Support the Global Strategic Marketing group in regards of the EU MDR compliance
Work closely with the functional business leads to ensure the efficiency and effectiveness of the solution deployed in support of the business goals and objectives.
Perform the required activities and generates the appropriate product development documents to ensure compliance with national and international regulations related to medical devices (EU MDR)
Perform MDR specific projects and functions as assigned by the group manager
Assures information exchange between internal partners, e.g Operations, PDEs, Regulatory Affairs, Design Transfer, etc.
Updating and reviewing: labeling material (LMD & IFU) using Agile, PLF process including F-S813 and Marketing Material using EOS
Drive the changes and facilitate release of the updated documents in PLM
Profound professional experience in related technical or scientific discipline
Proven exceptional written and oral presentation skills
Experience in an Medical Device regulated environment
A highly motivated team and an open way of communication
A very renowned company
Über Hays: With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
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