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1 VAGA DE Designer EM Blumenau / SC
Função/cargo da vaga:
Designer
Empresa:
Nome da empresa disponível para cadastrados.
Salário:
A combinar
Cidade/Estado:
Blumenau / SC
Tipo de Vaga:
Home Office
Regime de contrato:
Efetivo/CLT
Descrição da vaga:
Job titlequality specialistjob descriptionyou will be part of the emr&cm quality team, responsible for work in partnership with the development teams ensuring compliance throughout the whole development role:perform a wide variety of activities pertaining to compliance with applicable regulatory requirements, quality management system (qms) maintenance, improvement & harmonization, quality control and execution of processes and their deliverables in product development and subcontracting projects and report the findings to upper management as well as ensure and approval of designated project documentation in programs to program/business teams regarding the definition and implementation of product quality engineering activities, also in corrective and preventive upper management with respect to release for delivery of products, as well as execution of audits in all business processes and report the and represent quality discipline in design reviews, hazard analysis brainstorms, health risk stimulate, and support the implementation of process in the maintenance, improvement and deployment of the quality management regulations and standards to process artifacts for quality management system and deployment in the in and verification of changes to dhf/ dmr and approval of the and completes relevant sw quality engineering documents with/ without direct supervision. Provides sw quality engineering support, including assisting organizational units in addressing sw quality engineering for performing timely, detailed sw quality engineering tasks like: assessing software designs and reviewing test and other performance data, analyses market feedback, completing or assisting with in root cause analysis and sw quality problem solving. Provides effective oversight of: the execution of the sw quality plan and any risk management activities, and of all design related activities during the software as a single point of contact (person assigned to project team) responsible to ensure that software design quality related requirements/criteria are completed and meet sw quality standards for every the right fit if:bachelor or master degree in relevant knowledge domain, computer science electronics, electrical or information 6 to 8 years of professional experience with 3 to 4 years in medical device of relevant external standards for quality management systems for medical devices ( iso13485, iso 14971, mdd/mdr, fda-Qsr, iec62304, iec 62366, etc.)knowledge of software product development life experience in agile methodology enabling projects/ programs with regulatory communication skills in management knowledge and of product creation and (software) development methods & in using problem solving on product quality engineering metrics and philipswe are a health technology company. We built our entire company around the belief that every human matters, and we wont stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others. Learn more about our business. Discover our rich and exciting history. Learn more about our youre interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at philips. Learn more about our commitment to diversity and inclusion here.
Cód. 10007924
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