Quality Assurance Director

Abbott

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profile Job Location:

Santiago - Chile

profile Monthly Salary: Not Disclosed
Posted on: 08-11-2025
Vacancies: 1 Vacancy

Job Summary

JOB DESCRIPTION:

About Abbott

Abbott is a global healthcare leader creating breakthrough science to improve peoples health. Were always looking towards the future anticipating changes in medical science and technology.

Working at Abbott

At Abbott you can do work that matters grow and learn care for yourself and family be your true self and live a full life. You will have access to:

  • Career development with an international company where you can grow the career you dream of.
  • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
  • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity working mothers female executives and scientists.

Established Pharmaceuticals

We are committed to bringing the benefits of our trusted medicines to more people in the worlds fastest-growing countries. Our broad portfolio of high-quality and differentiated branded generic medicines reaches across multiple therapeutic areas including gastroenterology womens health cardiometabolic pain management/central nervous system and respiratory.

The Opportunity

The Quality Assurance Director role is based in Manufacturing Plant in Santiago de Chile. Its mission is to facilitate quality control of products manufactured in the unit from raw material to finished product packaging and validation of manufacturing processes ensuring compliance and implementation of policies and global and local standards and legislation.

What Youll Do

Strategic & Operational Planning

  • Participate in strategic planning for the unit to ensure short- medium- and long-term profitability and sustainability.
  • Contribute to sales and operations planning to align Quality Assurance with financial commercial and production goals.
  • Participate in projects related to the release of locally manufactured or imported products.

Quality & Compliance

  • Ensure compliance with medical and scientific standards for products.
  • Define criteria methods and procedures for chemical and microbiological analysis and validation of production processes.
  • Facilitate adherence to quality systems and legal requirements in production and packaging.
  • Ensure compliance with product and packaging specifications through raw material and process analysis.
  • Guarantee regulatory compliance throughout the manufacturing process.
  • Support internal and external audits by demonstrating procedures and operations.
  • Act as the companys technical representative before government agencies.

Process Improvement & Cost Optimization

  • Develop strategies to optimize budget improve resource utilization reduce maintenance costs and enhance quality standards.
  • Comply with internal policies and continuous improvement processes.
  • Conduct actions in line with the companys Code of Business Conduct.

Reporting & Documentation

  • Prepare all required reports as defined by the matrix or requested.
  • Support internal and external audits with proper documentation and procedures.

EHS & Sustainability

  • Support and participate in Environmental Health and Safety (EHS) policies and practices.

Team Management

  • Manage the team including planning attracting developing and overseeing personnel procedures.

Required Qualifications

  • Bachelors degree in Pharmacy or other science-related technical field.
  • MBA or Postgraduate degree in Business Management.
  • Minimum of 10 combined years of total experience in Quality Assurance (QA) in Pharmaceutical International Companies.
  • Total combined years: 8 in QA Quality Assurance Operations or Pharmaceutical engineering.
  • Excellent verbal and written communication skills in Business English.
  • People management experience and solid understanding of finance principles.
  • Knowledge of regulatory legislation and technical research expertise in the area of quality.
  • Familiarity with validation and quality methodologies.

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer committed to employee diversity.

Connect with us at on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.

The base pay for this position is

N/A

In specific locations the pay range may vary from the range posted.

JOB FAMILY:

Operations Quality

DIVISION:

EPD Established Pharma

LOCATION:

Chile > Santiago : E1-Office Building Avenida Carrascal 5650

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

No

MEDICAL SURVEILLANCE:

Not Applicable

SIGNIFICANT WORK ACTIVITIES:

Not Applicable


Required Experience:

Director

JOB DESCRIPTION:About AbbottAbbott is a global healthcare leader creating breakthrough science to improve peoples health. Were always looking towards the future anticipating changes in medical science and technology.Working at AbbottAt Abbott you can do work that matters grow and learn care for yo...
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Key Skills

  • Quality Assurance
  • FDA Regulations
  • ISO 9001
  • Root cause Analysis
  • Biotechnology
  • Clinical Trials
  • Quality Systems
  • Food Processing
  • Quality Control
  • Quality Management
  • cGMP
  • HACCP

About Company

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WHO WE ARE CREATING LIFE-CHANGING TECHNOLOGY From removing the regular pain of fingersticks as people manage their diabetes to connecting patients to doctors with real-time information monitoring their hearts, from easing chronic pain and movement disorders to testing half the world’s ... View more

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