Associate, Regulatory Projects

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...

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...

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...

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- 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 -...

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_22502...

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...

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- 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...

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...

Your Tasks- Collaborate with product owners, stakeholders, and cross-functional software teams to execute projects aligned with business objectives - Facilitate effective communication and coordination within the product team, ensuring clear goals and responsibilities - Track and lead progresses, milestones, and deliverables, providing regular stakeholder...

Are you ready for the next career step or looking for a career change? As Team Leader, Electronics Design (M/F/d), a responsible field of activity awaits you in a 10-member team, which is responsible for the design and development of electronics and firmware in the R&D group Emerging Applications. The task of this group is the development of new product...

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...

Th!nk Europe is a new spin-off of Th!nk E, a dynamically developing Belgian company in the energy sector, which will focus on cooperating with experts from EU member states and associated countries on European projects. Our multidisciplinary network will gather leading national experts in financing of energy projects, technical assistance to municipalities,...

Your Tasks - Perform clinical research project management activities including resource planning, timelines, and milestone management - Coordinate and manage multicentric submissions to regulatory authorities and ethics committees, including writing, editing, compiling, and maintaining documents related to pre - and post-market clinical trials according to...

**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 -...

Your 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 -...

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...

Aufgaben - Analyze and interpret frame-by-frame data to identify potential risk factors in aseptic processing - Contribute to expanding and organizing our data library, ensuring accuracy and accessibility - Employ problem-solving skills to troubleshoot and resolve aseptic processing and simulation data issues - Maintain consistent and precise documentation...