Quality Assurance Director

Abbott

Santiago, Chile
Quality control of products
Validation of manufacturing processes
Compliance with global standards
The Quality Assurance Director role is based in Manufacturing Plant in Santiago de Chile, with a mission to facilitate quality control of products manufactured in the unit, ensuring compliance and implementation of policies and global and local standards and legislation

Job Summary

  • The Quality Assurance Director role is based in Manufacturing Plant in Santiago de Chile, with a mission to facilitate quality control of products manufactured in the unit, ensuring compliance and implementation of policies and global and local standards and legislation.
  • Responsibilities include participating in strategic planning, ensuring compliance with medical and scientific standards, defining analysis methods, facilitating adherence to quality systems, and guaranteeing regulatory compliance throughout the manufacturing process.
  • Abbott offers career development with an international company, recognition as a great place to work globally, and opportunities to build your future and live your best life.

Matching Summary

The Quality Assurance Director role is based in Manufacturing Plant in Santiago de Chile, with a mission to facilitate quality control of products manufactured in the unit, ensuring compliance and implementation of policies and global and local standards and legislation.

Skills & Requirements

Must-have

  • quality control of products
  • validation of manufacturing processes
  • compliance with global standards
  • chemical and microbiological analysis
  • regulatory compliance
  • EHS policies and practices

Nice-to-have

  • strategic planning for unit
  • continuous improvement processes
  • team management and development
  • technical representative before government agencies

Key Requirements

  • Bachelor's degree in Pharmacy or science-related technical field
  • MBA or Postgraduate degree in Business Management
  • 10+ years total experience in QA
  • 8+ years in QA, Operations, or Pharmaceutical engineering
  • Excellent verbal and written communication in Business English
  • People management experience
  • Solid understanding of finance principles
  • Knowledge of regulatory legislation
  • Technical research expertise in quality
  • Familiarity with validation and quality methodologies

Work Rights

Not specified

Tailored Resume

Cover Letter