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Lifelancer
Lifelancer
51 – 200 Darbuotojai
KonsultavimasLogistikaSveikatos priežiūra
„Lifelancer“ yra dirbtiniu intelektu pagrįsta talentų samdos platforma, orientuota į gyvybės mokslų, farmacijos ir IT sektorius. Ji padeda kvalifikuotiems specialistams pristatyti savo patirtį, rasti tarptautinio darbo ir projektų galimybių bei susisiekti su darbdaviais, ieškančiais specializuotų talentų. Samdančioms komandoms „Lifelancer“ sujungia dirbtinio intelekto padedamą talentų paiešką su pagalba įdarbinant ir tvarkant darbo užmokestį keliose šalyse, taip pat padeda atsižvelgti į atitikties reikalavimus.
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Darbai įmonėje

Remote RDQA Clinical Quality Auditor — New Jersey

Conduct GCP audits and corrective-action follow-up for AbbVie, supporting clinical quality and compliance across global operations. Advise business partners on clinical regulations, quality systems, and inspection readiness.

USJungtinės ValstijosNJNaujasis DžersisNuotolinisVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųAuditorius
Google Cloud Platform

Aprašymas

  • Manage the Clinical audit program, including scheduling, planning, reporting, and audit resolution.
  • Maintain alignment with RDQA policies and procedures.
  • Help develop and implement the Clinical QA quality system.
  • Advise business partners on GCP and clinical quality matters.
  • Assess clinical processes through audits and quality-assurance oversight to verify compliance.
  • Lead and support the scheduling, planning, and execution of Clinical audits.
  • Perform investigator site, process, system, and Affiliate audits.
  • Deliver oral and written audit results within established timelines.
  • Review and approve Corrective Action Plans and monitor actions through completion.
  • Help develop and implement systems and processes that support global quality-assurance requirements.
  • Support the maintenance and development of quality standards for Clinical audits.
  • Participate in continuous-improvement initiatives and projects.
  • Support GCP inspections as needed.
  • Provide GCP regulatory guidance and consultation to RDQA and business partners.
  • Encourage ongoing education in quality, clinical guidelines, and regulations.

Reikalavimai

  • Bachelor’s degree in a physical, life, or health science; a healthcare profession such as nursing or pharmacy; or equivalent experience.
  • Three to five years of experience in the biopharmaceutical industry or with a regulatory authority.
  • Three to five years of experience in Quality Assurance and/or Clinical Research Development.
  • Strong analytical ability and skill in drawing conclusions from presented data.
  • Capacity to work effectively and efficiently in a dynamic environment with minimal supervision.
  • Working awareness of clinical-trial regulations, including ICH-GCP and the EU Clinical Trial Directive/Regulation, as well as industry best practices.
  • Flexibility to adapt to changing assignments and prioritize work effectively.
  • Strong project-management, interpersonal, and communication skills.
  • Ability to work independently and collaboratively within a team.
  • Willingness and ability to travel internationally.
  • Availability for travel of up to 40%.
  • Equivalent experience may be accepted in place of the stated bachelor’s degree.

Privalumai

  • Paid time off, including vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance.
  • 401(k) plan.
  • Short-term incentive programs.
  • Equal-opportunity employer benefits and reasonable-accommodation support for eligible applicants.

Susiję darbai

Jhpiego

Technical Director, Sustainable Health Systems and Private Sector Engagement

Jhpiego
1 001 – 5 000 Darbuotojai
KonsultavimasSveikatos draudimasSveikatos priežiūra
USJungtinės ValstijosMDMerilandas
127 874 $ – 162 786 $ / metai
Darbas vietojeVisas etatasVadovasPrivaloma Kalba: anglųDirektorius

Lead Jhpiego’s work to build sustainable, market-enabled health systems. Develop private-sector partnerships, innovative financing, and scalable solutions across global health programs.

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3Shape

Tier 2 Support Consultant, English – Kyiv Hybrid

3Shape
1 001 – 5 000 Darbuotojai
GamybaKonsultavimasLogistika
UAUkrainaHibridinisVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųPrivaloma Kalba: ukrainiečiųKonsultantas

Troubleshoot 3Shape dental scanners and software for customers worldwide, handling support through digital sessions, phone, and email. Based in a hybrid Kyiv role, you’ll document CRM cases and pass customer feedback to relevant teams.

Atidaryti