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Dirección Técnica - Medical Devices Barcelona


  • Barcelona
  • Inscripción cerrada
  • 0 inscritos
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Jornada Completa - Contrato Indefinido - Retribución sin especificar - Al menos 3 años de experiencia

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Empresa

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National company that manufactures and packages medical devices
Descripción de la oferta

Descripción de la oferta

Duración de la oferta: hasta el 16/08/2022

Funciones

Company that manufactures medical devices is looking for a Technical/Regulatory Affairs Manager - Medical Devices


Descripción de la oferta

* Maintain up-to-date and follow all Company Quality Assurance System ensuring alignment with regulatory requirements as per Quality Standard EN ISO 13485:2016, the Medical Device Directive 93/42/EEC and new Regulation (EU) 2017/745 requirements
 * Manage the EC Certificates, the EN ISO 13485 Certificate and the Manufacturer License issued by NB 0318-AEMPS (Spanish Health Ministry)
 * Report and manage of complaints, vigilance system, non-conformities, CAPAs, supplier evaluation, management review, internal audits, labelling, product compliance, KPIs, risk management, projects, pest control, documents and records control
 * Provide technical customer support
 * Responsible for the development and maintenance of product data sheets, technical files and registration dossiers
 * Lead and manage Quality Control Laboratory and two laboratory technicians, maintaining laboratory workflow, developing performance standards (such as ISO 4074) for analytical testing, quality compliance, SOP's, calibrations, equipment maintenance and other lab support functions
 * Manage regulatory affairs responsibilities: product registration to establish regulatory strategies, authoring and/or reviewing regulatory documents (technical files, submissions), monitoring status of registrations, providing support for currently-marketed products, including review and update of product/ manufacturing process changes, supplier changes, new and revised reports, and product labelling
 * Reviewpromotional material andlabellingtoensureapplicableregulatoryrequirements are met


Perfil del candidato

* Training in Health Sciences (Pharmacy,Chemistry...)
 * Experience working with ISO 13485
 * Experience in a similar position (Technical Director, Regulatory Affairs...)
 * High Level of English


Oferta de empleo

* Immediate incorporation
 * Good salary conditions

Requisitos

Training in Health Sciences (Pharmacy,Chemistry...)
Experience working with ISO 13485
Experience in a similar position (Technical Director, Regulatory Affairs...)
High Level of English

Área - Puesto

Calidad, I+D, PRL y medio ambiente - Director de Calidad

Categoría o nivel

Dirección

Nº Vacantes

1

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