du die Kontrolle darüber behältst, findest du hier: Cookie-Richtlinie. Creation and maintenance of key regulatory deliverables of the projects. Agfa HealthCare GmbH, human Resources, konrad-Zuse-Platz Bonn m/dach/jobs, job Segment: Medical, Engineer, Law, Product Development, Patient Care, Healthcare, Engineering, Legal, Research. Operational experience with risk management processes. Identify ongoing training needs and provide training as required. Performing internal audits and defending Agfa premarket activities during external regulatory inspections and audits. You are accountable for the implementation of regulatory procedures, sound application of risk management principles, and the creation of documentation to achieve timely regulatory clearances in your projects. Specific Skills: Self-starter attitude, strong organizational skills, and the ability to meet deadlines. Very good German and English verbal and written language skills, French is an asset. Agfa HealthCare is a global leader in IT enabled clinical workflow and diagnostic imaging solutions, offering healthcare facilities a seamless flow of information and a 360 view of patient care.
E-mail our webmaster if you have questions. Bonn, DE Premarket qara Professional (m/w).
Your Profile: University Degree (Engineering, Computer Science or Science) or equivalent combination of education and experience. The company has a unique, holistic approach, enabling it to provide in-depth clinical know-how and fully integrated hospital-wide solutions. Regulatory and CE submissions in cooperation with regional qara organizations. We offer a rewarding career in a field that impacts lives, the opportunity to work with a talented, committed team of individuals, training and career development programs, and a competitive compensation and benefits package. Signing off key project related documentation and milestones. For our office in Bonn we are looking for. Taking actions on process issues for related premarket/design control processes. At least 3-5 years experience in a regulated industry preferably medical device or related holding a position in quality assurance, regulatory affairs, quality management, or project management. Team player with excellent interpersonal, collaboration, negotiation, conflict resolution, relationship-building, and communication skills. Definition of regulatory and product quality strategy. Ensuring the adherence to the medical device risk analysis process as risk moderator of the development team. Country SamoaAndorraAngolaAntigua and and VerdeCayman IslandsCentral African Democratic Republic of theCongo, Republic of theCosta RicaCôte d'IvoireCroatiaCubaCyprusCzech RepublicEast TimorEcuadorEgyptEl SalvadorEquatorial IslandsFijiFinlandFranceFrench KoreaSouth Mariana State ofPanamaPapua New Kitts and NevisSaint LuciaSaint Vincent and the GrenadinesSamoaSan MarinoSao Tome and PrincipeSaudi LeoneSingaporeSint MaartenSlovakiaSloveniaSolomon IslandsSomaliaSouth AfricaSpainSri LankaSudanSudan, and Arab EmiratesUnited.
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