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Alira Health

Quality Assurance Coordinator

Alira Health

. Maintain and update QA trackers and support follow-up of quality events, including deviations, CAPAs, complaints, and associated actions and due dates .

Posted 10/5/2026full-timeRemote • SpainJuniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Quality Assurance processes, including document control and Quality Management Systems, with a strong focus on accurate recordkeeping and organizational skills. Proficient in managing quality events and supporting training administration within regulated life sciences environments.

Highest-signal resume keywords
Quality Assurance ExperienceQuality Management System KnowledgeDocument Control ProficiencyStrong Organizational SkillsEffective Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Quality Management SystemDocument ControlQuality Metrics PreparationCAPA ManagementDeviation TrackingTraining AdministrationRecord ManagementQuality Event Follow-UpQuality DocumentationQuality Assurance Processes
Soft Skills
Attention to DetailIndependent WorkFollow-Up SkillsEscalation ManagementWritten Communication
Tools & Technologies
Qualio eQMSElectronic Quality Management System
Industry Keywords
PharmaceuticalBiotechnologyMedical DeviceCRORegulated Life Sciences

About the role

Key responsibilities & impact
  • Maintain and update QA trackers and support follow-up of quality events, including deviations, CAPAs, complaints, and associated actions and due dates
  • Follow up with relevant stakeholders on outstanding actions, documentation, approvals, and quality-related requests
  • Support migration of manual and legacy quality records into the Qualio eQMS, ensuring records are complete, accurate, and appropriately organized
  • Support ongoing administration and maintenance of records within Qualio
  • Triage requests received through the QA inbox and route requests to the appropriate QA team member when escalation or quality judgment is required
  • Support routine training administration, including processing training requests, maintaining training-related records, and following up on outstanding activities
  • Respond to or appropriately route routine Qualio user enquiries and administrative requests
  • Support document and record management activities, including filing, naming, organization, and maintenance of controlled quality records
  • Assist with preparation of quality metrics, status reports, and routine QA follow-up activities, as required
  • Support other administrative and operational Quality Assurance activities assigned by the Global Quality Assurance team

Requirements

What you’ll need
  • Approximately 1–2 years of experience in Quality Assurance, Quality Systems, document control, or a related role, preferably within the pharmaceutical, biotechnology, medical device, CRO, or other regulated life sciences environment
  • Basic understanding of Quality Management System concepts and quality processes such as deviations, CAPAs, complaints, training, and controlled documentation
  • Previous experience with an electronic Quality Management System is an advantage
  • Strong organizational skills with the ability to track multiple activities, deadlines, and follow-up actions
  • High attention to detail and commitment to accurate recordkeeping
  • Strong written and verbal communication skills
  • Ability to work independently on established processes while appropriately escalating questions requiring QA review or decision-making
  • Proficiency in English

Benefits

Comp & perks
  • Remote work arrangement
  • Contingency Workforce contract type