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Medtronic
Medtronic
H1B vizasi homiysiIshlab chiqarishSog‘liqni saqlashTibbiy sug‘urta
Medtronic murakkab tibbiy holatlar uchun yechimlar ishlab chiqadigan global sog‘liqni saqlash texnologiyalari va ishlab chiqarish kompaniyasidir. Uning faoliyati davolash usullari, terapiyalar va tibbiy texnologiyalardan foydalanish imkoniyatlarini yaxshilash uchun yirik xalqaro jamoalarni tibbiyot xodimlari bilan yaqindan hamkorlikda birlashtiradi. 150 dan ortiq mamlakatda 95 000 dan ziyod xodimga ega Medtronic o‘z faoliyatining barcha yo‘nalishlarida inklyuziya, xilma-xillik, tenglik va barqaror amaliyotlarni qo‘llab-quvvatlagan holda bemorlarga yordam ko‘rsatishni rivojlantirishga e’tibor qaratadi.
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Kompaniyadagi ish o‘rinlari

Associate Regulatory Affairs Specialist - Eindhoven, Netherlands (Hybrid)

Support Medtronic’s Benelux medical-device compliance program through vigilance, safety actions, quality systems, and regulatory coordination. Partner with regional teams and authorities to maintain compliant post-market and regulatory processes.

NLNiderlandiya
43 840 € – 65 760 € / yil
GibridTo‘liq stavkaJuniorO‘rta darajaTalab Qilinadigan Til: inglizchaTalab Qilinadigan Til: niderlandMuvofiqlik

Tavsif

  • Coordinate field safety corrective actions and product holds across the Benelux region, from preparation through follow-up.
  • Handle competent-authority inquiries concerning vigilance activities and field safety corrective actions.
  • Guide sales teams on compliant product complaint handling and product return procedures.
  • Contribute to Quality Management System activities covering suppliers, distributors, document control, and KPI monitoring.
  • Track regulatory changes and help implement new requirements affecting the Benelux region.
  • Manage shared regulatory inboxes and answer internal, tender, and customer requests.
  • Review promotional and marketing materials for regulatory compliance.
  • Work with regional and global Quality and Regulatory teams on compliance initiatives and process improvements.
  • Support post-market surveillance, safety actions, authority interactions, and Quality Management System processes across the Benelux region.
  • Coordinate with commercial, quality, regulatory, and operational stakeholders.

Talablar

  • Bachelor’s degree with at least 0 years of experience in Regulatory Affairs, Quality, Life Sciences, Biomedical Sciences, Healthcare, or a related field.
  • Fluent written and spoken English and Dutch.
  • Advanced proficiency with Microsoft Office applications and database systems.
  • Demonstrated ability to manage competing priorities with strong organizational and administrative skills.
  • High accuracy and attention to detail when working in a regulated environment.
  • French or German language knowledge is preferred.
  • Knowledge of medical-device regulations, post-market surveillance, or vigilance processes is preferred.
  • Experience with an ISO 13485-certified Quality Management System is preferred.
  • Experience supporting regulatory, quality, or compliance work in healthcare or medical devices is preferred.
  • A proactive approach and effectiveness in multicultural working environments are preferred.

Imtiyozlar

  • Flexible work arrangement.
  • Competitive salary with a flexible benefits package.
  • Broad benefits, resources, and competitive compensation plans supporting employees across career and life stages.
  • Short-term incentive through the Medtronic Incentive Plan (MIP).

O‘xshash ish o‘rinlari

Hamilton Medical

Account Manager, Respiratory Ventilation | Texas and Oklahoma

Hamilton Medical
501 – 1 000 Xodimlar
H1B vizasi homiysiIshlab chiqarishSog‘liqni saqlashTibbiy sug‘urta
USAmerika Qo‘shma ShtatlariTXTexasMasofaviyTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaMijozlar bilan ishlash menejeriSotuv

Lead hospital sales of Hamilton Medical respiratory ventilation products across Texas and Oklahoma. Oversee capital procurement, customer adoption, installations, training, and territory pipeline management.

Ochish