation and technical writing projects) Document management in our electronic document management system, maintenance of eIFU website The Individual Bachelor’s degree in technical communication, translation, engineering, or a related field.
Equivalent proven experience will also be considered.
Exceptional verbal and written English skills.
Proficiency in German or Italian is a plus but not required.
The ideal candidate will possess strong writing, editing and verbal abilities, as well as technical communication capabilities.
Familiarity with medical device operations or regulated environments (MedTech, biotech, or pharma preferred).
Experience with modular or structured documentation systems, including content management systems (e.
., Schema ST4, or similar), is a plus.
A technical understanding of medical devices, acquired through education or professional experience, is advantageous.
Demonstrated problem-solving skills, sound judgment, and the ability to build effective cross-functional relationships.
Enthusiastic about process improvement through standardization, automation, and digitization.
Willingness to travel occasionally to the site in Monaco, Germany.
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Nos comprometemos a garantizar que nuestro proceso de selección es justo, transparente y sin discriminación ilegal.
Nuestro proceso de selección se rige por las demandas/requisitos fundamentales para el puesto, y no por prejuicios o discriminación por motivos de sexo, edad, estado civil, condición de veterano, discapacidad o dolencia no relacionada con el empleo, situación familiar, orientación sexual, religión, color, origen étnico, raza o cualquier otra clasificación protegida por la ley.
Tenga en cuenta que no aceptamos currículos no solicitados de seleccionadores o agencias de empleo.
En ausencia de un contrato de servicios de selección firmado, no consideraremos, ni aceptaremos, el pago de ninguna compensación por recomendación ni honorarios para el seleccionador.
En el caso de que un seleccionador o agencia presente un currículo o candidato sin un contrato previamente firmado, nos reservamos explícitamente el derecho de buscar y contratar a esos candidatos sin ninguna obligación económica con el seleccionador o la agencia.
¿Está buscando desarrollar una carrera importante? Tanto si trabaja en Investigación y Desarrollo, Ventas, Recursos Humanos como en otra función de apoyo, formará parte de una empresa que está transformando verdaderamente la innovación médica en soluciones significativas y, en última instancia, en una vida mejor y más sana para nuestros pacientes.
Por eso siempre estamos buscando contratar a personas apasionadas y comprometidas, con la formación técnica y la perspicacia empresarial adecuada, para cumplir nuestra misión de mejorar la vida de nuestros pacientes en todo el mundo.
Únase a LivaNova y ayúdenos a ofrecer la innovación sanitaria que importa.
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Dettagli dell'offerta
- Company 281 Sorin Group Italia S.r.l.
- Tutta l'Italia
- Imprecisato - Imprecisato
- Imprecisato
- 30/12/2024
- 30/03/2025
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