Clinical affairs manager Jobs in Schechen
- Gesponsert
Regulatory Project Associate (m / f / d)
MED-ELRosenheim, DE(Senior) Manager, Medical Science Liaison, Therapy Development, Transcatheter Mitral and Tricuspid Therapies (Germany)
Edwards LifesciencesGermany, Bayern, Remote- Gesponsert
Sales Manager (m / w / d)
GOLDBECK Süd GmbHRosenheim, Oberbayern, Bayern, Germany- Gesponsert
(Senior) Online Marketing Manager •
CADFEM Germany GmbHGrafing bei München, DeutschlandFilialleiter / Store Manager
SnipesRosenheim, DE(Junior) Regulatory Affairs Coordinator (m / w / d)
Medi-Globe GroupRohrdorf / Achenmühle, BayernTerritory Sales Manager - South-Germany
ProclinicalBayern, GermanyAsset Manager PV
Approach People RecruitmentBavaria, State, Germany- Gesponsert
Gehaltsabrechnungs-Manager (m / w / d)
Hamberger Industriewerke GmbHStephanskirchen, Deutschland- Gesponsert
QA Test Manager (m / w / d)
Qnit AGRosenheim, Germany- Gesponsert
Sales Manager (m / w / d) Bayern
SoftTec GmbHBayern, DEMechanical Engineer Required in Munich, Germany New
Skills ProvisionBayern, GermanyAssistant Manager (m / w / d)
L'Osteria - Rosenheim - AdlzreiterstraßeRosenheim, Bayern, Deutschland- Gesponsert
Junior Alliance Manager (m / w / d)
ACP Gruppe DeutschlandKolbermoor, DeutschlandGIS Manager
The Green Recruitment CompanyBavariaSenior DMPK Expert (f / m / d)
Nuvisan GmbHGrafing bei München, Bayern, Deutschland- Gesponsert
Hotel Manager (m / w / d) - Festanstellung
Premier Inn HotelsRosenheim, Bayern, GermanyRegulatory Project Associate (m / f / d)
MED-ELRosenheim, DEAbout MED-EL
MED-EL is a leading manufacturer of innovative medical devices for the treatment of various types and degrees of hearing loss. Our unique portfolio of implantable hearing solutions benefits thousands of individuals in more than 140 countries worldwide. With headquarters in Innsbruck, Austria, MED-EL has over 2,800 employees around the world.
Your Tasks
Our Regulatory Affairs department ensures that products comply with applicable regulations and standards. This includes providing strategic input to product developments, obtaining and maintaining product registrations and approvals, communicating with authorities, and monitoring regulatory changes to ensure continued compliance.
- Lead, organise and support key regulatory projects / tasks and regulatory compliance initiatives
- Organise and support preparation of regulatory submissions, licence renewals, registrations and change notifications to international authorities
- Organise and maintain regulatory documentation to meet regulatory requirements
- Provide regulatory intel to product development projects
Your Profile
Your Benefits
Interested?
Want to join a company that helps bring the joy of sound to people with hearing loss? Apply now!
Your Contact Person
If you have any questions please contact Caroline Schenk.
Please apply in English!