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Thermo Fisher Scientific
Thermo Fisher Scientific
H1B vizos rėmėjasGamybaLogistikaSveikatos priežiūra
„Thermo Fisher Scientific“ kuria ir tiekia technologijas, laboratorijų produktus bei farmacijos paslaugas, padedančias vykdyti mokslinius tyrimus ir teikti sveikatos priežiūrą. Įmonės veikla apima gyvybės mokslų tyrimus, analitinių problemų sprendimą, laboratorijų našumo didinimą, diagnostiką, taip pat gydymo metodų kūrimą ir gamybą. Klientams visame pasaulyje ji teikia paslaugas pasitelkdama tarptautinę komandą ir prekių ženklų portfelį, kurį sudaro „Thermo Scientific“, „Applied Biosystems“, „Invitrogen“, „Fisher Scientific“, „Unity Lab Services“, „Patheon“ ir „PPD“. Įmonės karjeros galimybės apima su šiais pasiūlymais susijusias mokslo, sveikatos priežiūros, gamybos, logistikos ir paslaugų veiklas.
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Darbai įmonėje

Remote Pharmacovigilance Quality Manager – Serbia

Lead pharmacovigilance quality systems, audits, training, and compliance for Global Patient Safety operations. The role supports remote work from Serbia and other listed European locations.

BGBulgarijaESIspanijaGRGraikijaHRKroatijaHUVengrijaPTPortugalijaRSSerbijaNuotolinisVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųVadovas

Aprašymas

  • Run the Pharmacovigilance Quality Management System within Global Patient Safety.
  • Help expand the Global Patient Safety Quality Management function.
  • Maintain and deliver the comprehensive training program.
  • Oversee Global Patient Safety procedural documents.
  • Support audit and inspection readiness, coordination, and management.
  • Advance continuous improvement through issue management, process changes, and KPI development.
  • Support or manage GVP audits and inspections.
  • Prepare Global Patient Safety teams for inspections and keep supporting documents readily accessible.
  • Coordinate responses to audit and inspection findings.
  • Review issue trends and implement plans to address underlying causes.
  • Identify internal deviations and support corrective and preventive actions, including root-cause analysis.
  • Lead corrective and preventive action implementation with the client Quality function.
  • Develop, maintain, expand, and deliver pharmacovigilance training.
  • Help monitor and update Global Patient Safety training curricula.
  • Train relevant client staff and third parties when applicable.
  • Develop, review, and improve Global Patient Safety processes and procedures.
  • Take part in cross-functional procedural document work and forums.
  • Support document control in Veeva.
  • Help develop and assess key performance indicators.
  • Monitor third-party compliance with contractual obligations, PVAs, SDEAs, and other agreements.
  • Coordinate with the QA Department on Global Patient Safety quality and compliance needs and deliverables.
  • Monitor compliance with Global Patient Safety SOPs and controlled documents.
  • Carry out other duties assigned by the line manager or Global Patient Safety leadership.

Reikalavimai

  • Bachelor’s degree at minimum in pharmacy, nursing, healthcare, another life-science or technical discipline, or a country-equivalent combination of education and experience.
  • At least five years of experience in the pharmaceutical or biotechnology industry.
  • At least three years of experience in pharmacovigilance or drug safety.
  • A strong record of managing pharmacovigilance quality systems, processes, and teams.
  • Experience preparing for, hosting, and responding to global audits and regulatory inspections.
  • Working knowledge of pharmacovigilance regulations and guidance in Europe, the United States, and Japan.
  • Knowledge of GxP quality and compliance requirements, processes, and measures.
  • Strong planning and organizational skills.
  • Excellent spoken and written communication.
  • Ability to work in a global environment.
  • Solution-focused approach, with the ability to prioritize and work independently.
  • Strong presentation skills and ability to explain complex issues clearly.
  • Demonstrated skill in authoring and contributing to procedural documents.
  • Ability to motivate and collaborate with multidisciplinary teams.
  • Proficiency with Microsoft Office and tracking databases.
  • Fluent written and spoken English.

Privalumai

  • Fully remote work arrangement.

Susiję darbai

Bank of America

Risk Analysis Specialist III

Bank of America
H1B vizos rėmėjasBankininkystėFinansaiFintech
USJungtinės ValstijosNJNaujasis DžersisNCŠiaurės Karolina
114 500 $ – 174 800 $ / metai
Darbas vietojeVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųRizika

Improve data quality, business controls, and operational risk practices across Bank of America’s risk analytics and capital management work. Collaborate with teams across the organization to assess processes and deliver actionable insights.

Atidaryti
West Bend Insurance Company

Senior Manager, Underwriting Business Services

West Bend Insurance Company
1 001 – 5 000 Darbuotojai
KonsultavimasSveikatos priežiūraTeisė
USJungtinės ValstijosWIViskonsinas
139 735 $ – 174 669 $ / metai
HibridinisVisas etatasVyresnysis specialistasPrivaloma Kalba: anglųRizikos vertintojas

Lead underwriting quality, policy services, and technical operations at West Bend Insurance Company. Drive operational performance, risk management, team development, and cross-functional improvements.

Atidaryti
Highmark Health

Associate Actuary

Highmark Health
H1B vizos rėmėjasDraudimasKonsultavimasLogistika
USJungtinės ValstijosALAlabamaAKAliaskaAZArizonaCAKalifornijaCOKoloradasCTKonektikutasFLFloridaHIHavajaiIDAidahasILIlinojusIAAjovaKSKanzasasKYKentukisLALuizianaMEMeinasMDMerilandasMAMasačusetsasMIMičiganasMNMinesotaMSMisisipėMOMisūrisMTMontanaNENebraskaNVNevadaNHNaujasis HampšyrasNJNaujasis DžersisNMNaujoji MeksikaNYNiujorkasNCŠiaurės KarolinaNDŠiaurės DakotaOHOhajasOKOklahomaOROregonasRIRod AilandasSCPietų KarolinaSDPietų DakotaTNTenesisTXTeksasasUTJutaVTVermontasVAVirdžinijaWAVašingtonasWVVakarų VirdžinijaWIViskonsinasWYVajomingas
86 400 $ – 138 600 $ / metai
Darbas vietojeVisas etatasVidutinis lygisPrivaloma Kalba: anglųAktuaras

Highmark Health seeks an associate actuary to lead actuarial studies, analyses, and recommendations. The role also develops processes, supports stakeholders, and mentors junior staff.

Atidaryti
Acrisure

Pharmacy Benefits Claims Consultant

Acrisure
H1B vizos rėmėjasKonsultavimasRinkodaraSveikatos priežiūra
USJungtinės ValstijosMIMičiganasHibridinisVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųPrivaloma Kalba: ispanųKonsultantas

Resolve pharmacy benefit claims for self-funded employer health plans by investigating discrepancies and coordinating with stakeholders. Support accurate claims processing and improvements to plan performance and cost management.

Atidaryti