Quality Assurance Complaints Analyst – Hybrid (Mexico City)

Alcon

Ciudad de México

Híbrido

MXN 240.000 - 360.000

Jornada completa

Hace 2 días
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Ventajas ofrecidas por este puesto de trabajo

Flexible hours
Remote work possibilities (min 3 days/
International environment

Descripción de la vacante

Alcon seeks an Associate Complaints to support the Quality & Regulatory Affairs team in Mexico City. You will process and investigate product complaints, monitor trends, and ensure regulatory compliance through accurate documentation and cross-functional collaboration.

The role involves collaboration with Medical Safety and R&D on adverse events, adherence to GxP and ISO 13485, and ongoing training to meet job requirements. This hybrid role offers flexible hours and remote options.

Formación

  • Bachelor's degree in a scientific, pharmacy, or healthcare-related field.
  • 6 months of experience in Quality Assurance, Pharmacovigilance, Technovigilance, or Complaint Handling within medical device and/or pharmaceutical industry desirable
  • Fluency in English and Spanish
  • Knowledge of pharmacovigilance/technovigilance and ISO 13485 desirable

Responsabilidades

  • Process, investigate, and monitor product complaints.
  • Support trending and reporting of defects; expedite per policy.
  • Collaborate with Medical Safety and R&D on adverse events.
  • Ensure regulatory reporting compliance; follow GxP SOPs.
  • Maintain accurate documentation and training to meet requirements.
  • Support continuous improvement and cross-functional problem solving.

Conocimientos

English/Spanish fluency
Analytical
Communication

Educación

Bachelor's degree (scientific/healthcare)

Descripción del empleo

Alcon seeks an Associate Complaints to support the Quality & Regulatory Affairs team in Mexico City. You will process and investigate product complaints, monitor trends, and ensure regulatory compliance through accurate documentation and cross-functional collaboration.

The role involves collaboration with Medical Safety and R&D on adverse events, adherence to GxP and ISO 13485, and ongoing training to meet job requirements. This hybrid role offers flexible hours and remote options.

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