Alira Health
Alira Health
Alira Health este o companie globală de consultanță și tehnologie în domeniul sănătății, care oferă servicii organizațiilor din domeniul științelor vieții. Activitatea sa acoperă cercetarea și dezvoltarea clinică, conformitatea cu reglementările, consultanța managerială, implicarea pacienților și accesul pe piață, precum și soluții tehnologice concepute pentru a sprijini cercetarea în științele vieții. Compania pune accent pe empatie, excelență științifică, rezultate mai bune pentru pacienți, sustenabilitate ecologică, implicare comunitară și inițiative ESG.

Quality Assurance Coordinator – Spain (Remote)

Support Alira Health’s global Quality Management System by maintaining Qualio records, tracking quality events, and coordinating quality requests. This full-time remote role is based in Spain, with work centered on Barcelona.

Descriere

  • Maintain QA trackers and follow up on quality events, including deviations, CAPAs, complaints, actions, and due dates.
  • Coordinate with stakeholders to resolve outstanding actions, documentation, approvals, and quality-related requests.
  • Help migrate manual and legacy quality records into the Qualio eQMS, keeping records complete, accurate, and well organized.
  • Administer and maintain quality records within Qualio.
  • Review requests submitted to the QA inbox and direct those requiring escalation or quality judgment to the appropriate QA team member.
  • Assist with routine training administration by processing requests, maintaining related records, and monitoring pending activities.
  • Answer routine Qualio user questions or route them to the appropriate contact.
  • Maintain controlled quality documents and records through accurate filing, naming, organization, and upkeep.
  • Help prepare quality metrics, status reports, and routine QA follow-up materials as needed.
  • Perform additional administrative and operational Quality Assurance duties assigned by the Global Quality Assurance team.

Cerințe

  • Bring approximately 1–2 years of experience in Quality Assurance, Quality Systems, document control, or a related field, ideally in a regulated pharmaceutical, biotechnology, medical device, CRO, or life sciences setting.
  • Understand core Quality Management System concepts and processes, including deviations, CAPAs, complaints, training, and controlled documentation.
  • Experience using an electronic Quality Management System is advantageous.
  • Organize and monitor multiple activities, deadlines, and follow-up actions effectively.
  • Demonstrate meticulous attention to detail and a strong commitment to accurate records.
  • Communicate clearly in writing and verbally.
  • Work independently within established processes and escalate matters that require QA review or decision-making.
  • Demonstrate proficiency in English.

Beneficii

  • Remote work arrangement.
  • Contingency Workforce contract type.

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