¡Activa las notificaciones laborales por email!

Quality Operations Specialist - Supplier Quality Managment

Novartis Farmacéutica

Mazatlán

Presencial

MXN 40,000 - 80,000

Jornada completa

Hace 14 días

Mejora tus posibilidades de llegar a la entrevista

Elabora un currículum adaptado a la vacante para tener más posibilidades de triunfar.

Descripción de la vacante

An established industry player is seeking a Quality Operations Specialist to oversee supplier quality management in the Americas. This role involves ensuring GxP compliance, managing quality projects, and executing batch releases while addressing technical complaints. The ideal candidate will thrive in a collaborative environment, driving continuous improvement and operational excellence. Join a passionate team dedicated to making a difference in people's lives through innovative solutions and quality assurance in the pharmaceutical sector.

Formación

  • Experience in QC/QA within the pharmaceutical or biotechnology industry.
  • Functional breadth and international collaboration experience.

Responsabilidades

  • Manage GxP suppliers and support exception investigations.
  • Execute batch releases in compliance with registration requirements.

Conocimientos

Technological intelligence
Quality Assurance (QA)
GMP procedures
Quality standards
Quality control testing (QC)
Ability to handle ambiguity
Self-awareness
Continuous learning
Technological experience

Descripción del empleo

Quality Operations Specialist - Supplier Quality Management

Job ID REQ-10038974

Date: May 06, 2025

Location: Mexico

Summary
About the Role

This position involves managing GxP suppliers in the Americas region, supporting exception investigations, and contributing to OpEx improvement projects. The qualified person executes batch releases in compliance with registration requirements, and reports technical complaints, adverse events, or special case scenarios related to Novartis products within 24 hours of receipt.

Key Performance Indicators
  • Manage quality aspects and projects within the area of responsibility.
  • Ensure and support overall GxP compliance and adherence to Novartis quality management systems.
Work Experience
  • Experience in QC/QA within the pharmaceutical or biotechnology industry, including environmental control and cleanroom zones.
  • Functional breadth and international collaboration experience.
Skills
  • Technological intelligence
  • Quality Assurance (QA)
  • GMP procedures
  • Quality standards
  • Quality control testing (QC)
  • Ability to handle ambiguity
  • Self-awareness
  • Continuous learning
  • Technological experience
Language

English

Why Novartis?

Helping people with diseases and their families requires more than innovative science; it requires a community of passionate, collaborative individuals like you. Join us to create breakthroughs that change lives. Learn more: Novartis Strategy & Culture

Join Our Novartis Network

If this role isn't the right fit, sign up to our talent community to stay connected and be the first to hear about new opportunities: Talent Network

Functional Area: Quality

Job Type: Full-time

Employment Type: Regular

Shift Work: No

Consigue la evaluación confidencial y gratuita de tu currículum.
o arrastra un archivo en formato PDF, DOC, DOCX, ODT o PAGES de hasta 5 MB.