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Senior Regulatory Affairs Specialist - New Product Development - JNJKJP00035766 (m/f/d)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Engineering, Support, Plm
Projektbeschreibung
REFERENCE NUMBER:
410493/29
MY DUTIES:
-Support preparation of technical documentation or design dossier documentation for submission to and review by Notified Bodies, as required (both MDD and MDR) and as assigned
-Support compliance execution work in collaboration with local Regulatory Team
-Provide regulatory support
-Work in concordance with MDR requirements regarding required content of Technical Documentation (focus on ANNEX II of Regulation (EU) 2017/745)
MY QUALIFICATIONS:
-Profound and in-depth experience in the Medical Device industry and Regulatory Affairs
-Understanding of MDR requirements regarding required content of Technical Documentation (focus on ANNEX II of Regulation (EU) 2017/745)
-Understanding of requirements of current Council Directive 93/42/EEC
-Experience with creation and maintenance of Technical Documentation in PLM Systems preferred
-Experience in IT system documentation and database management preferred
-MS Office skills (Excel, Access) for data analyses and comparisons
-Ability to comprehend principles of engineering, physiology and medical device use
-Strong analytical skills and proficiency in English written and spoken (German would be an asset)
MY BENEFITS:
-A very renowned company
-A highly motivated team and an open way of communication
-You will work in an international environment
PROJECT INFORMATION:
As a modern company, our client manages to constantly develop further and break new ground.
ABOUT 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.
410493/29
MY DUTIES:
-Support preparation of technical documentation or design dossier documentation for submission to and review by Notified Bodies, as required (both MDD and MDR) and as assigned
-Support compliance execution work in collaboration with local Regulatory Team
-Provide regulatory support
-Work in concordance with MDR requirements regarding required content of Technical Documentation (focus on ANNEX II of Regulation (EU) 2017/745)
MY QUALIFICATIONS:
-Profound and in-depth experience in the Medical Device industry and Regulatory Affairs
-Understanding of MDR requirements regarding required content of Technical Documentation (focus on ANNEX II of Regulation (EU) 2017/745)
-Understanding of requirements of current Council Directive 93/42/EEC
-Experience with creation and maintenance of Technical Documentation in PLM Systems preferred
-Experience in IT system documentation and database management preferred
-MS Office skills (Excel, Access) for data analyses and comparisons
-Ability to comprehend principles of engineering, physiology and medical device use
-Strong analytical skills and proficiency in English written and spoken (German would be an asset)
MY BENEFITS:
-A very renowned company
-A highly motivated team and an open way of communication
-You will work in an international environment
PROJECT INFORMATION:
As a modern company, our client manages to constantly develop further and break new ground.
ABOUT 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.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Sonstiges