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Regulatory Affairs Medical Devices Jobs

1 - 15 von 77
1 - 15 von 77
Suchergebnisse - Regulatory Affairs Medical Devices Jobs
MyMenopauseRx, LLC-Deutschland
Senior Regulatory Affairs Manager (m/w/d) Medical Devices Apply At Job Full Name First Name Last Name Email WhatsApp Number Upload CV Please upload CV in pdf format only. CV PDF Link User Profile We are an agile healthcare company that is...
appcast.io -
PAUL HARTMANN AG-Herbrechtingen
medical device environment or another regulatory field of work  •  Knowledge in regulatory requirements, MDR and relevant MDCGs, rel. MEDDEVs  •  Experience in literature search and review required as well as knowledge of regulatory medical writing  •  Knowledge...
Novanta Inc.-Berlin
and systematic way of working. Additional qualifications:  •  Manager Regulatory Affairs - Medical Devices.  •  Independent use of English (CEFR-B2)*. *) Common European Framework of Reference for Languages (CEFR). Novanta is proud to be an equal employment...
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PAUL HARTMANN AG-Herbrechtingen
medical device environment or another regulatory field of work  •  Knowledge in regulatory requirements, MDR and relevant MDCGs, rel. MEDDEVs  •  Experience in literature search and review required as well as knowledge of regulatory medical writing  •  Knowledge...
VSY Biotechnology GmbH-Stuttgart
registration of products in different countries, including international and European approvals of our own medical devices. Qualifications:   1.  BSc degree in Life Science or related fields.   2.  At least 3 years of experience in Regulatory Affairs and R&D...
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PAUL HARTMANN AG-Herbrechtingen
medical device environment or another regulatory field of work  •  Knowledge in regulatory requirements, MDR and relevant MDCGs, rel. MEDDEVs  •  Experience in literature search and review required as well as knowledge of regulatory medical writing  •  Knowledge...
KARL STORZ SE & Co. KG-Tuttlingen
Health & Regulatory Affairs Responsibilities  •  You will prepare and compile regulatory submission dossiers for new medical device registrations and changes to existing products, in accordance with regulations.  •  Monitoring new legislations, policies...
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Carl Zeiss AG-München
Regulatory / Clinical Affairs (RA/CA) Team Lead (m/f/x) Seeing beyond - future of medical technology For more than 100 years, ZEISS medical technology has been driving progress in ophthalmology and microsurgery. In ophthalmology, our solutions help...
connecticum.de -
Barrington James Limited-München
Job Opportunity: Quality Assurance & Regulatory Affairs (QA/RA) Manager Barrington James' QARA division is seeking a proactive and experienced Quality Assurance & Regulatory Affairs (QA/RA) Manager. This role is pivotal in maintaining and improving...
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PAUL HARTMANN AG-Herbrechtingen
medical device environment or another regulatory field of work  •  Knowledge in regulatory requirements, MDR and relevant MDCGs, rel. MEDDEVs  •  Experience in literature search and review required as well as knowledge of regulatory medical writing  •  Knowledge...
Merz Aesthetics-Frankfurt am Main
and maintaining the skin's beauty. Would you like to become part of our success story? Then join Merz Aesthetics! Medical Affairs & Science Liaison (m/f/d) Distribution Partner Management EMEA Aufgaben  •  You support the overall distribution partner business...
stepstone.de -
PAUL HARTMANN AG-Herbrechtingen
medical device environment or another regulatory field of work  •  Knowledge in regulatory requirements, MDR and relevant MDCGs, rel. MEDDEVs  •  Experience in literature search and review required as well as knowledge of regulatory medical writing  •  Knowledge...
bess AG-Berlin
instruments and innovative device systems, we serve clients across the fields of ENT, head and neck surgery, pulmonology and gastroenterology. For over 30 years, we have also been providing custom-made devices and supporting medical innovation, building a...
stepstone.de -
StudentJob DE-Heidenheim an der Brenz
in natural science, life science or engineering Knowledge in scientifc and/or clinical working (e.g. Chemical, microbiological or quality lab) Knowledge in the field of medical devices, regulatory affairs or quality management desired Willingness to learn...
studentjob.de -
Otsuka Pharma GmbH-Frankfurt am Main
experience, preferably including Quality Management for GxPs  •  Expert knowledge and experience in relevant regulations and guidance documents, e.g. in the area of Clinical Development, Medical Devices, IMP management, Regulatory Affairs or Pharmacovigilance...
stepstone.de -
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