Regulatory Affairs Associate, Global Registrations

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. RA_12502...

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...

RA_12502 Regulatory Project Associate (m/w/d) Regulatory Affairs Innsbruck, Österreich Fachkräfte Vollzeit 38,5 h Befristet 31.07.2027 Bewerben Unsere Regulatory Affairs Abteilung stellt sicher, dass die Produkte den geltenden Vorschriften und Normen entsprechen. Dazu gehört die Bereitstellung von strategischem Input für Produktentwicklungen, die...

RA_12502 Regulatory Project Associate (m/w/d) Regulatory Affairs Innsbruck, Österreich Fachkräfte Vollzeit 38,5 h Befristet 31.07.2027 Bewerben Unsere Regulatory Affairs Abteilung stellt sicher, dass die Produkte den geltenden Vorschriften und Normen entsprechen. Dazu gehört die Bereitstellung von strategischem Input für...

RA_12502 Regulatory Project Associate (m/w/d) Regulatory Affairs Innsbruck, Österreich Fachkräfte Vollzeit 38,5 h Befristet 31.07.2027 Bewerben Unsere Regulatory Affairs Abteilung stellt sicher, dass die Produkte den geltenden Vorschriften und Normen entsprechen. Dazu gehört die Bereitstellung von strategischem Input für...

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. RA_32502 . click...

CEO_22501 Specialist, Tender and Opportunity Support (m/w/d) CEO Team / Administration Innsbruck, Österreich Fachkräfte Vollzeit 38,5 h Unbefristet Bewerben Ihre Aufgaben * Operative Abwicklung internationaler Ausschreibungen im Bereich Medizintechnik * Ausarbeitung und fristgerechte Zusammenstellung aller relevanten Angebots- und...

CEO_22501 Specialist, Tender and Opportunity Support (m/w/d) CEO Team / Administration Innsbruck, Österreich Fachkräfte Vollzeit 38,5 h Unbefristet Bewerben Ihre Aufgaben * Operative Abwicklung internationaler Ausschreibungen im Bereich Medizintechnik * Ausarbeitung und fristgerechte Zusammenstellung aller relevanten Angebots- und...

Regulatory Affairs Associate, Global Registrations (m/w/d) Regulatory Affairs Innsbruck, Österreich - FachkräfteVollzeit 38,5hUnbefristet - BewerbenShare- Unsere Regulatory Affairs Abteilung stellt sicher, dass die Produkte den geltenden Vorschriften und Normen entsprechen. Dazu gehört die Bereitstellung von strategischem Input für...

Your Tasks - Support and organize submissions to Notified Body - Support and organize submissions, license renewals and registrations to international authorities - Organize and maintain regulatory documentation to meet regulatory requirements - Provide regulatory input to product development, product changes and manufacturing changes Your Profile -...

Regulatory Project Associate (m/w/d) Regulatory Affairs Innsbruck, Österreich - FachkräfteVollzeit 38,5hBefristet 31.07.2027 - BewerbenShare- Unsere Regulatory Affairs Abteilung stellt sicher, dass die Produkte den geltenden Vorschriften und Normen entsprechen. Dazu gehört die Bereitstellung von strategischem Input für Produktentwicklungen, die...

Regulatory Affairs Specialist (m/w/d) Regulatory Affairs Innsbruck, Österreich - FachkräfteVollzeit 38,5hUnbefristet - BewerbenShare- Unsere Regulatory Affairs Abteilung stellt sicher, dass die Produkte den geltenden Vorschriften und Normen entsprechen. Dazu gehört die Bereitstellung von strategischem Input für Produktentwicklungen, die Einholung und...

Your Tasks- Responsible for multiple aspects of office management for the Regulatory Affairs Department - Management of informational lists and databases - Certificate ordering and legalization - Sales area communications - General regulatory submission support - Your Profile- Written and verbal fluency in English - Attention to detail and excellent...

Wir sind international und Landwirtschaft ist unsere Leidenschaft. Unser Familienunternehmen produziert und vertreibt unter eigenen Marken hochwertige Produkte für naturverbundene Menschen und Landwirte weltweit. Dafür brauchen wir motivierte Mitarbeiter, die wir langfristig fördern. Für die Unterstützung unseres R&D Teams am Firmensitz Innsbruck...

Your Tasks- Regulatory dossier compilation and submission - Regulatory assessment and submission strategy development - Regulatory itelligence gathering - Management of informational lists and databases - Sales area communications - Your Profile- Written and verbal fluency in English - Attention to detail and excellent organizational skills - Strong...

This position is responsible for activities concerned with the review, development, remediation, and approval of Device History Files and/or Technical Documentation of medical devices. Activities will also include the preparation of regulatory submissions in all markets. Essential responsibility includes ensuring compliance to the applicable Quality...

Your Tasks - Manage coordination of transition of devices to the new Medical Device Regulation - Coordinate, organise and support key regulatory projects / tasks and regulatory compliance initiatives - Ensure timely delivery of project deliverables Your Profile - Project Management experiences as well as an interest in studies around bio-medical/engineering...

Your Tasks- Notified Body Coordination (meetings & protocols / projects & submission lists) - Preparation of Notified Body Application Appendices - Management of nomenclature and classification systems for medical devices - Support on Medical Device Regulation (MDR) transition conversions and related projects - Support on UK Conformity Assessment procedure -...

Your Tasks - Follow defined procedures for entering complaint reports into the company’s database in a timely and accurate manner (Both procedures and complaint reports are in English) Processing of Competent Authority and device investigation reports into PDF format Your Profile - Excellent communication skills in written and spoken English are a must....

Your Tasks- Operational handling of international tenders in the medical device sector - Elaboration and timely compilation of all relevant proposal/tender documents - Communication and coordination with the responsible departments in the company (product management, regulatory affairs, logistics, R&D, sales, etc.) - Review and control of all agreements and...

SOS Children's Villages, founded in 1949 by Hermann Gmeiner, is the world's largest non-governmental organization focused on supporting children and young people without parental care, or at risk of losing it.- Child neglect, abuse and abandonment is everywhere. Families are at risk of separation. Locally led, we work in more than 130 countries and...

**Company Description**: At Intuitive, we are united behind our mission: we believe that mínimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse...

Specialist, Tender and Opportunity Support (m/w/d) CEO Team / Administration Innsbruck, Österreich - FachkräfteVollzeit 38,5hUnbefristet - BewerbenShareIhre Aufgaben Operative Abwicklung internationaler Ausschreibungen im Bereich MedizintechnikAusarbeitung und fristgerechte Zusammenstellung aller relevanten Angebots - und...

Your Tasks - Conduct monitoring activities for clinical investigations - Generate monitoring plans and assist with completion of other clinical investigation documents - Ensure clinical investigations are conducted in accordance with the protocol, standard operating procedures, ISO14155, the Medical Device Regulation and all applicable regulatory...

- What you will be doing Always be courteous and helpful to World Courier customers and consignees. - Pick up and deliver goods as requested. - Ensure required paperwork is completed by customer/consignee. - Use initiative and anticipate problems that may occur with deliveries. - Keep Dispatch Officer informed of progress of deliveries and any delays. -...

- What you will be doing - Under broad supervision of the Customer Service Manager, you will become an integral part of our team, acting as first point of contact for our customers on an international level. Our Customer Service teams works closely with other offices around the world as well as vendors and governmental agencies to find optimal solutions for...

Your Tasks - Global product management of cochlear implants and surgical systems, with focus on in-life management - Preparations for products market entry - support of trials activities, validate fit for market and operational readiness, provide input for regulatory strategy & approval - Support of launches & products in-life activities - launch, establish...

**Main Tasks** - Global product management of cochlear implants throughout their complete life cycle - Support shaping future products - perform market research to uncover market trends, perform customer innovation research and discovery activities to uncover user needs, support the Research & Development during all the development phases of new products -...