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Auditor & Product Expert For Ivd Expert Devices
hace 1 semana
Job DescriptionAs a Product Specialist / Expert you evaluate IVD Expert medical products in accordance with European guidelines and standards.
You are responsible for the review of the technical documentation of selected product groups in non-active products area in your field of expertise Sterilize and non-sterilize devices, Implantable devices as orthopedic and dental implants, mesh and instruments, etc.
Experience & Further QualificationsDegree course in Natural Sciences / Biology, Biotechnology, Biomedical EngineeringDegree course in Natural Sciences / Biology, Biotechnology, Biomedical EngineeringAt least 4 years professional experience in design & development, production, quality assurance, regulatory affairs or quality management of medical devices (related to IVD Expert ).Four years of professional experience is a plus, which can be partially substituted by the work at TÜV Rheinland.
Auditor training is a plus ISO 13485 or ISO 9001.Knowledge of relevant guidelines, norms, and product specific standards; Fluent in Spanishand English, Portuguese is a plus.
Local and international business trips are required (depending on job position focus as Auditor and / or Product Expert 20 to 50% per month) and driver's license.
Working Location / Branch :
Barcelona or Madrid#J-18808-Ljbffr
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Auditor & Product Expert For Ivd Expert Devices
hace 1 semana
Barcelona, Barcelona, España Tüv Rheinland Group A tiempo completoAuditor & Product Expert for IVD Expert Devices As a Product Specialist/Expert you evaluate IVD Expert medical products in accordance with European guidelines and standards. You are responsible for the review of the technical documentation of selected product groups in non-active products area in your field of expertise – Sterilize and non-sterilize...
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Barcelona, Barcelona, España Sdi Digital Group A tiempo completoJob DescriptionAs a Product Specialist / Expert you evaluate IVD Expert medical products in accordance with European guidelines and standards.You are responsible for the review of the technical documentation of selected product groups in non-active products area in your field of expertise Sterilize and non-sterilize devices, Implantable devices as orthopedic...
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