Quality Assurance Coordinator

alirahealth; España; Presencial; EUR 26.000 - 38.000; Jornada completa

Descripción de la vacante

alirahealth is seeking a Quality Assurance Coordinator in Spain to provide operational and administrative support to the Global Quality Assurance function, ensuring QA activities are documented and completed in line with procedures.

You will track deviations, CAPAs, and complaints, assist with migrating records into Qualio eQMS, and coordinate training and QA inquiries, partnering with the Global QA team to maintain quality records and metrics.

Formación

• 1–2 years of QA or quality systems experience.
• Familiar with QA processes such as deviations, CAPAs, complaints.
• Experience with electronic QMS is an advantage.
• Strong organizational and communication skills; English proficiency.

Responsabilidades

• Maintain QA trackers and follow-up of quality events (deviations, CAPAs, complaints).
• Follow up with stakeholders on outstanding actions, documentation, approvals, and QA requests.
• Support migration of records into the Qualio eQMS, ensuring accuracy and organization.
• Support ongoing administration and maintenance of records within Qualio.
• Triage QA inbox requests and route to the appropriate QA team member.
• Support routine training administration and maintain training records.
• Respond to Qualio inquiries and administrative requests.
• Support document and record management and naming conventions.
• Assist with preparation of quality metrics and status reports.

Conocimientos

Quality Assurance

Document control

Quality metrics

Quality Systems

Herramientas

Qualio eQMS

Descripción del empleo

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don't limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.

Job Description Summary

The Quality Assurance Coordinator will provide operational and administrative support to the Global Quality Assurance function, helping ensure the effective maintenance, tracking, and administration of Quality Management System activities. Key responsibilities will include supporting the tracking and follow‑up of quality events such as deviations, CAPAs, and complaints; assisting with the migration of existing quality records into the Qualio electronic Quality Management System (eQMS); supporting the administration and maintenance of quality records and trackers; and triaging requests received through the QA inbox, including training requests, Qualio enquiries, and other routine Quality Assurance support needs. The role will work closely with members of the Global Quality Assurance team to ensure requests and quality activities are appropriately documented, routed, followed up, and completed in accordance with established procedures and timelines. The ideal candidate will have previous experience in Quality Assurance, Quality Systems, or a related role within the pharmaceutical, biotechnology, medical device, CRO, or other regulated life sciences environment. Familiarity with electronic Quality Management Systems, document control, training administration, deviations, CAPAs, and other quality processes is preferred. Strong organizational skills, attention to detail, follow‑up capabilities, and proficiency in English are essential.

ESSENTIAL JOB FUNCTIONS

• 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.

PREPARATION, KNOWLEDGE, SKILLS & ABILITIES

• 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.

Contract Type

Contingency Workforce

Salary Range

The final offer will be determined within the applicable location‑specific range and will depend on the candidate's confirmed work location, relevant experience, skills, qualifications, internal equity, and role scope.